Week 1: transport across membranes Flashcards

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1
Q

Primary vs secondary active transport?

A

Both:

  • Transport molecules AGAINST conc. gradient
  • Often work together

1
- uses ATP hydrolysis directly to power transport (e.g. using carrier proteins).

2
- uses ion conc. gradient established by ATP hydrolysis as to use electrochemical gradient to counter conc. gradient.

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2
Q

What are the key types of movement across the cell membrane?

A

Passive: no energy needed

  • Osmosis
  • Diffusion
  • Facilitated transport

Active: uses energy

  • Primary active transport
  • Secondary active transport

Endo/exocytosis

  • Endocytosis
  • Pinocytosis
  • Receptor-mediated endocytosis

Signal transduction

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3
Q

What is pinocytosis?

A

Pinocytosis (“cellular drinking”) is a type of endocytosis that takes up fluids across the plasma membrane.
- Affects small molecules, non-specific

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4
Q

What are the main types of membrane proteins? What are they used for?

A
  • Transport proteins => Facilitated transport
  • Signalling proteins => signal transduction
  • Joining cells => intercellular joining
  • Enzymes => enzymatic activity (active site exposed to external substances
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5
Q

What are the two main types of transport protein involved in facilitated transport/diffusion

A

Transport proteins in facilitated diffusion/transport:
+ Carrier protein (changes conformationally)
+ Channel protein (provides gateways x membrane)

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5
Q

What are the two main types of transport protein involved in facilitated transport/diffusion

A

Transport proteins in facilitated diffusion/transport:
+ Carrier protein (changes conformationally)
+ Channel protein (provides gateways x membrane)

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6
Q

What are the characterisitics of bilayer permeability?

A

Lipid bilayer is variably permable depending on solute, which allows osmosis and diffusion.

  • MOST permeable to small hydrophobic (non-polar uncharged) molecules (e.g. O2, CO2, N2). Quite fast crossing allowed
  • LEAST permeable to larger or hydrophilic molecules; ions (regardless of size) or polar uncharged molecules. Either slow and relatively imperable or essentially impermeable.
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7
Q

Diffusion vs osmosis?

A

Both:

  • Passive (no energy needed)
  • Levels out extremes of gradient
  • Stop when equilibrium is reached
  • Fairly slow

Diffusion:
- Solutes move across membrane to area of lower conc.
- For molecules that CAN cross membrane
(small, non-polar)
- Occurs at level of specific solute type (e.g. conc. of Na+ doesn’t affect diffusion of K+)

Osmosis:

  • Solvent moves across membrane to area of higher conc.
  • For molecules that CAN’T cross membrane (large or polar)
  • Needs selectively/semi-permeable membrane so solute can’t cross + fluid can
  • Driven by TOTAL solute conc. so composition doesn’t matter (Na+ conc. and K+ BOTH affect change from osmosis).
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8
Q

Facilitated transport vs diffusion?

A

Diffusion is generally the movement of solute towards low conc. areas across the membrane. Diffusion often plays a role in facilitated diffusion.

Facilitated diffusion is when this happens using transport proteins specifically (e.g. diffusion but through channel protein. Same process but made faster). Facilitated transport can also mean using ATP in active transport. Facilitated transport acts on hydrophilic and large molecules that can’t simply cross the plasma membrane.

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9
Q

How do contractile vacuoles relate to osmosis?

A

Contractile vacuoles can control water levels in the cell which can trigger changes in overall cell water content as it has to increase or decrease to restore equilibrium relative to outside

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10
Q

Isotonic vs hypotonic vs hypertonic? Relative to outside.

A

Isotonic: solute conc. equivalent either side

Hypotonic outside: lower conc. outside (water wants to flood cell)

Hypertonic outside: higher conc. outside (water wants to leave cell, shrivelling it up)

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11
Q

How do cells regulate the conc. of larger or polar molecules?

A

Conc. of larger + polar molecules can’t be controlled through diffusion across membrane because the membrane is (relatively) impermable to them, so controlled by…

  • osmosis
  • Facilitated diffusion (can recognise specifics)
  • endo/exocytosis
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12
Q

What is a symport protein?

A

Symport proteins move two types of ion in the same direction. Can be useful in creating electrochemical gradient changes to power 2ndary active transport.

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13
Q

Example of 1 and 2 active transport working together?

A

Na+ and K+ pumped into cell against conc. gradient, (inside: high K+ low Na+, outside: low K+ and high Na+), maintaining +ve charge inside and -ve charge outside. This electrochemical gradient of + and - charge then drives 2 active transport of glucose against conc. gradient towards higher conc. inside

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14
Q

Example of 1 and 2 active transport working together?

A

Na+ and K+ pumped into cell against conc. gradient, (inside: high K+ low Na+, outside: low K+ and high Na+), maintaining +ve charge inside and -ve charge outside. This electrochemical gradient of + and - charge then drives 2 active transport of glucose against conc. gradient towards higher conc. inside

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15
Q

What type of molecules act as ID tags for cell-to-cell recognition?

A

Proteins act as ID tags in cell to cell recognition

16
Q

What sort of molecules are usually transported with exo/endocytosis?

A

Endo.exocytosis is often used for molecules that are too large or hydrophilic (polar or charged) to pass through membrane.

17
Q

Endo vs exocytosis?

A

Exo: exit from cell
Endo: entry into cell

For endo: part of plasma membrane pinches off to make endocytotic vesicle.

For exo, vesicles and lipids from trans golgi fuse to plasma membrane and are reabsorbed to release contents to outside world.

18
Q

What sort of molecules are used in pinocytosis (“cellular drinking”)?

A

Pinocytosis is a type of endocytosis used for small, non-specific molecules of fluid.

19
Q

How does receptor-mediated endocytosis work?

A

Endocytosis relies on specific proteins in membrane recognising and triggering uptake of specific materials and transporting with vesicles coated in receptors.