Antibody Binding Epitope Mapping (AbMap) of Hundred Antibodies in a Single Run

作者
Huan Qi,Ming‐liang Ma,Chuansheng Hu,Zhao‐wei Xu,Fan-lin Wu,Nan Wang,Dan‐yun Lai,Yang Li,Hainan Zhang,He‐wei Jiang,Qingfeng Meng,Shujuan Guo,Yani Kang,Xiaodong Zhao,Hua Li,Sheng‐ce Tao
出处
期刊:Molecular & Cellular Proteomics [Elsevier BV]
卷期号:20: 100059-100059 被引量:51
标识
DOI:10.1074/mcp.ra120.002314
摘要

Antibodies play essential roles in both diagnostics and therapeutics. Epitope mapping is essential to understand how an antibody works and to protect intellectual property. Given the millions of antibodies for which epitope information is lacking, there is a need for high-throughput epitope mapping. To address this, we developed a strategy, Antibody binding epitope Mapping (AbMap), by combining a phage displayed peptide library with next-generation sequencing. Using AbMap, profiles of the peptides bound by 202 antibodies were determined in a single test, and linear epitopes were identified for >50% of the antibodies. Using spike protein (S1 and S2)-enriched antibodies from the convalescent serum of one COVID-19 patient as the input, both linear and potentially conformational epitopes of spike protein specific antibodies were identified. We defined peptide-binding profile of an antibody as the binding capacity (BiC). Conceptually, the BiC could serve as a systematic and functional descriptor of any antibody. Requiring at least one order of magnitude less time and money to map linear epitopes than traditional technologies, AbMap allows for high-throughput epitope mapping and creates many possibilities.

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