压电1
MyoD公司
细胞生物学
生物物理学
门控
频道(广播)
化学
离子通道
生物
心肌细胞
生物化学
机械敏感通道
受体
计算机科学
计算机网络
肌发生
作者
Z. Zhou,Xiaonuo Ma,Yiechang Lin,Delfine Cheng,Navid Bavi,Genevieve A. Secker,Jinyuan Vero Li,Vaibhao Janbandhu,Drew L. Sutton,Hamish S. Scott,Mingxi Yao,Richard P. Harvey,Natasha L. Harvey,Ben Corry,Yixiao Zhang,Charles D. Cox
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2023-08-17
卷期号:381 (6659): 799-804
被引量:24
标识
DOI:10.1126/science.adh8190
摘要
Piezo channels are critical cellular sensors of mechanical forces. Despite their large size, ubiquitous expression, and irreplaceable roles in an ever-growing list of physiological processes, few Piezo channel-binding proteins have emerged. In this work, we found that MyoD (myoblast determination)-family inhibitor proteins (MDFIC and MDFI) are PIEZO1/2 interacting partners. These transcriptional regulators bind to PIEZO1/2 channels, regulating channel inactivation. Using single-particle cryogenic electron microscopy, we mapped the interaction site in MDFIC to a lipidated, C-terminal helix that inserts laterally into the PIEZO1 pore module. These Piezo-interacting proteins fit all the criteria for auxiliary subunits, contribute to explaining the vastly different gating kinetics of endogenous Piezo channels observed in many cell types, and elucidate mechanisms potentially involved in human lymphatic vascular disease.
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