Lesson 1 - Transport Mechanisms Flashcards

1
Q

what is the cell membrane composed of and what molecules can diffuse readily

A
  • Cell membrane = composed of Phospholipid bilayer
  • Lipid-soluble molecules and gases diffuse through readily
  • Water-soluble molecules cannot cross without help
  • Impermeable to organic anions (proteins)

–> selective permeability

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2
Q

what does cell membrane permeability depend on? (3)

A

Permeability depends on molecular size, lipid solubility, and charge

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3
Q

explain simple diffusion

  • what molecules pass through?
  • what direction does it move in?
  • what is the rate of diffusion
  • what energy is needed, if any?
A
  • Small, lipid-soluble molecules and gases (e.g. O2, CO2, ethanol, urea etc…) pass either directly through the phospholipid bilayer or through pores
  • Movement of substance is down its [ ] gradient
  • The relative rate of diffusion is roughly proportional to the [ ] gradient across the membrane
  • Passive: No energy input required from ATP
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4
Q

explain facilitated diffusion

  • what is it?
  • what molecules pass through?
  • what direction does it move in?
  • what energy is required, if any?
A
  • Process of diffusion, where molecules diffuse across membrane, with the assistance of carrier protein
  • Carrier protein aid the movement of polar molecules (e.g. sugars and amino acids) across cell membrane
  • Movement of substance is down its [ ] gradient
  • The energy comes from the [ ] gradient of the solute
  • Passive: No energy input required from ATP
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5
Q

how do channel proteins work?

A
  • one gate is open
  • molecule enters
  • undergoes a conformational change
  • first gate closes and second opens to release the molecule
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6
Q

what is active transport?

  • what is it?
  • how does it work
  • what energy is needed and how is it acquired?
A
  • Active Transport is a mechanism to move selected molecules across cell
    membranes, against their [ ] gradient
  • Substance binds to protein carrier that changes conformation to move substance across membrane
  • Active Requires energy from ATP hydrolysis
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7
Q

what are ATPases and what is a famous example?

A
  • ATPases are a group of enzymes that catalyze the hydrolysis of a phosphate bond in adenosine triphosphate (ATP) to form adenosine diphosphate (ADP)
  • the sodium potassium pump is a famous example of how ATP is used to transport Na out and K in
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8
Q

what is secondary active transport?

  • what is it?
  • how does it work?
  • what does sequential binding do?
A
  • when a substance is transported up/against its concentration gradient without using ATP
  • it works by harnessing the kinetic energy that one substance generates from moving down its [ ] gradient to move its substance against the [ ] gradient
  • Sequential binding of a substance and ions to specific sites in the transporter protein induces a conformational change in the protein
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9
Q

what are channels?

  • what is it made of?
  • what does it look like in the membrane?
  • is it selective? if so how?
  • what are pores also called?
A
  • membrane spanning protein (around 4-5 protein subunits) creates a central pore for which specific ions can diffuse
  • These ‘Pore loops’ of the protein molecules dangle inside the channel
  • Physical properties of the pore loops create a selectivity filter
    –> Only specific molecules can diffuse through (by means of size and electric charge)
  • These ‘pores’ are called Membrane Channels
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10
Q

what are gated channels

  • what does the protein shape of gated channels mean for the diffusion of a substance?
  • what are the two types of gated channels that determine protein shape?
A
  • Membrane channels (these holes in the membrane) generally are not kept open
  • Channels can be closed off by a branch of the protein structure = ‘Gate’
  • gate closes = no diffusion, gate open = diffusion (remember that it is still selective)
  • The protein components switch between 2 shapes; one creates an open pore, the other blocks the pore
  • Factors determining channel protein shape (aka when it opens and when its closed):
    – ligand gates channels = binding of chemical agent
    – voltage gated channels = voltage across the membrane
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11
Q

ligand gates channels

  • what body system are cell membrane receptors part of?
  • what does the channel need in order to change shape?
A
  • Cell membrane receptors are part of the body’s chemical signaling system
  • The binding of a receptor with its ligand usually triggers events at the membrane, such as activation of an enzyme
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12
Q

voltage gated channels

  • explain membrane potential and what it usually is like in a cell?
  • how does voltage gated channels work depending on the membrane potential
  • what is the voltage sensing mechanisms on these gated channels?
A
  • all cells generate a membrane potential
  • usually the voltage inside the cell is negative and outside the cell is positive
  • Some membrane channels are sensitive to the potential difference across the membrane (e.g. depolarization) - polarized = gate is open, depolarized = back to natural position - closed
  • The voltage sensing mechanism is in the 4th transmembrane domain of the protein, the S4 segment. the S4 segment is what changes its shape
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13
Q

voltage gated channels - S4 segment

  • where is the s4 segment and what does it look like naturally and in a polarized cell?
  • what does the s4 segment look like in a depolarized cell?
A
  • S4 sticks out to the side of the protein (like a wing)

Naturally:
* The natural position of the S4 ‘wing’ is up towards the outer surface of the cell membrane.

Polarized:
- When the membrane is polarized, the positively charged wing is attracted downwards to the negatively charged inner surface of the membrane

Depolarized:
- when the membrane is depolarized (around -50 mV) (inside is more positive), inner region no longer provides sufficient electrical attraction to hold the S4 wing downwards, so it migrates back-up
* In the up position, S4 removes a structural occlusion from the pore (gate is open) such that ions can now diffuse through it (from inside of the cell to outside)

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14
Q

define endo/exocytosis generally

A
  • Endocytosis (outside to in): inward ‘pinching’ of membrane to create a vesicle; usually receptor- mediated to capture proteins, from outside to inside.
  • Exocytosis (inside to out): partial or complete fusion of vesicles with cell membrane for bulk trans-membrane transport of specific molecules, from inside to outside.
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15
Q

how many types of exocytosis are there?

A

two

exocytosis 1: the more rapid mechanism had been dubbed the ‘Kiss and Run’

exocytosis 2: full exocytosis

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16
Q

explain exocytosis 1 / kiss and run method

  • where does this occur specifically?
  • what is this method?
  • when is this method used?
A
  • The secretory vesicles dock and fuse with the plasma membrane at specific locations called ‘fusion pores’
  • Vesicle connects (kiss) and disconnects (run) several times
  • Since only part of the contents are emptied in one ‘Kiss’, the process can be repeated several times before the vesicle is depleted
  • This exocytosis is used for low rate of signaling
17
Q

explain exocytosis 2 / full exocytosis

  • what is it
  • how do proteins play a role
  • how is the action that proteins play become counterbalanced
  • when is this method used?
A
  • This involves complete fusion of the vesicle with the membrane, leading to total release of vesicle contents at once
  • sometimes the vesicle that will be performing exocytosis has proteins attached to it which will then fuse with the membrane
  • However, this must be counterbalanced by endocytosis to stabilize membrane surface area (so it doesn’t become too loose)
  • used for high levels of signaling
18
Q

what is membrane potential ?

what happens if the MP is 0 on the inside?

A
  • All cells in the body generate Membrane Potential (MP) (potential difference in a cell)
  • if the membrane potential is 0 inside the cell and not negative (-70 mV), it is likely to be dead
19
Q

what are the two conditions needed to create an Membrane potential?

A
  • To generate MP we need 2 conditions:
    1. A concentration gradient: created via an enzyme ion pump (functions as an ATPase) – this pump actively transports certain ion species across the membrane to create the concentration gradient
  1. Semi-permeable membrane: allows one ion species to diffuse across the membrane more than others
    * Diffusion of that ion species down its conc. gradient creates an electrical gradient
20
Q

Sodium potassium pumps (Na+/K+)

  • where are they found
  • what does it do
  • how much energy does it need in body vs neuronal cells
  • what value potential difference does it create?
A
  • all cells are loaded with Na+/K+ pumps – staple for all living cells
  • Na+/K+ dependent ATPase is enzyme that moves 3 Na+ out of cell, and 2 K+ into cell for each ATP molecule that is broken down (concentration gradient)
  • takes energy to do so (1/3 of energy needs in body cells and 2/3 of energy in neurons)
  • Na/K inequality –> potential difference of -10 mV (more neg on inside vs outside – extra cations on the outside)
21
Q

why is the resting membrane potential not -10 mV as indicated by the numerous Na+/K+ pumps everywhere?

A
  • the resting membrane potential is closer to -70 mV
  • this is due to the semi-permeable membrane of cells which contains K+ leakage channels along its membrane (at rest the membrane is permeable to K+ ions - not others)
  • these channels allow K+ to travel along its concent gradient (in to out - more to less) thus making the inside of the cell more negative (loosing positive charge)
22
Q

why doesn’t the membrane potential decrease forever

A
  • This efflux of K+ ions leaving the cell will occur until there is such a build up of “+” charge on the outside of the membrane that further diffusion of K+ is repelled by the electromagnetic force (more K+ cant leave because the positive charge around the membrane will repel the leaving ions, making it stay in) = i.e. we reach an equilibrium situation
23
Q

define what the equilibrium potential is

thus, what is membrane potential based on then?

what formula helps us calculate this?

A
  • when the electrical force of repulsion is equal in magnitude by the chemical force of diffusion down the [] gradient
  • in other words, at equilibrium, electrical work to repel outward cation diffusion equals chemical work of diffusion down conc. gradient
  • keep in mind these forces are equal in mag but opposite in direction
  • Membrane potential at equilibrium is determined by the concentration gradient - because without it there will be no movement of K+ ions in the first place
  • Can be calculated using the Nernst Equation
24
Q

what does the nernst equation describe

when is this only valid?

A
  • In the ideal situation, the Nernst equation, describes the balance between the chemical work of diffusion with electrical work of repulsion
  • The equation gives the potential difference across the membrane, inside with respect to outside, at equilibrium
  • The result is valid if and only if one ion species (ex. K+ in this case) is diffusing across the membrane (ideal situation)