1.3 Membrane structure Flashcards

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1
Q

What is the difference between a triglyceride versus phospholipid?

A

Phospholipid: One fatty acid is replaced with a phosphate head

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2
Q

What is an Ester bond? What is it between?

A

It is condensation between 0H group on the glycerol molecule and on OH group on phosphoric acid

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3
Q

What can be different between a phospholipids two tails?

A

One is a saturated fatty acid and the other is unsaturated

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4
Q

Are individual phospholipids bonded to one another?

A

Individual phospholipids are not bonded to one another. It’s the hydrophobic and hydrophilic attractions that keep them together.

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5
Q

What do phospholipids form when submerged in water?

A

Phospholipids form micelles when submerged in water.

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6
Q

What does it look like when phospholipids are at an air-water interface?

A

An air-water interface, tail stick out of the water

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7
Q

Why do phospholipids form a bilayer in plasma membrane?

A

Due to the amphipathic properties (hydrophobic and hydrophilic) of the phospholipid, the tails repel water and will be attracted to other hydrophobic tails. This is the same for the hydrophilic phosphate heads. Since the tails will distance itself from water, it will position itself between the two phosphate heads. The heads on either side of the tails were for me bilayer.

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8
Q

Explain why the model for membrane structure is known as the fluid mosaic model?

A
  • It is fluid because the phospholipids and proteins are free to move around within the bilayer
  • It is Mosaic because proteins are distributed throughout the phospholipid in a mosaic pattern (different shapes and sizes)
  • It’s a model because it is a agreed structure based on experimental and chemical evidence
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9
Q

Why must plasma membranes be flexible? (2)

A
  • To allow membranes to change shape e.g. for exocytosis and endocytosis
  • Allows movement of organelles within cells e.g. vesicles fused with the Golgi apparatus
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10
Q

Why can phospholipid molecules in a bilayer only move within the plane of the bilayer?

A

Phosphate heads cannot pass through the hydrophobic tails in the center of the bilayer and vice versa

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11
Q

What did Davson and Dannielli propose of the membrane?

A

They proposed the ‘lipo-protein sandwich’ model that said there were layers of protein adjacent to the phospholipid bilayers, on both sides of the membrane.

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12
Q

What did Daveson and Dannielli mistake the micrograph for?

A

It was actually the plasma membranes of TWO adjacent cells

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13
Q

What proved the Davson-Danielli model wrong (3)?

A
  • Freeze-fracturing electron micrographs -> found globular structures scattered through the centre of membranes
  • Structure of membrane proteins -> Extracted the proteins and found they varied in size and globular shape
  • Flourescent antibody tagging -> fluorescent markers were attached to antibodies that bind to membrane proteins. Showed that membrane proteins are free to move within the membrane rather than fixed in a peripheral layer
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14
Q

What did the freeze-etched electron micrograph tell us about the Davson-Danielli model?

A
  • Daniel Branton used freeze fracturing to split cell membranes between the two lipid layers, revealing a 3D view of the surface texture. It suggests that the proteins are on the inside, not outside.
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15
Q

How did Davson-Danielli’s model suggest for proteins?

A
  • Structure of membrane proteins. Proteins were extracted from the membranes. Analysis shows the variation in shape and size of proteins – they were not uniform. Some of hydrophobic region suggesting they were embedded it within the bilayer.
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16
Q

What showed that proteins are free to move within the membrane?

A
  • Fluorescent antibody tagging. Florescent markers were attached to antibodies that bind to membrane proteins. Cell with different markers fused together and markers were mixed throughout the membrane. It showed that proteins are free to move within the membrane rather than being fixed within the peripheral layer (attached) of the phospholipids.
17
Q

What is the difference between the Davson-Danielli model and the Singer-Nicolson model?

A

Davson-Danielli model showed proteins form distinct layers (sandwhich)

Singer-Nicolson model showed proteins embedded within bilayer (fluid-mosaic)

18
Q

What are the two groups in which the position of proteins can be divided into?

A

Peripheral and intergral proteins

19
Q

What are peripheral proteins?

Where are they? What anchors it to the membrane surface?

A

Peripheral (extrinsic proteins): outside, are embedded in one side of the bilayer - either in the outside or the cytosolic side (inside).

They have hydrophilic amino acids on the outer surfaces and interact with heads of the phospholiipids or with integral proteins. Some have a single hydrocarbon chain attached to them which is insert it into the membrane, anchoring the protein to the membrane surface.

20
Q

What are integral proteins?

A

Integral proteins spend a whole width of the membrane, across both layers of the bilayer.
Hydrophobic amino acids interact with the hydrophobic phospholipid tails in the bilayer, keeping them in place.

Hydrophilic amino acids line the part of the channel that forms the pore, allowing soluble materials to pass through.

21
Q

What are the key functions of membrane proteins (6)?

What is the mnemonic? What do each do?

A

TRACIE
Transport - Channel proteins (facilitated diffusion) and carrier proteins (active transport)
Receptors - of peptide-based hormones to allow cell to cell communication i.e. neurotransmitters at synapses
Anchorage: Cytoskeleton attachments and extracellular matrix
Cell recognition: MHC proteins and antigens
Intercellular junction: cell adhesion to form tight junctions between groups of cells in tissues and organs
Enzyme: immobilized enzymes with the active site on the outside e.g. small intestine

22
Q

Why do some membranes have a higher protein content and why?

A

Mitochondria - aerobic respiration -> require enzyme on membranes
Chloroplasts - photosynthesis -> require enzymes on membranes
White blood cells - antibodies
Root hair cells - active transport of minerals

23
Q

What is cholesterol?

A

It is a steroid (not a protein) with a hydrophilic end and a hydrophobic end, like a phospholipid

24
Q

Where is cholesterol found?

A

Cholesterol is found in animal cell membranes.

25
Q

How is cholesterol positioned in the membrane?

A

Cholesterol molecules are positioned between phospholipids and a membrane bilayer, with the hydrophilic end interacting with the heads and hydrophobic and interacting with the tails, pulling the phospholipids together and reducing the lateral movement of phospholipids

26
Q

What is the function of cholesterol?

A
  • Add stability to membranes without making them too rigid
  • Regulates permeability of the membrane - making membranes less fluid (more rigid) and hence less permeable, preventing leakage of ions or small polar molecules
27
Q

Why is cholesterol adapted in the cells of living organisms at high temperature?

A

Cells have an increased cholesterol content to maintain stability of the bilayer as high temperatures can denatured proteins making the membrane too permeable.

28
Q

What affects the rate of diffusion? (5)

A

Temperature, diffusion distance, surface area, concentration gradient, sides of diffusing molecules