Sickle Cell Anemia Concepts

Sickle Cell Anemia Concepts

Assessment

Interactive Video

Biology

9th - 10th Grade

Hard

Created by

Patricia Brown

FREE Resource

Dr. Alice explains sickle cell anemia, a genetic condition affecting red blood cells. Normal red blood cells are disc-shaped, aiding oxygen transport and flexibility. In sickle cell anemia, a genetic mutation changes a nucleotide, altering hemoglobin's structure. This mutation replaces glutamate with valine, causing hemoglobin to form long strands, leading to sickle-shaped cells. These cells struggle with oxygen transport and flexibility, causing health crises. The video covers the genetic basis, protein structure changes, and the overall impact on red blood cells.

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10 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the primary function of normal red blood cells?

To fight infections

To transport oxygen

To produce hormones

To store nutrients

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What causes the sickle shape in sickle cell anemia?

A deficiency in vitamin D

An excess of white blood cells

A mutation in the DNA

A lack of iron

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which amino acid is incorrectly incorporated in sickle cell anemia?

Lysine

Serine

Valine

Glutamine

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

How does the mutation in sickle cell anemia affect hemoglobin?

It makes hemoglobin more soluble

It causes hemoglobin to form long strands

It increases hemoglobin's oxygen capacity

It makes hemoglobin resistant to degradation

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the primary structure of a protein?

The interaction with other proteins

The folding pattern of the protein

The sequence of amino acids

The 3D shape of the protein

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the quaternary structure of hemoglobin in sickle cell anemia?

A free-floating four-piece protein

A single protein chain

Long protein strands

A double helix structure

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What happens to hemoglobin proteins in sickle cell anemia?

They become more flexible

They clump together

They increase in number

They dissolve in water

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