Transporters and Channels Flashcards

1
Q

What are 5 transport ‘channels’ types ?

A
  • simple diffusion ( bilayer)
  • aqueus diffusion ( channels )
  • Facilitative transport ( may involve coupling of solute movements )
  • active transport ( energy dependent) / against concentration( may involve coupling of solute movements )
  • coupled transport -( eg exchange ) ( two solutes going opposite directions ) ( antiport !!!)

N.B. diffusion is independent of different molecules ( e.g. sodium and glucose )

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2
Q

Transmembrane solute fluxes : - what can increase solute movement across a membrane/ cell layer

A
  • increase in microvilli absorbance
  • decrease in membrane thickness ( membrane is already thin !)
  • increase in cell metabolism - helps generate gradients
  • increase in pores ….
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3
Q

What are two types of pores?

A
  • water filled channels

- facilitative transporters

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4
Q

cell membranes have …

A

low Diffusional permeability to many vital biological solutes including inorganic ions , sugars and amino acids.

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5
Q

What are some important charachteristics of pores? ( transporters /channels )

A
  • solute flux — predicted by passive diffusion ( avoids bilayer )
  • substrate specific ( e.g. amino acids )
  • transporters are saturable ( theoretiically - since diffusion is not saturable )
  • specific inhibitors / inactivators
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6
Q

what is the Transportome ?

A

it is the collection of all 1289 genes which are transporters and channels (406 ion channels / 883 transporters )
- it is 4% of human genome !

  • these genes are classified into structurally related super- families and families !!!!
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7
Q

how are ions moved ?

A

by an electrochemical gradient and concentration.

N.B. transporters(a.k.a carriers or permeases ) have much lower rate of transport than ion channels !!!

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8
Q

A Gated Channel

A

voltage gated K+ channel

  • various ligands open some gates
  • large / fast solute flux when open !!!
  • selectively related to size and charge of hydrated ion

e. g. Ca++ has bigger hyrdration in comparison to K+ and Na + since it has an increased charge !
- smaller ions have higher hydrated radius - since charge is higher in smaller ions !!!

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9
Q

3 basic transporter mechanisms ?

A
  • UNiport - one solute from one side to the other ( cis to trans direction- into cell )
  • symport - two different solutes in same direction
  • antiport - two different solutions in opposite directions ( quicker than Uniport !)
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10
Q

what are some charachteristics of a basic transporter mechanism ? and what is this also called ?

A
  • relatively small / slow solute flux
  • selectivity ( tighter than channels ) - related to molecular interactions between solute ‘substrate’ and binding site on carrier protein.

the alternative access model

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11
Q

differences between transporters and channels?

A
  • transporters - work with solutes on both sides !
    channels- dont care if any solute is on any side - solute independent!

transport mechanisms are reversible ! ( N.B. facilitative transport )

substrate - loaded transporters change conformation quicker

therefore antiporter is quicker than uniport, leading to trans-stimulation and counter - transport ( TRANSPORTERS ONLY ,NOT CHANNELS !!)

counter transport - only occurs iwhen heteroexchange occurs
trans-simulation - only occurs when homoexchange occurs.

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12
Q

there are two types of Antiport ?

A
  • Antiport- Homoexchange - two solutes of same type

- Antiport - heteroexchange - two different solutes in different directions !

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13
Q

Kinetic Characteristics of transporters ( using example of uniport )

A

(a) Cis - effects: -
- saturability :- substrate molecules ‘ compete ‘ for transporter binding sites
- stereospecificity - certain stereoisomers are better ‘ fit’ to binding site (e.g. D - sugars , L- amino acids ( biologically important forms )

(b) trans - effects
- exchange diffusion:- ( trans- substrate accelerates exchange)
- counter - transport :- trans-acceleration by a different substrate ( hetero- exchange )

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14
Q

Channels vs Transporters ( Quantity vs Specificity )

A

Channels :

  • selectively related to size and charge of hydrated ion
  • conformational change ? ( but may be gated !!)
  • diffusion - single file - through narrow point of channel ( saturable )

Transporters /Carriers:

  • selectively related to molecular interaction between solute ‘ substrate ‘ and binding site on carrier protein (‘recognition criteria’)
  • conformational change predicited
  • carriage requires ‘ adsortpotion’ of solute from bulk fluid phases
  • requirement for co-substrates in many cases
  • exhibit counter transport
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15
Q

What is the Michaelis - Menton ?

A
  • Saturable Transport -

enzyme activity related to substrate concentration

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16
Q

what is the michaelis menton equation?

A

v= vmax (S) /// km +(S)

v= velocity 
vmax= maximum velocity (mol/min) all binding sites occupied 
(S)= substrate concentration on CIS face of membrane (mol/l ) 
Km = michaelis constant (mol/l) - where 50% of sites occupied 

diffusion - shows linear line
transport - shows curve . which tails off.!

at low substrate concentration :

(S) < Km
V proportional to (S)
(v=Kx(S) )

At high substrate concentrations:

(S) > Km
V= Vmax

substrates show competitive inhibition with one another

( other molecules may exhibit non - competitive inhibition )

17
Q

Competitive vs non competitive competition ?

A

Competitive inhibitor :

  • increase of substrate Km
  • unchanged Vmax

non competitive inhibition :

  • decreased Vmax
  • unchanged Km
18
Q

in real cells….

A
  • multiple transport components
  • nature of dependence on any ‘co-substrate’ ( e.g. Na+ )
  • binding of multiple substrates may be ordered
  • diffusional components of flux
19
Q

there are three types of active transport ?

A
  • primary
  • secondary
  • tertiary

coupling of solute transporter fluxes to create specific directional flows through facilitative transporters

(e. g. amino acids - eg glutamine (Gln) - non essential -
e. g. leucine (leu) essential - needed within the cell.

20
Q

What is endocytosis?

A
  • may involved saturable receptor binding
  • transmembrane movement
  • no Trans - effects ( NO CIS and TRAN situation ! )