Protein-Membrane Interactions in Regulated Exocytosis

调节胞吐作用中的蛋白质-膜相互作用

• 批准号: 8792541
• 负责人: Jingshi Shen
• 金额: $ 28.98万
• 依托单位: UNIVERSITY OF COLORADO
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-04-01 至 2016-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8792541
• 关键词: Address; Adipose tissue; Binding; Biochemical; Biological Assay; Biological Models; Blood Glucose; C2 Domain; Cell membrane; Cell surface; Cells; Chimeric Proteins; Complex; Data; Development; Diabetes Mellitus; Disease; Electrons; Elements; Epilepsy; Event; Exocytosis; GLUT4 gene; Glucose Transporter; Goals; Health; Human; Image; Immune System Diseases; Insulin; Intracellular Membranes; Kinetics; Knowledge; Lipid Bilayers; Lipids; Mediating; Membrane; Membrane Fusion; Membrane Proteins; Microscopic; Molecular; Molecular Mechanisms of Action; Muscle Fibers; Non-Insulin-Dependent Diabetes Mellitus; Pathway interactions; Phosphorylation; Physiological; Physiological Processes; Physiology; Process; Proteins; Pulmonary Surfactants; Reaction; Research; Role; S-nitro-N-acetylpenicillamine; SNAP receptor; Site; Stimulus; Stress; System; T-Lymphocyte; Therapeutic Intervention; Vesicle; Work; base; biophysical properties; blood glucose regulation; human disease; in vivo; insight; mutant; novel; novel therapeutics; proteoliposomes; receptor; reconstitution; syntaxin 4; syntaxin binding protein 1; trafficking; uptake; vesicular SNARE proteins

DESCRIPTION (provided by applicant): Regulated exocytosis is a stimulus-dependent membrane fusion event of fundamental importance to a range of physiological processes. The membrane fusion reaction involves substantial lipid rearrangements and is opposed by the powerful hydrophobic force. For fusion to occur, a high energy barrier must be overcome. The overall goal of this proposed research is to determine the functional roles of membrane bilayer remodeling in overcoming the energy barrier of exocytic vesicle fusion, using the trafficking of the glucose transporter GLUT4 as a model system. To achieve this goal, we will employ a unique combination of complementary approaches including biochemical reconstitution, electron microscopic imaging, and biophysical measurements. First, we will define how two membrane bilayers are brought into close apposition by the SNARE-SM complex to prepare for the subsequent steps of membrane remodeling and merging. Next, we will assess the functional role of vesicle membrane bending in the fusion reaction. Finally, we will examine how the fusion reaction is regulated by local remodeling of the plasma membrane. We hypothesize that the fusion of exocytic vesicles with the plasma membrane involves a novel dual-curvature-induction mechanism: while the amphipathic motif of the v-SNARE bends the vesicle membrane, the hydrophobic loops of C2-domain molecules penetrate into the plasma membrane and induce local membrane curvature. Together, these membrane-bending activities are expected to create curvature stresses at the fusion sites to overcome the energy barrier for the fusion reaction. Successful completion of this proposed research will provide key insights into the molecular mechanisms of exocytic vesicle fusion. This work will also serve as a paradigm for understanding the general principles of intracellular membrane fusion. Ultimately, our findings will facilitate the development of novel therapeutic strategies for diseases associated with dysfunctional regulated exocytosis including diabetes, epilepsy, and immune disorders.

描述（由申请人提供）：调节胞吐是一种依赖刺激的膜融合事件，对一系列生理过程具有重要意义。膜融合反应涉及大量的脂质重排，并受到强大的疏水力的反对。要发生核聚变，必须克服一个高能垒。本研究的总体目标是利用葡萄糖转运蛋白GLUT4作为模型系统，确定膜双分子层重塑在克服胞外囊泡融合的能量屏障中的功能作用。为了实现这一目标，我们将采用独特的互补方法组合，包括生化重建，电子显微镜成像和生物物理测量。首先，我们将定义两个膜双分子层如何通过SNARE-SM复合体紧密结合，为随后的膜重塑和合并步骤做准备。接下来，我们将评估囊泡膜弯曲在融合反应中的功能作用。最后，我们将研究如何融合反应是由局部重塑的质膜调节。我们假设胞外囊泡与质膜的融合涉及一种新的双曲率诱导机制：当v-SNARE的两亲基序弯曲囊泡膜时，c2结构域分子的疏水环穿透到质膜并诱导局部膜曲率。综上所述，这些膜弯曲活动有望在融合位点产生曲率应力，以克服融合反应的能量垒。这项研究的成功完成将为胞外囊泡融合的分子机制提供关键的见解。这项工作也将作为理解细胞膜内融合的一般原理的范例。最终，我们的研究结果将促进与功能失调的胞外分泌相关疾病（包括糖尿病、癫痫和免疫疾病）的新治疗策略的发展。