Membranes L3 Flashcards

1
Q

What drives transmembrane transport?

A

Dissipating a concentration gradient and increase entropy

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2
Q

How can you write out the Gibbs energy change

A

G = Go + RTln[X]i/[X]o

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3
Q

For uncharged species Keq= ?

A

1 because conc on both sides same at equilibrium

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4
Q

uncharged species Go=?

A

0

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5
Q

If conc inside is lower than conc outside of an uncharged species… (in terms of delta G)

A

delta G negative, spontaneous, exergonic transport occurs

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6
Q

What is a typical membrane potential for an animal cell?

A

-80mV

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7
Q

What is Gibbs change for CHARGED solute?

A

G = RTln[X]i/[X]o + zFEm

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8
Q

How can you predict the conc gradient that forms passively at Em?

A

Rearrange gibbs change for delta G =0

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9
Q

What is the full Nernst equation and the one at 20 degrees?

A
Em = RT/zF.ln[X]o/[X]i
Em = 58/z.log[X]o/[X]i
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10
Q

What is the lipid partition coefficient?

A

amount dissolving in test lipid/ amount dissolving in water

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11
Q

Draw permeability coefficient vs lipid partition coefficient

A

Straight line with urea then water as outliers above curve

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12
Q

What is Fick’s first law?

A

Rate of diffusion of small uncharged solute = permeability coefficient x conc gradient

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13
Q

How is lipid permeability of cells good?

A

In anearobic resp in fungi and plants ethanol leaves cell down conc gradient

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14
Q

What is bad about lipid permeability?

A

Renders cell vulnerable to pollutants from industrial activities

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15
Q

What characteristics do protein-mediated transport reactions show? (4)

A
  • Highly specific
  • Rate can be inhibited by structurally similar solutes
  • Rate higher than could be mediated by diffusion (proteins lower activation energy)
  • Shows saturation kinetics
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16
Q

Is protein-medicated transport intrinsically vectoral?

A

No, if conc gradient reversed transport direction reverses

17
Q

What is a typical carrier?

A

12 alpha-helices spanning membrane, especially useful for glucose and amino acid transport

18
Q

Draw “ping-pong” model

A

see notes

19
Q

Why do fungi and RBC phosphorylate glucose as soon as it reaches cytoplasm?

A

so it no longer fits binding site of carrier to prevent its release

20
Q

What is a typical channel and what is its speed of catalysis?

A

Usually 24 alpha helices, fastest enzymes known catalysing ~10^7 molecules per second, make small conformational changes

21
Q

What is patch clamp electrophysiology?

A

Glass microelectrode with 1 micrometer aperture blunt end is pushed against membrane, electrically isolating patch of membrane in electrode tip, tiny currents that form when ion chennel open can be measured

22
Q

What gets observed in patch clamp?

A

Channel openings observed on step increases of 1pA lasting less than 1 msec, represents passage of ~6000 ions

23
Q

Link in to ion channels…

A

Calcium signalling

24
Q

What are ionophores?

A

Bacterial peptides secreted to kill competing bacteria

25
Q

How does the ionophore valinomysin work?

A

see notes

26
Q

What are 3 modes of water transport?

A

via aquaporins, bulk flow, osmosis

27
Q

phi (overall water potential)=?

A

Solute potential (dissolving solutes reduces this) plus pressure potential (negative pressure reduces this) plus gravitational potential

28
Q

What are aquaporins?

A

can be regulated by phosphorylation to control water flow, made up of 4 subunits with many alpha-helices

29
Q

Why does ATP hydrolysis release energy for primary active transport?

A

At physiological pH, ATP can be extensively dissociated, as negative charges repel electrons in P=O bonds making O d- and P d+ therefore ATP holds energy to keep P atoms together, which gets released upon hydrolysis

30
Q

What does the end bit of ATP look like?

A

see notes