Introduction to cell membranes (2) Flashcards

Semester 1 year 1

1
Q

Why do red blood cells have a biconcave structure?

A

To increase their surface area for gas exchange

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2
Q

What do optical tweezers show?

A

Tensile strength of red blood cell membranes

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3
Q

What happens to red blood cells in hypertonic, isotonic and hypotonic solutions?

A

-hypertonic = water leaves cell + cell becomes crenelated (spiky)
-isotonic = no water moves + cell remains round
-hypotonic = water enters cell + cell eventually bursts

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4
Q

What are red blood cell ghosts?

A

Predominantly plasma membrane as the haemoglobin is washed away

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5
Q

Why do red blood cells have relatively simple protein compositions?

A

-they’re terminally differentiated cells
-protein composition is reflective of their function

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6
Q

What do mutations in spectrin cause?

A

Certain types of haemolytic anaemia

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7
Q

What do integral membrane proteins do?

A

-anchor cytoskeleton to plasma membrane
-provide structure to the cell
-allow it to change shape

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8
Q

What are key features of biological membranes?

A

-membranes are asymmetric
-proteins always have the same orientation in the membrane
-lipid composition of each of the 2 halves of the bilayer is different

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9
Q

What is the asymmetry of membranes important for?

A

-blood groups
-coagulation (clot formation)
-cell recognition + clearance

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10
Q

What blood groups can individuals have?

A

-O
-A
-B
-AB

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11
Q

What is blood group determined by?

A

Structure of oligosaccharides attached to sphingomyelin in the red blood cell membrane + to proteins in plasma + other body fluids

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12
Q

Which blood group is the universal donor and which is the universal acceptor?

A

-O = universal donor
-AB = universal acceptor

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13
Q

What is coagulation?

A

-clot formation
-phosphatidylserine on platelets + cell membrane provide nucleation site for coagulation

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14
Q

What do macrophage plasma membranes contain and where are they transferred to?

A

-contain receptors that recognise aminophospholipids
-transferred to outer leaflet of plasma membrane on apoptotic cells

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15
Q

What are liposomes?

A

Phospholipids form spherical structure in aqueous solution

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16
Q

What is passive transport?

A

-solutes move down a concentration gradient
-involves channels or carriers

17
Q

What is active transport?

A

-solutes move against a concentration so requires energy
-only carriers involved

18
Q

What can active transport be mediated by?

A

-coupled carrier
-ATP driven pump
-light driven pump

19
Q

What produces the ion concentration difference on either side of the membrane that results in an electrochemical gradient?

A

Produced through action of ion channels + carriers/pumps

20
Q

Do channels or carriers transport solutes more rapidly and why?

A

-channels
-carrier proteins directly bind to solute, whereas channels interact very weakly with solute

21
Q

How does passive transport by a carrier occur?

A

-solute binds to carrier in state A
-carrier converts into state B
-releases solute on other side of membrae

22
Q

What are the types of ion channel?

A

-voltage gated
-ligand gated with extracellular ligand
-ligand gated with intracellular ligand
-mechanically gated

23
Q

What are the types of carrier-mediated transport?

A

-uniport
-symport - cotransported ion on same side of transported mol.
-antiport - cotransported ion on opposite side of transported mol.

24
Q

What is the difference in what drives transport across mammalian plasma membrane and bacterial/yeast intracellular membranes?

A

-mammalian - driven by Na+ gradients
-bacteria/yeast - driven by H+ gradients

25
Q

Describe the transcellular transport of glucose

A

-moves against conc. grad.
-driven by glucose/Na+ symporter at apical surface - coupled uptake of glucose
-results in high Na+ conc. in cell that prevent symporter working
-Na+ moves out of cell into blood by Na+/K+ pump at basal surface
-high glucose conc. in cell - moves into blood using glucose carrier at basal surface