| Literature DB >> 21499952 |
Sung Ah Moon1, Min Kyung Ki, Sungyoung Lee, Mi-Lim Hong, Misook Kim, Sungsub Kim, Junho Chung, Sue Goo Rhee, Hyunbo Shim.
Abstract
Target-specific antibodies can be rapidly enriched and identified from an antibody library using phage display. Large, naïve antibody libraries derived from synthetic or unimmunized sources can yield antibodies against virtually any antigen, whereas libraries from immunized sources tend to be smaller and are used exclusively against the antigen of immunization. In this study, 25 scFv libraries made from the spleens of immunized rabbits, each with a size ranging from 10(8) to higher than 10(9), were combined into a single large library with > 10(10) individual clones. Panning of this combined library yielded target-specific rabbit scFv clones against many non-immunizing antigens, including proteins, peptides, and a small molecule. Notably, specific scFv clones against a rabbit self-antigen (rabbit serum albumin) and a phosphorylated protein (epidermal growth factor receptor pTyr1173) could be isolated from the library. These results suggest that the immune library contained a significant number of unimmunized clones and that a sufficiently large immune library can be utilized similarly to a naïve library, i.e., against various non-immunizing antigens to yield specific antibodies.Entities:
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Year: 2011 PMID： 21499952 PMCID： PMC3887623 DOI： 10.1007/s10059-011-2268-8
Source DB: PubMed Journal: Mol Cells ISSN： 1016-8478 Impact factor: 5.034