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磷脂酰肌醇-4,5-二磷酸(PIP2)对瞬时受体电位香草酸亚型4(TRPV4)通道的调节:结合位点与动态偶联

PIP2 regulation of TRPV4 channels: Binding sites and dynamic coupling.

作者信息

Huang Jian, Chen Jianhan

机构信息

Department of Chemistry, University of Massachusetts, Amherst, Massachusetts.

Department of Chemistry, University of Massachusetts, Amherst, Massachusetts.

出版信息

Biophys J. 2025 Aug 6. doi: 10.1016/j.bpj.2025.08.006.

Abstract

Transient Receptor Potential subfamily V4 (TRPV4) is a nonselective cation channel that plays important roles in thermo-sensing, osmoregulation, nociception, and bone homeostasis. The activities of TRV4 channels are known to be regulated by phosphatidylinositol 4,5-bisphosphate (PIP2), even though its molecular basis remains poorly understood at present. Existing studies reveal great uncertainty or even controversy on the binding sites as well as functional effects of PIP2 on TRPV4. Analysis of available cryo-EM structures suggests that the previously proposed sites on the N-terminal domain and the ankyrin repeat domain are too distal from the membrane interface and thus unlikely to be the primary sites for PIP2 regulation. Instead, we have identified two possible PIP2 binding sites near the cytosolic membrane interface using structural analysis and molecular docking. Atomistic simulations and free energy analysis reveal that these two sites belong to a single broad binding groove, where PIP2 binding is dynamic and can sample multiple configurations of interactions with positively charged side chains within the groove. These local free energy minima are separated by small free energy barriers and offer ∼4 kcal/mol stability with respect to the membrane bulk. Furthermore, dynamic network analysis suggests that PIP2 binding in the predicted groove can modulate the dynamic coupling between various domains of TRPV4, potentially priming the channel for responding to various stimuli. Together, these results provide important new insights on the possible molecular basis of PIP2 binding and regulation of TRPV4 activities.

摘要

瞬时受体电位V4亚家族(TRPV4)是一种非选择性阳离子通道,在温度感知、渗透压调节、痛觉感受和骨稳态中发挥重要作用。尽管目前对其分子机制仍知之甚少,但已知TRV4通道的活性受磷脂酰肌醇4,5-二磷酸(PIP2)调节。现有研究表明,PIP2对TRPV4的结合位点以及功能影响存在很大的不确定性甚至争议。对现有冷冻电镜结构的分析表明,先前在N端结构域和锚蛋白重复结构域上提出的位点距离膜界面太远,因此不太可能是PIP2调节的主要位点。相反,我们通过结构分析和分子对接在胞质膜界面附近确定了两个可能的PIP2结合位点。原子模拟和自由能分析表明,这两个位点属于一个单一的宽结合槽,其中PIP2的结合是动态的,可以与槽内带正电的侧链形成多种相互作用构型。这些局部自由能最小值由小的自由能垒隔开,相对于膜本体提供约4千卡/摩尔的稳定性。此外,动态网络分析表明,预测槽内的PIP2结合可以调节TRPV4各个结构域之间的动态偶联,可能使通道做好响应各种刺激的准备。总之,这些结果为PIP2结合和TRPV4活性调节的可能分子基础提供了重要的新见解。

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