Goldberg Flashcards

1
Q

What is the consequence of deficiencies in lysosomal enzyme lipid degradation?

A
  • accumulation of harmful quantities of gangliosides

- nerve cell death.

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2
Q

What is the function of actin in the cytoskeleton?

A
  • cell shape and organisation
  • cell movement
  • mutations in actin = cardiomyopathy
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3
Q

What are microtubules important for in the cytoskeleton?

A
  • Mitotic spindle
  • target for anti-cancer drugs
  • intra-cellular movements: vesicles, organells
  • driven by motor proteins
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4
Q

What is the function of intermediate filaments in the cytoskeleton?

A
  • Strucutral proteins

Defects > skin blistering

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5
Q

What does a convex Lens do?

A
  • converges parallel beams to the focal point
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6
Q

What does a concave lens do?

A
  • diverges parallel light.

- focal pint is the point they would have converged to.

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7
Q

What is the effect is decreasing the focal length?

A
  • increases the magnification.
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8
Q

What is the magnification strength of long focal length compared to short?

A
  • long = less magnifying
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9
Q

If the object is closer to the focal point what happens?

A
  • single lens produces an enlarged virtual image
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10
Q

What are the 2 components of a microscope?

A
  1. An objective lends to produce a magnified real image

2. An eyepiece to produce a magnified virtual image of the real image (that you see with your eye).

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11
Q

What are phase contrast microscopes useful for?

A
  • can amplify refractive index differences in cell components- excellent for live cells.
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12
Q

What is fluorescence microscopy used for?

A
  • diff parts in cell can be specifically stained

- or using antibodies, usually to individual proteins attached to fluorescent molecules.

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13
Q

How do fluorescence microscopes work?

A
  • specimen is illuminated with light of a specific wavelength (e.g. Green) whcih excites flurophore.
  • this then emits light of another wave elgnth (e.g. Red)
  • image is magnesia iced and focused on retina or detector.
  • the chromatic beam splitter reflects and transmits light of different wavelengths differently.
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14
Q

What is the purpose on confocal microscopy?

A

Pinhole prevents out-of-focus light reaching the detector.

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15
Q

What is the difference in information given by TEM and SEM microscopes?

A
  • TEM = 2D projection of image of a thin specimen

- SEM = unlimited thickness of specimen

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16
Q

What are the 4 stages of SEM?

A
  1. Primary beam is focused to a fine point
  2. Beam scanned across sample surface
  3. Secondary electrons emitted from specimen as the beam passes over it.
  4. Secondary e- are collected by detector and picture is build up.
17
Q

Explain the permeability of membranes.

A

Dynamic lipid and protein content of membrane.
gases = permeable
Small uncharged polar molecules = permeable/slightly permeable.

18
Q

What is the importance of membrane compartments?

A
  1. For cell function
  2. In disease and disorders
    > contains and organise genome- nuclear membranes
    > localise and facilitate ATP synthesis
    > general degradation of unwanted components.
19
Q

What is a phosphoglyceride?

A
  • the most common phospholipids.
    Head = alcohol; phosphate; glycerol
    Tail = hydrocarbon chains
20
Q

Where do phospholipid orientate to hide tails from water?

A
  • at the interface between oil and water.

- if forced into an aq enviroments it is energertaiclly favourable to form spherical vesicles

21
Q

What happens to hydrophobic molecules in water?

A
  • they do not interact with water they therefore prevent water-water interactions. And this imposes order on the water molecules.
22
Q

What is the effect of place a hydrophobic molecules in water?

A
  • decreases entropy. As it is theromodynamically unfavourable to increase order.
23
Q

What is the effect of aggregation?

A
  • decreases order and increases entropy - favourable
    > water forms ‘ice like’ cages around hydrophobic molecules
    > aggregation reduces hydrophobic molecules
    > therefore reduces order in the water > less water in cage
    > therefore increases entropy.
24
Q

Why do water molecules form cages around hydrophobic molecules?

A
  • reduced H-bonding increases bond strength
  • there are less H-bonds available to each water molecule
  • the fore they are stronger and hence more stable
  • surface area of 2 separate hydrophobic molecules is greater than two aggregated ones.
    » aggregation releases water molecules and increases entropy.
25
Q

How can lateral diffusion be demonstrated and measured?

A
  • By fluorescence recover after photobleaching (FRAP)
26
Q

What are sphingolipids?

A
  • bases on sphingosine
  • long chain amino alcohol
  • equivalent to glycerol and one fatty acid tail of phospholipid
  • second hydrocarbon tail added by amide bond.
  • Phosphate + alcohol head group added to C1.
  • they have a similar sharpe to glycerophospholipid
  • usually saturated
  • usually have one unsaturated fatty did chain
  • therefore sphingolipids pack closer together and have stronger van dear walls
27
Q

What is the structure of cholesterol?

A
  • Amphipathic
  • Small head group (OH)
  • does not form bilateral on its own (too hydrophobic)
  • but can insert into membrane
  • riding 4 ring structure
  • cholesterol interacts mainly with fatty acid tail of phospholipids.
  • they stiffen the fatty acid tails and thicken membrane
  • introduces order in tail region
    But maintains fluidity
28
Q

Why does cholesterol prefer to interact with sphingolipids?

A
  • more stable interaction between stiff flat steroid of cholesterol and long unsaturated fatty acid tail of sphingolipids
  • therefore cholesterol and sphingolipids partition from phospholipids.
29
Q

What are microdomains?

A
  • known as lipid rafts- concentrated thicker domains rich sphingomyelin and cholesterol
    > rafts are thicker than the rest of membrane
    -proteins with long transmembrane domains partition to rafts.
    . short domains partition to phospholipid containing domains
  • recruit proteins with lipid anchors