Cell Biology Flashcards

1
Q

9 Differences between Prokaryotes and Eukaryotes

A
  1. Size: P = 1-2 microns, E = 5-100 microns
  2. Nucleus
  3. DNA P = circular + single, E = linear, multiple + proteins
  4. Cell division P = binary fission
  5. Internal membranes P = rare E= lots
  6. Ribosomes P = 70s (50 + 30), E= 80s (60 +40)
  7. Cytoskeleton P = absent, E = microtubules
  8. Motility P= rotary motor -> flagellum, E= dynein drives eukaryotic flagellum, cilia, kinesin, myosin
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2
Q

3 categories of organisms

A

Eubacteria, Archae and Eukaryota

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3
Q

Taxonomy:

  1. B___
  2. S____
  3. Kingdom
  4. Phylum
  5. S____
  6. S____
  7. Class
  8. S____
  9. Order
  10. S____
  11. I_____
  12. P____
  13. S____
  14. Family
  15. Genus
  16. Species
A

Biota, Superkingdom, Subphylum, Superclass, Superorder, Suborder, Infraorder, Parvorder, Superfamily

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4
Q

3 types of globin protein

A

Hemoglobin, Myoglobin, Leghemoglobin

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5
Q

Evolutionary trees of proteins are

A

Gene trees

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6
Q

Outline cell cycle

A
G1 -> S -> G2 -> M 
In between G1 + S = G0 where resting cells lie 
G = RNA + protein synthesis
S = DNA replication
M = Mitosis
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7
Q

Ploidy

A

Number of sets of chromosome in a cell

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8
Q

Euploidy

A

Having an integral number of sets

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9
Q

Aneuploidy

A

Not having Euploidy e.g. trisomy 21

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10
Q

Differentiated cells are produced by

A

Asymmetric cell division

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11
Q

Parent cell =

A

Stem cell

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12
Q

Peroxisomes

A

Convert H2O2 to H2O

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13
Q

Cytoskeletal fibers

A
  1. Forms networks: microtubules, microfilaments and intermediate filaments
  2. Support membranes, organize organelles
  3. Important for cellular movement
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14
Q

Why do different membranes have different phospholipids?

A

Different phospholipids are different lengths. Length determines formation of hydrophobic tails. Tails determine fluidity and organization of phospholipids.

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15
Q

Types of centrifugation

A
  1. Differential

2. Density-gradient

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16
Q

Differences between types of centrifugation

A
  1. Differential -> organelles are separated in homogenate by size -> not pure
  2. Density-gradient -> Organelles separated by slight changes of density e.g. use of sucrose to create resistance for organelles which they push against when centrifuged
17
Q

How to measure electrophysiology?

A
  1. Patch-clamp

2. Radioactive tracers

18
Q

Outline fluorescence-activated cell sorting (FACS)

A
  1. Rapid separation of large number of cells
  2. Purify -> every cell is enclosed into a charged jar dependent on cell charge
  3. Isolate depending on market
19
Q

Outline flow cytometry analysis

A
  1. Measures the levels of various markers on large number of cells
  2. How light is being separated -> focuses on live cells
20
Q

How is intracellular signaling measured?

A

Ca2+ sensitive dyes are used to measure Ca2+ conc. In cells -> a.p.

21
Q

Benefits of GFP

A
  1. Label neurons + transgenic animals

2. Brainbow demonstrates how brain is used -> every neuron and interaction seen

22
Q

How is FRAP used?

A

Fluorescence recovery after photobleaching measures the mobility of proteins in cells

23
Q

6 Differences between Light, TEM and SEM microscopy

A
  1. Resolution: L 200 nm, T 1 nm, S 10 nm
  2. Depth of focus + Field of view: L low, T medium, S high
  3. Ease: L + S easy, T - requires skill
  4. Speed: L+S - rapid, T - slow
  5. Cost: L low, T + S high
24
Q

Outline electron microscopy

A

Relies on GFP or fluoroform. All the beams that pass through cause a white pattern.

25
Q

Outline SEM

A

Looking at how electron bounces back -> metal replica created by evaporated platinum + carbon

26
Q

Outline super-resolved microscopy

A

Extra detail beyond light microscopy using tricks to resolve light interference