BIOL 435 Ch. 3 Part Two (Recognition and Response) Flashcards

1
Q

5 distinct classes of Ab (isoptopes)

A
  1. IgA: alpha H
  2. IgD: delta H
  3. IgE: epsilon H
  4. IgG: gamma H
  5. IgM: mu H
    * based on differences in heavy chain structure
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2
Q

Ab class in B-cell

A
  • first IgM and IgD

- if activated, switch of classes at constant region

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3
Q

light chain isotopes

A
  1. Kappa
  2. Lambda
    *determined when Ab is made
    >tries one of them, than the other, if neither works=dies
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4
Q

Ab structure

A
-puzzled it together
>Papain
>Pepsin
>beta mercapto EtOH
-CHO on heavy chains
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5
Q

papain

A

-digest an Ab into 3 segments
>2 same (Ag binding= Fab)
>1 different (fragment crystalizable= Fc)
-150,000 Da

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6
Q

pepsin

A

-digest Ab into a single fragment with 2 Ab binding sites (F(ab)2)

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7
Q

beta mercapto EtOH

A
  • 2 H. chains: 50,000 Da each

- 2 L. chains: 22,000 Da each

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8
Q

IgG

A
  • 4 Ig domains in H chain
  • 2 disulphide bonds
  • most common
  • hinge region
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9
Q

IgD

A
  • 4 Ig domains in H. chain
  • 1 disulphide bond
  • hinge region
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10
Q

IgE

A
  • 5 Ig domains in H. chain
  • 2 disulphide bonds
  • no hinge
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11
Q

IgA

A
  • 4 Ig domains in H. chain
  • hinge region
  • can be secreted: dimer joined by J-chain
  • monomer in blood
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12
Q

IgM

A
  • original
  • secreted version=pentamer
  • 5 Ig domains in H-chain
  • no hinge
  • disulphide bonds between subunits to form pentamer
  • J-chain
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13
Q

type of Ab to produce

A
  • signals will tell what type

- variable region/specificity remains the same

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14
Q

BCR complex

A
  • molecules involved in signal transduction
    1. Ab/BCR molecules
    2. Ig alpha and Ig beta
    3. CD19, CD81, CD21
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15
Q

Ig alpha and Ig beta

A

-transduce signals via ITAMs

>tyrosines available to be phosphorylated

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16
Q

ITAMs

A

-immunoreceptor tyrosin-based activation motifs

17
Q

CD19, CD81, CD21

A
  • transmit and relay signals to cell interior

* CD12: co-receptor, binds to An indirectly via C3d

18
Q

TCR structure

A

-similar to Ig domains
-2 subunits (alpha and beta)
>constant region
>variable region
*always membrane bound: no soluble form

19
Q

2 TCR types

A
  • alpha beta
  • gamma delta
  • have diverse An binding characteristics
20
Q

variable regions (TCR)

A

-have 3 CDRs forming peptide-specific binding site

21
Q

constant regions (TCR)

A

-each contain transmembrane signals

22
Q

TCR respond to soluble An

A
  • can’t do like BCR can
  • need MHC help peptides
  • peptide sources can be from endogenously (ex. virus, cancer) or exogenously (put onto surface) processed An
23
Q

MHC

A

-major histocompatibility complex

24
Q

TCR complexes

A
  • with co-receptor involved in An recognition
  • want many safeties
    1. CD3
    2. CD4, CD8
    3. CD28
25
Q

CD3

A
  • contains ITAMs that transmit signal to cell

- 6 molecules on cell surface (3 dimers)

26
Q

CD4, CD8

A
  • function on increasing avidity of peptide binding by TCR

- bind to MHC (if not=wont be activated)

27
Q

CD28

A
  • engages CD80 or CD86 on APC to fully activate a naive T-cell
  • co-receptor
28
Q

3 dimers

A
  • delta-epsilon
  • gamma-epsilon
  • zeda-zeda / zeda-mu
  • ITAMs on intracellular side to pass signal in