Molecular Determinants of L-type Calcium Channel Gating

L 型钙通道门控的分子决定因素

• 批准号: 7316974
• 负责人: Henry M. Colecraft
• 金额: $ 2.14万
• 依托单位: JOHNS HOPKINS UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2002
• 资助国家: 美国
• 起止时间: 2002-04-15 至 2007-09-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7316974
• 关键词: Arrhythmia; Autistic Disorder; Behavior; Binding; Biological Assay; Biological Process; Cardiac; Cell membrane; Coupling; Cyclic AMP-Dependent Protein Kinases; Data; Detection; Disease; Engineering; Fluorescence Resonance Energy Transfer; Gene Expression; Heart; Heart Atrium; Hormones; Hypertension; Immunofluorescence Immunologic; Knowledge; L-Type Calcium Channels; Life; Mediating; Molecular; Muscle Contraction; Night Blindness; Numbers; Pathogenesis; Phosphorylation; Physiological; Process; Property; Protein Isoforms; Proteins; Public Health; Range; Recombinants; Regulation; Research Personnel; Role; Site; Structure; System; Therapeutic; Transcriptional Activation; Up-Regulation; base; cellular targeting; deafness; heart cell; insight; programs; reconstitution; research study; response; therapeutic target; trafficking

DESCRIPTION (provided by applicant): Ca2+ entry through plasma membrane L-type (Cav1.2) Ca2+ channels regulates many essential biological functions including muscle contraction, hormone release, and gene expression. Dysregulation of L-type channel functional expression underlies a wide range of diseases including life-threatening atrial arrhythmias, autism, night blindness, and deafness. Moreover, L-type channels are important therapeutic targets for a number of diseases that constitute a significant detriment to the public health such as hypertension, angina, and arrhythmias. Nevertheless, there are significant gaps in knowledge regarding the precise role of L-type channels in the pathogenesis of various diseases, and their full therapeutic potential remains largely unrealized. A key contributor to the impasse is lack of fundamental mechanistic insights into processes underlying L-type channel sub-cellular targeting and gating behavior. Our long-term objective is two fold: first, to increase fundamental molecular understanding of structure-function mechanisms underlying L-type channel functional expression; second, to bridge these basic insights to a new realization of the (patho)physiological roles and therapeutic potential of L-type channels. We combine electrophysiological assays of recombinant and native L-type (Cav1.2) channels, FRET detection of protein interactions, and immounofluorescence detection of channel subunits in 4 Aims: 1. Clarify the role of auxiliary Cav¿ structural determinants underlying trafficking and gating-modulation of recombinant L-type channel a1C subunits. 2. Clarify a1C structural determinants important for interacting with Cav¿s, and define their role in channel trafficking and gating-modulation. 3. Define the structural determinants underlying targeting of L-type Ca2+channels to dyadic junctions in heart. 4. Elucidate molecular determinants and mechanisms of protein kinase A modulation of cardiac L-type Ca2+channels.

描述（由申请人提供）：Ca 2+通过质膜L型（Cav1.2）Ca 2+通道进入调节许多基本生物学功能，包括肌肉收缩、激素释放和基因表达。L型通道功能表达失调是多种疾病的基础，包括危及生命的房性心律失常、自闭症、夜盲症和耳聋。此外，L-型通道是许多疾病的重要治疗靶点，这些疾病对公众健康构成重大损害，例如高血压、心绞痛和心律失常。然而，关于L型通道在各种疾病发病机制中的确切作用的知识存在重大差距，其全部治疗潜力在很大程度上仍未实现。造成僵局的一个关键因素是缺乏对L型通道亚细胞靶向和门控行为的基础过程的基本机制见解。我们的长期目标有两个方面：第一，增加对L型通道功能表达的结构-功能机制的基本分子理解;第二，将这些基本见解与L型通道的（病理）生理作用和治疗潜力的新认识联系起来。我们将重组和天然L型（Cav1.2）通道的联合收割机电生理检测、蛋白质相互作用的FRET检测和通道亚基的免疫荧光检测结合在4个目的中：1.阐明辅助Cav结构决定子在重组L型通道a1 C亚基运输和门控调节中的作用。2.阐明a1 C结构决定因素与Cav的相互作用的重要性，并定义其在通道运输和门控调制的作用。3.定义L型钙通道靶向心脏二元连接的结构决定因素。4.阐明蛋白激酶A调节心脏L型钙通道的分子决定因素和机制。