Transporters Flashcards

1
Q

How have gene families of transporters evolved?

A

There are 1289 genes for transporters and channels, together termed the TRANSPORTOME (4%of genome) with 406 ion;883 transporters

These are organized into super families such as the solute carrier family (SLC)

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2
Q

What is the Michaelis-Menten equation

A

describes SATURABLE TRANSPORT.

V= Vmax x [S]/Km + [S]

[S] of the CIS face

At V max; all the binding sites are occupied.

At Km (the constant) 50% of all sites occupied.

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3
Q

How do Km and V max provide information about the transporters function?

A

Facilitate transport is more rapid than simple diffusion, BUT it is SATURABLE (at Vmax)

At low substrate concentration, lower than the Km value volume of solute taken up is proportional to solute concentration.

Where he solute concentration is greater the the Km value, volume will EQUAL VMAX

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4
Q

Competitive effects on the transporter

A

INCREASES Km; as graph is initially more steep;

NO Change in V max (as it levels off at same level as control)

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5
Q

Non-competitive effects on the transporter

A

DECREASES v max (as it levels off below the maximium volume of the control)

NO CHANGE in Km

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6
Q

Describe different channel types in the membrane

A

Diffusion, facilitative Cell membranes have LOW diffusional permeability to many vital biological solutes including inorganic ions, sugars and amino acids. via different types of channels:

TRANSPORTERS (carriers/permeases/pumps)

water filled (aqueous diffusion)

facilitative

active transport (ATP dependent)

COUPLED transport (exchange)

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7
Q

How can the flux equation J1-2 = D.A.(change in c)/x

be used to increase solute movement across the membrane?

A

INCREASE Area (microvilli, alveoli)

DECREASE x Thickness (membrane already thin!)

INCREASE CHANGE IN CONCENTRATION (cell metabolism helps generate gradients)

INCREASE D (alter bilayer composition OR introduce “pores”)

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8
Q

Give some characteristics of pores

A

1) specific for certain substrates
2) saturable
3) specific inhibitors too
4) mediates the FLUX of a solute

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9
Q

How doe the rate of an ion channel compare to the transporter?

A

ion channel is MORE rapid (10-8 ions/s) and transporters 10-4/s.

This is due to greater specificity of the ion channel

ATP pumps even slower.

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10
Q

Give an example of a voltage gated ion channel?

A

Voltage-gated K+ channel when activated to OPEN allows for FAST/High flux of selected K+ IONS (singlefile)

ions are hydrated when selected and as a result the radius swells and increases.

Selectivity determined by the ions CHARGE AND SHAPE

channels can change shape or be gated,

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11
Q

What is the realtionship between ion diameter and mobility?

A

The larger ions are less mobile.

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12
Q

Why do smaller ions increase more when hydrated?

A

The smaller the ion radius means there is greater ion charge and so the greater the lattice enthalpy i.e. more exothermic. This effectively means the ions are closer together, so the centres of charge are closer together, hence a greater attractive force and more water molecules are attracted

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13
Q

Where is the CIS and TRANS interfaces in terms of ion transport?

A

CIS face is the side the ION is delivered

TRANS side, on the opposite face.

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14
Q

Describe symport/antiport transport (transporters)

A

When activated through substrate binding, there is a SLOW AND SMALL solute flux.

Selectivity determined by solute and BINDING-site on carrier protein.

It is slow because the transported has to REORIENTATE which is rate limiting.

Thus the reason (ion) channels are faster than transporters.

However, the antiport is faster than uniport)

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15
Q

Give details of the characteristic properties of uniport substrate binding site on the CIS and TRANS faces?

A

Cis-effects:

Saturability:- substrate molecules COMPETE for transporter binding-sites.

Stereospecificity:- Certain stereoisomers are BETTER FIT to binding site; very high affinities (like glucose) always taken in.

Trans-effects:
Exchange diffusion:- trans-substrate accelerates exchange

Counter transport:- trans-acceleration by a different substrate (hetero-exchange)

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16
Q

What happens if two solutes (X and Y) share the same affinity for a transporter?

A

X would compete against Y for binding sites.

The competition would decrease the overall rate of enzyme saturation (it would take longer for all the binding sites to fill)

As a result the solute concentration not bound remains high for longer, rate is less steep so Km increases (moves up x axis)

17
Q

In what way can binding be ordered in real cells? What are the the consequences of coupling (e.g. exchange) of substrate fluxes through a carrier?

A

Transports often require co-substrates such as Na+ which binds first then glucose.

This is shown by the L system and the A system involving tertiary transport.

1) ATPase pump transports 3NA+ out and 2K+ in;
2) Na+ transported back in WITH GLN (secondary symport system A)
2b) Na+ transported back in and A PROTON OUT (secondary antiport)
3) Gln transported out of cell, LEU transported IN (tertiary antiport system L)
3b) H+/proton back into cell WITH AMINO ACIDS (tertiary symport)

18
Q

What cell process does not involve any TRANS effects?

A

ENDOCYTOSIS; involves receptor binding of the membrane.