cell membrane

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63 Terms

1
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Membranes are made of —

lipids

2
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t or f

Proteins are a component of membranes

t

3
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• Proteins are involved with moving — across membranes

molecules

4
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• Cells are surrounded by a membrane that—

separates the contents of a cell from the external environment

5
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what is the point of having a cell membrane?

Contains and protects cellular contents, otherwise you’d just have soup

6
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describe what a cell membrane looks like

bilayer of lipids with the polar heads on the outside and the inside has the lipid tails

<p><span><span>bilayer of lipids with the polar heads on the outside and the inside has the lipid tails</span></span></p>
7
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can lipids can make other biologically relevant structures other than bilayer membranes?

yes

8
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name 3 other biologically relevant structures that lipids can make

Micelle •

Extracellular vesicles (EV)

• Liposome

9
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liposomes are normally man-made, but what do they resemble more?

a) micelles

b) extracellular vesicles

b) extracellular vesicles (double lipid bilayer)

10
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describe the structure of a micelle

knowt flashcard image
11
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describe the structure of a liposome

knowt flashcard image
12
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what were liposomes used for?

vaccines, covid vaccine used rna inside liposome because it doesnt mater where Rna gets expressed, it will make antigens

13
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what was the problem for liposomes in drug delivery?

The liposome would always get taken up by the liver first

14
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why can an etxracellular vesicle trasnport things like rna, dna, drugs but a micelle cannot?

the stuff its transporting is actually in the middle, so its non polar there

<p>the stuff its transporting is actually in the middle, so its non polar there</p>
15
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what unique thing do phosphoglycerides have in them

glycerol

16
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what unique thing do sphingolipids have in them?

sphingosine

17
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what unique thing do sterols have in them?

rings

18
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do all species have the same membrane lipid composition?

no

19
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whats one big difference between humans and e coli lipid membranes?

e coli have no cholesterol

20
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t or f

even human membranes depending on where they are they have different compositions

t

21
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different thicknesses, different levels of fluidity uh and different shapes are acheived by—

different lipid compositions change the structure

22
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t or f

even if you're looking at the same cell, it's not going to have the same exact same lipid composition at all parts of that surface

t

23
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in what ways can lipids move within a membrane? (they’re not static)

  • they can flip flop to the other leaflet (rare)

  • they can rotate around

  • they can do lateral diffusion 

<ul><li><p>they can flip flop to the other leaflet (rare)</p></li><li><p>they can rotate around</p></li><li><p>they can do lateral diffusion&nbsp;</p></li></ul><p></p>
24
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what is one way he mentioned to study the movement of lipid membranes

photobleaching

25
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explain the photobleacing thing

  • Label lipids (or proteins) in the cell membrane with a fluorescent tag.

  • Photobleach a small region with a focused laser beam (this destroys fluorescence only in that area).

  • If the lipids move around then this patch shouldnt exist anymore, theyll get spread out

  • this means that the fluorescence in that bleached area should return cause its not all concentrated in one area anymore

<ul><li><p><strong>Label</strong> lipids (or proteins) in the cell membrane with a fluorescent tag.</p></li><li><p><strong>Photobleach</strong> a small region with a focused laser beam (this destroys fluorescence only in that area).</p></li><li><p>If the lipids move around then this patch shouldnt exist anymore, theyll get spread out</p></li><li><p>this means that the fluorescence in that bleached area should return cause its not all concentrated in one area anymore </p></li></ul><p></p>
26
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In addition to the cell surface membrane, cells have many internal membranes, name 5

• Nuclear membrane

• Mitochondria

• Endoplasmic reticulum

• Golgi

• Lysosomes

27
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t or f

There's not the same lipid composition on both sides of the lipid bilayer leaflets

t

different needs for different environments and communication

28
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• Excess hydrophobic lipids in cells can be stored as —

droplets

29
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fats accumulate inside the membrane of the Endoplasmic reticulum, then what happens to them?

  • they bud off into the CELL CYTOPLASM

  • not into the ER lumen

  • thats why he says “droplets are generated from membranes” 

<ul><li><p>they bud off into the CELL CYTOPLASM</p></li><li><p>not into the ER lumen</p></li><li><p>thats why he says&nbsp;“droplets are generated from membranes”&nbsp;</p></li></ul><p></p>
30
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membranes need to contain a cell and stop things from getting in and out, but why is it bad to do that TOO much?

because you need some things to get in and out like nutrients and waste out and you need communication

31
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what are 3 examples of things that are permeable through the cell mebrane?

  • carbon dioxide

  • oxygen

  • ethanol

32
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most sugar and proteins are impermeable to the cell membrane, so how do they get in?

through the proteins that are in the membrane surface

33
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name a few ways proteins can be associated with the cell membrane

  • channels

  • trasnporters

  • receptors

  • some are just associated with the membrane or other proteins

34
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in simple channels, what is the flow of movement

Molecules move with the concentration gradient (passive, no ATP)

35
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Uniporters

Transport single type of molecule with the gradient

<p>Transport single type of molecule with the gradient </p>
36
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explain a symporter

  • you want to move one molecule in but its against its concentration gradient

  • proteins have evolved to let that molecule of interest hitch a ride on a molecule thats coming in WITH its concentration gradient 

<ul><li><p>you want to move one molecule in but its against its concentration gradient</p></li><li><p>proteins have evolved to let that molecule of interest hitch a ride on a molecule thats coming in WITH its concentration gradient&nbsp;</p></li></ul><p></p>
37
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antiporter

Catalyze movement of one molecule against a gradient, driven by a second molecule going WITH its gradient – molecules move in opposite directions

<p>Catalyze movement of one molecule against a gradient, driven by a second molecule going WITH its gradient – molecules move in opposite directions </p>
38
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explain how pumps work

it breaks down ATP (hydrolysis) to generate energy to allow the movement of a molecule against its gradient

<p><span><span>it breaks down ATP (hydrolysis) to generate energy to allow the movement of a molecule against its gradient </span></span></p>
39
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why is secreting proteins such a focus?

because proteins are usually hydrophilic or hydrophobic, so it dfeintely wont want to move ACROSS a membrane, either it wont want to go near it, or it will want to stay in it

thats why the cell needed to evolve these secretion pathways to find ways to get proteins In and out of cells

40
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if you have a ribosome freely floating in the cytoplasm, it will make a — protein

cytosolic (stays in cytoplasm, or is hydrophylic at least, I think)

<p>cytosolic (stays in cytoplasm, or is hydrophylic at least, I think)</p>
41
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if you want to make a protein that needs to get across a membrane, whats something you could do?

use an attached ribsosome that gets secreted into lumen directly

<p>use an attached ribsosome that gets secreted into lumen directly </p>
42
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So if a protein is to be secreted using the canonical secretion pathway, ribosomes attach the first attach the mRNA start to translate. It produces an —

end terminal peptide which is a signal peptide

<p><span>end terminal peptide which is a signal peptide  </span></p>
43
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. what happens with this signal recognition peptide?

it is recognized by a signal recognition protein

44
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what happens when the signal recognition protein recognized the signal sequence?

it directs that ribosome to the endoplasmic reticulum

<p><span><span>it directs that ribosome to the endoplasmic reticulum </span></span></p>
45
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this signal recognition protein is not just made out of protein. It also contains an RNA called the 7 SL RNA which is also Important for.

the Alu repetitive DNA element which is found super freqeuntly in the genome, is derived from this RNA

46
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So the docking of the signal recognition protein with proteins on the endoplasmic reticulum allows —

insertion of the newly synthesized AA chain (signal sequence) through the translocon

<p><span>insertion of the newly synthesized AA chain (signal sequence)  through the translocon </span></p>
47
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Once that signal sequence comes through the translocon, what happens?

the signal peptide is immediately cleaned off by the protein signal peptidase

<p><span>the signal peptide is immediately cleaned off by the protein signal peptidase </span></p>
48
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t or f

If it's going to be a secreted protein, it's generally modified

t

glycolsylation is common

49
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if you see a protein with a lot of disulfide bridges, what can you assume about it?

  • that it is a secreted protein (extracellular, like hormones, insulin, albumin, collagen) because intracellular proteins don’t have a lot of them

50
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okay so it can be glycosylated, disulfide bridge, whats one more thing he mentioned that can happen to modify?

proteolytically processed

51
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when hes talking about transmembrane proteins, which end of the protein is usually inside the cell and which end is usually outside the cell?

N terminus usually OUTside

C terminus usually inside

thats why he thought type 2 were so weird

<p>N terminus usually OUTside</p><p>C terminus usually inside</p><p>thats why he thought type 2 were so weird</p>
52
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whats different about secreted proteins to type 1 proteins? like how do they get stuck in the membrane?

  • they have a hydrophobic part of their chain which acts as a “stop trasnfer” signal to the translocon, so the rest of tit never goes through 

<ul><li><p>they have a hydrophobic part of their chain which acts as a&nbsp;“stop trasnfer” signal to the translocon, so the rest of tit never goes through&nbsp;</p></li></ul><p></p>
53
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explain what happens with type 2 membrane proteins

  • free ribsome starts trasnlating

  • then theres a “signal anchor sequence” which is hydrophobic

  • this drags it to the translocon

  • it cant put the N terminal end in because its too far away now 

<ul><li><p>free ribsome starts trasnlating </p></li><li><p>then theres a “signal anchor sequence” which is hydrophobic</p></li><li><p>this drags it to the translocon</p></li><li><p>it cant put the N terminal end in because its too far away now&nbsp;</p></li></ul><p></p>
54
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how do you get a type 3?

its like type 1 but the hydrophobic sequence is very early on so most of it doesnt go through

<p>its like type 1 but the hydrophobic sequence is very early on so most of it doesnt go through </p>
55
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how do you get type 4?

it starts like a type 2 but the hydrophoic signal is very late, so the whole thing almost gets trasnlated first

<p>it starts like a type 2 but the hydrophoic signal is very late, so the whole thing almost gets trasnlated first</p>
56
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t or f

type 2 and 3 (and 4 I think) have Cytosolic translation initially

true

57
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<p>when hes showing you this slide, what is he referring to, Iike what are you predicting? </p>

when hes showing you this slide, what is he referring to, Iike what are you predicting?

by looking at the sequence, you can see if it has

  • stop trasnfer sequence

  • where/if hydrophobic anchor sequence

so , this helps you determine the shape of the protein and where it will be

58
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what does he mean when he says that some membranes funciton as fucntional sites?

  • like the inner mitochondrial membrane is the site where ATP is produced

59
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what does he mean by internal membranes?

• Nucleus • Mitochondria • Lysosomes

60
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t or f

the nuclear membrane and the endopplasmic reticulum are actually attached to each other.

t

<p>t </p>
61
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okay so eukaryotes have these internal membranes right like nucleus and mitochondria, but prokaryotes have NO internal membranes right like no nucleus

right right

62
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whats the hypothesis for how the nucelur enveloppe came about?

a prokarrotic cell started getting plasma membrane invaginations in such a way that surrounded the nucleus to protect it 

<p>a prokarrotic cell started getting plasma membrane invaginations in such a way that surrounded the nucleus to protect it&nbsp;</p>
63
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whats the hypothesis for how mitochondria came about?

  • early prokaryote (or maybe the same cell that just got the nucelus?) engluphed a bacteria which becomes the mitochondria

  • because it engulphed it, it was put isnide a vesicle whihc became its second membrane