module 9 Flashcards

1
Q

what are the membrane functions?

A

-separate cells from external environment: create unique intracellular environment
-allow selective transport of substrates in and out of cell
-provide location for specialized pathways and processes
-rapid changes in electric potential across the membranes of neurons
-localization of receptors to facilitate response to physiological signals
-mediate cell-to-cell recognition and interaction

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2
Q

membranes are: (membrane characteristics)

A

-sheet-like structures, two molecules thick, between compartments
-consist mainly of lipid and proteins, with carbohydrates linked to them
-build from amphipathic molecules
-impermeable to polar molecules (pretty much all biomolecules)
-self-assembling, non-covalent structures
-fluid and dynamic structures
-highly specialized in their composition and distribution (assymetric; outer and inner face)

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3
Q

specific membrane proteins mediate ______________

A

particular biological functions

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4
Q

what is the basic structural element of membranes?

A

LIPID BILAYER
-membrane formation is from amphipathic nature of the membrane lipid
-self-assemble through the hydrophobic effect

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5
Q

what causes membranes to have different structures?

A

the structure formed depends on the ratio of cross-sectional areas of the polar head group and the hydrophobic tai
-fatty acids favor micelle formation
-lipids with two hydrocarbons tails (glycerophospholipids and sphingolipids) tend to form bilayers

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6
Q

how do lipid bilayers form membrane vesicles?

A

-exposure of hydrophobic tails at the edge of the bilayer to water is energetically unfavorable
-flat bilayer sheets are unstable and spontaneously form membrane vesicles with an internal volume
-these vesicles are the basic of cells and organelles

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7
Q

what are membranes permable to?

A

-bilayers have a very low permeability to ions and most polar molecules
-permeability of small molecules is correlated with their relative solubility in water
-some small non-polar gases (O2 and CO2) and small hydrophobic molecules (like the fat soluble hormones) can pass directly through the membrane
-NOT WATER, use aquaporin

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8
Q

what are vesicles for drug delivery?

A

-cell membrane can represent a critical barrier for polar drugs intended for intracellular targets
-encapsulation of a drug within a liposome can facilitate transport across the membrane
-liposomes can also be used to target specific cells or organelles

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9
Q

why are ratios different from membrane to membrane?

A

-membranes are primarily composed of lipids and proteins
-more active membranes have a higher ration of protein to lipid
-composition of membrane components can be dynamic, in particular for prokaryotes

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10
Q

what is the fluid mosaic model?

A

SHOW FREEDOM OF LATERAL DIFFSUSION
-membranes are dynamic structures due to the nature of the non-covalent interactions
-lipids and proteins freely diffuse in the plane of the membrane
-lateral movement of proteins and lipids within the membrane is very rapid
-movement across the membrane is restricted

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11
Q

is the composition of the inner and outer sheets the same?

A

-lipid composition of the inner and outer sheets of the bilayer can be different, allowing for specialization of the membrane faces

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12
Q

transbilayer movement requires ________

A

CATALYSIS

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13
Q

how does transbilayer movement happen?

A

-requires a polar head group to pass through hydrophobic environment
-uncatalyzed rate of lipid molecule crossing from one sheet to the other (flip-flop diffusion) is very slow
-translocation of lipids from one side of bilayer to the other is catalyzed by enzymes called flippases

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14
Q

what is membrane fluidity? what are examples of composition

A

-cells need to maintain appropriate levels of membrane fluidity

cells can adjust membrane composition to maintain liquid-ordered state
-bacteria vary the length and saturation of the hydrocarbon tails of membrane lipids
-animals use cholesterol to mediate membrane fluidity

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15
Q

what are the phase transitions of membrane fluidity?

A

membranes undergo temperature-dependent phase transitions
-below the phase trans temp, membrane is too solid
-above the phase trans temp, membrane is too fluid
-at the phase trans temp, the hydrocarbon chains are partially ordered but lateral diffusion still possible (just right)

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16
Q

what is the table of examples of temperature-dependent changes to membrane composition

A
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17
Q

what is the specialization of membrane structure and function ?

A

-composition of membrane components: lipids and proteins
-distribution of membrane components: static and dynamic
-specialized membrane regions: lipid rafts

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18
Q

what are the specialized compositions of distribution of lipids in membranes?

A

-varies across species and cell types
-this include dynamic changes to composition and/or positioning to regulate biological events
-for example, the movement of phosphatidylserine to outer leaf functions in initiating cell destruction (apoptosis) (kills itself)

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19
Q

what do lipid rafts arise from?

A

-the spontaneous association of lipid molecules whose hydrocarbon tails are of similar length

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20
Q

what is an example of something that creates lipid rafts?

A

-sphingolipids (with longer tails) form clusters that exclude glycerophospholipids
-the longer, saturated hydrocarbons of sphingolipids form stable associations making the rafts thicker and more ordered than the rest of the membrane

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21
Q

what are lipid rafts?

A

-rafts are docking points in lipid-anchored proteins that contain long-chain saturated fatty acid anchors
-the lipid-linked proteins that associate with rafts often serve signaling functions

22
Q

active roles of membranes often performed by __________

A

PROTEINS
-receptors and transporters

23
Q

what are the three categories of membrane proteins? how are they defined?

A

defined based on different mechanisms of association with the membrane
-peripheral (c and d)
-lipid anchored (e)
-integral membrane proteins (a and b)

24
Q

what are peripheral membrane proteins?

A

-associate with membrane through electrostatic or hydrogen-bonding interactions (easy to get off)
-can dock to either membrane lipids or integral proteins
-the bulk is in the cytosol or extracellular space
-changes in pH or ionic strength often release these proteins from the membrane

25
Q

what are lipid-anchored membrane proteins?

A

-covalently attached lipids can anchor proteins to the membrane
-these protein modifications are sometimes reversible, allowing for regulation of cellular location
-GPI anchored proteins always at outer layer
-proteins with single chain hydrocarbons always to inner face

-diff fatty acid attach to diff part of the membrane (amino aicd)

26
Q

what are integral membrane proteins?

A

-immersed in, and usually span, the membrane
-protein positioning withing a membrane is specific and directional
-tend to be of three varieties: single pass a-helical, a-helical bundles (7), and B-barrels

27
Q

what is the distribution of amino acids in integral membrane proteins?

A

-blue=charged residues, mostly within the intra and extracellular portions of the protein
-white= residues with non-polar side chains, dominate inside the hydrophobic slab of the bilayer
-red=tryptophan
-orange=tyrosine
cluster at the interface between the hydrocarbon chain and polar head group region

28
Q

how can we predict membrane spanning regions of integral proteins?

A

-predicted from the amino acid sequence
-stretch of 20 hydrophobic residues in a row are likely membrane spanning
-a hydropathy index look at the hydrophobic characteristics of a protein to predict transmembrane regions

-magnificent 7

29
Q

what is hydrogen bonding within membrane-spanning regions?

A

-side chains within the transmembrane region tend to be non-polar, however the carbonyl and amid groups of each peptide bond are polar
-polar unpaired carbonyl and amide groups in the bilayer core are energetically unfavorable
-carbonyl and amide groups of the proteins backbone within the bilayer have to be hydrogen-bonded

30
Q

what is the big graph of transport across membranes?

A
31
Q

what is the table of transport across membranes?

A
32
Q

what is simple diffusion?

A

-non-polar gases (O2 and CO2) and hydrophobic molecules can directly cross the membrane
-their direction and rate of movement is determined by their concentrations on either side of the membrane
-can only result in the net movement down a concentration gradient

33
Q

what is facilitated diffusion?

A

-membrane transporters lower the activation energy barrier of crossing the bilayer
-activation energy for removing the hydration shell from a polar solute and transferring it into the non-polar environment in the core of the bilayer is very high
-membrane transporters lower the activations energy for crossing the membrane by replacing the hydration shell with interactions with polar groups along the transfer path in the protein interior

34
Q

what are channels?

A

-membrane pores to transport molecules down concentration gradient
-high conductance rates because they bind the substrate very weakly
-do not saturate

35
Q

what are carriers?

A

-membrane proteins that undergo substrate-induced conformational change, or membrane positioning, to release substrate to the other side of the membrane
-slower because they bind the substrate quite strongly
-can saturate

36
Q

what is glucose permease of erythrocytes (red blood cells)?

A

facilitated diffusion through a carrier
-facilitated diffusion of glucose at 50,000X faster than simple diffusion
-specific for D-glucose
-the rate of uptake follows a pattern resembling M-M kinetics
-Kt about 1/3 the concentration of blood glucose so the transporter is nearly saturated and operates near V-max (75% of max capacity)

37
Q

how is co-transport used in diffusion and secondary active?

A

-in diffusion, co-transport through antiport or symport depends on the charge of the molecules in order to have a net neutral change
-in secondary active co-transport, system couples a molecule moving down its gradient to one moving up its gradient

38
Q

what is coupled transport?

A

-uniport=transport of a single molecules
-antiporters= move molecules in different directions
-symporters=move molecules in same direction

39
Q

what is active transport?

A

-input of energy allows movement of molecules against concentration gradients
-primary active and secondary active

40
Q

what is primary active transport?

A

-driven by direct source of energy (ATP)
-includes P-type, V-type and ABC transporters

41
Q

what is secondary active transport?

A

-couples the movement of one molecules up its conc gradient within the movement of another molecule down its gradient

42
Q

what is V-type ATPases?

A

vacuoles
-use the energy of ATP to move protons against a concentration gradient
-acidification of organelles
-in chloroplasts and mitochondria, F-type ATP synthases reverse this reaction to use proton gradient to generate ATP

43
Q

what are ABC transports?

A

-contain ATP-binding domains (ATP-Binding-Cassette)
-transport a variety of biomolecules out of the cell against a concentration gradient
-multi-drug resistance protein pumps drugs (chemotherapeutic) out of the cell, rendering the drugs ineffective
-detoxifying system

44
Q

what is P-type ATPase?

A

-Na, K ATPase uses the energy of ATP hydrolysis to pump three Na out of the cell and two K into the cell
-called a P-type transporter as it undergoes a phosphorylated intermediate

45
Q

what is Na and K in the cell?

A

-cells maintain high gradients of Na outside the cell and K inside the cell
-this gradient controls cell volume, electrical excitability, and enables uptake of nutrients through secondary active transport systems
-maintaining the activity of Na K pump requires about a third of your energy

46
Q

what is an example of secondary active transport?

A

-glucose uptake into intestinal epithelial cells

47
Q

what is glucose uptake into intestinal epithelial cells?

A

-in intestinal epithelial cells, glucose uptake from the gut is driven through symport with Na
-the movement of glucose up its concentration gradient is enabled by the movement of Na ions down their concentration
-active transport of glucose from the gut depends on the action of the Na K ATPase to establish the gradient of Na ions

48
Q

what are ion channels?

A

-enable rapid movement of ions across the membrane
-actions of ion channels can cause changes in membrane potential (action potentials) in neurons
-tightly regulated; voltage-gated channels and ligand-gated channels
-are highly selective for the molecule to be transported

49
Q

ion channels differ from ion transporters (like Na, K ATPase) in three ways:

A

-faster
-no saturation limits
-gated/regulated (open and close in response to signal)

50
Q

what is the specificity of ion channels (K channel)?

A

-K channels allows rapid movement of K ions out of cells
-although Na is smaller, the channel is 100-fold more permeable to K
-selectivity filter discriminates K and Na based on their ability to shed water molecules to form electrostatic interactions within backbone carbonyls

51
Q

what is the speed of ion channels (K channel)?

A

-selectivity filter has four equivalent binding sites for K
-as K ions enter the filter, the electrostatic repulsion from other incoming K ions helps to push the flow of ions from inside to outside of the cell