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            ヤマウチ アキラ
            Akira Yamauchi
           山内 明 所属 川崎医科大学 医学部 基礎医学 生化学 職種 教授  | 
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| 論文種別 | 原著 | 
| 言語種別 | 英語 | 
| 査読の有無 | 査読あり | 
| 表題 | Fine definition of the epitopes on the human gp91phox/NOX2 for the monoclonal antibodies CL-5 and 48 | 
| 掲載誌名 | 正式名:Journal of Immunological Methods 略 称:J Immunol Methods ISSNコード:00221759  | 
| 掲載区分 | 国外 | 
| 巻・号・頁 | 501 | 
| 著者・共著者 | Kawai C, Miyano K, Okamoto S, Yamauchi A, Kuribayashi F. | 
| 発行年月 | 2022/02 | 
| 概要 | Superoxide-producing NADPH oxidase, gp91phox/NOX2, in phagocytes plays a critical role in the host defenses against pathogens. Moreover, gp91phox/NOX2 contributes to the oxidative stress in endothelial cells. Therefore, investigating the level of gp91phox/NOX2 with immunoblotting is important for estimating the amount of superoxide produced. Here, we showed that the epitopes in human gp91phox/NOX2 recognized by monoclonal antibodies (mAbs) CL-5 and 48 were in amino acids 132–147 and 136–144, respectively. Although the epitopes were close to the N-glycosylation sites, N-glycan maturation did not affect mAbs recognition. When Pro-136 was substituted with Arg, the corresponding mouse residue, human gp91phox/NOX2 was not recognized by mAbs CL-5 and 48; however, the substitution did not affect gp91phox/NOX2-based oxidase activity. This finding explains why these mAbs specifically recognize the human but not mouse gp91phox/NOX2. Hence, these mAbs are useful for investigating the level of gp91phox/NOX2 without amino acid substitutions in the epitopes. | 
| DOI | https://doi.org/10.1016/j.jim.2021.113213 | 
| PMID | 34971634 |