Cell Biology Final Exam FA21 - PART II (CH12 & CH13) Flashcards

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1
Q

What are the models of cell membrane structure?

A
  1. Overton
  2. Langmuir
  3. Gorter and Grendel
  4. Davson-Danielli
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2
Q

Describe the overton cell membrane model

A

1890
Put plant root cells in - lipid soluble could cross membrane and water soluble could not
Results: cell membrane made of lipids

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3
Q

Describe the Langmuir cell membrane model

A

1900
Dissolved phospholipids in benzene then layered onto a water surface
let the benzene evaporate and phospholipids left behind
Results: postulated the membrane is a single layer of phospholipids

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4
Q

Describe the Evert Gorter and Grendel cell membrane model

A

1925
Same experiment as Langmuir, but measured chemicals and everything at careful rate
Postulated the double layer of phospholipids
Used thermodynamics to propose that hydrophobic regions point away from water and hydrophilic head groups point towards water
[Hydrophillic heads outside, hydrophobic fatty acid tails inside]

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5
Q

Describe the Davson-Danielli cell membrane model

A

1935
Stated issues with Gorter and Grendel’s model (surface tension, protein extraction, etc.)
EXPERIMENT – Postulated proteins may coat the outer sides of the bilayer forming a protein lipid protein sandwich
- Protein layer on each outer side of phospholipid bilayer
- Molecules must be able to penetrate (sugars, proteins, amino acids)
People arguing there are proteins of all shapes and sizes, and how are things going to get across
RESULTS – Davson-Danielli added a polar pore to their model of the membrane

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6
Q

What did Singer-Nicolson say the issues were with Davson-Danielli?

A

a. Protein extraction, some proteins you have to destroy the membrane to get out (extremely hydrophobic)
b. Protein to lipid composition ratio should be the same – it is not
- Protein:lipid composition of various membranes varied greatly

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7
Q

What was the Singer-Nicolson experiment on showing a fluid membrane?

A

FRAP (fluorescence recovery after photo-bleaching)

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8
Q

What was the FRAP experiment?

A
  • Put fluorescent label on the protein
  • Take laser and bleach area of the cell (white)
    Follow area over an hour
  • See the bleached area recovers
    Proteins are moving about in the membrane
  • (There are some proteins that cannot move about)
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9
Q

Results of FRAP experiment?

A

The membrane is fluid – proteins and phospholipids are moving around

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10
Q

What was the Singer-Nicolson experiment on showing a mosaic membrane?

A

Freeze Fracture

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11
Q

What was the Freeze Fracture experiment?

A

Took membrane from cell and quick-froze, add liquid nitrogen, use knife (microtome) to peel back phospholipid bilayer to look inside
Spray with electron-dense material to actually look at surface (i.e. platinum)
- Used scanning EM to see a bunch of bumps and valleys inside the bilayer
Hills – proteins embedded in layer
Valleys – protein area
- Theorize proteins are in/go through the membrane

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12
Q

Results of Freeze Fracture experiment?

A

Membrane is a mosaic of phospholipids and proteins that are interspersed throughout
Protoplasmic P face – interior
Ectoplasmic E face – exterior

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13
Q

What was the third experiment performed by Singer Nicolson to show fluidity in the membrane?

A

Cell fusion

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14
Q

What was the cell fusion experiment?

A

Labeled mouse cell with red dye (rhodamine)
- Labeled human cell with green dye (fluorescein)
Fused two cells together using polyethylene glycol or Sendei virus and allowed to incubate

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15
Q

Results of cell fusion experiment?

A

Within 40 minutes, red and green diffuse throughout the cell

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16
Q

What is the influence of the length of fatty acid tails on the lipid bilayer?

A

Longer tails = less fluid

Shorter tails - more fluid

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17
Q

What is the influence of saturation on the lipid bilayer?

A

Unsaturated = more fluid, saturated= less fluid

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18
Q

What is the influence of temperature on the lipid bilayer?

A

higher temp = more fluid

lower temp = less fluid

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19
Q

What is the influence of Cholesterol on the lipid bilayer?

A

more cholesterol = less fluid (stiffens membrane)

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20
Q

What class of membrane proteins transport into and out of the cell. As seen in Na+/K+ movement?

A

Transporters

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21
Q

What class of membrane proteins helps fold proteins and link intracellular actin filaments to extracellular matrix proteins?

A

Anchors

22
Q

What class of membrane proteins detect signals on outside of cell and transmit the message inside of the cell. Can direct cell growth and division.

A

Receptors

23
Q

What class of membrane proteins can catalyze the production of small intracellular signaling molecule cAMP .

A

Enzymes

24
Q

What is a single-pass membrane protein?

A

Passes membrane once

25
Q

What is a multipass membrane protein?

A

Passess membrane meaning they traverse the membrnae several times. Dimers, trimers, tetramers

26
Q

What are alpha helices (membrane protein)

A

Crosses bilayer by interacting with side chains
Hydrophobic side chains interact with phospholipid
Hydrophilic- H bonds- form backbone

27
Q

What are beta barrels (membrane protein)

A

Interact to form a channel in membrane

28
Q

What are the principles of membrane transport?

A
  1. Synthesis
  2. Addition of Sugars
  3. Orientation
  4. Movement through cell membrane
  5. Asymmetry
29
Q

Describe synthesis (memb transport)

A

Lipids are made in the ER and added

30
Q

Describe addition of sugars (memb transport)

A

Sugars are added with a block of about 10 sugars

sugars modified and sized in golgi

31
Q

Describe orientation (memb transport)

A

Cytosolic side always on cytosolic side. Non-cytosolic will be on luminal side.

32
Q

Movement through cell membrane (memb transport)

A

Phospholipids are distributed between two bilayers. The membrane trafficking moves from ER to Golgi to Membrane

33
Q

Asymmetry - Scamblase

A

Phospholipids synthesis adds to cytosolic half of the bilayer
Lipid bilayer of endoplasmic reticulum
Found in the ER membrane
`Randomly flips the phospholipids from one side to the other
Scramblase catalyzes transfer of random phospholipids from one monolayer to another
Symmetric growth of both halves of bilayer

34
Q

Asymmetry - Flippase

A

Asymmetric lipid bilayer of plasma membrane
Delivery of new membrane from ER
Flippase catalyzes transfer of specific phospholipids to cytosolic monolayer
Now in golgi apparatus- it is assymetric
Flips specific phospholipids to the other side
Asymmetry lipid bilayer of plasma membrane

35
Q

What are the types of transport?

A

Uniport - only 1 molecule pumped out
Symport - both molecules transferred together in the same direction, the energy that is released drives the transport
Antiport - molecules being pumped in different directions (Na+/K+ pump)

36
Q

How are molecules transported across the membrane?

A

Passive diffusion
Facilitated diffusion
Active transport

37
Q

Describe carrier proteins

A

bind specific molecules, undergo conformational change, like sugar and amino acid
Only a few molecules can go across at a time

38
Q

Describe channels in the membrane

A
Form open pores 
Allow free diffusion through open pore
Appropriate size and charge
Ex. Ions
Lots of molecules can go across
39
Q

Ligan gated vs voltage gated vs mechanical/stress-gated

A

-ligand gated
Hormone or neurotransmitter bind to open the channel
-Voltage gated
-mechanical/ stress-gated
There is movement against it to open the pore (seen in hearing)

40
Q

What are the properties of ion channels?

A

rapid transport
selective for size and charge
pore will close at some point

41
Q

Types of ion channels

A

Ligand-gated
Voltage-gated
Mechanical/stress

42
Q

Voltage Gated -Membrane potential

Nerve cells

A

K+ can leak through to give a negative membrane potential, sodium on outside of the membrane and potassium on the inside of the membrane
Inorganic ions cause negative charge
Chloride balances out

43
Q

Nerve Impulses / action potential

-process

A

When K+ and Na+ channels close they are refractory for a few seconds
We want nerve impulses to move down, that way they don’t open too soon b/c then nerve impulses could move back up

44
Q

How do Na+ and K+ select for the ions?

A

Na+ ion has to have at least 1 h2o molecule to get across, K+ with with water is too big to get across the Na+ channel (10x more permeable to Na)
K+ can get across with water because it can interact with the carbonyl oxygens that are lining the channel. Na+ is not big enough to interact with the carbonyl oxygens that line the membrane

45
Q

How are electrical signals converted to chemical signals?

A

Ca2+ channels convert electrical signals to chemical signals
When the Ca2+ channels opens, the synaptic vesicle fuses to the membrane and the neurotransmitter releases a chemical signal into the synaptic cleft. The neurotransmitter signals are then converted from an electrical to a chemical signal. This chemical signal will eventually return to an electrical signal
The nerve cell is designed to turn an electrical signal into a chemical signal
The whole point is to get the signal to the next cell that it needs to go to

46
Q

Active Transport

-sodium / Potassium pump

A

3 Na+ ions bind from the cytoplasmic side. The pump gets phosphorylated and ATP is converted to ADP. There is a conformational changed and the pump opens on the other side of the cell. The 3 Na+ are released and 2 K+ come into the pump. The pump is dephosphorylated which causes a conformational change to the pump and it opens on the inside of the cell. The K+ is released into the cell where there is a low gradient of K+ inside of the cell and a high gradient of Na+ inside the cell. The cycle repeat

47
Q

Importance of Na/K pump in active transport

A

Propagates electrical impulses in nerve and muscle cells (brings back equilibrium in the nerve cell)
Drives active transport of variety of molecules
Maintains osmotic balance and cell volume

48
Q
  • ABC transporters (ATP-binding cassettes)

- Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)

A

Produces a mucus that is abnormally thick and sticky within the lungs. It is a great place for bacteria to grow and creates lots of lung infections. There is a defect in the Cl- ion transport. When the R domain is phosphorylated, the pore opens which allows Cl- ions, Na+ ions, and h2o to come out of the cell. The h2o being removed causes the thick mucus layer on the lungs

49
Q
  • contribution to disease

- Cholera toxin?

A

Cholera activates the normal CFTR. Cholera acts as a selective pressure on heterozygotes. Heterozygote advantage is if there is a defective allele, not as much h2o can be pumped out

50
Q

glucose transporter

A

One glucose and two Na+ enter the glucose transporter pump. Those causes a conformational change and the glucose and Na+ are pumped into the cell. Once they are released, the pump has another conformational change outside of the cell and the cycle continues.