Humoral Immunity And The Genrstion of Antibody Diversity Flashcards

1
Q

What is the variable region within an antibody specialised for?

A

In the variable region the amino acid sequence varies from one Ig molecule to another to allow binding to various antigens

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What is the constant region within a antibody responsible for?

A

The constant region is responsible for its effector actions such as activating complement and binding to phagocytes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is the antibody made out of?

A

2 heavy chain and two light chain, those light chain can be either lambda or kappa

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What is the complementary determining region?

A

These are hyper variable region on the variable region which is part of the V that bind to antigens.

Side note CDR3 is the most variable region

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

How is the CDR different in primary structure and tertiary structures

A

The CDR are separated when in primary structure but they are adjacent when in 3D form

The rest of the V structure form the framework allows all the CDR to face the antigen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

How much antibodies are there and where do they rest?

A

The body generates 100million B cells and each generates a different random Ig. These B cells just sit in the lymph nodes not doing much.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What happens to B cells during infections?

A

During an infection a few B cell will happen to make Ig that can Bing to the foreign antigens which then result in the activation of the B cell and it multiply. This is colonal selection

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

How do B cells get activated

A

Activation of a B cell require its Ig to bind with a foreign antigen then we need help from CD4+ T helper cell and the cytokines released from said T helper cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

How many genes do we have coding for antibodies?

A

We inherit no complete Ig gene, it’s all segmented. By arranging these segments in different combination we can generate many Ig sequence.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What does the Germ line kappa light chain contain?

A

The kappa light chain have one constant region 35 variable region and 5 short joining segments

V1-v25…….j1-5…….C…..germ line DNA…..

The J segment are quite close to the C segment but the V segment are a long way away from the constant region on the DNA.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Where can a ending keys enzyme attach within the antibody gene segments?

A

There are binding sites after each V segment and one before each J segment.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

How does the endonucleus enzyme work?

A

It will cut at random after one V segment and before one J segment. The free end then ligature together and join together.

This process is not splicing but dsDNA joining. This is due to the fact that the resulting segments are not one functioning gene.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

How is gene diversity generated?

A

Gene diversity can be enervated by rearranging the gene segment.
We have 1C, 5J and 35V so the number of different variable is 175 (35*5)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What happens during recombination with V and J segment

How is junction so diversity created?

A

RAG recombinase cut and remove intervening DNA and ends are processed before joining together.

Exonuclease will mess around with the free ends before they are ligature together.

Terminal deoxynucleotidyl transferase randomly add a few nucleotides to the free end before they are added together. This creases junction all diversity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Why is TdT terminal deoxynucleotidyl transferase important?

A

They are important for generating Ig diversity, it is also important as a leukaemia marker l and a useful enzyme in genetic engineering

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

How much difference antibodies we can make?

A

Each kappa chain we have 35 variable and 5 joining segment. With junction modification we can add at least 10 more variable ways. So more than 1750

Heavy chain have 45V, 6J and 20 diversity segments and with junction variable of at least 10 and there is two junctions V-D and D-J. This amount to 466201010= 540,000

We know CDR is made up of heavy and light chain so 1750*540,000 =9,450,000,000 different combinations

17
Q

What is allelic exclusion?

A

Any B cell is diploid, it have two alleles of the Ig heavy chain so t theory it can make two heavy chain but third never happens due to allelic exclusion.

This is because as soon as one allele successfully rearranges and start making heavy chain protein the Feb rearrangement process for heavy chain is switched off. This is the same for light chains, we have two kappa and lambda light chains.

18
Q

How many light chains do B cells make?

A

One B cell will only make one light chain, either kappa or lambada