The long term objective of this study is to attain an understanding of how the amino acid sequence of antibody variable regions leads to antibody specificity and affinity for antigen, and to idiotypic expression. Oligonucleotide-directed mutagenesis of antibody genes will be used to introduce mutations in the complementarity determining regions (CDRS) of a mouse antibody specific for p-azophenylarsonate (Ars). Mutant antibodies will be expressed following transfection of the mutagenized genes into myeloma or hybridoma cell lines, and transfectomas will be recovered either in liquid microcultures or in soft agarose. Secreted antibodies, in supernatants or in situ, will be screened by standard immunological assays. The hypothesis that antibody affinity is particularly sensitive to changes at certain positions will be tested by introducing all possible substitutions at each of four positions that have been found to affect affinity of the anti-Ars antibody. Minimal requirements for improved antibody affinity and for changed specificity will be determined by introducing one or a few random mutations at a time in the CDRs of the anti-Ars antibody, and screening for mutants with increased affinity for Ars or with new antigen specificities. To probe the roles of each of the six CDRs of the anti-Ars antibody in antigen binding and idiotypic expression, the CDRs will be individually """"""""blanked out"""""""" by replacement with glycine residues. The reconstruction of an anti-Ars combining site will then be attempted by introducing into such glycine-replaced CDRS, the amino acid residues that have been implicated in Ars contact. The glycine-replaced CDRs will also be randomly mutagenized at low frequency, to obtain antibodies specific for Ars or for other antigens. Insights gained from the proposed studies should further our understanding of protein folding in general and of antibody complementarity in particular, and should bring us a step closer to the long term objective of tailoring antibodies for research and medical purposes.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI023909-07
Application #
3136466
Study Section
Allergy and Immunology Study Section (ALY)
Project Start
1986-07-01
Project End
1995-07-31
Budget Start
1992-08-01
Budget End
1993-07-31
Support Year
7
Fiscal Year
1992
Total Cost
Indirect Cost
Name
Boston University
Department
Type
Schools of Medicine
DUNS #
604483045
City
Boston
State
MA
Country
United States
Zip Code
02118
Liebman, Meredith A; Roche, Marly I; Williams, Brent R et al. (2007) Antibody treatment of human tumor xenografts elicits active anti-tumor immunity in nude mice. Immunol Lett 114:16-22
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Chen, Liyan; Liebman, Meredith A; Teodorescu-Frumosu, Sanda et al. (2003) Expression of a prototypic anti-colorectal cancer polyclonal antibody library in mammalian cells. Immunol Lett 88:135-40
Sharon, Jacqueline; Sompuram, Seshi R; Yang, Chiou-Ying et al. (2002) Construction of polyclonal antibody libraries using phage display. Methods Mol Biol 178:101-12
Williams, Brent R; Sharon, Jacqueline (2002) Polyclonal anti-colorectal cancer Fab phage display library selected in one round using density gradient centrifugation to separate antigen-bound and free phage. Immunol Lett 81:141-8
Williams, Brent R; Sompuram, Seshi R; Sharon, Jacqueline (2002) Generation of anti-colorectal cancer fab phage display libraries with a high percentage of diverse antigen-reactive clones. Comb Chem High Throughput Screen 5:489-99
Sharon, J; Sarantopoulos, S; Den, W et al. (2000) Recombinant polyclonal antibody libraries. Comb Chem High Throughput Screen 3:185-96
Santora, K E; Sarantopoulos, S; Den, W et al. (2000) Generation of a polyclonal fab phage display library to the human breast carcinoma cell line BT-20. Comb Chem High Throughput Screen 3:51-7
Sompuram, S R; Den, W; Sharon, J (1996) Analysis of antigen binding and idiotypic expression by antibodies with polyglycine-replaced complementarity-determining regions. J Immunol 156:1071-81

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