Midterm 1 recap Flashcards

1
Q

What is a snare?

A

family of membrane proteins responsible for selective fusion of vesicles with a target membrane

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2
Q

What are transport vesicles?

A

membrane proteins that carries proteins form one intercellular compartment to another

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3
Q

What is vesicular transport

A

movement of material between organelles via membrane-enclosed vesicles.

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4
Q

What are clathrin?

A

protein that makes up a coat for transport vessicles that bud towards cystolic side of cell from plasma mebrane (inward endoycitic pathway) or golgi apparatus (outward exocytic pathway)

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5
Q

What are Rab Proteins?

A

GTP binding proteins on surface of transport vesicles and organelles

Serves as molecular marker to ensure vesicles fuse with correct membranes

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6
Q

What are tethering proteins?

A

filamentous transmembrane protein involved in docking of transport vesicles to target membranes

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7
Q

Explain how transport vesicles are created from receptor-mediated endocytosis

A

Coat Assembly:
- cargo receptors bind to a molecule which then changes confirmation to also bind to adaptin proteins on cystolic side

Bud formation:
The adaptin protein allows for clathrin proteins to bind to it

Vessicle Formation:
Protein dynamin forms around neck of plasma membrane and through GTP hydrolyis, pinches it off

Uncoating
- clathrin proteins are removed and transport vesicle is able to fuse with membranes of other organelles

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8
Q

Role of Adaptin

A
  1. secures clathrin to vesicle
  2. selects cargo molecules for transport via trapping the specific receptor proteins and forming a vesicle containing the receptor proteins and their bounded molecules
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9
Q

Explain mechanics of Vesicle Docking

A

Rab and tethering proteins

The GTPases Rab proteins on the vesicles are binded to tethering proteins on the membrane of the organelle destination
(each specific vesicle and membrane have their own unique Rab and tethering protein combo)

Snares
V-snares on vesicle and T-snares on membrane interact to firmly dock vesicle in place.

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10
Q

How do snares facilitate the fusing of vesicles to organelle membranes?

A
  • snares wrap around each other and act like a winch, pulling the vesicle towards the membrane protein
  • this allows for fusions because the lipid bilayers can get within 1.5 nm from eachother
  • also, due to water being in between the vesicle and membranes, random fusion is higherly energetically unfavorable
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11
Q

What is receptor-mediated endoycytosis

A

selective uptake of material in which macromolecule binds to a receptor in plasma mebrane and enters cell in clathrin-coated vesicles

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12
Q

What is an endosome (function)

A

membrane-enclosed compartment through which material ingested by endocytosis passes on it ways to lysosomes

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13
Q

Explain how cholesterol from bloodstream is taken up by cells

A

receptor-mediated endocytosis:
1. cholesterol in blood bind to proteins and from LDL (low-density lipoproteins)
2. LDL binds to LDL receptors (adaptin binds to these receptors on cytosolic side, clathrin binds to adaptin and dynamin hydrolyzes GTP to pinch off a clathrin-coated vesicle)
3. vesicle fuses with endosome
(endosome’s acidic pH separates LDL receptors from LDL)
4. LDL is transferred to lysosome while LDL receptors bud off in vesicles that fuse back to plasma membrane
5. lysosome breaks down LDL via hydrolytic enzymes and cholestrol is released into cytosol to synthesize new membranes

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14
Q

Function of Cytosol

A

contains many methabolic pathways (protein synthesis and cytoskeleton

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15
Q

Function of Nucleus

A

contains main genome, DNA + RNA synthesis

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16
Q

Function of mitochondria

A

ATP synthesis by oxidative phosphorylation

17
Q

Function of Golgi Apparatus

A

modification, sorting and packaging of lipids for secretion or delivery to organelles such as lysosomes

18
Q

Function of endoplasmic reticulum
(smooth vs rough)

A

synthesis of lipids (smooth)
synthesis of proteins for distribution to many organelles and to plasma membrane (ER)

19
Q

function of endosome

A

sorting of endocytosed material

20
Q

function of lysosome

A

intracellular degradation
(involved in phagoytosis, pinocytosis, and autophagy)

21
Q

function of peroxisome

A

oxidative breakdown of toxic molecules

22
Q

Desribe the Na+ K+ pump

A

transfers Na+ against electrochemical gradient (towards high concentration and positive polarity outside of cell)
transfers K+ against chemical gradient (towards high concentration and negative polarity inside of cell)
- brings three Na+ and 2 k+
- uses 30% of totoal ATP consumption

23
Q

What happens during refractory period of nerve conduction

A

voltage gated Na+ channels
- changes into an inactive conformation (b/c energetically favorable) where Na+ cannot enter or leave cell membrane

K+ leak channels
- becomes depolarized and opens to allow potassium ions to leave the cell membrane thereby bringing cell potential to negative intracellularly

24
Q

What occurs when an action potential reaches presynaptic nerve terminal

A
  1. Ca2+ ion channels on presynaptic membrane depolarized and changes into open conformation (influx of Ca2+ ions)
  2. synaptic vesicles are triggered and results in being exocytosed out of presynaptic membrane into synaptic cleft
  3. neurotransmitters from synaptic vesicles bind to neurotransmiter receptors
  4. transmitter-gated ion channels then undergo conformation change that allows for ion transport (acetylcholine –> excitatory –> Na+ into cell) (norepinepherine –> inhibitory –> K+ out cell)
25
Q

Why are both electrical and chemical signals used during neuronal transmission

A

electrical signals help propagate nerve impulses from dendrite to axons quickly (action potential moves and is amplified by voltage gated Na+ channels)

electrical signals CANNOT pass synaptic cleft therefore must be converted to chemcial signals (neurotransmitters)

26
Q

what are gamma (y) tubulins?

A

gamma tubulin ring complexes make up nucleating sites on centrosome matrix

–> where microtubules grow (polymerizes) from alpha to beta (minus to positve side)

27
Q

Compare and contrast microtubules and actin

A

microtubules
- 13 parallel protofilaments made from tubulin dimers (alpha pos, beta minus)
- grows at both ends but more rapidly on alpha end (dynamic instability powered by GTP)

actin
- grows faster at plus end than minus end
- when there is intermediate concentration of free actin monomers, tread miling occurs (polymerization at plus end occurs at same rate as depolymerization at minus end
- uses ATP for polymerization

28
Q

Describe dynamic instability

A

controled by GTP hydrolysis

Growing:
rate of GTP hydrolysis is slower than rate of tubulin dimer polymerization

Shrinking
rate of GTP hydrolysis is faster
- protofilaments contianing GDP tubulin peel away + GDP tubulin is released into cytosol

29
Q

How is skeletal muscle contraction triggered and controlled

A

Trigger:
- T-tubules connect plasma membrane to sarcoplasmic reticulum (specialized ER
- When T-Tubule polarizes –> voltage gated Ca2+ channels open up
- causes conformation change in Ca2+ release channels on Sarcoplasmic reitculum
- Ca2+ released into the cytosol to cause myofibril contraction

Control
troponin: protein complex that includes Ca2+ sensitive protein
initally: tropomyosin binded to actin and troponin complex keeps it there
influx of Ca2+: calcium ions bind to troponin complex –> conformatin chanage on both troponin and tropmyosin
Myosin heads can now bind to actin