Structure and Function of a Bacterial Na Channel

细菌Na通道的结构和功能

• 批准号: 6913553
• 负责人: DAVID E. CLAPHAM
• 金额: $ 35.64万
• 依托单位: BOSTON CHILDREN'S HOSPITAL
• 依托单位国家: 美国
• 财政年份: 2003
• 资助国家: 美国
• 起止时间: 2003-07-01 至 2007-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6913553
• 关键词: X ray crystallography; cell line; electrophysiology; membrane permeability; membrane structure; protein structure function; sodium channel; structural biology; voltage gated channel

DESCRIPTION (provided by applicant): Ion channels govern the activity of the thinking brain, beating heart, contracting muscle, and every cell of the body. They are targets of many therapeutic agents; mutations of ion channel genes are the cause of dozens of inherited diseases, including cardiac arrhythmias and neurological illnesses. Many of these ion channels are opened in response to changes in voltage across the cell membrane. The central long-term aim of this proposal is to understand the molecular mechanism of voltage gating of ion channels. We recently discovered an ion channel in bacteria (NaChBac) that has many of the properties of an important class of ion channels in humans: it is selectively permeant to sodium, opened (gated) by changes in membrane voltage, and inactivated in a time-dependant manner after voltage-dependant gating.NaChBac is unique in being the only voltage-dependent ion channel that can be expressed and studied in a mammalian cell line. This is important because bacterial channels are the most likely sources of sufficient protein for high-resolution structural studies (X-ray crystallography). The NaChBac protein has been crystallized and is likely to yield high-resolution structural data. It is thus crucial to investigate the structure and function of this ion channel through a combination of mutagenic and electrophysiologic studies. Information gained about its ion selectivity, voltage gating, and inactivation can then be directly correlated to the structure when obtained. Understanding this relatively simple ion channel will help us understand how the larger class of channels function, and eventually how we might target them with therapeutic agents.

描述（由申请人提供）：离子通道控制思维的大脑、跳动的心脏、收缩的肌肉和身体的每一个细胞的活动。它们是许多治疗药物的靶点;离子通道基因的突变是数十种遗传性疾病的原因，包括心律失常和神经系统疾病。这些离子通道中的许多响应于跨细胞膜的电压的变化而打开。这项建议的中心长期目标是了解离子通道电压门控的分子机制。我们最近在细菌中发现了一种离子通道（NaChBac），它具有人类中一类重要离子通道的许多特性：它选择性地渗透钠，通过膜电压的变化打开（门控），并在电压依赖性门控后以时间依赖性方式失活。NaChBac是唯一可以在哺乳动物细胞系中表达和研究的电压依赖性离子通道。这一点很重要，因为细菌通道是高分辨率结构研究（X射线晶体学）最有可能获得足够蛋白质的来源。NaChBac蛋白质已经结晶，很可能产生高分辨率的结构数据。因此，通过诱变和电生理学研究相结合来研究该离子通道的结构和功能是至关重要的。获得的关于其离子选择性、电压门控和失活的信息然后可以在获得时与结构直接相关。了解这种相对简单的离子通道将有助于我们了解更大类别的通道如何发挥作用，以及最终我们如何用治疗剂靶向它们。