G-protein regulation of exocytotic transmitter release

G 蛋白调节胞吐递质释放

基本信息

批准号：
7651094
负责人：
KEVIN P CURRIE
金额：
$ 33.54万
依托单位：
VANDERBILT UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2006
资助国家：
美国
起止时间：
2006-08-01 至 2011-07-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7651094
关键词：
Address Adenovirus Vector Adrenal Glands Binding Binding Sites Biochemical Biological Assay C-terminal Catecholamines Cells Chromaffin Cells Complex Coupled Data Disease Distal Electric Capacitance Electrophysiology (science)Event Exocytosis G Protein-Coupled Receptor Signaling G-Protein-Coupled Receptors G-protein Beta gamma GTP-Binding Proteins Goals Hormones In Vitro Investigation Knowledge Left Maps Mediating Membrane Modeling Molecular Neurons Neurotransmitters Peptide Mapping Peptides Physiological Play Point Mutation Process Proteins Recombinants Regulation Regulation of Exocytosis Relative (related person)Reporting Research Personnel Role SNAP receptor Signal Pathway Staging Stimulus Stress Synaptic Transmission Synaptic plasticity Testing Vesicle Work base carbon fiber chemical release controlled release flash photolysis information processing insight intercellular communication interest millisecond mutant neuroregulation novel overexpression patch clamp receptor response sensor synaptotagmin synaptotagmin I syntaxin syntaxin 1 syntaxin 1A tool voltage

项目摘要

DESCRIPTION (provided by applicant): Release of chemical transmitters by regulated exocytosis underlies many forms of intercellular communication, including hormone release and synaptic transmission. G protein-coupled receptors (GPCRs) orchestrate complex regulation of exocytosis, and in particular inhibit transmitter release from neurosecretory cells. Inhibitory GPCRs can be auto- or hetero-receptors, are typically Gi/o coupled, and work by release of G protein beta-gamma subunits (Gbeta-gamma). The most intensively studied mechanism of inhibition involves modulation of voltage-gated Ca2+ channels (Ca-channels), but direct effects on the exocytotic apparatus have also been reported. Our preliminary data show that Gbeta-gamma binds to SNAP25 and syntaxin-1A, suggesting that Ca-channels and SNAREs might be targeted in parallel by Gbeta-gamma to inhibit exocytosis. The central goal of this proposal is to dissect the molecular basis by which Gbeta-gamma controls exocytotic transmitter release in neurosecretory cells. To enable the precise biophysical analyses required to address this goal, we will use adrenal chromaffin cells, a neurosecretory model that provides significant experimental advantages. Furthermore, catecholamines released from chromaffin cells play important physiological roles in the coordinated response to stress or danger. We will combine carbon fiber amperometry, patch clamp electrophysiology, and flash photolysis of caged compounds, along with novel molecular tools (mutant Gbeta-gamma subunits and inhibitory peptides) to dissect the roles of Ca-channels and SNAREs in Gbeta-gamma -mediated regulation of exocytosis. In aim #1 we will test the hypothesis that Gbeta-gamma acts in parallel at Ca-channels and other downstream targets to inhibit transmitter. In aim #2 we will characterize the interaction of Gbeta-gamma with the exocytotic machinery and test the hypothesis that Gbeta-gamma inhibits exocytosis by competing with synaptotagmin-l for binding to SNAP25. In aim #3 we will use mutational and peptide mapping to characterize the Gbeta-gamma - SNAP25 interaction and generate novel molecular tools to dissect its role in the regulation of chromaffin cell exocytosis. To summarize, our investigations will significantly advance knowledge of the molecular mechanisms that control neurotransmitter and hormone secretion, and provide insight into the pathological basis of diseases related to secretion and neuromodulation.

描述（由申请人提供）：通过受调节的胞吐作用释放化学递质是许多形式的细胞间通讯的基础，包括激素释放和突触传递。 G 蛋白偶联受体 (GPCR) 协调胞吐作用的复杂调节，特别是抑制神经分泌细胞释放递质。抑制性 GPCR 可以是自身或异源受体，通常是 Gi/o 偶联，并通过释放 G 蛋白 β-gamma 亚基 (Gbeta-gamma) 发挥作用。研究最深入的抑制机制涉及电压门控 Ca2+ 通道（Ca 通道）的调节，但也报道了对胞吐装置的直接影响。我们的初步数据显示，Gbeta-gamma 与 SNAP25 和 Syntaxin-1A 结合，表明 Gbeta-gamma 可能同时靶向 Ca 通道和 SNARE，以抑制胞吐作用。该提案的中心目标是剖析 Gbeta-gamma 控制神经分泌细胞中胞吐递质释放的分子基础。为了实现实现这一目标所需的精确生物物理分析，我们将使用肾上腺嗜铬细胞，这是一种具有显着实验优势的神经分泌模型。此外，嗜铬细胞释放的儿茶酚胺在对压力或危险的协调反应中发挥着重要的生理作用。我们将结合碳纤维电流分析法、膜片钳电生理学和笼状化合物的闪光光解，以及新型分子工具（突变的 Gbeta-gamma 亚基和抑制肽）来剖析 Ca 通道和 SNARE 在 Gbeta-gamma 介导的调节中的作用胞吐作用。在目标 #1 中，我们将测试 Gbeta-gamma 在 Ca 通道和其他下游目标上并行作用以抑制递质的假设。在目标#2中，我们将描述 Gbeta-gamma 与胞吐机制的相互作用，并测试 Gbeta-gamma 通过与突触结合蛋白-1 竞争与 SNAP25 的结合来抑制胞吐作用的假设。在目标#3中，我们将使用突变和肽图谱来表征 Gbeta-gamma - SNAP25 相互作用，并生成新的分子工具来剖析其在嗜铬细胞胞吐作用调节中的作用。总而言之，我们的研究将显着增进对控制神经递质和激素分泌的分子机制的了解，并深入了解与分泌和神经调节相关的疾病的病理基础。