2.1 Cell Structure Flashcards

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1
Q

Adv and Disadv of light microscopes

A

About :
- Impossible to resolve between 2 objects closer than half the wavelength of light (500-650nm)

-Adv :
- Small and easy to carry
- Cheap
- Easy sample preparation
- Easy to use
- Specimens can be alive or dead eukaryotic cells
- No vacuum needed
- Colour image

Disadv :
- Max resolution 200nm
- Max magnification 1500
- Cannot observe ribosomes, lysosomes or endoplasmic reticulum

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2
Q

Adv and Disadv of Transmission Electron Microscopes. How do they work?

A

Focus beam of electrons through specimen. denser parts absorb more electrons so appear darker on final image. Produces contrast between different parts of specimen.

Adv :
- High resolution
- Internal structures within cells can be seen
- High magnification

Disadv :
- Only thin specimens
- Cannot observe live specimens
- Vacuum needed
- Water must be removed from specimen
- Artefacts may be introduced due to lengthy preparation of specimens
- Not a colour image

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3
Q

Adv and Disadv of scanning electron microscopes. How do they work?

A

Scan beam of electrons over specimen. Electrons bounce of surface and detected to form an image

Adv :
- 3D external structures of specimen can be observed
- Thick or 3D specimens used

Disadv :
- Lower resolution than TEMs
- Cannot observe live specimens
- No colour

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4
Q

What are laser scanning confocal microscopes? Advantages and Disadvantages?

A

Cells stained with fluorescent dyes
Thick section of tissue scanned with laser beam
Reflected by dye
Multiple depths of tissue scanned to produce image
Adv :
- Thick or 3D (external) specimens
- External and internal structures observed
- High resolution
- Cytoskeleton can be observed
- High magnification

Disadv :
- Slow process
- Laser can cause photodamage
- Vacuum needed
- Length treatment process of sample
- Dead specimen

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5
Q

What are Microtubules

A
  • Eukaryotic
  • Cytoskeleton
  • Made of α and β tubulin combined to form dimers, the dimers are then joined into protofilaments
  • 13 protofilaments in a cylinder make a microtubule
  • Cytoskeleton provides support and movement of cell
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6
Q

Process of protein synthesis

A
  • DNA from nucleus copied to molecule of mRNA via transcription
  • mRNA strand leaves nucleus via nuclear pore
  • Attaches to ribosome on RER
  • Ribosome reads genetic instructions and synthesises a protein via translation
  • Protein passes into lumen of RER and is folded and processes
  • Processed proteins transported to golgi apparatus via vesicles
  • Golgi apparatus modifies protein
  • Leaves golgi apparatus via vesicle
  • Vesicle fuses with cell surface membrane and releases protein by exocytosis
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7
Q

What are microfilaments?

A

Solid strands
Made from actin
Cause cell movement and movement of organelles

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8
Q

What are microtubules?

A

Tubular hollow strands
Made of tubulin
Organelles move along these fibres using ATP to drive movement

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9
Q

Function of cytoskeleton

A

Strengthening and supporting cell
Intracellular movement
Cellular movement

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10
Q

How does the cytoskeleton provide strength and support?

A

Mechanical strength
Via scaffolding maintaining shape of cell
Supports organelles keeping them in position

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11
Q

How does the cytoskeleton provide intracellular movement?

A

Forms ‘tracks’ along which organelles can move
Movement of vesicles
Chromosomes to opposite ends in cell division

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12
Q

How does the cytoskeleton provide cellular movement?

A

Cilia and Flagella
Hair like extensions containing microtubules responsible for moving them

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13
Q

Structures unique to prokaryotic cells

A
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14
Q

Comparison of prokaryotic and eukaryotic cells

A
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