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Proc Natl Acad Sci U S A. 2009 Dec 1;106(48):20216-21. doi: 10.1073/pnas.0909775106. Epub 2009 Oct 29.

Precise determination of the diversity of a combinatorial antibody library gives insight into the human immunoglobulin repertoire.

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1
Research Informatics, Rinat-Pfizer Inc., 230 East Grand Avenue, South San Francisco, CA 94080, USA.

Abstract

Antibody repertoire diversity, potentially as high as 10(11) unique molecules in a single individual, confounds characterization by conventional sequence analyses. In this study, we present a general method for assessing human antibody sequence diversity displayed on phage using massively parallel pyrosequencing, a novel application of Kabat column-labeled profile Hidden Markov Models, and translated complementarity determining region (CDR) capture-recapture analysis. Pyrosequencing of domain amplicon and RCA PCR products generated 1.5 x 10(6) reads, including more than 1.9 x 10(5) high quality, full-length sequences of antibody variable fragment (Fv) variable domains. Novel methods for germline and CDR classification and fine characterization of sequence diversity in the 6 CDRs are presented. Diverse germline contributions to the repertoire with random heavy and light chain pairing are observed. All germline families were found to be represented in 1.7 x 10(4) sequences obtained from repeated panning of the library. While the most variable CDR (CDR-H3) presents significant length and sequence variability, we find a substantial contribution to total diversity from somatically mutated germline encoded CDRs 1 and 2. Using a capture-recapture method, the total diversity of the antibody library obtained from a human donor Immunoglobulin M (IgM) pool was determined to be at least 3.5 x 10(10). The results provide insights into the role of IgM diversification, display library construction, and productive germline usages in antibody libraries and the humoral repertoire.

PMID:
19875695
PMCID:
PMC2787155
DOI:
10.1073/pnas.0909775106
[Indexed for MEDLINE]
Free PMC Article
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