Sung Ah Moon" /> Sung Ah Moon, Min Kyung Ki, Sungyoung Lee, Mi-Lim Hong, Misook Kim, Sungsub Kim, Junho Chung, Sue Goo Rhee*, and Hyunbo Shim*" /> Sung Ah Moon, Min Kyung Ki, Sungyoung Lee, Mi-Lim Hong, Misook Kim, Sungsub Kim, Junho Chung, Sue Goo Rhee*, and Hyunbo Shim*. Mol. Cells 2011;31:509-13. https://doi.org/10.1007/s10059-011-2268-8">
Mol. Cells 2011; 31(6): 509-513
Published online April 15, 2011
https://doi.org/10.1007/s10059-011-2268-8
© The Korean Society for Molecular and Cellular Biology
Correspondence to : *Correspondence: rheesg@ewha.ac.kr (SGR); hshim@ewha.ac.kr (HS)
Target-specific antibodies can be rapidly enriched and identified from an antibody library using phage display. Large, na?ve 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 108 to higher than 109, were combined into a single large library with > 1010 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 na?ve library, i.e., against various non-immunizing antigens to yield specific antibodies.
Keywords antigen specificity, immune library, non-immunizing antigen, phage display, scFv
Mol. Cells 2011; 31(6): 509-513
Published online June 30, 2011 https://doi.org/10.1007/s10059-011-2268-8
Copyright © The Korean Society for Molecular and Cellular Biology.
Sung Ah Moon1, Min Kyung Ki1, Sungyoung Lee2, Mi-Lim Hong2, Misook Kim2, Sungsub Kim2, Junho Chung3, Sue Goo Rhee1,*, and Hyunbo Shim1,4,*
1Division of Life and Pharmaceutical Sciences, The Graduate School, Ewha Womans University, Seoul 120-750, Korea, 2Young In Frontier, Anyang 431-836, Korea, 3Seoul National University College of Medicine, Seoul 110-799, Korea, 4Department of Life Science, College of Natural Sciences, Ewha Womans University, Seoul 120-750, Korea
Correspondence to:*Correspondence: rheesg@ewha.ac.kr (SGR); hshim@ewha.ac.kr (HS)
Target-specific antibodies can be rapidly enriched and identified from an antibody library using phage display. Large, na?ve 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 108 to higher than 109, were combined into a single large library with > 1010 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 na?ve library, i.e., against various non-immunizing antigens to yield specific antibodies.
Keywords: antigen specificity, immune library, non-immunizing antigen, phage display, scFv
Hye Young Yang, Kyung Jae Kang, Julia Eunyoung Chung, Hyunbo Shim
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