MHC Class I Flashcards

1
Q

What is the function of MHC Class I molecules?

A

To present endogenous antigens from within cells to CD8 plus cytotoxic T lymphocytes CTLs

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2
Q

What types of antigens are presented by MHC Class I molecules?

A

Endogenous antigens such as viral proteins and defective ribosomal products DRiPs

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3
Q

What is the structure of MHC Class I molecules?

A

One alpha chain with three domains alpha 1 alpha 2 and alpha 3 and a beta-2 microglobulin

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4
Q

Where are MHC Class I molecules expressed?

A

On all nucleated cells

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5
Q

What is the role of cytotoxic T lymphocytes CTLs?

A

To recognize and destroy infected or abnormal cells by interacting with MHC Class I molecules that are presenting endogenous antigens

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6
Q

What happens to viral proteins in the cytosol during antigen processing?

A

They are degraded into peptides by the proteasome

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7
Q

What is the proteasome?

A

A multi-catalytic protease complex that breaks down proteins into peptides for antigen presentation

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8
Q

What is the role of TAP in the MHC Class I pathway?

A

TAP1 and TAP2 form a transporter that moves peptides from the cytosol into the endoplasmic reticulum ER

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9
Q

What is the role of beta-2 microglobulin in MHC Class I?

A

It stabilizes the structure of MHC Class I and assists in peptide binding

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10
Q

Where are peptides loaded onto MHC Class I molecules?

A

In the endoplasmic reticulum ER

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11
Q

What is the peptide-binding groove of MHC Class I molecules?

A

A cleft between the alpha 1 and alpha 2 helices where peptides of 8 to 9 amino acids are tightly bound

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12
Q

What is the immunoproteasome?

A

A modified version of the proteasome that generates peptides optimized for MHC Class I binding

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13
Q

What are anchor residues in peptides presented by MHC Class I?

A

Specific amino acids in peptides that interact with the MHC binding pocket

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14
Q

What is cross-presentation or cross-priming?

A

The process by which exogenous antigens are presented on MHC Class I molecules by professional antigen-presenting cells such as dendritic cells

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15
Q

What happens to peptides after they are transported into the ER by TAP?

A

They are trimmed by ER aminopeptidases to fit the MHC Class I binding groove

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16
Q

What is the role of the peptide-loading complex?

A

To assist in the assembly of MHC Class I molecules with peptides in the ER

17
Q

How does MHC Class I antigen presentation enable immune surveillance?

A

It allows the immune system to detect and respond to infections or abnormalities inside cells

18
Q

What happens to MHC Class I peptide complexes after assembly in the ER?

A

They are transported through the Golgi apparatus to the cell surface for presentation to CD8 plus T cells

19
Q

What are defective ribosomal products DRiPs?

A

Abnormal or misfolded proteins generated during translation that are rapidly degraded and presented by MHC Class I molecules

20
Q

What is the dual role of MHC Class I molecules in viral infections?

A

To present viral peptides to CTLs and to allow the immune system to detect virally infected cells

21
Q

How are peptides selected for binding to MHC Class I molecules?

A

Peptides with specific anchor residues and lengths are selected to fit the MHC Class I binding groove

22
Q

What is the impact of viral evasion on MHC Class I antigen presentation?

A

Some viruses produce proteins that interfere with MHC Class I expression or peptide loading to evade immune detection

23
Q

What is the importance of cross-presentation in immunity?

A

It allows professional antigen-presenting cells to initiate CD8 plus T cell responses against pathogens not directly infecting them

24
Q

How does the MHC Class I pathway contribute to adaptive immunity?

A

By presenting intracellular antigens it activates CD8 plus T cells which are crucial for the adaptive immune response

25
Q

What is the order of the MHC Class I Pathway?

A

1- Synthesis of MHC Class I Molecules
2- Antigen Processing in the Cytosol
3- Peptide Transport to the ER
4- Peptide Loading
5- MHC Class I Complex Formation
6- Transport to the Cell Surface
7- Presentation to CD8+ T Cells