pack Flashcards

1
Q

What is a folded protein?

A

A folded protein is a functional protein

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2
Q

Is the process of protein folding random?

A

NO, it is an active process that isn’t random.

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3
Q

What is the function of chaperone?

A

Promote protein folding

and

Prevent protein misfolding and aggeregation.

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4
Q

How does chaperone promote protein folding? How does it prevent misfolding?

A

Folding:It binds to unfolded proteins using atp, after the atp is hydrolyzed, it releases folded (native) protein

Protection: shields out bad influnces

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5
Q

What is melting temperature of proteins?

A

T m is the temperature at which 50%
of the protein is unfolded

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6
Q

What is the typical melting temp for proteins?

A

Typical T m = 40-60 o C for proteins

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7
Q

What is denaturation?

A

unfolding and distruption of the secondary and tertiary structure without hydrolysis of peptide bonds

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8
Q

Can a denatured protein usually recover?

A

NO, they usually remain unfolded

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9
Q

Why is the aggregation of misfolded proteins a bad thing?

A

Bc they are very stable so too big to break down and too big to transport, and they become toxic.

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10
Q

What causes protein misfolding?

A
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11
Q

What is the molecule that is formed from aggregating proteins called?

A

Amyloid

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12
Q

What is amyloidosis?

A

a disease that
occurs when amyloid builds up in organs

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13
Q

What is an example of a disease that is caused by amloydosis?

A

alzheimer and parkinsons disease

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14
Q

What causes alzheimers?

A

An abnormal cleavage by secretase enzyme of the amyloid precursor protein which forms amyloid b-pleated sheets.

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15
Q

What protein forms the amyloid plaques in alzheimer?

A

amyloid β (Aβ) protein

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16
Q

What protien that is misfolded causes parkinsons disease?

A

Misfolding of alpha-synuclein (sy like see you bc the nuclei of the brain dissapear) (alpha wolves park in misfolded dens)

17
Q

How are Prion Diseases caused?

A

Infectious abnormal prion (PrP sc) (sc = scrapie) interacts with a normal prion (PrP c) (c = cellular) altering its 3rd formation and changing it into an abnormal prion

18
Q

What causes Transmissible spongiform encephalopathies?

A

infectious prions

19
Q

What is the Transmissible spongiform encephalopathies called in humans?

A

Creutzfelt-Jacob disease (bc the affected can feel cruel bc of personality changes)

20
Q

What is the Transmissible spongiform encephalopathies called in sheep?

A

Scrapie (bc you scrape them بتجمعهم in the herd)

21
Q

What is the Transmissible spongiform encephalopathies called in cows?

A

Bovine Spongiform Encephalopathy (mad cow disease) (bc cows can be funny so they put them on vine)

22
Q

What is HSP70?

A

Heat shock protein (chaperone) that promotes protein folding and fixes misfolded proteins due to stressful conditions

23
Q

what is special about taq dna

A

has high melting temp and is used to amplify dna

24
Q

What causes huntington disease?

A

An abnormal polyglutamine (CAG) repeat in the huntington protein which causes aggregation and in turn neuron death.

(bc the hunter needs a long and large rifle )

25
Q

Why are protein aggregates so stable?

A

bc the hydrophobic parts are getting hidden so it misfolds and becomes stable

(like hemoglobin S)

26
Q

What is another protein that causes Alzehimer?

A

Tau protein which gets hyperphosphorylated causing it to deattach from microtubules and form aggregates.

(old people like tahoes) (tahoes aggregates to you in the highway)

27
Q

What protein causes cardiac amyloid?

A

Misfolding of transthyretin causing amyloids. (transport)