T Cell Receptor Flashcards

1
Q

What is the function of MHC?

A

Monitor IC environments by presenting short peptide fragments on surface of cell to T cell to either signal response against foreign protein

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2
Q

How do you get diversity of TCR? (5)

A
  1. recombination of VDJ segments
  2. recombination of different number of gene segments
  3. imprecise joining by RAG
  4. P and N nucleotide addition by TdT
  5. Assembly of different combos of rearranged TCR chains (alpha/beta or delta/gamma)
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3
Q

Does TCR have affinity maturation?

A

No, because it doesn’t have somatic hypermutation

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4
Q

What do cytosolic peptides bind to? What are they presented to? What is the effect on presenting cell?

A

-binds MHC class I, present to CD8, and causes cell death

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5
Q

What do intravesciular pathogens bind to? What are they presented to? What is the effect on presenting cell?

A

-binds MHC class II, presents to CD4, and activates the APC to kill intravesicular bacteria and parasites

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6
Q

What do extracellular pathogens and toxins bind to? What are they presented to? What is the effect on presenting cell?

A

-binds MHC class II, presents to CD4, activates B cells to secrete IG to eliminate EC pathogen

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7
Q

Is this affinity of TCR for Ag weak or strong compared to Ab?

A

weak

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8
Q

What region of the MHC protein do CD4 and CD8 recognize?

A

constant region, can interact with any MHC class II or class I protein respectively

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9
Q

What does gamma-delta TCR recognize?

A

3D shape of MHC molecule or Ag, not dependent on peptide held by MHC

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10
Q

How do superantigens work?

A
  • recognizes outside constant regions of TCR and MHC to bind both in a nonspecific manner
  • increases frequency of T cell response from 1 in 10^4 to 10^5 to 1 in 4 to 20 to get huge cytokine release
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11
Q

Does superantigen have any specificity?

A

-has specificity for certain VB segments, increases susceptibility for certain people

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12
Q

What HLA types make up class I MHC? class II?

A
for class I, HLA-A, HLA-B, HLA-C (homodimer)
for class II, HLA-D (heterodimer)
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13
Q

Where does the diversity come from for class I MHC? Class II?

A
for class I, diversity comes from number of alleles (6) since it's a homodimer
for class II, diversity comes from heterodimer arrangments
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14
Q

Which class of MHC is expressed on all nucleated cells?

A

MHC class I

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15
Q

What class of MHC is expressed on APCs?

A

MHC class II to allow interact with CD4 T cells so it can secrete cytokines to help B cells

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16
Q

What is the structure of MHC class I? Which subunits make up the binding groove?

A
  • alpha 1, 2, 3 (transmembrane), beta 2

- alpha 1 and 2 make up binding groove

17
Q

What is the structure of MHC class II? Which subunits make up the binding groove?

A
  • alpha 1, 2 (transmembrane), beta 1, 2 (transmembrane)

- alpha 1 and beta 1 make up the binding groove

18
Q

Which MHC class has a closed off binding groove that fits smaller peptides only?

A

class I

19
Q

Which class of MHC do extracellular pathogens present from?

A

class II

20
Q

What is the processing pathway for IC pathogens?

A
  • pathogen in cytosol degraded in proteasome to peptides

- transported into ER where they bind MHC previously held by chaperones, and are exported to cell surface