Lecture 2 Flashcards

1
Q

What is electrochemical gradient?

A

net flow of ions accross membrane.

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2
Q

What is the resting membrane potential in - mV? how potassium and Na reacting to that number?

A
  • The resting membrane potential is -70 mV which means neither potassium (-90 mV) or sodium (+65 mV) are at equilibrium.
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3
Q

What is a diffusive driving force?

A

generated by the concentration difference

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4
Q

What is an electrical driving force?

A

the force generated by a potential difference in an electrical field.

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5
Q

What governs the specific ion movements across PM?

A

-The driving force and number of open channels.

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6
Q

The chemical and electrical forces are complementary in the case of sodium because?

A

-Both the charge and concentration are higher extracellularly and lower inside the cell so it increases the potential of Na wanting to enter the cell.

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7
Q

The chemical and electrical forces are offset incompletely in the case of Potassium because?

A

-Potassium is in a high concentration inside the cell so the chemical forces wants to take it out but the electrical forces offset that because it needs K+ to stay inside the cell.

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8
Q

The chemical and electrical forces of Cl- are offset completely because?

A

The concentration of Cl- inside the cell is low so concentration wants more inside the cell but the cell is already negative so the electrical forces do not Cl- to go in. So the two forces offset each other.

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9
Q

What are the uses of the Nernst equation?

A

-If you have the concentration gradient of an ion then you can calculate the electrical gradient.

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10
Q

How is the driving force (Vm- Veq) is explained?

A

-The driving force is the difference between membrane potential and the equilibrium potential required. if the membrane potential for K+ is -90 and the cell resting potential is -70 then the difference is 20. 20 is the driving force and that is considered low driving force. On the other hand Sodium would have high driving force because its Veq = +60mV and since the Vm =-70 mV then the difference is 130 mV which is a large driving force.

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11
Q

What is conductance? What are the two meanings of conductance?

A
  • Opposite of resistance which means how easily the charges would go through.
  • Conductance can mean for one channel or for the whole cell.
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12
Q

What is a high conductance channel vs a low conductance channel?

A

High conductance channel will let more current through but low conductance channel will let less current through.

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13
Q

What is shunting inhibition?

A
  • Inhibitory Neurotransmitters such as GABA and glycine Open chloride channels but since the resting membrane potential is similar to the equilibrium potential of Cl- so
  • The opening of Cl- channels do not change the voltage of the cell but it “Shunts” responsiveness to Na+ channels.
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14
Q

What does the Goldman-Hodgkin-Katz equation explain?

A

-The permeability and equilibrium potential of each ion determines the membrane potential.

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15
Q

Which one is faster in terms of Ion movements channels or carriers?

A

-Channels.

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16
Q

What is gated diffusion?

A

-its dictated by voltage, ligand or mechanical force.

17
Q

What is selective diffusion?

A

Ions pass through channel based on size and charge.

18
Q

Whats the structure of the Na channel?

A

It has four domains and each has 6 Transmembrane segments that combine to form a barrel.
-It has an inactivation channel.

19
Q

Whats the structure of K channel?

A

Its made out of 6-TM peptide and its the combination of 4 of this peptide to form this channel.

  • The potassium channel 6 TM peptide has the S4 region which has lots of positive amino acids and its referred to as the voltage sensor.
  • S5 and S6 are known as the gate and between them, there is H5 which is the P loop and that determines which ion goes through.
20
Q

What is a Cyclic Nucleotide-gated channel?

A
  • They’re part of the 6 TM channel family and also has 4 domains. it is activated by cAMP or cGMP.
  • its involved in vision and olfaction
21
Q

What are TRP channels?

A

Also part of the 6 TM channel family and it varies in sensitivities from PH, Temperature, Menthol, Capsiacin and also involved in sweet, bitter and umami taste buds.

22
Q

What is an epithelial sodium channel? What is its structure?

A
  • It is always open and it detects salty taste. the sodium from NaCl that goes through help detect the taste.
  • These channels are also involved in salt excretion in the kidneys.

-Structure: made of 3 subunits (alpha, beta and gamma) and each subunit has 2 TM segment and a large Extracellular loop.

23
Q

What is the function of aquaporin? what is the structure and where is it prominent?

A
  • Water can diffuse through the PM but these channels facilitate the movement of water.
  • It also moves glycerol and urea but does not allow the passage of charged ions.

-The structure: 6 TM and 4 subunits and it’s also prominent in the kidneys.

24
Q

What are the ligand operated gates?

A

-They requiret the chemical binding of chemicals (mostly neurotransmitters) in ligand receptors.

25
Q

What are Ionotropic receptors? What excites these receptors and what inhibits them?

A
  • They bind ligand and rapidly activate the channel.
  • The channel itself is part of the receptor.

Excitation: Acetylcholine and Glutamate
Inhibition: GABA and glycine.

26
Q

What is a GPCR?

A

a G-Protein coupled receptor.

27
Q

What are the properties of GPCR? What are some examples?

A
  • it has 7 transmembrane proteins.
  • activates with a ligand but does not contain a channel.
  • It Activates a G-Protein within the cell and starts a 2nd messenger cascade.
  • Often regulates a channel and amplifies the response of a stimulus.

Examples:

  • Sweet, bitter, umami taste receptors
  • Neurotransmitter receptors
  • Rhodopsin (Photoreceptors)
  • Olfactory receptors.