Chaperone-Mediated Autophagy (CMA) | Selection, Mechanism and Regulation

Chaperone-Mediated Autophagy (CMA) | Selection, Mechanism and Regulation

Assessment

Interactive Video

Health Sciences, Biology

University - Vocational training

Hard

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The video explains chaperone-mediated autophagy (CMA), a selective degradation process targeting proteins with a KFRQ sequence. CMA is activated during prolonged fasting and decreases with aging and certain diets. It involves chaperone proteins like HSC70 and lysosomal proteins such as lamp2A. The process is crucial for cellular health, and its dysfunction is linked to diseases like Danon disease. Lamp2C plays a role in RNA/DNA degradation independently of HSC70. The video concludes with the importance of CMA in maintaining proteostasis.

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10 questions

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1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the primary function of the KFRQ consensus sequence in CMA?

To enhance protein synthesis

To select proteins for degradation

To stabilize cellular membranes

To promote cell division

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which chaperone protein is primarily responsible for recognizing the KFRQ sequence?

HSP 40

HSC 70

Bag 1

HSP 90

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What role does HSP 90 play in the CMA process?

It synthesizes new proteins

It degrades proteins

It prevents protein aggregation

It transports proteins to the lysosome

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which lysosomal protein is crucial for acidifying the lysosome?

Cathepsin A

Vpas

HSC 70

Lamp 1

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the primary function of cathepsins in the lysosome?

To transport proteins

To synthesize proteins

To break down protein cargo

To stabilize the lysosomal membrane

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the rate-limiting step in the CMA process?

Protein synthesis

Protein translocation through lamp 2A

Protein folding

Protein aggregation

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What disease is associated with a deficiency in lamp 2A?

Alzheimer's disease

Huntington's disease

Danon disease

Parkinson's disease

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