Molecular Mechanisms and Regulation Networks of TRPM8

TRPM8的分子机制和调控网络

• 批准号: 10396096
• 负责人: Wade D. Van Horn
• 金额: $ 37.68万
• 依托单位: ARIZONA STATE UNIVERSITY-TEMPE CAMPUS
• 依托单位国家: 美国
• 财政年份: 2021
• 资助国家: 美国
• 起止时间: 2021-05-01 至 2026-02-28
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10396096
• 关键词: Biological Process; Biophysics; Cells; Chemicals; Complement; Complex; Computational Technique; Data; Development; Disease; Drug Targeting; Electrophysiology (science); Explosion; Future; Genus Mentha; Goals; Health; Horns; Human; Ion Channel; Ion Channel Protein; Laboratories; Legal patent; Link; Maps; Membrane Proteins; Menthol; Modernization; Molecular; Obesity; Oncogenes; Outcome; Outcomes Research; Output; Pain; Physiology; Property; Proteins; Publications; Regulation; Research; Signal Transduction; Stimulus; Structure; TRP channel; Techniques; Therapeutic Intervention; base; cancer type; cold temperature; drug discovery; insight; interdisciplinary approach; patch clamp; prognostic; protein complex; protein function; research vision; sensor; stoichiometry; structural biology; therapeutic target; tumor progression

Project Summary/Abstract Overview of Research: The Van Horn lab primarily focuses on elucidating and understanding the molecular mechanisms that underlie membrane protein function in health and disease. To achieve these goals, the laboratory employs a modern state-of-the-art and interdisciplinary approach using biophysical, structural, computational, and functional techniques. We are experts in membrane protein biophysics and make use of advanced NMR studies combined with functional whole-cell patch-clamp electrophysiology. These orthogonal data are linked with Rosetta-based computational techniques to understand protein function. Our primary target is the TRPM8 ion channel which was initially identified as an oncogene that is prognostic for some types of cancer progression. More recently, it has become a focus for therapeutic intervention in pain and obesity. Complicating the potential application of TRPM8 therapies is that it is a molecular integrator that is activated by a number of diverse stimuli. For example, TRPM8 is the primary human cold sensor but is also activated by the chemical menthol from mint, both of which activate TRPM8 signaling networks. The ability to respond to several different stimuli in a polymodal manner makes TRPM8 studies crucial to delineate the independence and interdependence of molecular mechanisms that result in biological function and complicate its therapeutic targeting. In addition to direct stimulation by cold and menthol, TRPM8 is regulated by diverse proteins, including the membrane protein, PIRT, which in turn modulates TRPM8 activation by cold, menthol, and other stimuli. Beyond our research on direct activation of TRPM8 by cold and menthol, we focus on determining the mechanisms whereby PIRT modulates TRPM8 function. This has led to a number of contributions from our lab including, biophysical and structural characterization of TRPM8 and PIRT, TRPM8–PIRT complex stoichiometry, identification of species-dependent regulation, and central insight into molecular regulatory mechanisms. These efforts have led to strong scientific output, including publications, seminars, and patents. Five-year Goals: Broadly defined, we will identify how TRPM8 is directly activated by cold temperatures and other stimuli, map the allosteric networks that allow for polymodal function, and determine structures of TRPM8 and related membrane protein complexes of functional consequence. Research Vision: In the past 8 years, there has been an explosion of TRP channel structural biology with now ~100 discrete TRP channel structures. This represents tremendous development and output. Our research seeks to extend and complement the structural momentum to delineate fundamental mechanistic properties such as allostery, dynamics, and protein complex regulation that determines function. These TRPM8 outcomes are anticipated to have direct impacts on human health and disease but also to serve as a template that defines and identifies fundamental rules and properties of membrane protein function.

项目总结/摘要 研究概述：范霍恩实验室主要致力于阐明和理解 在健康和疾病中膜蛋白功能的基础机制。要实现这些目标， 实验室采用了现代国家的最先进的和跨学科的方法，利用生物物理，结构， 计算和功能技术。我们是膜蛋白生物物理学的专家， 先进的核磁共振研究结合功能性全细胞膜片钳电生理学。这些正交 数据与基于Rosetta的计算技术相关联，以了解蛋白质功能。我们的首要目标 是TRPM 8离子通道，最初被鉴定为一种致癌基因，对某些类型的肿瘤有预后作用。 癌症进展最近，它已成为疼痛和肥胖症治疗干预的焦点。 使TRPM 8疗法的潜在应用复杂化的是，它是一种分子整合剂，其被以下物质激活： 各种各样的刺激。例如，TRPM 8是主要的人体冷传感器，但也由温度传感器激活。 薄荷中的化学薄荷醇，两者都能激活TRPM 8信号网络。能够应对多个 不同的刺激以多模态的方式使TRPM 8研究至关重要，以描绘独立性， 导致生物学功能并使其治疗复杂化分子机制的相互依赖性 面向.除了受到冷和薄荷醇的直接刺激外，TRPM 8还受到多种蛋白质的调节，包括 膜蛋白，PIRT，反过来调节TRPM 8激活冷，薄荷醇，和其他刺激。 除了我们对TRPM 8被冷和薄荷醇直接激活的研究之外，我们还专注于确定TRPM 8的激活机制。 PIRT调节TRPM 8功能的机制。这使得我们的实验室做出了许多贡献， 包括TRPM 8和PIRT的生物物理和结构表征，TRPM 8-PIRT复合物化学计量， 物种依赖性调控的鉴定，以及对分子调控机制的核心见解。这些 这些努力带来了大量的科学产出，包括出版物、研讨会和专利。 五年目标：从广义上讲，我们将确定TRPM 8如何被低温直接激活， 其他刺激，映射允许多模态功能的变构网络，并确定TRPM 8的结构 以及功能性后果的相关膜蛋白复合物。 研究展望：在过去的8年里，TRP通道结构生物学已经爆炸，现在 ~100个离散TRP通道结构。这代表着巨大的发展和产出。我们的研究 寻求扩展和补充结构动力，以描绘基本的机械属性， 变构、动力学和决定功能的蛋白质复合物调节。TRPM 8的这些成果是 预计对人类健康和疾病有直接影响，但也作为一个模板， 识别膜蛋白功能的基本规则和特性。