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Allosteric mechanisms of CA-activated K channel gating

CA 激活 K 通道门控的变构机制

基本信息

批准号：
8045488
负责人：
FRANK T HORRIGAN
金额：
$ 32.91万
依托单位：
BAYLOR COLLEGE OF MEDICINE
依托单位国家：
美国
项目类别：
财政年份：
2001
资助国家：
美国
起止时间：
2001-09-30 至 2013-03-31
项目状态：
已结题

项目摘要

DESCRIPTION (provided by applicant): Ion channels dynamically regulate membrane permeability through their ability to open and close (gate) in response to various stimuli. Progress has been made in identifying and characterizing parts of channel proteins that are involved in this gating process including "sensors" that detect stimuli, and "gates" that regulate the flow of ions through the channel pore. However many questions remain concerning the conformational events and interactions that couple the action of sensors and gates. A comprehensive understanding of sensor/gate communication is likely to be of fundamental importance in understanding how channels normally work and how they are modulated by endogenous factors, drugs, or disease. To determine the nature of communication between sensors and gates we have studied the function of the BK-type Ca2+- activated K+ Channel (Slo1); a channel that senses both membrane voltage and intracellular Ca2+ as well as a variety of potential regulatory factors including intracellular Mg2+, Heme, and extracellular Cu2+. BK channels participate in physiologically important processes, and disruptions in their function or expression have been associated with diseases such as hypertension, epilepsy and cancer. Therefore an understanding of BK channel regulation may have direct implications for understanding disease mechanisms and developing more effective therapeutic options. Allosteric mechanisms exist by which the activation of sensors and the opening of the gate in BK channels appear to represent distinct events that strongly influence each other but can occur in isolation. Slo1 offers a unique opportunity to elucidate the functional properties and molecular mechanisms of sensor/gate communication. By studying the response of Slo1 to extreme stimuli and taking advantage of particular kinetic and steady-state properties of this channel we are able to study, in isolation, sensor activation, channel opening, and the coupling between sensor and gate. These methods and analytical tools will be applied to mutant Slo1 channels to identify residues and interactions that are involved in sensor/gate communication, and to understand how Mg2+, Heme and Cu2+ regulate BK channel activity. The results will be important, not only for understanding the gating and physiological regulation of BK channels, but also for elucidating how sensors and gates are coupled and gating is regulated in other ion channels.

描述（由申请人提供）：离子通道通过其响应各种刺激而打开和关闭（门控）的能力动态调节膜渗透性。在识别和表征参与该门控过程的通道蛋白的部分方面已经取得了进展，包括检测刺激的“传感器”和调节离子通过通道孔的流动的“门”。然而，许多问题仍然关于构象事件和相互作用耦合的传感器和门的行动。传感器/门通信的全面理解可能是理解通道如何正常工作，以及它们如何被内源性因素，药物或疾病调节的根本重要性。为了确定传感器和门之间的通信的性质，我们已经研究了BK型Ca 2+激活的K+通道（Slo 1）的功能;一个通道，既感测膜电压和细胞内Ca 2+，以及各种潜在的调节因子，包括细胞内Mg 2+，血红素，和细胞外Cu 2+。BK通道参与重要的生理过程，其功能或表达的破坏与高血压、癫痫和癌症等疾病有关。因此，对BK通道调节的理解可能对理解疾病机制和开发更有效的治疗方案具有直接意义。存在变构机制，通过该机制，BK通道中传感器的激活和门的打开似乎代表彼此强烈影响但可以孤立发生的不同事件。Slo 1提供了一个独特的机会来阐明传感器/门通信的功能特性和分子机制。通过研究Slo 1对极端刺激的反应，并利用该通道的特定动力学和稳态特性，我们能够孤立地研究传感器激活、通道开放以及传感器和门之间的耦合。这些方法和分析工具将应用于突变Slo 1通道，以确定参与传感器/门通信的残基和相互作用，并了解Mg 2+，血红素和Cu 2+如何调节BK通道活性。这些结果不仅对理解BK通道的门控和生理调节很重要，而且对阐明传感器和门控是如何耦合的以及门控在其他离子通道中是如何调节的也很重要。