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Molecular Mechanisms of Vesicular Glutamate Transport

囊泡谷氨酸转运的分子机制

基本信息

批准号：
7266852
负责人：
RICHARD J REIMER
金额：
$ 11.38万
依托单位：
STANFORD UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2003
资助国家：
美国
起止时间：
2003-08-01 至 2009-07-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7266852
关键词：
Address Anions Behavior Brain Carrier Proteins Cell Communication Cell membrane Cells Characteristics Charge Chloride Channels Computer information processing Coupled Coupling Cysteine Data Dependence Enzymes Epitopes Exhibits Exocytosis Functional disorder Glutamate Transporter Glutamates Goals Histidine Intervention Ions Kinetics Lead Measurement Mediating Modification Molecular Movement Nature Neuronal Injury Neurons Neurotransmitters Phosphate Activated Glutaminase Physiological Play Process Process Measure Property Proteins Protons Rate Regulation Research Personnel Role Signal Transduction Site Site-Directed Mutagenesis Structure Substrate Specificity Synaptic Cleft Synaptic Transmission Synaptic Vesicles Temperature Testing Transmembrane Domain Vesicle base driving force excitotoxicity glycosylation improved inorganic phosphate insight nervous system disorder novel programs protein expression protein function protein structure reconstitution uptake vesicular glutamate transporter 1

项目摘要

DESCRIPTION (provided by applicant): The broad long-term goal of this proposal is to define mechanisms involved in the regulation of information processing in the brain and how these mechanisms may impact on neuronal injury. Synaptic transmission, the major neuron specific mechanism for cell-to-cell communication, requires the concentration of neurotransmitters into synaptic vesicles to facilitate their rapid and precise release. Recently, the proteins responsible for the storage of the excitatory neurotransmitter glutamate in synaptic vesicles have been identified. However, the basic mechanisms by which these proteins (VGLUT1 and VGLUT2) function remain undetermined. Data suggests that VGLUT1 may also transport phosphate and function as a chloride channel. Since these additional functions will influence vesicular glutamate storage, it is important to clearly characterize the nature of the role that VGLUT1 plays in these processes. Three Aims are proposed to address these issues. The first Aim of this proposal is to define mechanism by which VGLUT1 catalyzes the accumulation of glutamate in synaptic vesicles. The second Aim is to determine if, in addition to transporting glutamate into vesicles, VGLUT1 also functions as a phosphate transport or chloride channel. The third Aim is to determine the secondary structure of VGLUT1 and the relationship of the structure to the functions of the protein. Progress in these Aims will lead to an improved understanding of the underlying molecular mechanisms of vesicular glutamate transport and insight into the role of VGLUT1 in vesicular storage of glutamate, synaptic transmission and excitotoxicity.

描述（由申请人提供）：本提案的长期目标是确定参与大脑信息处理调节的机制，以及这些机制如何影响神经元损伤。突触传递是细胞间通信的主要神经元特异性机制，需要神经递质集中到突触囊泡中以促进其快速准确的释放。最近，负责突触囊泡中兴奋性神经递质谷氨酸储存的蛋白质已被确定。然而，这些蛋白（VGLUT1和VGLUT2）功能的基本机制仍未确定。数据表明VGLUT1也可能运输磷酸盐并作为氯离子通道发挥作用。由于这些附加功能会影响谷氨酸囊泡储存，因此明确表征VGLUT1在这些过程中所起作用的性质是很重要的。为解决这些问题，提出了三个目标。本研究的第一个目的是确定VGLUT1催化谷氨酸在突触囊泡中积累的机制。第二个目的是确定VGLUT1除了将谷氨酸转运到囊泡中外，是否还作为磷酸盐运输或氯离子通道。第三个目的是确定VGLUT1的二级结构及其与蛋白功能的关系。这些目标的进展将有助于更好地理解谷氨酸囊泡运输的潜在分子机制，并深入了解VGLUT1在谷氨酸囊泡储存、突触传递和兴奋毒性中的作用。

项目成果

期刊论文数量（6）

专著数量（0）

科研奖励数量（0）

会议论文数量（0）

专利数量（0）

Synaptic Vesicle Protein NTT4/XT1 (SLC6A17) Catalyzes Na+-coupled Neutral Amino Acid Transport.

突触小泡蛋白 NTT4/XT1 (SLC6A17) 催化 Na 偶联中性氨基酸转运。

DOI：
10.1074/jbc.m806407200
发表时间：
2009
期刊：
The Journal of biological chemistry
影响因子：
0
作者：
Zaia,KimberlyA;Reimer,RichardJ
通讯作者：
Reimer,RichardJ

Vesicular uptake and exocytosis of L-aspartate is independent of sialin.

L-天冬氨酸的囊泡摄取和胞吐作用不依赖于唾液酸蛋白。

DOI：
10.1096/fj.12-206300
发表时间：
2013
期刊：
FASEB journal : official publication of the Federation of American Societies for Experimental Biology
影响因子：
0
作者：
Morland,Cecilie;Nordengen,Kaja;Larsson,Max;Prolo,LauraM;Farzampour,Zoya;Reimer,RichardJ;Gundersen,Vidar
通讯作者：
Gundersen,Vidar

The lysosomal sialic acid transporter sialin is required for normal CNS myelination.

DOI：
10.1523/jneurosci.3005-09.2009
发表时间：
2009-12-09
期刊：
The Journal of neuroscience : the official journal of the Society for Neuroscience
影响因子：
0
作者：
Prolo LM;Vogel H;Reimer RJ
通讯作者：
Reimer RJ

G328E and G409E sialin missense mutations similarly impair transport activity, but differentially affect trafficking.

G328E 和 G409E 唾液酸蛋白错义突变同样会损害转运活性，但对转运的影响不同。