Chemical Basis for Potassium Channel Modulation

钾通道调节的化学基础

• 批准号: 7092592
• 负责人: Pamela Michael England
• 金额: $ 29.32万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
• 依托单位国家: 美国
• 财政年份: 2003
• 资助国家: 美国
• 起止时间: 2003-07-15 至 2008-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7092592
• 关键词: SDS polyacrylamide gel electrophoresis; Xenopus oocyte; biophysics; free radical oxygen; long QT syndrome; matrix assisted laser desorption ionization; methionine; nuclear magnetic resonance spectroscopy; oxidation; oxygen; potassium channel; protein protein interaction; sulfoxide; voltage gated channel; western blottings

DESCRIPTION (provided by applicant): Ion channels are a class of proteins that play critical role in cellular signaling by mediating the excitability of cells. This activity of ion channels is not static, but constantly changes in response to various intracellular and extracellular signals and, in recent years, many of the factors that directly modulate the activity of ion channels have begun to be identified. Understanding the chemical basis for how the activity of these proteins is modulated represents one of the most important areas of modern science as it impacts our understanding of how the nervous system works as well as our ability to pharmacologically manipulate it. The proposed research seeks to characterize several potential modes of modulation of the human ether-a-go-go related gene (HERG) ion channel, a voltage-gated potassium channel found in brain and heart. The activity of HERG channels is modulated by oxygen (02) and reactive oxygen species (ROS) in vitro and it has been proposed that HERG channels function as direct sensors of O2/ROS in vivo. The hypothesis that O2/ROS sensing by HERG channels is mediated by the reversible oxidation of methionine residues within the channel will be evaluated by characterizing the biophysical effects of site-specifically incorporating methionine sulfoxide into the channel on channel biophysics. HERG channel activity is also modulated by various classes of small molecules in vivo. In all but a few cases, the binding site(s) for these compounds have not been identified, however. The hypothesis that small molecules modulate the activity of HERG channels by binding to the N-terminal (PAS) domain will be evaluated using NMR spectroscopy (to detect structural perturbations associated with ligand binding) and electrophysiology (to define biophysical changes associated with ligand binding). Finally, HERG channel activity also appears to be modulated by various protein-protein interactions. To determine the site(s) in HERG that interact with other proteins, photoreactive amino acids capable of forming protein cross-links will be site-specifically incorporated into the HERG.

描述（由申请人提供）：离子通道是一类通过介导细胞兴奋性在细胞信号传导中发挥关键作用的蛋白质。离子通道的这种活性不是静态的，而是响应各种细胞内和细胞外信号而不断变化，近年来，许多直接调节离子通道活性的因素已开始被识别。了解如何调节这些蛋白质的活性的化学基础是现代科学最重要的领域之一，因为它影响我们对神经系统如何工作的理解以及我们通过药理学操纵神经系统的能力。拟议的研究旨在描述人类 ether-a-go-go 相关基因 (HERG) 离子通道（大脑和心脏中发现的电压门控钾通道）的几种潜在调节模式。 HERG 通道的活性在体外受氧 (02) 和活性氧 (ROS) 调节，并且已经提出 HERG 通道在体内充当 O2/ROS 的直接传感器。 HERG 通道的 O2/ROS 传感是由通道内蛋氨酸残基的可逆氧化介导的假设将通过表征位点特异性地将蛋氨酸亚砜掺入通道中对通道生物物理学的生物物理影响来评估。 HERG 通道活性也受到体内各类小分子的调节。然而，除了少数情况外，在所有情况下，这些化合物的结合位点尚未确定。小分子通过与 N 末端 (PAS) 结构域结合来调节 HERG 通道活性的假设将使用 NMR 波谱（检测与配体结合相关的结构扰动）和电生理学（定义与配体结合相关的生物物理变化）进行评估。最后，HERG 通道活性似乎也受到各种蛋白质-蛋白质相互作用的调节。为了确定 HERG 中与其他蛋白质相互作用的位点，能够形成蛋白质交联的光反应性氨基酸将被位点特异性地掺入 HERG 中。