Yamada Shinji, Honma Ryusuke, Kaneko Mika K, Nakamura Takuro, Yanaka Miyuki, Saidoh Noriko, Takagi Michiaki, Konnai Satoru, Kato Yukinari
1 Department of Antibody Drug Development, Tohoku University Graduate School of Medicine , Sendai, Japan .
2 Department of Orthopedic Surgery, Yamagata University Faculty of Medicine , Yamagata, Japan .
Monoclon Antib Immunodiagn Immunother. 2017 Jun;36(3):129-134. doi: 10.1089/mab.2017.0016. Epub 2017 May 12.
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.
I型跨膜唾液酸糖蛋白血小板内皮细胞黏附分子(PDPN)在几种正常细胞中表达,包括肾足细胞、肺I型肺泡细胞和淋巴管内皮细胞。我们最近通过用牛PDPN的重组蛋白免疫小鼠,制备了一种抗牛PDPN(bovPDPN)单克隆抗体(mAb)PMab-44。在本研究中,我们使用bovPDPN的许多缺失突变体和点突变体确定了PMab-44识别bovPDPN的关键表位。流式细胞术分析显示,PMab-44的表位为Glu46-Thr50,其对应于血小板聚集刺激(PLAG)结构域3。确定PMab-44表位中的重要氨基酸为Glu46、Tyr48和Thr50。蛋白质印迹分析也证实了这些结果,表明bovPDPN的PLAG结构域在产生有用的抗PDPN单克隆抗体的免疫原性方面也很重要。