| Literature DB >> 31535919 |
Yukinari Kato1,2, Junko Takei1,3, Yoshikazu Furusawa1,2, Yusuke Sayama1, Masato Sano1, Satoru Konnai4,5, Atsushi Kobayashi6, Hiroyuki Harada3, Maki Takahashi7, Hiroyoshi Suzuki7, Shinji Yamada1, Mika K Kaneko1.
Abstract
Podoplanin (PDPN)/T1alpha is a type I transmembrane sialoglycoprotein, which is expressed on podocytes of the kidneys and type I alveolar cells of the lungs. PDPN is also known as Aggrus, a platelet aggregation-inducing factor, which comprises three platelet aggregation-stimulating (PLAG) domains (PLAG1, PLAG2, and PLAG3) in the N-terminus and PLAG-like domains (PLDs) in the middle of the PDPN protein. We have previously established a mouse anti-bear PDPN (bPDPN) monoclonal antibody (mAb) clone, PMab-247 using the Cell-Based Immunization and Screening (CBIS) method. PMab-247 is very useful in flow cytometry, Western blotting, and immunohistochemical (IHC) analyses; however, the binding epitope of PMab-247 has not been elucidated. In this study, we aimed to investigate the epitope of PMab-247 using enzyme-linked immunosorbent assay and IHC analyses. The results revealed that the critical epitopes of PMab-247 are Asp76, Arg78, Glu80, and Arg82 of bPDPN. The Glu80 and Arg82 are included in PLD of bPDPN. The findings of our study can be applied to the production of more functional anti-bPDPN mAbs.Entities:
Keywords: PDPN; PMab-247; epitope mapping; podoplanin
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Year: 2019 PMID: 31535919 DOI: 10.1089/mab.2019.0025
Source DB: PubMed Journal: Monoclon Antib Immunodiagn Immunother ISSN: 2167-9436