| Literature DB >> 28498096 |
Shinji Yamada1, Ryusuke Honma2, Mika K Kaneko1, Takuro Nakamura1, Miyuki Yanaka1, Noriko Saidoh1, Michiaki Takagi2, Satoru Konnai3, Yukinari Kato1,4.
Abstract
A type I transmembrane sialoglycoprotein podoplanin (PDPN) is expressed in several normal cells, including podocytes of the kidney, type I alveolar cells of the lung, and lymphatic endothelial cells. We recently produced an anti-bovine PDPN (bovPDPN) monoclonal antibody (mAb), PMab-44, by immunizing mice with recombinant proteins of bovPDPN. In this study, we determined the critical epitope of PMab-44 for the recognition of bovPDPN using many deletion mutants and point mutants of bovPDPN. Flow cytometric analyses revealed that the epitope of PMab-44 was Glu46-Thr50, which corresponds to platelet aggregation-stimulating (PLAG) domain-3. The important amino acids in the PMab-44 epitope were determined to be Glu46, Tyr48, and Thr50. Western blot analysis also confirmed these results, indicating that the PLAG domain of bovPDPN is also important in immunogenicity for producing useful anti-PDPN mAbs.Entities:
Keywords: PMab-44; bovine PDPN; podoplanin
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Year: 2017 PMID: 28498096 DOI: 10.1089/mab.2017.0016
Source DB: PubMed Journal: Monoclon Antib Immunodiagn Immunother ISSN: 2167-9436