Mechanisms of TRPV1 Channel Regulation

描述（由申请人提供）：TRPV 1离子通道是多模式受体，可被热、高[H+]o、电压、花生四烯酸代谢物、辣椒素（辣椒的辛辣提取物）和信号脂质PI（4，5）P2（PIP 2）激活。Ca ~（2+）/钙调素（Ca ~（2+）/CaM）和ATP也可调节其活性。我们的长期目标是了解TRPV 1整合这些多种生理刺激的分子机制。我们和其他人以前已经确定PIP 2直接激活TRPV 1。我们最近的工作表明，细胞内C-末端结构域的近端部分包括至少一部分的PIP 2结合位点。然而，无法控制天然膜的脂质组成，细胞和切除的斑块中存在无数的酶和其他蛋白质，以及难以特异性标记细胞内通道的细胞内结构域，这些都证明了理解PIP 2和其他激活方式对TRPV 1的调节存在严重的实验障碍。我们已经开发了一种新的方法来重建纯化的TRPV 1通道在高密度合成巨单层囊泡（GUV）。在这个建议中，我们将应用标准的膜片钳方法，膜片钳荧光测定法（PCF），和过渡金属离子FRET（tmFRET）研究纯化的TRPV 1通道的GUV的定义脂质组成。设计到我们的无半胱氨酸TRPV 1背景中的单个半胱氨酸将用于用荧光团位点特异性标记GUV中的通道，完全消除背景荧光问题。用于重构的GUV将包括结合过渡金属的合成脂质，其在我们开发的新型短程tmFRET方法中充当短程FRET淬灭剂。PCF允许我们同时记录电生理通道的功能和荧光通道的重排。这些新的工具将使我们能够测量与PIP 2激活以及与热，Ca 2 +/CaM和ATP激活相关的细胞内N-和C-末端结构域的动态。 公共卫生相关性：TRPV 1离子通道介导疼痛受体神经元对疼痛化学和热刺激的反应。我们将使用一些创新的新技术，我们已经开发出探测疼痛刺激调节这些离子通道的活动的机制。我们特别关注TRPV 1通过信号脂质调节的分子事件。

DESCRIPTION (provided by applicant): TRPV1 ion channels are multimodal receptors that can be activated by heat, high [H+]o, voltage, arachidonic acid metabolites, capsaicin (the pungent extract of hot chili peppers), and the signaling lipid PI(4,5)P2 (PIP2). Ca2+/Calmodulin (Ca2+/CaM) and ATP may modulate its activity as well. Our long-term goal is to understand the molecular mechanism by which TRPV1 integrates these multiple physiological stimuli. We and others have previously established that PIP2 directly activates TRPV1. Our recent work indicates that the proximal part of the intracellular C-terminal domain comprises at least part of the PIP2 binding site. However, the inability to control the lipid composition of native membranes, the presence of myriad enzymes and other proteins in cells and excised patches, and the difficulty of specifically labeling intracellular domains of channels within cells have proven serious experimental barriers to understanding regulation of TRPV1 by PIP2 and other activation modalities. We have developed a novel approach to reconstitute purified TRPV1 channels at high density in synthetic Giant Unilamellar Vesicles (GUVs). In this proposal we will apply standard patch-clamp methods, Patch-Clamp Fluorometry (PCF), and Transition Metal Ion FRET (tmFRET) to study purified TRPV1 channels in GUVs of defined lipid composition. Single cysteines engineered into our cysteineless TRPV1 background will be used to site-specifically label channels in the GUVs with fluorophore, completely eliminating the background fluorescence problem. The GUVs used for reconstitution will include synthetic lipids that bind transition metals which act as short- distance FRET quenchers in the novel short-range tmFRET approach we have developed. PCF allows us to simultaneously record the function of the channel with electrophysiology and the rearrangement of the channel with fluorescence. These new tools will allow us to measure dynamics of the intracellular N- and C-terminal domains associated with PIP2 activation as well as with activation by heat, Ca2+/CaM, and ATP. PUBLIC HEALTH RELEVANCE: TRPV1 ion channels mediate the response to painful chemical and thermal stimuli in pain- receptor neurons. We will use a number of innovative new techniques which we have developed to probe the mechanisms by which painful stimuli regulate the activity of these ion channels. We particularly focus on the molecular events that underlie TRPV1 regulation by signaling lipids.