Yuki Okada, Hiroyuki Suzuki, Tomohiro Tanaka, Mika K Kaneko, Yukinari Kato
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引用次数: 0
摘要
细胞表面的异位核苷酸酶 CD39 与另一种异位核苷酸酶 CD73 一起介导细胞外三磷酸腺苷转化为免疫抑制性腺苷。肿瘤微环境中升高的腺苷会削弱抗肿瘤免疫,从而促进肿瘤细胞的免疫逃逸和进展。抑制酶活性的抗 CD39 单克隆抗体(mAbs)可用于抗肿瘤治疗。因此,了解 mAbs 的抑制活性与表位之间的关系非常重要。我们之前利用细胞免疫和筛选方法建立了一种抗小鼠 CD39(anti-mCD39)mAb--C39Mab-1。在本研究中,我们利用流式细胞术确定了 C39Mab-1 的关键表位。我们进行了 PA 标记(12 个氨基酸 [aa])替代分析(命名为 PA 扫描)和 RIEDL 标记(5 个氨基酸)替代分析(命名为 RIEDL 扫描),利用流式细胞术确定了 C39Mab-1 的临界表位。通过结合 PA 扫描和 RIEDL 扫描,我们确定了横跨 mCD39 的 275-279、282-291 和 306-323 aa 三个片段的构象表位。这些分析有助于鉴定膜蛋白的构象表位。
Epitope Mapping of an Anti-Mouse CD39 Monoclonal Antibody Using PA Scanning and RIEDL Scanning.
A cell-surface ectonucleotidase CD39 mediates the conversion of extracellular adenosine triphosphate into immunosuppressive adenosine with another ectonucleotidase CD73. The elevated adenosine in the tumor microenvironment attenuates antitumor immunity, which promotes tumor cell immunologic escape and progression. Anti-CD39 monoclonal antibodies (mAbs), which suppress the enzymatic activity, can be applied to antitumor therapy. Therefore, an understanding of the relationship between the inhibitory activity and epitope of mAbs is important. We previously established an anti-mouse CD39 (anti-mCD39) mAb, C39Mab-1 using the Cell-Based Immunization and Screening method. In this study, we determined the critical epitope of C39Mab-1 using flow cytometry. We performed the PA tag (12 amino acids [aa])-substituted analysis (named PA scanning) and RIEDL tag (5 aa)-substituted analysis (named RIEDL scanning) to determine the critical epitope of C39Mab-1 using flow cytometry. By the combination of PA scanning and RIEDL scanning, we identified the conformational epitope, spanning three segments of 275-279, 282-291, and 306-323 aa of mCD39. These analyses would contribute to the identification of the conformational epitope of membrane proteins.