Lecture 7 - Lipids Part 2 Flashcards

1
Q

What are functions of a plasma membrane?

A

protection (cell shape), transport, communication (signaling/regulation), cell adhesion (movement)

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2
Q

What features does a plasma membrane have with regard to permeabillity and why is that the case?

A

impermeable to hydrophilic molecules b/c lipid bilayers with hydrophobic tails and hydrophilic heads

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3
Q

What are the 3 major transport types and do they require energy?

A

passive: no energy, uses concentration gradient (simple, osmosis, facilitated)
active: energy required to move against concentration gradient (primary and secondary)
bulk: energy required (endocytosis and exocytosis)

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4
Q

What is uniport, symport, and antiport (with regard to energy required and molecules moved)?

A

primary active transport = UNIPORT uses ATP to move 1 molecule against concentration gradient
secondary active transport: uses conc gradient of one moelcule (not ATP) to move another molecule
-symport: both molecules move in same direction
-antiport: both molecules move in diff direction

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5
Q

What are the 2 types of bulk transport and is energy required? What “vessel” is required?

A

vesicular transport of bulk materials - requiring membrane vesicles and energy
-endocytosis: phagocytosis
-exocytosis: neurons releasing NTs

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6
Q

What is an example for an uniporter found in rods, transporting what?

A

GLUT1 - glucose transporter 1 found in rods
PMCA: calcium ATPase transport Ca2+

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7
Q

What is an example for an antiporter found in rods, transporting what?

A

Na-K-Ca Exchanger (NCKX): antiporter found in retinal rods that uses conc gradient made from Na+/K+ ATPase to transport Ca2+ out of cell while Na+

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8
Q

Which 4 types of multiprotein complexes are found in a membrane involved in transport, signaling, adhesion, and protection?

A
  1. gap junctions: transport, signaling (within tissue/between cells)
  2. tight junctions: seal cells
  3. desmosomes: cell adhesion (hold neighboring cells together); allow molecule transport
  4. adherens junctions: cell adhesion to ECM
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9
Q

Which one is the membrane model that is still accepted today and what are the major features of that model?

A

fluid mosaic model - highly dynamic = fluid; diff molecule types = mosaic (phosphollipids, cholesterol, protein, carbs)

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10
Q

Which lipid classes are the main types found in plasma membrane?

A

glycerides (contain glycerol)
non-glycerides (sphingolipids, steroids like cholesterol)

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11
Q

Which lipid types are the most abundant?

A
  1. glycerophospholilpids/phosphoglycerides = glycerol + 2 FA tails + phosphate head (inositol, choline, ethanolamine)
  2. sphingolipids (raft) - non-glycerides
  3. cholesterol (raft) - influence lipid fluidity
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12
Q

Which 3 types of membrane protein exist (with regard to location and attachment features)?

A
  1. integral proteins: permanently incorporated
  2. peripheral proteins: temporarily attached to bilayer or integral proteins
  3. lipid-anchored proteins: permanently attached
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13
Q

What are the major features of the 3 membrane protein types?

A

integral proteins: in bilayer –> so hydrophobic parts interact with hydrophobic phospholipid tail
peripheral proteins: hydrophilic so not linked with hydrophobic bilayer interior
lipid-anchored proteins: hydrophillic; on surface of membrane; covalently attached

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14
Q

Which protein structure of TM-proteins is the predominant form in our membranes - alpha helix or beta barrel?

A

alpha helix (ex: rhodopsin)

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15
Q

What is an example for TM protein that’s required for enzymatic activity (type/kind, not specific molecule)?

A

integral receptor protein - required for enzymatic activity

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16
Q

What is an example for a TM-protein that’s required for cell recognition (type/kind, not a specific molecule)?

A

T-cell receptors and foreign antigens

17
Q

What is an example for a TM-protein that’s required for signal transduction/signaling (type/kind, not a specific membrane)?

A

GPCR - transmembrane receptors - ligand binds and G-protein changes shape and downstream effect occurs

18
Q

Where in the rod photoreceptor (structure/formation) is rhodopsin predominantly found and where in this structure is it located?

A

rhodopsin (alpha helical GPCR transmembrane protein) found in discs of PR rod outer segment which is embedded in RPE (retinal pigmented epithelium)

19
Q

Of which 2 components is rhodopsin made of (type of molecule and specific name)?

A

rhodopsin = opsin + 11-cis-retinal (chromophore = light absorbing pigment)

20
Q

What happens to these 2 components when light hits rhodopsin?

A

when light hits rhodopsin, 11-cis-retinal becomes 11-trans-retinal = activated rhodopsin

21
Q

What is the name of the G-protein that interacts with activated rhodopsin?

A

transducin = GPCR that interacts with activated rhodopsin

22
Q

What is the name of the ligand that keeps a special channel open to allow sodium to enter the rod? What is the name of the channel?

A

cGMP keeps cGMP gated Na+ channels open –> depolarized rod in the dark

23
Q

What is the name of the enzyme generating GMP and what is the substrate?

A

PDE: phosphodiesterase makes GMP from cCMP when activated alpha unit of G-protein interacts

24
Q

In the dark, the rod sodium channels are ____ resulting in ____ resulting in ____ resulting in ____?

A

In the dark, rod’s cGMP gated Na+ channels are OPEN, resulting in DEPOLARIZATION (increase conc positively charged ions) resulting in EPSP (excitatory post synaptic potential), resulting in RECEPTOR POTENTIALS

25
Q

When light is present, rod sodium channels are ____ resulting in ____ resulting in _____ resulting in ____?

A

When light is present, rod cGMP gated Na+ channels are CLOSED, resulting in HYPERPOLARIZATION (decrease in positive ions inside cell), resulting in IPSP (inhibitory post synaptic potential), resulting in FEW RECEPTOR POTENTIAL

26
Q

What is the visual cycle?

A

biochemical reactions that regenerate visual pigment (11-cis-retinal)

27
Q

Which enzymes/enzyme complexes are required in the visual cycle?

A
  1. light activates rhodopsin so (opsin + 11-cis-retinal –> opsin + all-trans-retinal)
  2. RDH8/12 (retinol dehydrogenase) reduces all-trans-retinal to all-trans-retinol in presence of NADPH
  3. LRAT (lecithein retinol-acyl-transferase): all-trans-retinol to all-trans-ertinyl esters
  4. RPE65 (retinol isomerase): all-trans-retinyl esters to 11-cis-retinol (retinol is vitamin A)
  5. RDH5/10/11 (11-cis-retinol dehydrogenase): 11-cis-retinol to 11-cis-retinal
28
Q

Starting with all 11-cis-retinal converted to all-trans retinal which products (3) are generated in the cycle until 11-cis-retinal is renewed (correct sequence)?

A
  1. 11-cis-retinal –> all-trans-retinal (via light activation)
  2. all-trans-retinal –> all-trans-retinol (via RDH8/12)
  3. all-trans-retinol –> all-trans retinyl esters (via LRAT)
  4. all-trans-retinyl esters –> 11-cis-retinol (via RPE65)
  5. 11-cis-retinol –> 11-cis-retinal (via RDH5/10/11)
29
Q

If proteins or enzymes in a retinal cell are not built or functioning, what will be the outcome?

A

results in congenital blindness in kids if RPE65 missing