11.3 Solute Transport Across Membranes Flashcards

1
Q

summary of transport types

A

-nonpolar compounds can dissolve in the lipid bilayer and cross a membrane unassisted
-polar compounds and ions require a specific membrane protein carrier

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2
Q

simple diffusion

A

movement of a solute from the region of higher concentration to the region of lower concentration

chemical gradient

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3
Q

membrane potential
Vm

A

a transmembrane electrical gradient that occurs when ions of opposite charge are separated by a permeable membrane

produces a force that:
-opposes ion movements that increase Vm
-drives movements that reduce Vm

electrical gradient

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4
Q

electrochemical gradient (electrochemical potential)

A

determines the direction in which a charged solute moves across a membrane

composed of:
-the chemical gradient
-the electrical gradient (Vm)

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5
Q

passive transporters

A

facilitate movement down a concentration gradient, increasing the transport rate

process is called passive transport or facilitated diffusion

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6
Q

active transporters

A

move substrates across a membrane against a concentration gradient or an electrical potential

process is called active transport

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7
Q

primary active transporters

A

use energy provided DIRECTLY by a chemical reaction

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8
Q

secondary active transporters

A

couple uphill transporter of one substrate with downhilll transport of another

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9
Q

transporter proteins reduce the ________ for diffusion by:

A

energy of activation by:
1. forming noncovalent interactions with the dehydrated solute
2. providing a hydrophilic transmembrane pathway

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10
Q

ion channels

A

provide an aqueous path across the membrane through which inorganic ions can diffuse at very high rates
-most have a “gate” regulated by a biological signal
-typically show some specificity for an ion
-are not saturable with their ion substrate
-flow stops either when the gate is closed or when there is no longer an electrochemical gradient

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11
Q

differences between ion channels and transporters

A

ion channels: single gate while a transporter (pump) ha alternating gates

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12
Q

the glucose transporter of erythrocytes mediates

A

passive transport

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13
Q

describe glucose transporter mechanism

A

enters the erythrocyte by passive transport via GLUT1

analogous with an enzymatic reaction where:
-glucose (“substrate”) outside is Sout
-glucose (“product”) inside in Sin
-transporter (“enzyme”) is T

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14
Q

GLUT1

A

integral membrane protein with 12 hydrophobic segments that form 12 membrane-spanning helices
-helices are amphipathic (residues are nonpolar on one side and polar on the other side)

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15
Q

the model of glucose transport into erythrocytes cycles between two extreme conformations:

A

T1 form
T2 form

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16
Q

T1 form

A

glucose-binding site exposed on the outer membrane surface

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17
Q

T2 form

A

glucose-binding site exposed on the inner surface

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18
Q

transport of glucose into a myocyte by GLUT4 is regulated by

A

insulin

know pathway

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19
Q

chloride-bicarbonate exchanger

A

anion exchanger essential in CO2 transport to the lungs from tissues

-passive transport system
-electroneutral exchange= no net transfer of charge

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20
Q

cotransport systems

A

simultaneously transport two solutes across a membrane
1. antiport
2. symport

21
Q

antiport

A

moves in opposite directions

22
Q

symport

A

moves in the same direction

23
Q

uniport systems

A

carry only one substrate

24
Q

active transport results in

A

the accumulation of a solute above the equilibrium point

thermodynamically unfavorable (endergonic)
-must be directly or indirectly coupled to an exergonic process

25
Q

primary active transport

A

solute accumulation is coupled directly to an exergonic chemical reaction

26
Q

secondary active transport

A

endergonic transport of one solute is coupled to the exergonic flow of a different solute that was originally pumped uphill by primary active transport

27
Q

free-energy change for transport of an uncharged solute

A

no bonds are broken and delta G is zero

28
Q

free-energy change for transport of an ion

A

without movement of an accompanying counterion, the process is electrogenic (produces an electrical potential)

29
Q

P-type ATPases

A

family of cation transporters that are reversibly phosphorylated by ATP as part of the transport cycle
-integral proteins with 8 or 10 predicted membrane-spanning regions
-sensitive to inhibition by the transition-state analog vanadate

30
Q

examples of P-Type ATPases include

A

Na+K+ATPase= animal cell antiporter for Na+ and K+
H+ATPase= plant and fungi transporter
SERCA pump

31
Q

SERCA pump

A

sarcoplasmic/ endoplasmic reticulum Ca2+ ATPase pump

uniporter for calcium ions

32
Q

general structure of the P-type ATPases

A

critical Asp residue in the P domain undergoes phosphorylation and dephosphorylation

33
Q

postulated mechanism of the SERCA pump

A

each catalytic cycle moves two calcium ions across the membrane and converts an ATP to ADP and Pi

two conformations of the transporter, E1 an E2 interconvert

34
Q

Na+K+ATPase

A

couples phosphorylation-dephosphorylation of the critical Asp resiue to the movement of Na+ and K+ against their electrochemical gradients
-maintains low sodium concentration and high potassium concentration in the cell
-essential to the conduction of action potentials in neurons

35
Q

V-Type and F-Type ATPases are

A

ATP-Driven proton pumps

36
Q

V-type ATPases

A

class of proton-transporting ATPases responsible for acidifying intracellular compartments
-V0 domain serves as a proton channel
-V1 domain contains the ATP-binding site and the ATPase activity

37
Q

F-Type ATPases

A

catalyze the uphill transmembrane passage of protons, driven by ATP hydrolysis

-F0 integral membrane protein complex provides a pathway for protons
-F1 protein uses energy of ATP to drive proteins uphill

38
Q

F-Type ATPases catalyze reactions in

A

both direction

a large proton gradient can supply the energy to drive ATP synthesis

when functioning in this direction, F-type ATPases are named ATP synthases

39
Q

ABC transporters

A

family of ATP-driven transporters that pump substrates across a membrane against a concentration gradient

they have 2 ATP-binding domains (“cassettes”) and two transmembrane domains

example substrates: amino acids, peptides, proteins, metal ions, various lipids, bile salts, and hydrophobic compounds including drugs

40
Q

mechanism of ABC transporters

A

substrates move across the membrane when two forms of the transporter intercovert
-driven by ATP hydrolysis

41
Q

ion gradients provide the energy for

A

secondary active transport

42
Q

Na+-glucose symporter

A

takes up glucose from the intestine in a process driven by the downhill flow of Na+

strong thermodynamic tendency for Na+ to move into the cell provides the energy needed for the transport of glucose into the cell

43
Q

ionophores

A

“ion bearers”
compounds that shuttle ions across membranes in this way

acts as a shuttle, carrying K= across the membrane down its concentration gradient and deflating that gradient

44
Q

aquaporins (AQPs)

A

provide channels for movement of water molecules across plasma membranes
-each protein has a specific location and role
-low activation energy suggests that water moves in a continuous stream
-do not allow passage of protons (hydronium ions)

45
Q

ion-selective channels

A

move inorganic ions across membranes
-the rate of flux can be orders of magnitude greater than the turnover number for a transporter
-not saturable
-gated in response to cellular event

46
Q

ligand-gated channels

A

binding of an extracellular or intracellular small molecules forces an allosteric transition in the protein, which opens or closes the channel
-generally oligomeric

47
Q

voltage-gated ion channels

A

a change in transmembrane electrical potential (Vm) causes a charged protein domain to move relative to the membrane, opening or closing the channel

48
Q

patch-clamping

A

currents are measured through a region of the membrane surface containing only one or a few ion-channel molecules