6 Flashcards

(80 cards)

1
Q

what caused membrane formation

A

decrease in ionic interactions with water (hydrophobic effect). H-bonding between head groups and water, and van der waal’s for the tails

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2
Q

what can’t go through biological membranes

A

polar or charged molecules

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3
Q

what do membrane proteins do

A

move shit across and transmit signals

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4
Q

why do you need membrane fluidity

A

because you need to change protein conformation in order to signal and move stuff, therefore you need the membrane to move

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5
Q

what is membrane fluidity caused by

A

noncovalent bonds breaking and forming essentially. this is in turn from the lipids (such as cholesterol) in the membrane

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6
Q

fluid mosaic model proposed when and where

A

early 1970s by singer and nicolson

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7
Q

what makes a membrane fluid and mosaic

A

membrane components move rapidly. diverse mixture of lipids, embedded and peripheral proteins, carbohydrates on the surface

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8
Q

recent modifications to the lfuid mosaic model

A

movement of lipid and membrane proteins differ in pure lipid and biological membrane. in biological membranes there are more restrictions

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9
Q

FRAP

A

label cell surface molecules (lipid or protein) with fluorescent fluorophore. use high intensity laser to bleach it in a small part, measure the mobility of other molecules into affected region. so you get a curve

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10
Q

single molecule tracking fluorescence microscopy

A

antibody on a single molecule, and you see how fast it moves

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11
Q

what tends to trap proteins and lipids into interacting

A

lipid rafts

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12
Q

lateral diffusion of protein depends on what aside from lipid rafts

A

cytoskeleton (anchored on it) or extracellular components

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13
Q

what would SDS do on a FRAP experiment

A

denature the proteins. fluorescent proteins, lipids are now all in solution, and you ahve no results

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14
Q

what would a crosslinker do on a FRAP experiment

A

decrease fluidity while keeping cell intact, decreasing recovery of fluorescence (or completely remove recovery)

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15
Q

which side are sugars/oligosaccharides present on a double layered membrane

A

they are added on the exterior side onto lipids and proteins. this is because it is mediated by enzymes in the ER and golgi

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16
Q

why do you need sugars on lipids and proteins

A

membrane insertion and cell recognition

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17
Q

what is a type of post translational modification for membrane proteins

A

adding sugars

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18
Q

how fast is moving lipids from one leaflet to another, why

A

very slow. flip flop diffusion is slow because of the polar head group making it energetically unfavorable

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19
Q

flippase. what does it move, what does it need

A

a membrane protein that moves PE and PS from outer to inner leaflet. needs ATP

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20
Q

floppase. what does it move, what does it need

A

moves PC SM from cytosolic to outer leaflet, needs ATP

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21
Q

scramblase. what does it do, what does it need

A

does not need ATP. moves stuff down the concentration gradient, so reduces assymmetry

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22
Q

what are lipids. what do they do?

A

type of molecule that provides structural support for cells and organelles. stores carbons for energy, plays a role in info transduction and signalling.

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23
Q

solubility properties of lipids.

A

not soluable in water, very soluable in nonpolar solvents.

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24
Q

how does diversity affect lipids?

A

they can be hydrophobic or amphipathic, depending on the diverse chemical structures and functional groups.

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25
what are micelles made of
single tailed lipids. cam be inside out or normal (inside out has water inside)
26
monolayer vs bilayer. when does each form
bilayers have water on both side, monolayer only one side
27
unilammelar vescicle is also known as __. what is it
a liposome. it is a double layered circle thing
28
fatty acid numbering from the terminal methyl uses what symbol
omega
29
double bonds numbered from the carboxylic acid uses what symbol
the triangle
30
free fatty acids are
not bound to a headbone or backbone via ester bonds. known as FFAs
31
monosaturated fatty acid
1 double bond
32
polysaturated fatty acid (pufa)
more than 1 double bond
33
what would you call an 18 carbon chain with a double bond 9 carbons from the carboxylic acid
18:1 omega 9
34
which fatty acids are essential
omega 3 and omega 6
35
are omega 3 and 6 mono or polyunsaturated
poly
36
bad vs good fats
saturated (TAG triacylglyceride) and unsaturated trans are bad. unsaturated and cis are good
37
what decreases membrane fluidity
saturated fatty acids (closely packed), longer chains (van der waals)
38
what does lower membrane fluidity do to melting temperature
higher melting temperature. melting temperature is an index of membrane fluidity
39
what type of fatty acids have kinks
cis
40
why do cis kinks increase membrane fluidity
decreases van der waal's by making the bottom of the fatty acid no longer interact
41
how do membrane lipids melt
it goes from a gel-like solid phase to a liquid crystalling phase
42
what is the ideal temperature for a membrane lipid
slightly above melting temperature so you can have conformational changes
43
phase transitions for pure lipid samples and native membranes
pure lipid has sharp and well defined transition temperatures, native membranes have broad peaks
44
tri-acyl glycerol are used for what and where
efficient, unlimited energy reserve of reduced carbon chains (saturated to pack more). a dehydrated storage form of lipids in adipocyte cells used to store energy
45
structure of TAG
3 fatty acids bound to glycerol backbone through ester linkages. fatty acid tails contain double bonds creating mixed triglycerides
46
2 types of amphipathic lipids
glycerophospholipid and sphingolipids
47
most common steroid in membranes
cholesterol
48
glycophospholipid structure
2 fatty acid chains, phosphate and a head group (polar). the head group can be ethanol or serine. 3 carbon backbone
49
sphingolipid structure
a long fatty acid with a sphingosine group (amine that connects to the carbonyl carbon in the fatty acid). also has a 3 carbon backbone and a polar head group.
50
examples of sphingolipid
sphingomyelin and ganglioside (sugar head group)
51
cholesterol metabolism
cortisol, testosterone, bile salts
52
why do you need cholesterol
dietary lipid absorption, moderate membrane fluidity and signal transduction.
53
what does cholesterol form complexes with
sphingolipids, glycolipids, some lipid anchored proteins to form lipid rafts
54
cholesterol effects on membrane fluidity and melting temperature
decreases melting temperature by disrupting noncovalent bonds. modulates membrane fluidity
55
why are lipid compositions on membranes different
cells control synthesis of different kinds of membrane lipid and target them to certain organelles and leaflets.
56
peripheral membrane proteins adhere to what
surface of lipid membrane OR integral membrane proteins through noncovalent interactionsh
57
how to remove peripheral membrane proteins
increasing salt, changing pH (milder conditions)
58
integral membrane proteins location
span membrane with TMs
59
removing integral membrane proteins
harsh conditions (detergents that swap places with proteins to solublize or organic solvents)
60
will detergents remove peripheral proteins
yes of course
61
lipid anchored proteins removal
harsh detergents or solvents
62
issues with harsh detergents and solvents
may break protein structure
63
how are lipid anchored proteins kept in place
lipid chains covalently attached to amino acid functional groups and side chains
64
what is the fatty acid present and what atom is the fatty acid linked to for S-palmitoylation
palmito group is the fatty acid, linked to sulfur (cysteine bond)
65
where are GPI anchored proteins
outside of the cell because they are linked in the ER
66
how are GPI proteins kept in place
covalently linked through a sugar chain to a lipid anchor
67
what do you do after you get a mixture of integral and peripheral proteins
chromatography to separate the 2
68
how do detergents solublize membrane proteins
by creating miscelles around hydrophobic regions
69
physical properties of detergents
amphipathic molecules
70
CMC critical micelle concentration
how much is needed for detergent to spontaneously form stable micelle structure
71
why do you want to be above the CMC to solublize proteins
because then micelles can form
72
methods to deduce primary sequence
DNA sequencing, protein prediction algorithms
73
how many AAs for alpha helix TM
20
74
how wide is the membrane in angstroms
30
75
how wide is an amino acid in angstroms
1.5
76
how is the hydropathy index determined
average ktye-doolittle hydrophobicity values within a segment. move window one residue and redo. plot on central amino acid
77
what does window size do for hydropathy plot
smaller window is noisier, larger is smoother
78
how many amino acids must you average for the hydropathy plots
odd numbers so you can attribute to center AA
79
requirements for finding a TM in hydrophobic plot
above 0 (means hydrophobic), 20 AA wide and 1-1.5 tall.
80
do hydrophobic plots predict or confirm structure
predict