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直接选择功能性De Novo宏循环来激活细胞上胰岛素受体
Yun-Hsuan Kuo1, Emiko Mihara2, Junichi Takagi2
1Department of Chemistry, Graduate School of Science, The University of Tokyo, Tokyo, Japan.
Angewandte Chemie (International ed. in English)
|March 12, 2026
概括
新的RaPID-ExCells系统通过在细胞内部进行查,可以直接发现功能性宏循环. 这种方法确定了HL4,一种强大的胰岛素受体激动剂,展示了它对功能性发现的实用性.
科学领域:
- 生物化学 生物化学
- 分子生物学分子生物学
- 药物发现 药物发现 药物发现
背景情况:
- 随机非标准集成发现 (RaPID) 系统使用mRNA显示用于体外选择宏环结合剂.
- 然而,结合亲和力并不总是与细胞环境中的功能活性相关.
研究的目的:
- 开发一个升级系统,RaPID-ExCells,通过细胞查直接发现功能活跃的宏循环.
- 确定胰岛素受体 (IR) 的新型宏循环激动剂.
主要方法:
- 将mRNA显示与用于细胞查的遗传重编程 (RaPID-ExCells) 的整合.
- 基于亲和力的体外选择,然后进行细胞功能测试.
- 在发现的宏循环中对非蛋白质原性氨基酸进行深度突变扫描.
主要成果:
- 发现了一种新的宏循环,HL4,该宏循环专门对细胞上的胰岛素受体 (IR) 产生作用.
- 拉皮德-ExCells促进了深度突变扫描,以阐明HL4的激进活性必不可少的残留物.
- 证明了非蛋白质原性氨基酸可以在不影响活性的情况下被纳入.
结论:
- 拉皮德-ExCells系统是一个强大的平台,用于直接选和发现功能活跃的宏循环.
- 这种方法可以识别诸如胰岛素受体之类的细胞标的强大调节剂.
- 阐明了一种新型胰岛素受体激动剂的结构-活性关系.
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