Lecture 18 Flashcards

1
Q

Ig Superfamily Members

A
  1. Antibodies
  2. B-Cell Receptors
  3. T-Cell Receptors
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2
Q

Antibodies

A

Soluble B-Cell Receptors

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3
Q

B-Cell Receptors

A

Membrane-Anchored Antibodies

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4
Q

T-Cell Receptors

A

Membrane-Anchored MHC-ligand Receptor

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5
Q

b-Pleated Sheet

A
  1. Laterally packed
  2. Anti-parallel or parallel
  3. Peptide-backbone
  4. R groups above/ below
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6
Q

Immunoglobulin Domains

A
  1. Hydrogen bonding along peptide backbones
  2. A.A. in b-strands alternate hydrophobic or hydrophilic
    3.
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7
Q

Hydrophobic

A

Residues ‘sandwiched’ between folds

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8
Q

Disulfide Bonding

A

Between b-stands on opposite folds

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9
Q

Antibody Molecules

A
  1. Two IDENTICAL Heavy Chains
    • 4/5 Ig Domains per Heavy Ch.
  2. Two IDENTICAL Light Chains
    • 2 Ig Domains per Light Ch.
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10
Q

Structure of Antibody Molecules 1

A
  1. Disulfide bonds covalently link the LIGHT and HEAVY chains
  2. Forms HETERODIMERS
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11
Q

Structure of Antibody Molecules 2

A
  1. Disulfide bonds covalently link the two HEAVY chains
  2. Forms HETEROTETRAMERS
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12
Q

Hinge Region

A
  1. Center of the HEAVY chains
  2. provide ‘molecular flexibility’
    • multivalent antigens
  3. IgA, IgD, and IgG
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13
Q

Glycosylation

A

Spreads antibodies for better receptor access
– tails of antibodies

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14
Q

Glycosylation 2

A
  1. CH2 domains of IgA, IgD, and IgG
  2. CH3 domains of IgE and IgM
  3. CH-CH spacing
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15
Q

Variable Region

A

Present in the NH2-terminal Ig domain of LIGHT AND HEAVY chain

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16
Q

Variable Regions

A
  1. Linking segments between b-strands are markedly more variable
  2. Linking segments: more accommodations
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17
Q

Linking Segments

A

Site responsible for specifying antigen binding

18
Q

CDR

A

Complimentary-determining region

19
Q

IgM

A
  1. Primary immunoglobulin
    – “on go”
  2. NO hinge region
  3. Generally found in serum
  4. Pentamer has 10 potential antigen binding sites
20
Q

IgD

A
  1. Expressed on a subset of naïve B-Cells
  2. Alternative mRNA splicing
  3. Hinge Region
21
Q

IgG

A
  1. Class switching
  2. Hinge region
  3. Most abundant immunoglobulin
  4. Crosses placenta
  5. “Work Horse”
22
Q

IgG: Four isotopes

A
  1. IgG1
  2. IgG2
  3. IgG3
  4. IgG4
23
Q

IgA

A
  1. Class Switching
  2. Hinge Region
  3. Mucosal antibody
24
Q

IgA: Two isotopes

A
  1. IgA1
  2. IgA2
25
Q

IgE

A
  1. Class switch
  2. NO hinge region
  3. Least abundant immunoglobulin
  4. Allergic reactions
26
Q

B- Cell Receptors

A
  1. Membrane-bound Ab isoform
  2. ‘Activates’ B-Cells after antigen binding
27
Q

B-Cell Signal Transduction

A

Iga and Igb

28
Q

B-Cell Antigen Binding

A

CR2 (CD21) and CD19

29
Q

B-Cell Receptor Complex

A
  1. Transduces antigen binding into intracellular signals
  2. B-Cell Proliferation
  3. B-Cell Differentiation
30
Q

B-Cell Receptor: What does it make

A

Germinal Center OR Antibodies

31
Q

T-Cell Receptor-Signaling Complex

A
  1. Immunoglobulin Superfamily
  2. One constant Ig region
  3. One variable Ig region
  4. Single transmembrane spanning domain
  5. Truncated cytoplasmic domain
32
Q

gd-TCR

A
  1. Often concentrated in mucosa
  2. Break the binding rules
  3. Can include lipid/glycolipid antigens
33
Q

V Domains

A

Three HyperVar regions
CDR

34
Q

C Domains

A

Single b sheet
Disulfide link

35
Q

TCR-CD3 Complex

A
  1. zz (zeta-zeta)
  2. ge (gamma-epsilon)
  3. ed (epsilon-delta)
36
Q

TCR-CD3 Complex

A

Promotes complex clustering within the plane of the membrane

37
Q

CD4

A
  1. Binds antigen-bound MHC II
  2. Phosphorylated tail
  3. Expressed in TH cells
38
Q

CD8

A
  1. a-b heterodimer or a-a heterodimer
  2. Binds antigen-bound MHC I
  3. Expressed in TC cells
39
Q

T-Cell Receptor Complex

A
  1. T-Cell Receptor
  2. Signal Transduction: CD3 Complex
40
Q

T-Cell Receptors: MHC recognition

A
  1. CD4 - MHC II
  2. CD8- MHC I
41
Q

CD28

A

Co-receptor
- required for full activation

42
Q

T-Cell Activation Results

A
  1. Transduction of binding into the cell
  2. Initiation of signaling pathways
  3. Immediate responses
  4. Long-term responses