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00:01 Yeah, okay. So we are now. Well not live like in

00:06 but live as in recording and um for those of you who, who

00:11 just joining the class. This is of the big orientation summary. So

00:15 to black boy, familiarize yourself know I record my lecture so you can

00:19 go back and listen to the orientation . There is an assessment that you

00:23 to do. That comes due next . That right? That that next

00:27 the third. Yeah, I think . All right. You want to

00:30 the book? Uh, you can the book cheap from the publisher.

00:33 what do we decide? $96, . That's that's insane. And weighs

00:41 did we did anyone bother me wearing ? The easy way to weight is

00:45 get on a scale, hold the , see what the way it

00:48 Then get us to put the book and weigh yourself differences the weight of

00:51 book. All right. Remember we pre reading for class. The next

00:57 reading quiz or assessment will open at o'clock on monday. It closed at

01:01 right before class. So you have the weekends you have more time to

01:05 than you do during the week. just by its nature. Remember each

01:08 these assessments will have 10 questions there minutes. You get two attempts on

01:13 . So watch the video, do orientation assessment. I'm tired of you

01:19 your quiz. Um, and then you have questions, you can email

01:22 . Of course. I'm not going ignore you. Although sometimes during the

01:26 two weeks takes me a little bit time. Usually about 24 hours to

01:29 around. So you're here for right? Physiology, That's why you

01:39 taking the class. You want to what the body does. And so

01:43 essence, what we're gonna do today we're gonna look at a brief overview

01:48 of what the body is and what gonna do is we're gonna start very

01:53 . All right. So this is for every class you always have the

01:56 couple of days, right? Where like he's gonna repeat everything I've learned

01:59 all these other classes. Yeah, true. That's what's going to happen

02:02 physiology for the first six lectures or you're gonna see stuff that you've seen

02:06 , not necessarily in the detail that gonna show it to you, but

02:09 definitely seen this stuff. So everyone . But what we're trying to do

02:11 to make sure that those of you have never seen this stuff are on

02:15 same page as those that you have this stuff. Okay, so that's

02:18 of what the goal is. And once we create that foundation that allows

02:21 to move into the different systems. so right now, I just want

02:25 just briefly time what is physiology is study of normal function of living

02:29 Now, most of you are in class because you want to study how

02:33 are broken. Right? I mean want to go and go into our

02:38 most of you, not all but of you. And so you're trying

02:41 figure out if something is broken, is it broken? And how does

02:44 supposed to work so I can fix ? What just happens? I'm afraid

02:52 you better behave yourself. Yes. was scared to go on this side

02:59 the room. Right? All So basically what you're thinking about is

03:06 which is called pathology? Alright. are studying how things are broken,

03:11 systems don't work and really how do go about figuring out why it's

03:16 All right. But we're interested in how things work. So, if

03:19 come up to me and trust some of you will have these questions

03:22 come up to me after class, doctor Wayne, I've been working in

03:24 lab in the er and the operating , blah blah blah. And I

03:28 this and it's like some horrible disease has like seven initials and I you

03:34 pronounce it. I can't pronounce And you're like, what's going on

03:36 ? And I'm gonna do this? don't know because why? I don't

03:42 how things are broken. All I've never studied pathology to that

03:47 Now I can guess my way through based on what I know how things

03:51 . But the pathology stuff is a different fields something that I don't know

03:55 lot about. And when you hear . So I don't know a lot

03:59 something. That's a good thing. right. So what does it

04:03 Well, we're looking on how That's the big picture. The system's

04:07 our way down all the way down the molecules, how all those things

04:11 , the chemical and physical aspects of things and how they get your body

04:14 function the way that they do. right. Now, this is a

04:17 discipline. And biology. When you Biology one on one and one or

04:21 or here at the University of which we've now changed to 1306 and

04:27 . Very confusing. I know. you learned the basic six disciplines of

04:33 . All right. So this is subset of that and then you can

04:36 further divided even further than that. , for example, I was a

04:41 biologist. I studied reproductive physiology. area of focus was first male reproductive

04:48 . How do we make sperm? then when I graduated got my P

04:52 , I went and studied how female worked. And so I'm this little

04:57 itsy bitsy narrow slice of pie in broader picture of physiology. That makes

05:03 . So physiology is kind of the term that talks about the entire

05:09 All right now, no matter what study though, ultimately the central theme

05:13 all of this is homeostasis. And , we're going to get to that

05:16 just amendment minute. But just to something that we're all walking in here

05:21 some knowledge. I just want you shout out what each of these systems

05:25 in the most basic sense. What the integra mint do? Do you

05:28 segments your skin protects good? What the muscular system do? Move?

05:34 skeletal system do support? What does impulses control? I think I

05:41 So, basically controls other systems. system hormones signaling very good circulatory

05:50 What does blood do? Yeah, a transport That's actually the best.

05:55 it's a transport system. It is our logistics system in our body.

06:00 really kind of cool. Alright. is one that a lot of people

06:02 know to anyone here know. Lymphatic it's great. It's kind of like

06:08 , kind of like the immune It's kind of a combination of the

06:13 together. All right. And we don't spend a lot of

06:15 So, I think we have like slide way back in the middle of

06:18 semester. It's like here's lymphatic. , let's kind of ignore for right

06:21 . But when you deal with the , you spend a lot of time

06:24 about. All right. But it . It serves as part of transport

06:27 , part of defense, respiratory Here's an easy one breathing gas exchange

06:33 system. Something I wish I did this moment, which was eat before

06:38 came. Right. It's processing materials energy and for fuel and for building

06:46 system. What you wish you had right before class. Right, remove

06:52 from the body. So, I'm sitting here doing the dance about 30

06:55 in. And then finally, reproductive did the name? What does it

06:59 reproduction? Make new offspring so that can uh So the species can can

07:05 on. All right. So, going to cover almost all of these

07:09 in this class. Trying to see don't even have immune system up

07:12 So, this is basically what we're to be dealing with over the course

07:16 the semester. All right. to start this all off, we've

07:20 to start with a chemistry lesson. right. First off, we need

07:24 understand the body is an open Alright? And it's an open system

07:28 the external environment, meaning that things come from the external environment and I

07:32 things back to the external environment. not a closed system. There's a

07:36 of exchange going off. All And the point of the body,

07:41 the process of the body that we is that it's responsible for maintaining homeostasis

07:47 is simply maintaining a constant internal environment all these changes. Now, the

07:53 lesson here has to do with The principle of mass balance or the

07:57 of mass action. You ever heard term in chemistry, right? Basically

08:01 it says. Do you know how balance your equations? That's that's in

08:05 what it is. It's basically the that go in must equal the things

08:08 come out. And that's what you your entire Kim won and Kim two

08:12 doing right. Remember those horrible equations and over and over again.

08:17 But you can think of it in of simple nous. All right.

08:20 , what do I do? I food in and I drink stuff.

08:23 that's easy. And then what I is I poop and pee everything out

08:26 I don't use and I burned things . That's easy mode. But it's

08:31 more complicated than that. All So, you can think about it

08:34 this. Everything that you produced through is um is something that you're adding

08:38 the body, right? So even you have these building blocks, you're

08:43 things to the body from the building . You're creating new things. But

08:46 you build the new things, you're taking things away from the body.

08:50 that anabel is um is both in and subtraction, right? And when

08:55 break things down, like when you things into your body, okay,

08:58 easy. I'm adding things in from external environment. But when I break

09:02 down, I'm also losing things just I'm creating energy. So there's this

09:08 and subtraction that we don't think quite much about. It's easy to

09:12 I put in a cheeseburger in my , I get the energy plus the

09:17 material that I don't use and I that. That's easy. It's this

09:21 stuff that we kind of forget And so when we're looking at

09:25 we're going to be dealing with maintaining just the addition of subtract that were

09:31 commonly used to, we're talking about these large systems that are mostly invisible

09:36 us that we don't think about all much. So homeostasis is maintaining constant

09:43 environment despite change. Now the easy to think about is what we all

09:48 . On the way over here, walked off my offices and start to

09:52 across campus wasn't too bad until I that like 100 ft from the this

09:57 . And all of a sudden it like I was in the Sahara,

10:02 ? And so I walk in the and I'm just at this point I'm

10:06 . So what's my body doing, , right? I'm trying to cool

10:10 to maintain that constant internal environment because all the exertion, it really was

10:16 coming into the building. And then come in this building as well,

10:20 conditioned and all of a sudden now body temperature is now starting to

10:24 So what's my body going to start , it's going to start shivering,

10:28 to produce heat to maintain that So, here in the States,

10:33 the easiest way to think of his . Homo states has noticed. It's

10:37 maintaining that constant internal environment despite the . Now, your body is really

10:44 of interesting because what we've done or the body is, remember, you

10:48 off as an individual cell and then became many, many cells attached to

10:52 other that became very, very But what we've done in this in

10:56 process is we've created these unique And so, what we can say

11:00 that the body consists of two major compartments. Now, your book talks

11:05 a third compartment. This trans cellular that we're not going to talk

11:08 So, we're just gonna ignore It does exist, but we're ignoring

11:12 . Okay. It's kind of like monster that sleeps under your bed.

11:16 I pretend it's not there, it's there. Right. Okay.

11:21 the first compartment, it's the compartment cells. So, collectively, all

11:26 cells together, they have an internal outside of the cells. That's the

11:30 compartment and the boundary between the external and that external compartment is basically the

11:36 of my body. So, basically skin. All right. So,

11:39 do these things have? Well, fluid in them. So, we

11:42 to the fluid inside the cells intracellular refer to the fluid outside the

11:47 Extra cellular fluid so far. Right. It's like dr Wayne.

11:52 you just get to the point. right. Why do we have these

11:57 ? Anyone want to wager a guess tell me the reason why I

12:01 you don't have to guess. You want to look If I ask a

12:06 . If you ask, give it dumb answer. I'm not going to

12:09 fun of you unless it's like really dumb, like, you know,

12:13 . But, you know, don't afraid to kind of like,

12:16 I think it's this. Why do think? Well, this thing different

12:21 . Hi. Perfect. You can the thought so. So, I'm

12:27 you go ahead. Mhm. don't need that. Mhm.

12:38 let me put it into words that can understand. We need compartments because

12:42 environments to do different chemical reactions. ? That's easy enough. That And

12:48 what you're saying. All right. need different compartments for different chemical

12:52 And so, what we've done is created unique little environments for these chemical

12:58 to occur. Now, this shouldn't terribly foreign to you live in a

13:02 that is divided into compartments, Whether you're in a dorm or whether

13:05 in an apartment or whether you live a mansion. Right? You have

13:09 that are designated for certain things. example, the kitchen is designated for

13:16 . The living room is native for . That's see that's actually that's

13:21 The bedroom is designated for I want to say betting come on bed,

13:25 betting, But it's for sleeping right , the bathroom is for business,

13:32 ? And whatever that business happens to , whether using the restroom or use

13:35 and bathing whatnot, it's your business now. Can you do your business

13:39 the kitchen? You can But you . Right. That's that's absolutely

13:47 right? The bedroom, you can all sorts of things in the

13:50 Can you shower in the bedroom, ? No, because it does.

13:53 lacks the machinery to do so. . Can you sleep in the living

13:58 ? Yes, but when you wake at 4:00 AM, with that Crick

14:01 your neck, you're gonna be wishing were in your bed. Right?

14:04 , we have compartmentalized our spaces around for the greatest efficiency for whatever the

14:11 is at hand. And that's what body has done as well. It's

14:14 these unique compartments. And actually, inside the cell itself, there's a

14:18 compartments. That's what the organelles All right now, the compartments that

14:24 are the boundary of the barrier that these two things is the plasma

14:29 And this is where a lot of conversation is going to be today.

14:31 if you're sitting there rolling around, can't believe he's going to talk the

14:34 time about the plasma membrane. I blame you, But it's actually one

14:38 the most important structures in the body it creates this barrier for this

14:43 All right. So, if you at the extra cellular fluid,

14:48 we have a barrier between these That's plasma membrane. But if you

14:50 just at the extra cellular fluid, actually divided into two compartments as

14:54 We have the compartment that is the directly around the cells. And then

14:59 have the compartment which is the fluid flows through the body. That's

15:03 So, that's really the fluid that's the blood. So, the part

15:06 in the blood is called the The stuff that's around the cells is

15:10 the interstitial fluid. Interstitial means in the cells. That's why it's interstitial

15:15 . All right now, the barrier those two compartments is very permeable.

15:21 can mix between the plasma and interstitial . But that barrier is your capillaries

15:27 are part of the cardiovascular system. , the blood circulates. But when

15:31 comes into the capillaries, it mixes allows for interstitial fluid to go into

15:35 plasma and allows for plasma to mix interstitial fluid. All right.

15:40 there's an exchange there. All Now, coming back to that term

15:48 . Homeostasis is sometimes confused with the of equilibrium equilibrium means balance,

15:56 When we think homo state says I'm to find a state of balance,

16:00 it's not balance in the sense that two sides are equal, right?

16:05 I'm hungry, I'm putting cheeseburgers in body to provide fuel and nutrients but

16:10 haven't created added into the system so I can get things right equilibrium says

16:17 A. Has to equal side And that's not what's going on

16:21 All right. So if you, if you look at these compartments

16:28 And that's what this picture is and a fantastic picture from your book.

16:31 can look at and you can count the concentrations the osmolarity is and all

16:35 of fun stuff of all the different . And if you look at those

16:38 you go, wow, they're relatively same. Especially in terms of

16:43 If you don't know what osmolarity osmolarity simply the number of salutes per unit

16:48 solution. All right. They don't what the salutes are. It's just

16:52 in it. Okay, there's the number of particles and so you can

16:56 look inside the cell about 290. in the interstitial space, number 2

17:01 over here in the plaza about 2 great. So we have balance.

17:06 have equilibrium in terms of the number particles. But if you look at

17:10 absolute particles you're going to see that are very different. So inside the

17:14 here, I don't know if you read. It says 15 million molar

17:18 120 millimeter potassium gotta gotta gotta up , sodium is 145. Almost a

17:25 full difference Over here, potassium is . That's a 20fold difference. It's

17:32 . Yet this is home a static . All right. In other

17:37 while the number of particles are the , the types of particles are

17:43 And so the body finds that this state is what it wants to be

17:50 because it can use this disequilibrium. we call chemical disequilibrium to do

17:56 All right. It's to its So, part of the job of

18:00 plasma membrane is to ensure that this here is different than that compartment there

18:07 which salutes happen to be present. , so, right now, it's

18:12 important which solids. We're going to to that in a couple of

18:15 but you'll eventually learn if you haven't to memorize yet. sodium high and

18:19 sodium low outside cells. potassium high cells. I'm sorry, just flip

18:23 flip that all around. Sorry, my blue little rewrite inside cells,

18:29 is low potassium high outside cells, is high, potassium is low.

18:35 , now, our bodies are not in chemical disequilibrium but osmotic equilibrium,

18:42 it's also chemical or excuse me, neutral. How do we know

18:46 I can touch you and you don't electrocuted. Now I can go rub

18:50 feet around the room and come up and shock you. But that's not

18:54 electrical state. That's just me building a charge on my external surface.

18:59 . And it's a lot of fun do, especially when people aren't expecting

19:03 . All right, our cells artist state of electrical disequilibrium.

19:09 you can see right here in this is just a graph representation of where

19:14 particular ions are located. You can I've got my sodium high outside the

19:21 inside the cell. Very low. ? And so, what we're seeing

19:25 is we're seeing an imbalance and we're to study why this imbalance exists when

19:29 talk about the electrical communication of But this electrical disequilibrium means that the

19:36 because they're not in equilibrium on either of the membrane want to move and

19:41 they want to move, that means they have charged that goes with

19:46 And that charge can then be used do things like move muscles or have

19:54 . Okay, so, the point all of this that I'm trying to

19:58 at is that when we talk about , this state right here, that

20:03 looking at is in home a static . Even though you look at these

20:07 and you can see there's dis So, we're all clear on

20:11 that good. That kind of makes , sort of All right. So

20:19 equilibrium chemical electrical disequilibrium refer to as dynamic steady state dynamic. What does

20:25 mean dynamic means things are always moving state means things are not changing,

20:32 ? So things are moving. But not changing. Kind of like your

20:35 right? Before you have the Right. We're moving. Things are

20:39 . Good. Things seem to be of stagnant and we have the

20:46 All right now, the reason we have dynamic movement why we can have

20:51 steady state where things don't change is we have these unique transport mechanisms and

20:57 have selective permeability in the plasma Notice we're coming right back to this

21:02 membrane. All right, selective permeability that we have an ability to choose

21:08 passes back and forth across the membrane the cells get to choose. All

21:12 now, this is a picture of plasma membrane and electron micrografx.

21:16 sir. Forget it. Mhm. , what we're going to see is

21:23 they are mechanisms used by the So, I don't want to define

21:26 like that. It's mechanism used by cells so that they can accomplish their

21:31 . All right. They And if ask me where do they develop

21:34 They developed over eons and eons of to be just systems that worked.

21:40 . So, for example, we're to talk about the sodium potassium hcPS

21:44 . Someone asked one semester as well did this come from? He

21:47 I don't know. It just happened develop the cells found that it kind

21:50 worked and over time it fixed So, that was really, really

21:56 just as those are terrible answers to a class when you're supposed to sound

22:00 smart. It just is We don't the answer to that group? I

22:05 jump too far. All right. , let me come back to the

22:08 . So, there's an electron You're looking at two cells here.

22:10 number B. Here's or Selby Selby here. Here, sell A on

22:15 side. You can see right there's the plasma membrane or the space

22:19 the two. This little space that putting my finger in that would be

22:23 interstitial space. Just to give you sense of how itsy bitsy teeny tiny

22:26 interstitial um actually is. Right. , that line right there in that

22:30 , right there represents the plasma membrane this side and the plasma membrane on

22:34 side. And so we've blown it . Uh five fold, right?

22:39 , you can see here here's the um here's the plasma membrane for sell

22:43 That is the plasma membrane for Alright, so plasma membranes have this

22:48 structure we're going to look at But basically, what is the platinum

22:51 ? What does it do? it serves as physical isolation, it

22:54 creates the barrier between that cell and surrounding environment. All right.

22:59 that's the easy one. It's a . All right. So, if

23:03 a barrier, what that means is it can serve as a regulator of

23:08 internal environment. It decides what gets come in and go out.

23:12 So, how does it determine that determine that based on what's actually in

23:16 membrane. What's embedded in the Right. It serves as a point

23:21 communication. So what embeds in the ? What proteins happen to be there

23:26 what sugars have to be happening beyond service allows or serves as an interaction

23:31 that cell and that surrounding environment. . It also allows that sell to

23:37 with other cells. So, if one has proteins on that side and

23:39 one has cells, proteins on that that are capable of interacting, those

23:43 cells can talk to each other. , So, that's when we say

23:47 , that's what we're talking about. also serves as a point of structural

23:52 . All right. What that means is what we can't see in this

23:55 . Is that all on the inside this plaza member. And both cells

23:59 a whole bunch of proteins that serve sido skeleton. Alright. In other

24:04 , they created a structure that allows the cell to have a specific

24:09 That specific shape then allows that cell function in the way that's supposed to

24:14 . And it's being maintained by that membrane and that protein structure that's associated

24:20 it that would be on the internal . So, the membrane all of

24:26 sudden becomes pretty important. It's not a barrier. It allows for this

24:31 and communication with other cells and with environment. All right. So,

24:39 deserves attention when it is capable of many different things. Here's a cartoon

24:46 of it. You can see here mostly lipids and some proteins injected and

24:52 fact, the ratio of protein to . The more proteins there are the

24:58 activity that cell is said to All right. There's a there's a

25:03 relationship there. All right. if you look at it, You

25:07 see that the the lipids. So are fossil lipids are arranged in a

25:13 specific way. Now, many of said they're going to learn this in

25:16 one. Yes, you did. go over this very carefully here.

25:20 . We have a fossil lipid. lipid has two parts to it.

25:24 has a hydrophobic tail and it has hydro filic head. All right.

25:29 hydrophobic head is attracted to the So that points towards where water

25:34 The hydrophobic tail is excluded by the and so it's forced or pointed away

25:39 the water. And so you get of these things and they will arrange

25:43 in the sheets so that you have two membranes or these two sheets,

25:48 . Which is called a bi And so the head portion is always

25:54 towards water. The tail push portion always being excluded from the water.

25:59 so you have a barrier. Now is impermeable to water soluble substances because

26:07 tail portion sits there and says I like things that like water. I

26:13 know why it's so rude, but is so nothing can pass through that's

26:17 soluble. But if your lipid soluble can pass through just fine.

26:22 the proteins are going to bed themselves all the way through or to the

26:26 . And we're going to see all different types of proteins. And what

26:28 looking at here is from your This is what a fossil lipid looks

26:32 . And I want you to kind see this structure a little bit more

26:35 . All right. I'm not gonna you the chemistry. I'm not gonna

26:38 you to memorize structure. But one the things you need to start doing

26:41 terms of learning things is putting things categories. And then being able to

26:45 all the things that are related to that looked like it. Okay,

26:49 , you can see here with the lipid, there's your fatty acid tails

26:51 here. This is the foster lipid of the hydra filic head. And

26:58 it has this unique kind of Like I said, where that's what

27:01 gonna look like and arrange itself in by later. Here are some common

27:07 lipids. Do you think you need memorize these fossil lipids? No,

27:11 you for shaking your head like you make me. All right.

27:15 But can you look at them and see a structure that is common between

27:19 right tails. Uh basically a fossil that is has some sort of charge

27:27 it. Usually primarily because of the charge. But you can see their

27:32 . Uh there again. You can a charge so on and so

27:35 So those are going to range themselves water. Now, I do want

27:39 point out one thing for you because going to deal with this thing.

27:42 probably a couple of days when we with communication. So, if I

27:44 out to you now, you oh , I remember him talking about

27:47 This one right here. You don't to memorize this name. But is

27:49 fossa title in hospital? All We're going to see this one

27:54 And we're going to see that it from the plasma membrane in the

27:57 Or the cell uses it as a molecule, breaks it up and uses

28:00 of it as a signaling molecule. , when you look at this

28:03 while you're not going to go, is this all coming from? It's

28:06 there. It's right there in the membrane. Now, that's the first

28:10 of lipid that you're going to find a plasma membrane. There's actually more

28:14 one type. The next type is single lipid. They were heard of

28:18 single lipid Before teaching this class. had never heard of one because why

28:24 I what's his finger lipids? a single ip, it is a

28:28 acid tail. Got to make sure doing this right? So here's the

28:31 acid tail. So that would be fatty acid tail. And then it

28:34 a finger seen to it. Now of you probably noticed finger senors some

28:39 you or the rest of you like were like I have no idea what

28:42 is is what is referred to as amine alcohol. You don't need to

28:47 that. I'm not going to say is this finger scene. But it's

28:50 really really long structure that has this lipid and then kind of this head

28:56 , right? And I said foster but this water loving head that is

29:01 has a phosphate to it. And what you do is you attach a

29:05 acid to the mid right next to . And all of a sudden,

29:08 does it look like, What does look like? Yeah. Uh

29:15 So that's why they exist. Now happen to be a little bit longer

29:19 regard to the tales region than fatty are. And so that causes them

29:23 kind of bump themselves up and single kind of accumulate together with some proteins

29:29 they create what are called lipid You may have heard of lipid rafts

29:34 lipid rafts or where you might find whole bunch of receptors and they kind

29:37 move together as a group. And it serves as a mechanism to congregate

29:43 receptors together. So it's finger lipids found in the plaza remembering and you

29:48 probably see why. Right. And I'm trying to show you it can

29:53 have a sugar attached the end so becomes like a lipid. So it's

29:57 lipid or like a lipid. All . Third type cholesterol. How many

30:02 been told cholesterol bad for you? course. I mean at some point

30:06 life someone said cholesterol battery. no. You want cholesterol cholesterol good

30:10 you cholesterol important for you. Don't cholesterol. Bad things will happen.

30:15 right. This is cholesterol on its . You can see it has these

30:20 . It has its long tail. is basically the primary structure from which

30:24 your steroids come from. So this from vitamin D. Comes from

30:28 It's based cholesterol is really important for whole bunch of signaling molecules and other

30:33 that we build cholesterol likes to find way into plasma membranes and it's one

30:37 these really really unique proteins that does really cool thing. Alright, so

30:42 lipids can have tails that are straight this. Right? So that's what

30:48 refer to as being saturated. Or can have double bonds which would make

30:52 unsaturated. And when you have a bond that's going to create a kik

30:56 that the hill goes off to the like so all right. So you

31:00 see kind of um you can imagine here, you can see all the

31:04 and all this bending and stuff like . And so when everything is

31:08 what's going to happen is all those ass details can get really, really

31:11 together and everything jam up nice and and something that are a bunch of

31:16 like that will then become a right? Can you picture that a

31:21 of things that can get close then get really, really close.

31:24 there's no elbow room and so it's , really tight. And that's where

31:27 would be an example of a solid when you have a whole bunch of

31:30 . So imagine me, I'm a olympic. Here's my tale, right

31:35 off to the side. You can't close to me. Now. Now

31:37 got elbow room, there's more I can become a liquid,

31:41 So those are the kind of the that we have to kind of deal

31:44 . The problem is you want liquid membranes. That would be very bad

31:49 then you can't create a structure that things from moving through it,

31:54 And you don't want things jam together well because things are jammed together,

31:59 nothing can move through it. So have a mechanism through cholesterol to kind

32:04 to find a happy medium and I'm to go ahead and answer the question

32:07 see if I yes. So let see if I can do this was

32:14 really, really briefly. So remember is not gonna be on the

32:17 I'm going to do it over So if you can imagine here's my

32:20 lipid head, if I have nothing saturated bonds. So in other words

32:26 every carbon that's in that fatty acid basically has its two hydrogen,

32:32 So it be carbon hydrogen going this , hydrant going that way, then

32:36 connects to the next carbon, next . Each of them would have their

32:39 . So that would be referred to saturated. All right. And so

32:42 you get a double bond right, move forward like that, you cannot

32:50 two Hydggen. Right? How many can you have for each of these

32:55 ? Right. And so that's basically it's unsaturated because it doesn't have every

33:04 Thank you every Yes. Every carbon have 4, 4 connections. And

33:11 should. Well, it does. mean it's a double bond, but

33:13 get what I'm saying, right? understand my basic organic chemistry still is

33:19 from 20 years ago. Look at . I don't know even I don't

33:27 know what that means right now. , I mean, you know again

33:31 when we say language it's like if you don't use 20 years, it's

33:35 fully conjugated. I'm thinking verbs and not trying to be silly, but

33:39 really how bad it is, So when you're fully saturated, you're

33:44 to be basically creating a series of bonds that look like this,

33:49 Because the arrangements of the angles of carbons and the hydrogen is right.

33:53 to do that. Right? But you have a saturated, you're going

33:57 get that sister that trans And so you go. And then all of

34:00 sudden it's there's that double bond, can go off this way and now

34:04 kicking off to one side or the . And so that's what I'm saying

34:08 that when you're dealing with these unsaturated , you're forcing the chain away from

34:13 parallel structure. So if you have bunch of these with a bunch of

34:18 to get nice and close, If throw in an unsaturated, they can't

34:24 close. Do you see that? now this thing is more permeable things

34:31 sneak in between there. Mhm. want a bad example. I have

34:36 young kids. I used to have young kids as I've aged. They've

34:39 as well. I don't know how works. But we have four kids

34:45 so you can imagine four kids and adults, what do the four kids

34:48 to do? North south east west can catch two of them but two

34:51 them are always gonna escape and it's gonna be this to smallest.

34:55 Because in a crowd of adults, can sneak in between everybody, they're

34:59 fat and big like their father. ? They can run between legs.

35:04 shocking. But they can do Right. And so when you have

35:10 unsaturated fatty acids in the way or your plasma membrane, it creates a

35:16 which means that the plasma membrane is more more liquid state. Right?

35:22 a little bit of heat. Heat that. And what are those uh

35:25 are those fatty acids going to What you had heat to anything?

35:29 do they do? Start moving a bit, right, and they start

35:33 around. Now, if you have whole bunch of fatty acids are fossil

35:37 that are close together, you they can't wiggle that much, but

35:40 can eventually start giving them enough They can separate from each other,

35:44 ? They're not bonded to each They're just jammed up together because of

35:48 conditions of being in water. But have enough heat to a fat in

35:53 . It will separate out as best can. Right? This won't will

36:00 a lot faster because it has more to move around. Okay,

36:07 we have a problem here, we in Houston out of a little bit

36:11 heat to a body. What's going happen to it? If you didn't

36:15 if you have these unsaturated bonds, melt like butter, You'd be like

36:18 wicked witch of the West. That's really obscure reference because none of you

36:22 have seen that was revived. Then need to nod your head and

36:27 oh, yeah, All right. , let me get back to the

36:33 . Have I explained that kind of enough? All right. So what

36:37 does is it can insert itself into spaces and so what it does is

36:45 makes it possible for a membrane that kind of shaky. In other

36:51 will melt fast. It increases or raises the temperature at which it's going

36:56 melt. So, it creates an where it's a little bit more

37:01 But at low temperatures, what it , it prevents those fatty acids was

37:06 lipids from getting really close together and and basically creating an impermeable barrier.

37:12 your body can survive at a wider of temperatures because cholesterol inserts itself into

37:18 membranes to change What range those fatty will disassociate or not? That kind

37:26 makes sense. That was a long to get through all that. But

37:31 a good question. Ask if you remember, there's a good place to

37:34 it. All right. So, we're doing is we're impressed. We're

37:37 flexibility. Now there are a bunch different proteins. I am going to

37:41 of jump through these pretty quickly. , sir. Go ahead. The

37:47 the Oh, so in terms of you talking about in terms of flipping

37:55 stuff like that? All right. , here's the rule. So remember

37:58 foster lipid is only really gonna stay the side that it's originally found?

38:03 that's what this is really kind of . It can spin around it can

38:06 places, it can high 51 of buddies and change places with it.

38:10 can dance. You can do all things. What it won't do is

38:13 won't flip to the other uh to other by layer. It can it's

38:19 difficult. It costs a lot of and it's difficult to do. In

38:23 , you see it primarily when cells going through apoptosis. You guys know

38:26 ? Apoptosis? Yeah, it's cell . Right? It's one of the

38:30 is there's a lot of foster lipids that takes place. So basically the

38:37 is creating a program. So that's of the signals that demonstrates that that's

38:41 on. So, that's what that really kind of dealing with.

38:44 There is basically saying they just they stay on one side. Yes,

38:51 . Mhm Thank you. So one the things you guys going to really

38:59 to speak up because one the masks prevent the sound coming forward. It's

39:04 . Just speak loudly. And if can't hear you know the sound of

39:09 project this way doctor project this So go ahead. Yeah.

39:17 so here that to talk about these types? Mm Uh huh.

39:24 I couldn't. Yes. So, yes. So the question is I

39:29 the question is, is that do cells have these different types of foster

39:34 ? The answer is yes. Is ratio a specific thing. I don't

39:39 right. But the idea is that are different types of fossil lipids that

39:42 be in different are in in the membrane. Okay, you'll find these

39:47 ones. All right. So, go to the proteins and again,

39:53 dealing with the generic explanation right We're not looking at specific molecules.

39:58 . The most common type one that's to understand is the integral one.

40:02 second one on the list. Not first one. But that's how I

40:05 . That's how I roll. Trying to freak you out.

40:08 so trends I mean, integral proteins trans membrane proteins are proteins that have

40:14 themselves across the lipid bi layer. have a region that is going to

40:18 hydrophobic. So that anchors them and them in place inside the plasma

40:24 Right? That doesn't mean they're attached anything. They can be on the

40:28 side, but they're not attached to within the membrane themselves so they can

40:32 around within the plasma membrane. It's kind of cool. When I was

40:36 grad school the uh lab down the worked on integrations which is a type

40:41 plasma membrane protein. And they were to see how integrated behaved in

40:47 It was really cool because they would cells that would were attached and they

40:51 a fluorescent dye attached to these proteins they could watch the proteins move along

40:56 surface like a tank track. it's basically like rolling. You can

41:00 it's like it's like it's stuck on on the plate and then it would

41:03 to the end and then it would sprint across the top and get on

41:06 other side and then stick itself. then it be So they move

41:11 just fine because they're not anchored in they are anchored in the sense that

41:14 can't escape from the plasma membrane All right. Um They can be

41:20 to cite a skeleton like I which is down here. So,

41:23 would be on the inside of the . All right. That can cause

41:27 to become immobile. All right, , steve Sadove skeletons in just a

41:32 we have peripheral proteins. Peripheral protein be like this right here and that

41:35 right there. They're attached to an protein that is inserted. So usually

41:39 attached to either the in or the terminus and it just allows you to

41:45 with that particular protein. Typically these gonna be enzymes. Or if we're

41:49 about the side of skeletons, structural proteins, basically holding things in place

41:54 anchored proteins. This is basically a that's anchored to some sort of

41:58 So you can see that right Here's our fossil lipid. You can

42:01 it has a a sugar moti right that's attached that then attaches itself to

42:07 protein. This would be a gyp glucose or a glad constipated integrated protein

42:15 think is Glynco jip for the sugar part. So, Glad cost cell

42:25 tricare. We'll get to the This is going to happen first couple

42:30 . All right. So, what want to do is I want to

42:32 through some of the big ones. things that you should know Ligand binding

42:37 . Alright, this one is like most common type we're going to

42:41 Uh there's about 5000 different seven trans Ligon receptors in the body.

42:50 once we learned one, we've learned all. So, what we have

42:54 , you can see it has seven membrane regions. It has a ligand

42:57 domain that's gonna be found on the the cell. It has a c

43:01 region which allows it to interact with on the inside of the cell.

43:04 , typically what happens is the chemical bind here on the lagoon in that

43:08 a conformational change or shift in the of the molecule which causes a change

43:14 the shape down here. So the that it interacts with is going to

43:18 as well. So whether it's already to something that's going to change its

43:21 or what it's gonna do is it's to change shape. So it can

43:24 in something and it's going to create cascade of events that occur inside the

43:29 . This is how you get an signal to become an inside signal.

43:32 right. Has a very very important in vesicular transport. But primarily we're

43:37 with chemical or uh cell to cell here. Here is that structural protein

43:43 promised you. So here this is extra cellular matrix. So, it's

43:47 of backwards from what I was telling . You can imagine down here they'll

43:50 cytoplasmic stuff. But what we've done we're anchoring a protein to the extra

43:55 matrix. Have you ever heard extra matrix? You've heard that term extra

43:59 means outside Matrix means a bunch of garbled together. Right, So,

44:05 what we're looking at here. this creates an uh a contact with

44:09 external environment. So, we're looking here for example, this might be

44:12 integrated. And what it's doing is interacting with its environment and anchoring it

44:17 place. So that cell doesn't get away from where it's located. Go

44:23 . I've got a story. But ahead. Okay, cheap.

44:30 You get an A. You can the class. Sorry, I worked

44:33 G protein coupled receptors so I get excited about them. So,

44:36 So seven trans membrane protein most of time. Or G protein coupled

44:41 You're jumping ahead of the game, is good. And we're going to

44:44 about them in a full lecture when talk about cell to cell communication.

44:48 right. So, if you know ahead of the game you already and

44:51 a so just awesome. All The G. P. Not jip

44:58 is having problems. All right. these um can be linked by fossil

45:04 or via foster lipids uh typically um though it's basically cell to cell adhesion

45:11 sell a matrix adhesion. So integrates one of the key ones that are

45:15 these adhesion molecules. Cams is an . You might see cell adhesion molecule

45:22 molecules is where we're gonna spend a of time to help us understand how

45:25 membrane works. Basically they allow for small islands and other small molecules to

45:32 verse across the membrane. So, you can imagine this by layer is

45:36 barrier. You need some way to through the barrier. This wall is

45:40 barrier for me getting out of this . How do I get out of

45:42 room through a door? All And we got really fancy names for

45:47 doors of cells. We call them or channels or carriers or pumps.

45:52 right. Now, there's basically two . The channel protein is basically a

45:57 filled poor. So, it would like having a door that's always open

46:01 you have water flowing through it. things can pass easily from one side

46:06 the membrane to the other. All . The specialized names are the pores

46:11 the channel. So you probably or have heard of aqua por ins,

46:14 you heard an aqua porn? so an aqua porn allows water to

46:18 through and they refer to those as . All right, the channels are

46:22 more common name. And so these the constantly open or even they can

46:27 have gates to them, right? can be channels that open and close

46:33 . On the other hand, carry in general are not always opened our

46:38 open the both sides at the same . All right. So the way

46:42 like to think about this is you been to one, Oh, you've

46:45 over to the Hilton College. Anyone to the Hilton college over here?

46:50 . Okay. You've got homework assignment . You've got across the desert of

46:54 campus, go past the student right? So it's literally south of

46:59 and then right across the street is Hilton um which is the hotel and

47:03 management College of Hotel and restaurant And I want you to walk through

47:06 front door and embrace the air conditioning that front door. But here's the

47:11 door. It's a rotating door. ever been in a rotating door.

47:17 go in and then at some point that door is rotating, you're no

47:21 outside, but you're not inside your that panic space. You know what

47:27 talking about? Right? It's like can I can thank goodness. I

47:32 go all the way through. That's a carrier in a pump work

47:36 Now. The carrier allows for an or a molecule to move down its

47:42 gradients. So carriers typically do not energy to move the materials that they

47:48 need or the materials that they allowed move, pumps on the other

47:52 do exactly what the opposite. They things in a direction they don't want

47:56 go. They require energy. I'm taking an eye on that's over

48:00 . That's happy because it's at the end of its concentration grade and you're

48:05 it against its concentration gradient. so that energy primarily comes from A

48:13 . P. But we're going to there's two different types of pumps and

48:16 these are some other ones. here's your G protein coupled receptors

48:20 You can see that we can have intracellular signaling that's associated with the So

48:24 got enzymes up here um that play role in this intracellular signaling. You

48:28 G proteins also here associated with that trans membrane. You don't have to

48:33 what that is. I'm just showing they play a role intracellular signaling.

48:37 those enzymes here's side of skeletons. this would be you can see here

48:41 our plasma membrane. Here's a whole of proteins in there. You can

48:44 there's a molecule called spectrum here's acting is probably one of the more familiar

48:49 but all together to create this network mesh work that helps to help maintain

48:53 shape of the self. All There are also carbohydrates. So we

49:00 proteins. We got fats and carbohydrates the plasma membrane. Now these are

49:06 attached to either proteins or to That doesn't make any sense. Since

49:10 are the only two things there. But this is going to be found

49:13 the outside of the plasma membrane. on the inside. Alright. And

49:19 job is to serve as a molecular for that cell. In other

49:23 it's a tag or an identifying marker the cells can use to identify one

49:28 but also plays a role in their . So if you take all the

49:33 , all the glycoprotein is all the lipids on the outside of the cell

49:37 collectively look at it. You call the Glick. Okay Alex. So

49:42 way to remember this lady's is that made of sugar and spice and

49:45 Nice guys. I don't know, , snails, puppy cocktail doesn't work

49:50 this. Whatever. All right. that's lipids, proteins, sugar

49:56 candy coat on the outside. One the ways that bacteria hide themselves from

50:02 system is with their Glick. Okay because it's hard to grab onto and

50:08 . But once you find them it's . Yes sir. It's not the

50:13 . Mhm. Yes. So typically we have is we have proteins on

50:19 outside that we referred to as the cellular matrix and then we have the

50:22 that kind of stick up and kind go all over the place. That's

50:26 sugar by itself is referred to as Black Okay Alex. Now, collectively

50:31 sugars and all the stuff, the cellmate are probably included together as extra

50:37 matrix. So in the they can all right, so they can play

50:44 role in holding cells together or they play a role in preventing interaction with

50:49 cells so they can be structural in nature of holding things together and interacting

50:54 them. They might actually even serve a signaling mechanism to have the cell

50:58 they interact with proteins in that extra matrix to do things on the inside

51:01 the cell. Yes sir, I can't I can't see Sorry.

51:09 that. Yeah. Uh So so regard to the proteins that are interacting

51:17 the two individual cells so that can the case. But typically what we're

51:21 to when we're talking about an extra matrix or we're talking about those types

51:26 interactions. They go beyond just the junctions. So, tight junction really

51:31 kind of like the ziploc portion of ziploc bag. It basically are proteins

51:35 two sides are on two different cells but creating a barrier from in between

51:40 two cells. So you can't pass them. Right. We have proteins

51:43 example that form um um See this I'm going one way. My brain

51:50 to go another way. Um That gap junction. See I finally got

51:55 it. And so gap junctions basically proteins from both cells they're interacting but

52:00 creating a tunnel between the two cells they're not really interacting with anything

52:06 Um But when you're looking at, example, like epithelium. So like

52:10 skin and stuff. And this is example I was going to go to

52:13 when someone gave you an indian you are either a younger sibling who's

52:18 is a younger sibling. All here's the older sibling. All

52:22 so all the people that just raise hand or the cruel people to their

52:26 siblings. You remember that? Do remember? Did you ever do pink

52:29 ? I'm looking at you guys right . Did you ever do pink

52:32 Where you pin someone down and get pink belly? Pink belly. Pink

52:35 screaming. All right. Did you give the indian burn? I don't

52:41 I'm in a different name. Indian . When you go up and grab

52:43 arm and you twist in two different . You remember that? So the

52:47 people are now thinking therapy. The ones are going right, why does

52:53 skin when you're doing the indian burn come off your body. It's because

52:58 these types of interactions. The Show your matrix and the interactions with

53:02 cells basically allow you. And granted Desmond zones and hemi Desmond zones and

53:07 other types of connecting uh anchoring type proteins. But the idea here is

53:13 the cells are connected to each And so when you're pulling on

53:17 you're pulling on all of them and creates a greater structure that doesn't want

53:22 rip if that makes sense. Just a lot of fun pain. I'm

53:27 . Just it's a cruel, cruel that you play on other people.

53:33 right. See what else we got . Oh, bulk flow. Everyone

53:39 in. Remember that? What just in and out of your body

53:46 Yeah, mask that. Alright. . What they're made up of

53:53 What else, nitrogen? What What else? A whole bunch of

53:57 stuff I didn't memorize are gone. , bunch Stephanie. Do you guys

54:01 the ratios so 80 20 and then rest right. It's really it's like

54:09 20 point something. And then everything is like 20.0.0. I think carbon

54:14 0.2% of their I don't remember But it's like really look all

54:21 Of all those things. What does body want in its body in your

54:25 your body, oxygen? What does do not want? Carbon dioxide?

54:29 when you breathe in your breathing in dioxide? All right, When you're

54:33 out, you're breathing out air. , you're breathing out oxygen. All

54:37 ? So, when air is moving and forth, all those components of

54:42 are moving with it. Now, are slight changes in the air that

54:45 in and goes out. We're going learn that later in the semester,

54:48 all of it moving together is what refer to as bulk flow. I

54:52 selectively go, oh, when I in, I just want the

54:54 You can keep that nitrogen don't need . It might be inert, but

54:59 don't need it. Okay, that's the fluid moving in mass.

55:05 , So bulk flow occurs. That's best example is primarily the respiratory

55:11 but within the body, bulk flow , for example, between the plasma

55:15 the interstitial fluid fluid mixes in and mixes out and it doesn't matter what's

55:21 that fluid. It might be something you desperately want. But that doesn't

55:25 . Things are going to follow that or flow as a result of boat

55:31 . All right. So, you're moving from an area of high

55:34 to an area of low pressure. of the things we're gonna be learning

55:37 lot about over and over again. gonna be so tired of It is

55:40 be uh gradients, you're gonna hear grading gradients. So, just get

55:45 to gradients. All right. And always moving down a gradient, whatever

55:48 gradient happens to be, energy requires to move up against the gradient.

55:53 , permeability is a term we We say something is when a membrane

55:57 permissible. What we're saying is it the passage of a particular substance if

56:02 impermeable, disallows the movement of that . So our membranes are semi

56:07 There are things that it will allow pass it will there are things that

56:09 allow to pass. All right. so that selective permeability, semi

56:15 selective permeability is going to depend upon proteins are actually found in the

56:21 All right. So, let's see else has an influence. Well,

56:27 scalability that protein or sorry, that in lipid. So, if you

56:33 uncharged like oxygen or carbon dioxide or non polar, like a fatty acid

56:38 back and forth across the membrane. sweat. Nothing's going to stop

56:43 Remember. This is fat loving. , it will permit things to go

56:48 . If your water soluble, on other hand, you can't pass through

56:54 because you basically have two layers mm these things saying no, you can't

57:00 by. All right. So, soluble. Itty matters. Anyone here

57:06 on farm school? No, No one. Okay, All your

57:14 , you have a patient that needs drug that needs to go to the

57:18 . What do you need to give ? You need to give them something

57:20 is water soluble and fat soluble. do you think? Fat soluble Because

57:24 has to pass through cells through other and other cells just to get there

57:30 . Can't give some of the So he was just going to sit

57:32 circulation. So that's why it becomes . Understanding what these things size

57:39 All right. Why large molecules have real difficult time getting through uh molecules

57:46 are close together. Goes back to example of my kids. My kids

57:50 escape me because they can weave in and out stuff. You know,

57:54 wife, on the other hand, escape me because it's a lot harder

57:57 get through other adults when she's trying run away from me. Because you

58:00 tell I'm just a horrible threat. right. Maybe maybe I should use

58:06 older kids there now, freshman in school. So they're bigger. All

58:11 , small molecules pass through things very easily. There needs some sort

58:16 force. It's either going to be or an active event. If it's

58:19 . What we're saying is that this doesn't require external energy to move

58:24 In other words, it's using the forces, the natural physical forces to

58:28 things down their concentration gradient. But sometimes you're going to need to

58:34 energy cause something to move and that be an active event. Now,

58:40 are different types of transport diffusion protein transport, which is broken down a

58:45 bunch of different types of particular transporting . We're going to get to these

58:49 In the next lecture. So, planning on getting through all these

58:52 I've got 20 minutes. We'll see that's possible. The fusion. This

58:57 real easy, basically get a whole of things close together, put them

59:00 an environment. What do they want do? They naturally want to spread

59:03 ? So they're equal distance from each . Alright, So, given an

59:06 amount of time, those particles, molecules will separate. They basically bounced

59:11 each other at the same rate. so basically, if you're moving

59:17 so they're they're equidistant, they're able do that. All right.

59:20 that's in essence what diffusion is. . This is an open environment.

59:24 , you can see if I drop dice cube. The cube just takes

59:27 and eventually spread out over there. diffusion can also occur across the

59:31 All right. So, you're moving membrane. What do you need to

59:34 with the membrane? The membrane has be permissible to that substance, but

59:38 will continue to move down that concentration until equilibrium is met. So,

59:45 fusion is passive. You always move an area of high to low

59:49 Hence the definition of passive. All , you're moving from an air

59:53 Is that high to low. You're go to a point where you can

59:56 equilibrium. And this is where some the really simple ideas that you learn

60:01 kindergarten are going to come into Think about this room, look at

60:05 slope in the room. If I on a skateboard in the back of

60:07 room when I go faster, go , slow. Thank you very

60:11 Let's take this room and let's make a little bit steeper. Am I

60:14 to go faster, slow, go ? What if I get it like

60:19 , like crazy fast. Right, all going to pull out your phones

60:24 film it because it's just gonna be things professors do in the classroom.

60:29 right, so you already have a , You understand the steeper, the

60:33 of the faster I go. All , so that's true for molecules.

60:36 steeper the concentration gradient, the more is over here in the last series

60:40 there, the faster diffusion is going take place. That's easy. Short

60:45 the distance. It doesn't take me to get the room next door.

60:51 . Going to take me a long to get to sec 100.

60:55 longer distance, shorter the distance, is it's going to be a good

60:59 . So, the fusion is faster shorter distances. Alright, higher

61:03 What am I doing with the higher ? We always talk about temperature is

61:06 like, oh, I'm adding in . You're adding an energy. So

61:10 I have more energy, that means cells are going to be in that

61:14 those molecules are gonna be more They're going to move more. So

61:17 easier to get things to move when have more energy. Easy example.

61:21 you grew up here in the I know texas isn't sometimes considered itself

61:25 it's hot like this? Yes. right. Have you ever made sweet

61:29 ? Some of you are sitting there , yeah, sweet tea is real

61:31 . What do you do? You water, you put in your you

61:35 in your your t you let it and then you take your sugar and

61:39 you dump it in and what happens all that sugar? Yeah, it

61:45 . Right. It diffuses. if you're in the north, you

61:51 down here and organized team. You order Sweden. All right. You

61:55 I want to sweeten their and they you some sugar and you put it

61:57 there. What does that sugar Sits right there at the bottom of

62:01 glass? Right. What do you to do? You have to

62:05 In other words, you have to energy into the system in order to

62:07 to diffuse, Right? That's the , temperature matters more temperature. More

62:14 cells quicker than the fusion. smaller molecules, as we mentioned

62:19 we said, that you can use system that has a barrier,

62:24 Or membrane, that membrane has to permeable to the substance fixed law of

62:29 , basically. Is that he's the that figured all this stuff out.

62:32 also said, look. So there's magnitude permeability. The membrane to that

62:36 . Here's a new one surface All right. If I have a

62:40 bit of area, it's very hard get a lot of things through

62:43 If I have a bigger air and more things through it. Right,

62:45 kind of makes sense. So that's of the things. And then thickness

62:49 the membrane is pretty much defined. the thicker you make that membrane,

62:52 heart is um you guys know you've heard of it. But do

62:58 know what? It is basically an of the lungs? The lungs start

63:02 extra fluid and then it becomes harder breathe. Why? Well, the

63:07 between the alveoli of the lungs and blood is actually very small. Couple

63:13 Put a layer of water on top that. Just, just a little

63:16 maybe. Let's say this is .3 , let's say we put .1

63:21 I've increased the distance that oxygen molecule to travel. Hence it's harder for

63:27 water or the air to diffuse or oxygen to diffuse. Why? It's

63:30 to breathe. Oh my goodness. . Please don't memorize equations for the

63:40 of doing them. I'm not going ask you a math question on the

63:43 for those who look forward to math on test. Sorry, that's what

63:46 three is for. All right. this does is it describes to you

63:51 relationship of finding um where that where ions equilibrium is going to be

63:59 It's called the nearest equation. I it was up there. It's down

64:03 . All right. And basically what says is look, I can figure

64:06 if I another concentration on the inside on the outside of the cell of

64:09 particular ion, that ion is going travel down the chemical grade in one

64:15 . It's going to travel the opposite with the equal or with the electrical

64:21 . And there's gonna be at some where that molecule can't decide which way

64:24 wants to go. Right? It the point of equilibrium and we can

64:28 out what that voltage is. If know what the concentrations are. All

64:33 , that's what this uh this equation . It does depend on the violence

64:38 some other fun stuff. But basically just the concentration in and out.

64:41 this is why we don't memorize and the math, right? We just

64:45 all right. If I have a that's 100 and 50 millimeter there and

64:49 million more there. It's a 10 1 ratio. The natural log of

64:55 Is going to be greater than Right? And so that will give

65:00 an answer that tells me. But I flip it around, it's going

65:03 give me an opposite answer is gonna a negative value, won't it?

65:06 guys remember that from math? So going to change the direction of

65:10 isn't it? So it's basically saying can figure out where that charges,

65:18 like in voltage, where that ion going to stop moving, well not

65:24 moving, but stop net movement. kind of makes sense now. Why

65:29 I bring this up now? Because going to see in a couple of

65:34 the movement of islands for um both movement and how neurons signaling and knowing

65:43 they, those ions kind of are to move because they have an equilibrium

65:48 they're trying to reach and they're not allowed to reach it. And all

65:52 got to do is give them an to try to reach it and that

65:56 is going to cause the current that's to allow the muscles to contract or

66:00 neurons to fire. Okay, So notice we're not going diving deep

66:06 yet. We're going to get Poor's always open no gates. So

66:13 here, there is a Poor channels gates. They can exist in close

66:19 or in an open state. They be always open, but they still

66:22 something I can close. All when they're always open. We call

66:27 leak channels because they're leaking when they're can open and close. We typically

66:33 refer to him as a gated Typically when we're looking at a channel

66:37 can open and close it opens and in response to something. If I

66:41 to open that door, what what it gonna take for me to open

66:44 door behind you behind us? You look at the door and see force

66:50 some sort. But if I just on the door will it open?

66:53 theory should because the little patches are there. But I see handles.

66:58 I have to mechanically manipulate the door order to open it. So I

67:03 a mechanically gated door back there, I? Right? If you go

67:07 a grocery store you have a motion so it detects motion. And so

67:12 we have in our bodies, we these channels that have different types of

67:18 that open and close the gates. right. It's different types of stimulate

67:22 we call modalities. So you can like chemically gated channels. That's the

67:26 one. You can think. Something to bind to the channel, like

67:29 key going into a keyhole that causes gate to open. That's easy

67:34 You get a little bit more The surrounding area has to have the

67:37 charge in order for us to change shape of the gate to open the

67:42 . All right, we'll make more when we started talking about them regularly

67:47 gated for example, this is where manipulate ever been poked and it

67:53 All right, that's mechanically gated channel you deform the skin. The detective

67:59 in the skin that caused the pain . Oh, I'm being poked,

68:04 the brain. Okay, so that's gated. So its selectivity for what

68:10 going to allow to go through. is dependent upon the diameter of the

68:14 poor and the electrical charge of amino inside. You guys remember your uh

68:23 periodic table, you're like no, memorized it. Which is higher sodium

68:28 potassium sodium. It's a smaller molecule potassium. Right, So you'd expect

68:34 I have a potassium channel, shouldn't allow sodium to come right on

68:37 Yes, but all right. It's size is right, but because of

68:42 charge on the inside, it can't pong its way through appropriately. So

68:46 how it's selective just for potassium and for potassium and sodium. If that

68:52 sense. In other words, it's of like a uh special tunnel that

68:57 potassium can go through. Yes, . You gotta speak up. Sorry

69:05 . Uh So you're talking about studying pes pump. Yeah, that would

69:12 the slide away. A couple slides . Here's a carrier. Remember what

69:17 said? The carrier is never open the outside. It's only open to

69:20 side, not to both sides at same time. This is just an

69:23 of it. You can see here my leg in it binds to the

69:26 site. Right? So there it bound to it that causes a change

69:30 the shape of the molecule when that changes shape or it changes. So

69:34 opens up the other side now. it does at the same time,

69:37 loses the affinity to binding to that Liggan. So it kicks it out

69:42 then when it kicks out it changes back to the original shape. And

69:45 is how the carrier works. All , it moves molecules much much slower

69:50 channel does because the channels just like up. It's like if I say

69:53 is dismissed, you'll get up and start running out of here like the

69:56 is on fire, Right? If had that little rotating door, you'd

70:00 be standing there going, okay, turn. Right? So while it

70:07 no continuous passage, it still allows to move down there gradient because of

70:12 way the shape changes over time it's confirmation of change now. Carrier media

70:18 , this stuff right here has specificity that it won't just buying anything.

70:23 binds usually a single molecule, it's a single molecule. A family of

70:28 . Remember, glucose and galactose. an awful lot of like, don't

70:32 ? Right, So glucose and galactose be able to bind the same type

70:35 carrier might be a hex us All right. So, it would

70:40 an example. And when that's the then you're going to have competition.

70:43 so they're basically to fighting for the seat, that's musical chairs, I

70:50 think about the name of the Right. So it's basically which everyone

70:54 a greater concentration, has a greater of actually being moved by that particular

70:59 . And then there's also a limited of carriers or in a limited number

71:03 sites. And so if you have whole bunch of stuff that needs to

71:06 carried, basically, you keep carrying until you reach a point of

71:11 So if I have 10 molecules in or I'm just going to say to

71:16 , then saturation point is when those carriers are moving to molecules at a

71:21 and you're basically hitting this maximum transport . If I have one molecule then

71:28 someplace way down here, it was terrible example. I shouldn't use bigger

71:33 , right? So saturation refers to limit with which you can carry things

71:39 so you can reach a maximum transport . I've got nine more minutes and

71:44 getting tough. It's very weird coming and having to speak as fast as

71:50 need to active transport. Remember we active requires energy energy in the form

71:56 a teepee. But there's two different of active transport. We have primary

72:00 and secondary active. Primary active is we use a teepee directly. So

72:05 we look at the sodium potassium https ATP comes along binds to the molecule

72:11 allows me to move things, I'm the energy directly to the carrier right

72:17 the pump. Secondary active transport is advantage of active transport. So,

72:23 active transport is moving things in a that that doesn't want to go.

72:27 it's a pump. I'm moving sodium where it doesn't want to go.

72:31 . Moving potassium where it doesn't want go. I can now use that

72:35 up energy to power something. All . It's like a capacitor. That's

72:40 secondary active transport. So, if need a visual image, if you

72:45 a ping pong ball, not one pong ball, you have 1000 ping

72:49 balls and you put them all in closet, carefully shutting the door after

72:52 time. When you open the door the ping pong ball is gonna want

72:55 come. Right, they're all stored the cloud. So that potential energy

72:59 want to open the closet, they'll out. That's kinetic energy. All

73:03 , So, what you're doing is using the Connecticut. You could use

73:06 type of kinetic energy to power Let's say at the bottom of the

73:10 there's something that allows those ping pong to go through. And all of

73:13 sudden Now you're able to power I know your T. V. Your

73:17 because we need to waste power up phones. Stupid example. But you

73:22 the picture. Yeah, I'm gonna examples here in a second. But

73:25 . But go ahead and ask the . Say like obviously the Mhm.

73:36 sodium interesting. Mhm. Mhm. something this is created. Yeah.

73:48 audience. Mhm. Bingo. You the a. two so far.

73:56 got two ways in the class. asking those questions. All right.

73:59 , let me let me show I'll show you the example. Let's

74:02 ahead. Mhm. Yes. no. So, ions are going

74:10 we're going to see. So with active transport, we're taking advantage of

74:14 energy. The startup energy to move that naturally is going against its concentration

74:19 . So oftentimes we're going to see in just a second. Oftentimes it's

74:24 ion moving a molecule that's not an on. But sometimes we're going to

74:29 that it's ions moving other islands. it's all sorts of really interesting.

74:33 , it depends on what which gradient actually taking advantage of. So you're

74:37 something from higher to lower. That's you're expending but you're moving things from

74:43 to higher. And that's what you're the energy to do. Alright,

74:48 , here's our friend sodium potassium https . The question you ask is always

74:52 and two. Right. And the is yes, it happens to be

74:56 all the pictures are terrible. But binding sites for showed even the binding

75:00 for potassium are in the exact same . So basically you can bind up

75:06 and then when you change the you kick out the three. Now

75:08 have a binding site for two All right. I don't think it's

75:12 Mueller ratio. I think it's an 3-2. All right, So,

75:17 is the big picture and it basically , look, here's my sodium binding

75:22 are available. See here's my sodium comes along binds to its three

75:26 that causes the cleavage of ATP. there goes the ADP there's the energy

75:32 the phosphate. Now I've got energy up. That energy causes a conformational

75:37 . So now I have a change the shape of the molecule sodium leaves

75:42 no longer has an affinity when sodium longer has an affinity. Now there's

75:46 potassium binding sites. It's in the same spot. Now potassium will bind

75:52 it now has an affinity for potassium then I just go back once potassium

75:56 it causes a change in the I can kick out the energy

75:59 right, I can kick out that and now I'm back to that other

76:03 . I opened up. Kick that . That makes it possible for me

76:06 buy the 80 P. Rinse So, for every 80 P I

76:10 three. So three sodium one direction potassium the other direction. Where am

76:14 putting the sodium? I'm kicking it of the cell. What am I

76:17 at the potassium? I'm jamming it much as I can into the

76:20 So, I've got all this potassium wants to escape. I got all

76:23 sodium that wants to come in. now have gradients that I can take

76:27 of. Yes, ma'am. So primary. So, what did we

76:33 here? Let me go back. . So, here's the 80p being

76:37 directly. Okay. And so the is transferred at this point and I'm

76:42 and expanding that energy so that eventually going to go back and redo that

76:47 over again. Sorry, I just to the wall. I should never

76:50 that. All right. So, I use ATP directly, that's how

76:54 do it. So, I created gradients and this is where the secondary

76:57 transport. This is a sodium Co transporter, sodium wants to go

77:02 glucose wants to go and you want bad example. I've got three

77:05 You want a really bad example? went to school in New Orleans every

77:09 at a different bar. It was night alright, every night if a

77:14 wanted to go in, he had come in um with uh let me

77:19 if I can get this right, guy wouldn't couldn't come in without a

77:23 charge. But if you came in a girl, there was no cover

77:27 . So, girls wanted to go the in the bars, but they

77:30 want to pay for drinks. So and girls would come outside the

77:34 Right? And they'd say, I want to go in. Will

77:37 go in with me, I'll buy a drink. So you take in

77:39 girl. So that was basically how got in without the cover charge.

77:43 ? Girl got a free drink guy into the place so they can maybe

77:47 up. All right. That's that the goal. And the bar was

77:52 because they got to sell drinks. the guy, here's the girl.

77:58 wants to go in because that's where the actions at writes down my concentration

78:04 glucose wants to go in because it's outside the cell. But glucose there's

78:07 of glucose inside cell. Very little outside the cell. Glucose can't go

78:11 without Expending energy. Now want to energy to move energy. No.

78:16 this is why you're going to use stored up energy. sodium comes

78:20 Makes the glucose binding site available. binds in. When they both bind

78:24 the molecule changes the shape that causes and glucose to be released. The

78:29 re changes its shape back in. have not spent an ounce of ATP

78:32 move anything. sodium is gone where wanted to go. Glucose got to

78:36 where you want to go and then pump is gonna grab the sodium and

78:38 it back out again and make it it all over again. That's an

78:42 of co transport now. Yes. . Tom. Mhm mm. All

78:54 . So, once it gets this . right? So once this transport

78:57 is a carrier. Once this transporters this direction it has no affinity to

79:01 like that. So it's rea changes shape back to the original and when

79:04 changes back to its original now it's up to the sodium again. So

79:09 it's a force cycle because each change shape causes the next step. I've

79:14 three slides here. It'll take me than a minute to go through all

79:17 them. Alright because what I really to deal with here is I want

79:21 show you these pictures you're going to these words co transporters. The one

79:24 just showed you is the most common . All right. But look there

79:28 so many different types. And when see a sim porter or co

79:33 what you're doing is you're moving things the same direction to answer your

79:37 Look one is going downhill. The one's going up. That's when we

79:40 looked at but every single one of is one's going down, one's going

79:44 against one's going against its greatest. when it's being moved you're expending one

79:50 its gradient. That's the energy that's in second secondary active. Now if

79:56 moving things in opposite directions you might it an anti porter or an

80:01 Okay that's the other term and basically the same principle one is moving down

80:05 you're moving something against its grading it sometimes be three hoops. So here's

80:12 , here's another one is three, one's a popular one in case C

80:16 might be one you might have heard . So basically you're always gonna at

80:19 generally speaking you're gonna exchange Catalans for ions and ions and fry and

80:24 But the idea is again it's the principle, one is uphill ones,

80:28 your and then I want to show these two slides because they're all

80:34 And so if you understand conceptually when introduced something that you've never seen

80:39 like here's in kate to L. . You'd be like oh well that's

80:44 a co transporter. I'm using sodium move to molecules that don't want to

80:49 uphill to move them uphill actually three in that case and that's all there

80:54 to this stuff. So if you conceptually what we're talking about secondary active

81:01 , you already understand how many of things a lot and that's it.

81:08 I went over for one minute, apologize.

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