Prion Diseases and Protein Structure

Prion Diseases and Protein Structure

Assessment

Interactive Video

Biology, Science, Chemistry

11th - 12th Grade

Hard

Created by

Patricia Brown

FREE Resource

The video tutorial explains the complex process of protein folding and the consequences of misfolding. It introduces prions, misfolded proteins that can cause diseases in humans and animals, such as mad cow disease and Creutzfeldt-Jakob disease. The tutorial details the mechanism by which prions misfold and aggregate, forming insoluble fibers that damage brain cells. It highlights the infectious nature of prions, which can be transmitted between individuals and species, posing significant health risks.

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10 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What determines the function of a polypeptide?

Its three-dimensional structure

The number of amino acids

The type of bonds it forms

Its primary sequence

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What are prions?

Bacterial cells

Viral particles

Misfolded proteins that form aggregates

Normal proteins

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which disease is caused by prions in humans?

Mad cow disease

Parkinson's disease

Alzheimer's disease

Creutzfeldt-Jakob disease

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What structural feature is predominant in prions?

Alpha helices

Beta-pleated sheets

Random coils

Disulfide bridges

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Why do beta-pleated sheets in prions have a high potential for bonding?

They are hydrophobic

They are linear and parallel

They are flexible

They are covalently bonded

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What happens when prions aggregate?

They break down into smaller units

They become inactive

They form larger fibers

They dissolve in water

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is an amyloid fiber?

A type of normal protein

A lipid molecule

A fiber formed by aggregated prions

A type of carbohydrate

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