Unit 1 - Cellular function Flashcards

1
Q

what is the role of the peroxisome?

A

break down of lipids by beta oxidation producing hydrogen peroxide which is neutralised by catalase to water and oxygen

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2
Q

what is the role of the golgi body?

A
  • modifies/ packages proteins for secretion

- transport vesicles from endoplasmic reticulum to golgi to fuse with the cis face

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3
Q

what chemical changes occur to proteins by the golgi body?

A

post-translational modification:

  • glycosylation (addition of oligosaccharides)
  • phosphorylation
  • sulphation (addition of sulphates)
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4
Q

where and how are vesicles budded off from the cisternae of golgi?

A

from trans face

- exocytosis

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5
Q

what model describes the cell membrane?

A
  • fluid mosaic model
  • fluid - phospholipids can move relative to one another
  • mosaic: embedding of proteins different size/shapes
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6
Q

what type of proteins are found in the membrane?

A
  • intrinsic/ integral: carrier proteins/ channels

- extrinsic/ peripheral: surface - receptors, recognition sites

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7
Q

what else is found on extracellular surface in cell membranes?

A

carbohydrates - form glycocalyx (cell coat) and also involved in cell recognition

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8
Q

what is the role of the cholesterol in the cell membrane?

A

interfere with hydrophobic interactions between tails so decreases the fluidity - sometimes causing crystallisation

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9
Q

what is the cytoskeleton?

- name four functions

A

flexible lattice of fibrous proteins - filaments

functions: mechanical structure/ support, intracellular transport, suspension of organelles, adhesion

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10
Q

what are the types of filament found in the cytoskeleton?

A
  • microfilaments: actin - dynamic structure
  • intermediate filaments - stronger/ more stable - keratin
  • microtubules - formed of alpha/beta tubulin provide strength, form spindle fibres, components of cilia and flagella, moves vesicles around cell by motor proteins that walk them along the tubules (dynein= towards centrosome/ kinesins=away)
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11
Q

what is another term for centrosome?

A

MTOC - microtubule organzing centre

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12
Q

What is the outer surface of cilia called and what is it composed of?

A
  • axoneme
  • nine doublet microtubules arranged around a pair of microtubules with protein links at regular intervals which provide attachment to the cytoskeleton by basal body
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13
Q

how does the rapid motion of cilia/flagella occur?

A

motor protein = ciliary dynein linked by polypeptide chain to one side of doublet microtubule and other free head interacts with neighbouring microtubule

  • ATP hydrolysis occurs so able to bind to next protein subunit
  • in this way it bends the cilium so bent region progresses along producing a rhythmic wave-like motion so material is swept across
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14
Q

what defect causes cystic fibrosis?

A

defect in chloride channel (CFTR) in apical membrane of epithelial cells so no chlorine transport

  • no osmotic gradient is formed - no water
  • mucus undiluted - difficulty breathing - leads to pneumonia - fertile environment for bacteria
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15
Q

what is lysosomal disease?

A

lack of lyzozymes so there is an accumulation of fats/sugars in lysosome which disrupts normal cell function leading to lsd

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16
Q

What is kartagener’s syndrome?

A

defective dynein gene so cannot sweep mucus from airways leads to respiratory infection

17
Q

what type of cell is an enterocyte?

A

absorptive cell

  • simple columnar epithelial cell
  • microvilli on surface to increase SA for absorption
18
Q

what is the difference between the secretory cells of exocrine and endocrine?

A
  • exo: mucus

- endo: hormones

19
Q

how does cell motility occur?

A
  • extends projection called lamellopodium in direction of movement and attaches to substrate that provides traction to allow cell to be pulled along by polymerisation and depolymerisation of actin