STRUCT BIOLOGY OF CELL SURFACE RECEPTORS RELEVANT TO HUMAN HEALTH & DISEASE: HIV

与人类健康相关的细胞表面受体的结构生物学

• 批准号: 7597916
• 负责人: K CHRISTOPHER R GARCIA
• 金额: $ 0.14万
• 依托单位: STANFORD UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-03-01 至 2008-02-29
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7597916
• 关键词: Address; Biology; Cell Surface Receptors; Cell surface; Cells; Complex; Computer Retrieval of Information on Scientific Projects Database; Coupled; Data; Disease; Funding; Generations; Grant; Health; Human; Institution; Laboratories; Ligands; Modeling; Molecular; Numbers; Physiological; Proteins; Receptor Activation; Research; Research Personnel; Resources; Signal Transduction; Source; Structure; System; United States National Institutes of Health; base; extracellular; molecular recognition; receptor

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. My laboratory is investigating structural aspects of cell-surface receptor recognition and activation, in receptor/ligand systems relevant to human health and disease. The molecular mechanisms by which information is communicated from the outside to the inside of a cell are still not well understood. Yet, cell-surface receptor activation is fundamental to essentially every vital physiological function. We are making progress in understanding molecular recognition between proteins through crystallographic studies of protein-protein complexes. However, the molecular bases for the subsequent transduction of an activation signal, upon receptor engagement, remains largely speculative for even the most intensively studied receptor systems. Models to explain the generation of an activation signal have been derived from structural analysis of receptor extracellular and intracellular domains which have been reconciled with functional data. The general question my laboratory is endeavoring to address is how the extracellular engagement of a ligand by a receptor is structurally coupled to the activation of intracellular signaling cascades. As such, my laboratory is attempting to carry out crystal structure determinations of a spectrum of receptors in complex with their ligands from a number of different systems.

这个子项目是许多研究子项目中的一个 由NIH/NCRR资助的中心赠款提供的资源。子项目和 研究者（PI）可能从另一个NIH来源获得了主要资金， 因此可以在其他CRISP条目中表示。所列机构为 研究中心，而研究中心不一定是研究者所在的机构。 我的实验室正在研究与人类健康和疾病相关的受体/配体系统中细胞表面受体识别和激活的结构方面。 信息从细胞外传递到细胞内的分子机制仍然没有得到很好的理解。 然而，细胞表面受体的激活是基本上每一个重要的生理功能。 通过对蛋白质-蛋白质复合物的晶体学研究，我们在理解蛋白质之间的分子识别方面取得了进展。 然而，在受体接合后，激活信号的后续转导的分子基础对于即使是最深入研究的受体系统也仍然是推测性的。 解释激活信号的产生的模型已经从受体细胞外和细胞内结构域的结构分析中得到，这些结构域已经与功能数据相协调。我的实验室正在努力解决的一般问题是，受体与配体的细胞外接合如何在结构上与细胞内信号级联的激活相耦合。 因此，我的实验室正试图进行一系列受体的晶体结构测定，这些受体与来自许多不同系统的配体形成复合物。