BC 5 Cell Membranes Flashcards

Understand Fluid Mosaic Model and Cell Membrane components.

1
Q

Cell Membrane Permeability

A

Restricts certain molecules.

Small Hydrophobic Molecules Allowed
Gases, oxygen, carbon dioxide

Small polar can as well but slowly

RESTRICTED: highly charged, ions, large molecules, sugars, amino acids (require transport proteins

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2
Q

Amphipathic

A

Hydrophobic and Hydrophilic ie Lipids

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3
Q

Major Cell Membrane Lipids (Structure)

A

Glycerophospholipids: 2 Fatty Acid Tails -> {{Glycerol -> Phosphate -> Choline}} Polar
- Phosphotidylcholine

Sphingolipids: 1 Fatty Acid Tail -> Sphingosine (1 FA + Head) Phosphate -> Choline

Cholesterol: Short Fatty Acid Tail -> Rigid steroid Ring Structure

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4
Q

Glycerophospholipids:

A

Most Abundant Lipid

14-24 Carbon Atom Chain

One hydrophobic tail usually has one or more Cis bonds (unsaturated)

Ester linkages to fatty acid tails (Choline also ester linked)

Named by head group: Phosphotidyleserine, choline etc…

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5
Q

Sphingolipids

A

Sphingosine Backbone instead of glycerol, already has one FA tail

Sphingosine + FA = Ceramide

Phospholipid bc contains phosphorous

major of outer leafelet

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6
Q

Glycolipids

A

Sphingolipids that contain carbohydrate (COH) chains

nerve Tissues

Only in outer leaflet, carb exposed

Cerebrosides: Nerve Tissue/Brain

Gangliosides (acidic glycosphingolipids) Ganglion cells, involve accumulation of NANA containing cells

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7
Q

Cholesterol

A

Amphipathic

Small poplar head, rigid steroid ring, non polar hydrocarbon tail

Membrane fluidity

Both leaflets

high in RBC/liver

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8
Q

5 Membrane Fluidity Actions

A

Lateral Diffusion: move in plane

Rotation: rotate on axis

Swing: Just Tail

Flexion: contraction of tail (cushion)

Transverse: flip flop, helped by flippases

  1. UNSATURATED(kinked) 2. length 3. high Temp 4. Cholesterol (rigid at high T/flex at low T) prevents freezing
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9
Q

4 Major Cell Membrane Activities

A

Transport
Catalysis: of membrane associated reactions (atp)
Structural Links: To cytoskeleton or ECM
Receptors

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10
Q

Peripheral Proteins & Membrane Protein Mobility

A

Loosely Associated to Membrane via H Bonds or Electrostatic Forces

Mobility: Restructed by rafts, tight junctions, ECM interactions, Cytoskeletal attachments

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11
Q

Membrane Carbohydrates

A

ONLY on the extracellular leaflet, covalently attached to proteins and lipids

Make up Glycocalyx (carb rich zone outside cell) (glycol-bound to sugar: glycolipids/glycoproteins etc)
-cell recognition/signaling occur here/absorbs water, becomes slimey (motile), narrow passes, cushion/ endothelial, RBC, platelet/determines ABO/blood clotting/sperm-egg int

Glycocalyx: Formed by enzymatic Glycosylation (non enzymatic, glycation)

microvilli covered by thick glycocalix in intestine, contains glycosylated enzymes for breakdown and absorbs, friction protection

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12
Q

Cell Membrane Defects (associated diseases)

A

Lipid Associated:
MS: Autoimmune Myelin Sheath (Sphingomyelin/Galactocerebrosides)

Niemann-Pick: hereditary, deficiency of sphingomyelinase, accumulation in liver, spleen, lunchs, bone marrow, brain, neuro problems
A. Infants, Jaundice, enlarged liver, brain damage 18mo
B. enlarged liver and spleen, preteen, brain not affected, less than 1% levels of enzyme compared to norm.
C. different mutation, buildup of cholesterol in liver, spleen and neural cells

Sphingolipidosis: Fabry X linked, Krabbe, Gaucher, Tay Sachs, Metachromatic leukodystrophy. Inherited
high in Ashkenazi Jews, enzyme replacement therapy helps lots, infantile fatal.

Cystic Fibrosis: Membrane protein, Cl- transporter defective-abnormally think mucus obstructs airways. CFTR gene ABC family

Congenital Disorders Glycolation : CDG- carbohydrate disorders. Either missing oligosaccharide chains or abnormal ones. Manifest broadly,.

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