Vanderbilt Screen Center- GPCRs, Ion Channels, and(RMI)
Vanderbilt Screen Center- GPCRs, Ion Channels, and(RMI)
批准号:
6950958
负责人:
C DAVID WEAVER
金额:
$256.7万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-07-01 至 2008-06-30
中文摘要
描述(由申请人提供):G蛋白偶联受体(GPCR)、离子通道和转运蛋白是密集的基础研究领域,并且是经证实的药物靶点。然而,仍然需要新的工具来更好地理解这些蛋白质在生物系统中的作用,并为发现治疗剂铺平道路。虽然配体的发现已经在这些蛋白质的制药公司进行,他们的零售产品的利益往往排除,或大大延迟,研究结果的出版或考虑的目标/小分子相互作用的许多可能的模式之一。尽管多个学术和工业实验室的强烈兴趣,但绝大多数GPCR,离子通道和转运蛋白的小分子配体并不存在。在分子图书馆和筛选中心网络(MLSCN)倡议的支持下,研究界有很好的机会开发新的工具来帮助理解这些蛋白质。因此,我们建议开发一个MLSCN筛选中心,专注于G蛋白偶联受体,离子通道和转运蛋白研究的化学工具的产生。我们将使用行业标准的仪器和筛选方法对这些蛋白质进行基于细胞的功能性HTS。我们将进一步提高我们的能力,快速发现和表征这些目标的新工具和信号通路/生理系统,它们是通过使用新技术的一部分,这将允许这些蛋白质和它们的合作伙伴之间的相互作用更多的生理相关的审讯。我们将开发专业知识,技术和方法,以了解和改善通过HTS发现的小分子的特性,以生产支持基础和转化研究的工具。范德比尔特大学非常适合支持MLSCN中心,因为它在拟议的目标领域结合了基础和工业研究专业知识,致力于转化和化学生物学,以及在建立和维护高度合作的实验室和核心设施方面的卓越传统。
英文摘要
DESCRIPTION (provided by applicant): G-protein coupled receptors (GPCRs), ion channels, and transporters are areas of intense basic research and are proven drug targets. However, there remains a need for new tools to develop a better understanding of the roles of these proteins in biological systems and to pave the way for discovery of therapeutic agents. Although ligand discovery has been performed on these proteins in pharmaceutical companies, their retail product interests often preclude, or greatly delay, the publication of research findings or consider only one of the many possible modes of target/small molecule interaction. Despite intense interest of multiple academic and industry labs, small molecules ligands do not exist for the vast majority of GPCRs, ion channels, and transporters. The research community, supported by the Molecular Libraries and Screening Centers Network (MLSCN) initiative, has an excellent opportunity to develop novel tools to aid in understanding these proteins. Thus, we propose to develop a MLSCN screening center focused on the generation of chemical tools for the study of G-protein coupled receptors, ion channels, and transporters. We will perform cell-based functional HTS for these proteins using industry-standard instrumentation and screening methods. We will further enhance our ability to rapidly discover and characterize novel tools for these targets and the signaling pathways/physiological systems of which they are a part by using new technologies that will allow more physiologically-relevant interrogation of interactions between these proteins and their partners. We will develop the expertise, technologies, and methods to understand and improve the properties of small molecules discovered through HTS to produce tools to support basic and translational research. Vanderbilt University is well suited to support an MLSCN center due to its combination of basic and industrial research expertise in the proposed target areas, its dedication to translational and chemical biology, and its tradition of excellence in the establishing and maintaining highly-collaborative laboratories and core facilities.
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海外基金