| Literature DB >> 34424763 |
Ren Nanamiya1, Masato Sano1, Teizo Asano1, Miyuki Yanaka1, Takuro Nakamura1, Masaki Saito2, Tomohiro Tanaka1, Hideki Hosono1, Nami Tateyama1, Mika K Kaneko1, Yukinari Kato1,2,3.
Abstract
The classic method for identifying the epitope that monoclonal antibodies (mAbs) bind uses deletion mutants and point mutants of the target protein. However, determining the epitope of mAbs-reactive membrane proteins is often challenging. We recently developed the RIEDL insertion for epitope mapping (REMAP) method to identify mAb-binding epitopes. Herein, we first checked the reactivity of an anti-epidermal growth factor receptor (EGFR) mAb (EMab-51) to several EGFR deletion mutants such as EGFR/dN152, EGFR/dN313, EGFR/dN370, EGFR/dN375, EGFR/dN380, and EGFR/dN482. We found the N-terminus of the EMab-51-binding epitope between residues 375 and 380 of EGFR. We next produced EGFR/dN313 mutants with the RIEDL peptide tag inserted at each possible position of 375-AFRGDSFTHTPPLDP-389. EMab-51 lost its reactivity with the mutants having a RIEDL tag inserted at each position of 377-RGDSFTHTPP-386, whereas LpMab-7 (an anti-RIEDL mAb) detected every mutant. Thus, using the REMAP method, we identified the EMab-51-binding epitope of EGFR as 377-RGDSFTHTPP-386.Entities:
Keywords: EGFR; EMab-51; RIEDL tag; epitope mapping; monoclonal antibody
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Year: 2021 PMID: 34424763 DOI: 10.1089/mab.2021.0010
Source DB: PubMed Journal: Monoclon Antib Immunodiagn Immunother ISSN: 2167-9436