| Literature DB >> 30213726 |
Henry D Wilson1, Xiuling Li1, Haiyong Peng1, Christoph Rader2.
Abstract
Phage display of combinatorial antibody libraries is a versatile tool in the field of antibody engineering, with diverse applications including monoclonal antibody (mAb) discovery, affinity maturation, and humanization. To improve the selection efficiency of antibody libraries, we developed a new phagemid display system that addresses the complication of bald phage propagation. The phagemid facilitates the biotinylation of fragment of antigen binding (Fab) antibody fragments displayed on phage via Sortase A catalysis and the subsequent enrichment of Fab-displaying phage during selections. In multiple contexts, this selection approach improved the enrichment of target-reactive mAbs by depleting background phage. Panels of cancer cell line-reactive mAbs with high diversity and specificity were isolated from a naïve chimeric rabbit/human Fab library using this approach, highlighting its potential to accelerate antibody engineering efforts and to empower concerted antibody drug and target discovery.Entities:
Keywords: antibody engineering; phagemid; site-specific programming; sortagging; whole-cell panning
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Year: 2018 PMID: 30213726 PMCID: PMC6186506 DOI: 10.1016/j.jmb.2018.09.003
Source DB: PubMed Journal: J Mol Biol ISSN: 0022-2836 Impact factor: 5.469