Fluid Mosaic Model of Cell Membranes Flashcards

1
Q

Membrane Functions

A
  • Site of biochem functions e.g. ETC in respiration
  • A permeable barrier, allowing certain molecules in
  • Organisation + localisation in the cell
    -Transport in/out of cell through proteins that regulate movement of substances
  • Detect + transmit chemical + electrical signals with proteins acting as receptors
  • Cell adhesion
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2
Q

The Fluid Mosaic Model for Membrane Structure - Brief Summary

A

By Singer and Nicolson (1973)

  • some proteins are embedded into the membrane so has an irregular structure
  • is very fluid
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3
Q

How did Ernst Overton conclude cells have a selectively permeable barrier?

A
  • Discovered that lipid-soluble substances crossed easily while water-soluble substances didn’t

=> Concluded that lipids were present in the barrier

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4
Q

How did Katharine Blodgett and Irving Langmuir discovered lipids are hydro -phobic/ -philic

A

1910s/1920s
- Added clean water to a trough
- Then added lipids, forming a layer on top with fatty acid tails orienting away from water

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5
Q

What did Gorter and Grendel do to discover membranes are bilayers?

A
  • Used red blood cells as they only have plasmid membrane
  • Mixed them with benzene to extract lipids, added then to trough so solvent evaporates
  • Area occupied were used to find surface area of cell

=> was double surface area of RBCs

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6
Q

Errors in Gorter and Grendel’s Methods

A
  • Assummed solvent would extract all lipids - was only 2/3
  • Ended up underestimating surface area

Bilayer organization confirmed by electron microscopy in the 1950s

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7
Q

Problems with the idea of a biological membrane being a simple lipid bilayer

A
  • Surface tension, electrical resistance, and solute permeability were different from a lipid bilayer
  • Couldn’t explain how selective a cell is e.g galactose can’t enter but glucose cant
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8
Q

Model for membrane structure proposed by Hugh Davson and James Danielli (1935)

A
  • Due to emerging concept (at the time) of enzyme-substrate specificity
  • Theoretical model of a bilayer of lipids coated in protein (‘Sandwich Model’)
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9
Q

Fluid Mosaic Model of Membrane Structure - In detail

A
  • Membranes containing lipids and proteins
  • Phospholipids form a bilayer due to their amphipathic nature
  • Phospholipids move freely causing membrane fluidity
  • Some proteins move, some are restricted
  • Proteins aren’t uniformly distributed (not an even coating)
  • Membranes are asymmetrical + selectively permeable
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10
Q

Membrane Topology (they have 2 sides)

A

Exoplasmic side faces the surrounding
Cytoplasmic side faces inside the cell

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11
Q

Membrane lipids

A

Predominant lipids are phospholipids (have glyceride backbone)
e.g. phosphatidylcholine, phosphatidylserine, phosphatidyletanolamine

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12
Q

Typical membrane phospholipid structure

A
  • Hydrophilic head: phosphate, glycerol + e.g. choline
  • Hydrophobic (fatty acid) tails: hydrocarbon tails (2)

Are amphipathic molecules - drives formation of lipid bilayers

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13
Q

Hydrophobic forces

A

Water forces hydrophobic groups together to minimise their disruptive effects on the hydrogen-bonded network

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14
Q

Formation of sealed spherical compartment

A
  • It is energetically unfavourable to have a planar phospholipid bilayer
  • The aqueous environment in and out is sealed by the bilayer => energetically favourable
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15
Q

Vanderwaals Forces in Membranes

A
  • At a short distance, 2 atoms show weak bonding interaction due to fluctuating electrical charge
  • If too close together, they repel each other

Individually, interactions are very weak but can form strong forces when macromolecules come close together

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16
Q

Membrane Asymmetry

A

Differs based on what side of membrane
Biological membranes are asymmetrical with respect to phospholipids

  • Exoplasmic: phosphatidylcholine (PC) and sphingomyelin (SM)
  • Cytosolic: phosphatidylserine (PS) and phosphatidylethanolamine (PE)
  • Asymmetry is established and maintained by scramblases and flippases
17
Q

Lipid bilayer synthesis: the role of Scramblases

A
  • New phospholipids are only added to cytosolic side
  • Transfers them from one side of bilayer to another to ensure equal growth of membrane
  • Not specific to certain phospholipids
18
Q

Lipid bilayer synthesis: the role of Flippases

A

Are head-group specific phospholipid translocators to transfer PS + PE from exoplasmic side to cytosolic side

  • Operate continuously to counteract scramblases in plasma membrane - ensure 2 sides of bilayer are balanced
19
Q

Cholesterol

A

Are abundant in eukaryotic cells - stabilises bilayer and thus regulates membrane fluidity

Structure
- Hydrophilic polar head group
- Rigid planar steroid ring structure
- Non-polar hydrocarbon tail