Title: Review
1Review
2You have isolated protein X, which you believe is
a new isotype of human immunoglobulin.
- You prepare rabbit antisera to whole human IgG,
human k chain, and human g chain. Assuming
protein X is in fact, a new immunoglobulin
isotype, to which of the antisera would it bind?
Why?
3You have isolated protein X, which you believe is
a new isotype of human immunoglobulin.
- Devise an experimental procedure for preparing an
anitserum that is specific for protein X
4Question 2
- According to the clonal selection theory, all the
immunoglobulin molecules on a single B cell have
the same antigenic specificity. Explain why the
presence of both IgM and IgD on the same B cell
does not violate the unispecificity implied by
clonal selection.
5Question 3
- IgG, which contains g heavy chains,developed much
more recently during evolution than IgM, which
contains m heavy chains. Describe two advantages
and two disadvantages that IgG has in comparison
with IgM.
6Question 4
- Explain why a VH segment cannot join directly
with a JH segment in heavy-chain gene
rearrangement.
7Question 5
- Considering only combinatorial joining of gene
segments and association of light and heavy
chains, how many different antibody molecules
potentially could be generated from germ-line DNA
containing 500 VL and 4 JL gene segments and 300
VH, 15 DH, and 4 JH gene segments?
8Question 6
- What mechanisms generate the three hpervariable
regions (complementarity determining regions) of
immunoglobulin heavy and light chains? Why is
the third hypervariable region (CDR3) more
variable than the other two (CDR and CDR2)
9Since CDR3 makes a major contribution to Ag
binding by the Ab molecule, amino acid changes
generated by junctional flexibility can make a
major contribution to Ab diversity.
107. You have generated a congenic A.B mouse strain
that has been selected for its MHC haplotype.
The haplotype of strain A was a/a and of strain B
was b/b.
- Which strain provides the genetic background of
this mouse? - Which strain provides the haplotype of the MHC of
this mouse?
11You have generated a congenic A.B mouse strain
that has been selected for its MHC haplotype.
The haplotype of strain A was a/a and of strain B
was b/b.
- To produce this congenic strain, the F1 progeny
are always backcrossed to which strain? - Why was backcrossing ot one of the parents
performed? - Why was interbreeding of the F1 and F2 progeny
performed? - Why was section necessary and what kind of
selection was performed ?
12Question 8
- You cross a BALB /c mouse (H-2d)mouse with a CBA
(H-2k) mouse. What MHC molecules will the F1
progeny express on its liver cells and its
macrophages?
13Question 9
- When does a B-cell becomes immunocompetent?
- A. Following productive rearrangement of variable
region heavy-chain gene segments in germ line DNA - B. Following productive rearrangement of variable
region heavy chain and light chain gene segments
in germ line DNA. - C. Following class switching
- D. During affinity maturation
- E. Following binding of T-helper cytokines to
their receptors. - F. All of the above
14Question 10
- What was the name of the scientist who along with
Gerald Edelman won the Nobel prize for deriving
the structure of antibodies? - a. Don Henley
- b. Rodney Porter.
- c. Gene Simmons
- d. Art Garfunkel
- e. Deborah Harry