Molecular underpinning of intracellular pH regulation on TMEM16F

被引:14
|
作者
Liang, Pengfei [1 ]
Yang, Huanghe [1 ,2 ]
机构
[1] Duke Univ, Med Ctr, Dept Biochem, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Dept Neurobiol, Durham, NC 27710 USA
来源
JOURNAL OF GENERAL PHYSIOLOGY | 2021年 / 153卷 / 02期
基金
美国国家卫生研究院;
关键词
CHLORIDE CHANNELS; TUMOR-CELLS; PHOSPHATIDYLINOSITOL 4,5-BISPHOSPHATE; DYSREGULATED PH; BREAST-CANCER; CL-CHANNELS; ANOCTAMIN; CRYO-EM; PHOSPHATIDYLSERINE; EXPOSURE;
D O I
10.1085/jgp.202012704
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
TMEM16F, a dual-function phospholipid scramblase and ion channel, is important in blood coagulation, skeleton development, HIV infection, and cell fusion. Despite advances in understanding its structure and activation mechanism, how TMEM16F is regulated by intracellular factors remains largely elusive. Here we report that TMEM16F lipid scrambling and ion channel activities are strongly influenced by intracellular pH (pH(i)). We found that low pH(i) attenuates, whereas high pHi potentiates, TMEM16F channel and scramblase activation under physiological concentrations of intracellular Ca2+ ([Ca2+](i)). We further demonstrate that TMEM16F pH(i) sensitivity depends on [Ca2+](i) and exhibits a bell-shaped relationship with [Ca2+]i: TMEM16F channel activation becomes increasingly pHi sensitive from resting [Ca2+](i) to micromolar [Ca2+](i), but when [Ca2+]i increases beyond 15 mu M, pHi sensitivity gradually diminishes. The mutation of a Ca2+-binding residue that markedly reduces TMEM16F Ca2+ sensitivity (E667Q) maintains the bell-shaped relationship between pHi sensitivity and Ca2+ but causes a dramatic shift of the peak [Ca2+](i) from 15 mu M to 3 mM. Our biophysical characterizations thus pinpoint that the pH(i) regulatory effects on TMEM16F stem from the competition between Ca2+ and protons for the primary Ca2+-binding residues in the pore. Within the physiological [Ca2+](i) range, the protonation state of the primary Ca2+-binding sites influences Ca2+ binding and regulates TMEM16F activation. Our findings thus uncover a regulatory mechanism of TMEM16F by pHi and shine light on our understanding of the pathophysiological roles of TMEM16F in diseases with dysregulated pH(i), including cancer.
引用
收藏
页数:20
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