MSIC Flashcards

1
Q

What are characterics of molecules that can traverse the plasma membrane via simple diffusion?

A

fat-soluble, small, and uncharged

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2
Q

Carrier proteins and channel proteins transfer what kind of molecuels?

A

small, water-soluble molecules

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3
Q

Channel proteins are regulated by what 3 factors?

A

Membrane potential, neurotransmitters, mechanical stress

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4
Q

What is the major mechanisms by which large molecules move, enter/leave the cell?

A

Vesicle budding

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5
Q

What is the classification of pinocytosis?

A

Clathrin independent

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6
Q

What is the classification of phagocytosis?

A

Clatherin independent, actin dependent

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7
Q

What are PAMPs, what do they play a role in?

A

Pathogen associated molecular patterns, activate nuclear factor kappa B –> regulates cell phagocytosis

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8
Q

What are Fc?

A

non-antigen binding domains

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9
Q

What is involved in movement of cargo material from plasma membranes to early endosomes and Golgi apparatus to early and late endosomes?

A

Clathrin-coated vesicles

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10
Q

COPII coated vesicles are transported from where to where?

A

rER–> Golgi apparatus

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11
Q

COPI transports vesicles where?

A

Golgi apparatus –> rER

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12
Q

What are multivesicular bodies (MVB)?

A

highly selective transporters that transport proteins from early to late endosomes and seperate proteins that are destined to be recyclin

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13
Q

What organelle is well defined in secretory cells?

A

Golgi apparatus

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14
Q

What types of cells do not have mitochondria?

A

RBC and terminal keratinocytes

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15
Q

What are three functions of proteins in mitochondria cristae?

A
  1. oxidation reaction
  2. synthesizing ATP
  3. regulating transport
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16
Q

Cytochrome c is located in what part of the mitochondria?

A

intermembrane space

17
Q

What is the major products of the mitochondrial matrix?

A

CO2 and reduced NADH (source of electrons)

18
Q

What do matrix granules store and what is their function?

A

Ca2+ – they increse in number and size when concentration of cation increases in cytoplasm.

19
Q

What does the matrix contain?

A

mitochondrial DNA, ribosomes, tRNAs

20
Q

What is chemiosmotic coupling?

A

movement of protons back to mitochondrial matrix, against H gradient

21
Q

MERRF is a defect in what structure?

A

mitochondrial DNA coding for lysine

22
Q

Describe the mitochondria orthodox configuration

A

cristae are prominent and the matrix compartment occupies a large part of the total mitochondrial volume, IT IS LOW LEVEL of oxidative phophorylation

23
Q

Describe the mitochondrial condensed configuration

A

cristae are not easily recognized the matrix is concentrated –> HIGH LEVELS of oxidative phosphorylation

24
Q

What initiates the cascade of protelytic enzymes that lead to cell apoptosis?

A

Bcl-2 –> release of cytochrome c

25
Q

Beta-oxidation of fatty acids is a major function of what structure?

A

peroxisomes

26
Q

Where are peroxisomes most abundant?

A

liver and kidney cells

27
Q

Zellweger syndrome is a disorder caused by what?

A

unfunctional peroxisome bc of lack of necessary enzymes (targeting signal is mutated)