Antibody biology Flashcards

1
Q

which response do B cells activate

A

humoral response, responsible for producing antibodies.

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2
Q

where do b cells originate and mature

A

bone marrow

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3
Q

what happens to the B cells upon activation with antigens

A

they differentiate into plasma cells which are antibody-producing factories

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4
Q

what do plasma cells secrete

A

antibody of the same specificity as the membrane-bound immunoglobulin expressed by their B cell precursor

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5
Q

FAB

A

fragment antigen binding - responsible for binding antigen

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6
Q

FC

A

fragment crystallisable - responsible for effector function

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7
Q

what does the flexible hinge of IgG allow

A

allows for both arms to bind to many arrangements of antigens on pathogen surfaces

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8
Q

what are the two types of light chains

A

Lambda and Kappa

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9
Q

In any individual antibody molecule, are the chains the same or different

A

both light chains

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10
Q

which chain determines the class of antibodies

A

heavy chain

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11
Q

what do antibodies fold into

A

globular domains with distinctive 3d structure

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12
Q

what do the globular domains comprise of

A

2 beta sheets with a total of 7 or 8 antiparallel beta strands which are linked by disulphide bridge to form a beta parallel.
this folded structure is known as the “immunoglobulin fold”

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13
Q

what do hypervariable loops form

A

antigen binding site

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14
Q

what are hypervariable loops known as

A

complementarity-determining regions (CDRs)

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15
Q

what happens when VH (variable heavy) and VL (variable light) domains are paired

A

their 6 CDRs creae the antigen-binding site

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16
Q

what is an epitope

A

An epitope, also known as an antigenic determinant, is the specific region on an antigen that is recognized and bound by an antibody, a B cell receptor, or a T cell receptor.

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17
Q

what is a linear epitope

A

epitopes in protein antigens may comprise a single stretch of polypeptide chain

18
Q

what is a discontinuous epitope

A

3D folded like structure where the polypeptide chain is not continuous

19
Q

what can epitopes bind to

A

pockets, grooves, extended surfaces or projections in antigen binding sites

20
Q

each individual has an antibody repertoire (available antigen specificities) of approximately how many

A

1011

20
Q

epitopes for antibodies are exposed where

A

on pathogen surfaces

21
Q

how is the antibody repertoire achieved

A

Ig genes are organised differently to other genes, in all cells except B cells, Ig genes are in fragmented form that cannot be expressed
Ig heavy and light chain loci consist of families of gene segments, arrayed sequentially along the chromosome
* They are inherited in this form through egg and sperm (germline)Therefore their arrangement is termed “germline configuration”
* In developing B cells, Ig gene segments must be rearranged to assemble functional light and heavy chain gene

22
Q

VH domain is encoded by what

A

V (encodes most of the V domain) ,D (diversity segment) and J (Joining segment) gene segments

23
Q

VL domain is encoded by what

A

V (encodes most of the V domain) and J (Joining segment) gene segments

24
Q

at which point in B cell development does Ig gene rearrange in the H chain

A

early pro-b cell: D-J rearranging
late pro - b cell: V-DJ rearranging

25
Q

at which point in B cell development does Ig gene rearrange in the L chain

A

small pre b cell: V-J rearranging

26
Q

when is the DNA spliced out

A

during early development of the B cell

27
Q

what is the D gene segment joined to and what is the DJ segment joined to

A

D is joined to J and V is joined to DJ

28
Q

what is recombination coded by

A

recombination signal sequences
12 and 23 base pair sequences

29
Q

what is the 12/23 rule

A

genes with the 12 base pairs can recombine with 1 with the 23 base pair spacer

30
Q

what is the mediator to organise the splicing

A

VDJ recombinase

31
Q

what is the VDJ recombinase made of

A

RAG (recombination activating gene) 1 and RAG2 RAG-1 and RAG-2 proteins work together to initiate the recombination process by recognizing specific recombination signal sequences (RSS) flanking the variable (V), diversity (D), and joining (J) gene segments.

32
Q

how does the RAG complex work

A

The RAGS bind to the 12 and 23 base pairs on the V and J RSS. The RAG complexes then come together and align the RSSs and cleaves the DNA at ends of gene segments.
That forms a DNA hairpin and a clean break at the heptemer ends. The RAG complexes hold the DNA in place while broken ends rejoined by DNA repair enzymes = nonhomologous end-joining. Coding joint formed in chromosome, signal joint removed piece of circular DNA.

33
Q

what creates the palindromic nucleotides

A

a nick that opens the hairpins can occur at several different positions

34
Q

diversity of Ig repertoire generated by main processes
Combinatorial diversity

A

many of the copies of each gene segment type which can combine in many different ways

35
Q

diversity of Ig repertoire generated by main processes
Junctional diversity

A

nucleotides added or subtracted at joints between gene segments during enzymatic steps

36
Q

diversity of Ig repertoire generated by main processes
combinations of light chain heavy chain

A

many different combinations of light and heavy chains v regions that pair to form antigen binding site

37
Q

diversity of Ig repertoire generated by main processes
somatic hypermutation

A

somatic hypermutation introduces point mutations into rearranged V region genes of activated B cells

38
Q

in the CH gene what do the exons code for

A

individual Ig domain

39
Q

s

A