Proteomic analysis of synaptic ribbons in the inner ear

内耳突触带的蛋白质组学分析

• 批准号: 7638419
• 负责人: WILLIAM F SEWELL
• 金额: $ 18.88万
• 依托单位: MASSACHUSETTS EYE AND EAR INFIRMARY
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-07-01 至 2011-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7638419
• 关键词: Acoustic Nerve; Amaze; Anatomy; Auditory; Cattle; Cells; Characteristics; Chemicals; Chimeric Proteins; Complex; Coupled; Data; Development; Disease; Electron Microscopy; Electrons; Enzymes; Hair Cells; Hearing; Labyrinth; Learning; Molecular; Molecular Structure; Mus; Nerve Fibers; Noise-Induced Hearing Loss; Play; Procedures; Protein Analysis; Protein Isoforms; Proteins; Proteome; Proteomics; Research Personnel; Retina; Retinal Photoreceptors; Role; Sampling; Shapes; Structure; Subcellular structure; Surface; Synapses; System; Time; Tinnitus; Two-Dimensional Gel Electrophoresis; Work; base; immunoreactivity; insight; interest; neurotransmission; presynaptic; protein purification; public health relevance; ribbon synapse; transmission process

DESCRIPTION (provided by applicant): Both the structure and the function of the hair cell's synaptic ribbon have been enigmatic since its discovery in the early days of electron microscopy. It is assumed that it plays a key role in determining the amazing temporal and dynamic characteristics of afferent neurotransmission between the hair cell and the auditory nerve fiber, but whether it has other functions is not known. In the half-century since its discovery, we have learned relatively little about its molecular anatomy or its function. Though many proteins known to be important in conventional synapses are present at the ribbon, we know little about the dominant components of the structure itself. The recent development of mass-spectrometric-based proteomics approaches for protein identification, coupled to a relatively complete proteome for the mouse, allows identification of hundreds of proteins in very small samples. Thus revisiting protein identification in purified samples of synaptic ribbon should yield most if not all of the proteins in and associated with the synaptic ribbon. The work is straightforward, the procedures are in place, the mouse proteome is highly developed, and the proteomic analysis of mass spec data is routine. The specific aims are to (1) Identify protein components in purified synaptic ribbon complexes, and in the electron dense core of the ribbon. (2) Immunochemically verify presence of candidates in synaptic ribbons of the mouse inner ear and in ribbon complexes purified from bovine retina. It seems evident that a prerequisite to understanding function of a structure as complex as the ribbon is to define the structure of the ribbon at the proteomics level. For many proteins identified, function will be implicit, based on analysis of the protein in other systems. Others may need some thought or experimentation to determine what they do. There seems no question that this straightforward quest to identify proteins in the synaptic ribbon should generate many hypotheses for what the ribbon is doing that could keep investigators busy for some time to come. Identification of the molecular components of the synaptic ribbon will be a fundamental step towards understanding its specific function at the afferent synapse. PUBLIC HEALTH RELEVANCE: The synaptic ribbon's role in transmission at the hair cell synapse has been enigmatic since its discovery over a half century ago. Recent advances in proteomics will allow identification of the molecular structure of this unusual subcellular structure that is essential for normal hearing. Because most proteins have specific molecular functions, knowing the panel of players in this structure should engender specific, testable hypotheses as to its function that may provide insights into a range of auditory disorders, including tinnitus and noise-induced hearing loss.

描述（由申请人提供）：毛细胞突触带的结构和功能自电子显微镜早期发现以来一直是个谜。据推测，它在决定毛细胞和听神经纤维之间传入神经传递的惊人的时间和动力学特性方面起着关键作用，但它是否还有其他功能尚不清楚。自发现以来的半个世纪里，我们对它的分子解剖学或功能了解得相对较少。虽然许多已知在传统突触中重要的蛋白质都存在于带状结构中，但我们对结构本身的主要成分知之甚少。最近发展的质谱为基础的蛋白质组学方法的蛋白质鉴定，再加上一个相对完整的蛋白质组的小鼠，允许在非常小的样品中识别数百种蛋白质。因此，在纯化的突触带样品中重新进行蛋白质鉴定应该产生大多数（如果不是全部的话）突触带中和与突触带相关的蛋白质。这项工作是简单的，程序到位，小鼠蛋白质组是高度发达的，质谱数据的蛋白质组分析是常规的。具体目标是：（1）鉴定纯化的突触带复合物中的蛋白质组分，以及突触带的电子致密核心。(2)免疫化学验证小鼠内耳的突触带和从牛视网膜纯化的带复合物中候选物的存在。很明显，理解像丝带这样复杂的结构的功能的先决条件是在蛋白质组学水平上定义丝带的结构。对于许多已鉴定的蛋白质，基于对其他系统中蛋白质的分析，功能将是隐含的。其他人可能需要一些思考或实验来确定他们做什么。毫无疑问，这种对突触带中蛋白质的直接探索应该会产生许多关于突触带功能的假设，这可能会让研究人员在未来一段时间内保持忙碌。识别突触带的分子成分将是理解其在传入突触中的特定功能的基本步骤。公共卫生关系：自从世纪前被发现以来，突触带在毛细胞突触传递中的作用一直是个谜。蛋白质组学的最新进展将允许鉴定这种对正常听力至关重要的不寻常亚细胞结构的分子结构。由于大多数蛋白质具有特定的分子功能，因此了解该结构中的参与者小组应该产生关于其功能的特定，可测试的假设，这些假设可以提供对一系列听觉障碍的见解，包括耳鸣和噪声引起的听力损失。