Voltage-driven Structural Transitions in Voltage-Gated Calcium Channels

电压门控钙通道中电压驱动的结构转变

• 批准号: 9389512
• 负责人: Riccardo Olcese
• 金额: $ 32.5万
• 依托单位: UNIVERSITY OF CALIFORNIA LOS ANGELES
• 依托单位国家: 美国
• 财政年份: 2014
• 资助国家: 美国
• 起止时间: 2014-12-01 至 2020-09-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9389512
• 关键词: Accounting; Address; Amino Acid Sequence; Architecture; Arrhythmia; Attenuated; Binding Sites; Blood Vessels; Calcium Channel; Calmodulin; Cells; Charge; Coupling; Data; Data Set; Dependence; Disease; Drug usage; Environment; Exhibits; Fluorescence; Fluorometry; Formulation; Gene Expression; Health; Human; Hypertension; Immobilization; Individual; Ion Channel; Ions; Kinetics; Knowledge; L-Type Calcium Channels; Label; Left; Measurement; Membrane; Methodology; Modeling; Molecular; Molecular Conformation; Movement; Muscle Contraction; Mutagenesis; Myocardial Contraction; Nerve; Oocytes; Optics; Pathologic; Periodicity; Physiological; Physiological Processes; Process; Property; Proteins; Regulation; Research Proposals; Role; Scheme; Series; Signal Transduction; Structure; Techniques; Thermodynamics; Time; Timothy syndrome; Ursidae Family; Voltage-Clamp Technics; Work; analytical tool; conformational conversion; design; fluorophore; innovation; insight; mutant; neurotransmitter release; novel therapeutics; operation; polypeptide; public health relevance; response; sensor; tool; voltage; voltage clamp

DESCRIPTION (provided by applicant): A depolarization-initiated influx of Ca through voltage-gated Ca (CaV) channels gives rise to a plethora of physiological responses such as neurotransmitter release, muscle contraction and gene expression. Membrane depolarization is sensed by four transmembrane structures, the voltage sensor domains (VSDs), which surround and control the activation, deactivation and inactivation properties of a central Ca-selective pore governing the amount and timing of Ca influx. In contrast to homotetrameric KV channels, the CaV pore and four VSDs are encoded by a single long polypeptide chain (alpha1). Thus, each VSD has a unique primary amino acid sequence, suggesting distinct voltage-sensing properties. Critically, the voltage-sensing processes coupling membrane depolarization to Ca influx are still poorly understood and the molecular mechanisms by which auxiliary subunits, such as beta and alpha2delta, alter the voltage dependence of the channel, still need to be elucidated. This lack of knowledge persists in part because ionic and gating current measurements have not thus far captured the properties of individual VSDs in CaV channels. Using Voltage Clamp Fluorometry (VCF), we have resolved that the time- and voltage-dependent properties of each of the four VSDs of human CaV1.2 revealing their highly distinct functional properties. We now have the experimental tools and theoretical formulation to answer key unresolved questions on the operation of CaV1.2 channels, as delineated in four specific aims: (1) To establish the contribution of individual voltage sensing domains to CaV1.2 channel activation. (2) To establish the molecular mechanism by which accessory subunits regulate voltage-dependent activation of CaV1.2 channels. (2a) regulation by alpha2delta subunits (2b) regulation by beta subunits (3) To determine the role of each VSD in Voltage- and Ca-dependent Inactivation and (4) To develop a CaV1.2 model accounting for the operation and role of the four distinct VSDs. CaV1.2 channels specifically labeled at each VSD with small, environment-sensitive fluorophores will be voltage-clamped using the cut-open oocyte technique, so that voltage-evoked fluorescence changes will reflect local conformational rearrangements. A series of physically-relevant models consistent with the CaV1.2 structure and accounting for all experimentally- resolved aspects of CaV1.2 voltage-dependent operation, including the interactions governing excitation- evoked Ca influx. The innovative aspects of this proposal include (1) the experimental approach, unprecedented for the CaV superfamily; (2) the hypothesis that VSDs are the targets of regulation by modulatory subunits; (3) the premise, supported by striking preliminary results, that CaV1.2 VSDs are drivers and regulators for inactivation; (4) the theoretical approach proposes the first model consistent with the molecular architecture and asymmetry of CaV channels. Finally, this study will contribute to the understanding of the molecular mechanisms of pathological states caused by altered CaV1.2 voltage dependence, such as Timothy Syndrome.

描述（由申请人提供）：去极化引发的钙通过电压门控钙（CaV）通道内流引起过多的生理反应，如神经递质释放、肌肉收缩和基因表达。膜去极化是通过四个跨膜结构——电压传感器结构域（VSDs）来感知的，这些结构域围绕并控制着控制钙内流量和时间的中心钙选择孔的激活、失活和失活特性。与同四聚体的KV通道相比，CaV孔和4个vsd由一条长多肽链（alpha1）编码。因此，每个VSD都有一个独特的初级氨基酸序列，表明不同的电压感应特性。关键的是，耦合膜去极化和Ca内流的电压传感过程仍然知之甚少，辅助亚基（如β和α 2 δ）改变通道电压依赖性的分子机制仍然需要阐明。这种知识的缺乏部分是因为离子和门控电流的测量到目前为止还没有捕捉到CaV通道中单个vsd的特性。使用电压箝位荧光法（VCF），我们确定了人类CaV1.2的四种vsd的时间和电压依赖特性，揭示了它们高度不同的功能特性。我们现在有实验工具和理论公式来回答关于CaV1.2通道运行的关键未解决的问题，如四个具体目标所述：(1)建立单个电压传感域对CaV1.2通道激活的贡献。(2)建立辅助亚基调控CaV1.2通道电压依赖性激活的分子机制。（2a） α 2delta亚基的调控(2b) β亚基的调控(3)确定每个VSD在电压和钙依赖性失活中的作用；(4)建立一个CaV1.2模型，解释四种不同的VSD的运作和作用。使用切开卵母细胞技术，在每个VSD上用小的、环境敏感的荧光团特异性标记的CaV1.2通道将被电压夹住，因此电压引起的荧光变化将反映局部构象重排。一系列与CaV1.2结构一致的物理相关模型，并解释了CaV1.2电压依赖操作的所有实验解决的方面，包括控制激发引起的Ca内流的相互作用。该提案的创新之处包括：(1)实验方法，这对于CaV超家族来说是前所未有的；(2) vsd是调节亚基调控的目标假说；(3) CaV1.2 vsd是失活的驱动因子和调控因子，这一前提得到了惊人的初步结果支持；(4)理论方法提出了第一个符合CaV通道分子结构和不对称性的模型。最后，本研究将有助于理解CaV1.2电压依赖性改变引起的病理状态（如Timothy综合征）的分子机制。