Epitope Mapping of an Anti-ferret Podoplanin Monoclonal Antibody Using the PA Tag-Substituted Analysis.

Yu Isoda, Mika K Kaneko, Tomohiro Tanaka, Hiroyuki Suzuki, Yukinari Kato
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Abstract

In small animal models of severe acute respiratory syndrome coronaviruses (SARS-CoV and SARS-CoV-2) infection, ferrets (Mustela putorius furo) have been used to investigate the pathogenesis. Podoplanin (PDPN) is an essential marker in lung type I alveolar epithelial cells, kidney podocytes, and lymphatic endothelial cells. Monoclonal antibodies (mAbs) against ferret PDPN (ferPDPN) are useful for the pathological analyses of those tissues. We previously established an anti-ferPDPN mAb, PMab-292 using the Cell-Based Immunization and Screening (CBIS) method. In this study, we determined the critical epitope of PMab-292 using flow cytometry. The ferPDPN deletion mutants analysis revealed that the Val34 is located at the N-terminus of the PMab-292 epitope. Furthermore, the PA tag-substituted analysis (PA scanning) showed that Asp39 is located at the C-terminus of PMab-292 epitope. The epitope sequence (VRPEDD) also exists between Val26 and Asp31 of ferPDPN, indicating that PMab-292 recognizes the tandem repeat of the VRPEDD sequence of ferPDPN.

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利用 PA 标签替代分析法绘制抗铁锈色斑鬼臼毒素单克隆抗体的表位图。
在严重急性呼吸系统综合征冠状病毒(SARS-CoV 和 SARS-CoV-2)感染的小动物模型中,雪貂(Mustela putorius furo)被用来研究发病机制。Podoplanin(PDPN)是肺I型肺泡上皮细胞、肾脏荚膜细胞和淋巴内皮细胞的重要标志物。针对雪貂 PDPN(ferPDPN)的单克隆抗体(mAbs)可用于这些组织的病理分析。我们之前利用细胞免疫和筛选(CBIS)方法建立了一种抗雪貂 PDPN 的 mAb--PMab-292。在本研究中,我们利用流式细胞术确定了 PMab-292 的关键表位。ferPDPN缺失突变体分析表明,Val34位于PMab-292表位的N端。此外,PA 标记替代分析(PA 扫描)显示,Asp39 位于 PMab-292 表位的 C 端。表位序列(VRPEDD)也存在于 ferPDPN 的 Val26 和 Asp31 之间,表明 PMab-292 可识别 ferPDPN 的 VRPEDD 序列的串联重复。
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CiteScore
4.80
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发文量
49
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