STRUCTURAL STUDIES OF MACROMOLECULES USING SYNCHROTRON RADIATION

利用同步辐射进行大分子结构研究

• 批准号: 7370345
• 负责人: Alfonso Mondragon
• 金额: $ 0.02万
• 依托单位: STANFORD UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-03-01 至 2007-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7370345
• 关键词: STRUCTURAL; STUDIES; MACROMOLECULES; USING; SYNCHROTRON

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. This proposal is concerned with the study of several different systems: a) type I DNA topoisomerases; b) chicken brain a-spectrin; c) domain I of the RNA component of RNase P, and d) several DNA binding proteins. The work is based on X-ray crystallography. We have been studying E. coli DNA topoisomerase I and III for a number of years and have proposed a catalytic mechanism. We are now in the process of studying the interactions of topoisomerase I with DNA and also the structure of mutant proteins that could shed light on the details of the reaction. We solved the structure of two repeats of chicken brain a-spectrin in 1997 using data collected at SSRL. We are now studying new crystals that contain three consecutive repeats. The third project is concerned with the structure of domain I of the RNA component of RNase P. This domain is 154 bases long and the crystals diffract to 3.3 ¿¿at a synchrotron source. The final project is concerned with the structure of ZntR, a metal-dependent transcriptional activator of E. coli. The crystals are small and we require synchrotron radiation for MAD phasing.

该子项目是利用NIH/NCRR资助的中心赠款提供的资源的许多研究子项目之一。子项目和研究者（PI）可能从另一个NIH来源获得主要资金，因此可以在其他CRISP条目中表示。所列机构为中心，不一定是研究者所在机构。该建议涉及几种不同系统的研究：a）I型DNA拓扑异构酶; B）鸡脑α-血影蛋白; c）RNase P的RNA组分的结构域I;以及d）几种DNA结合蛋白。这项工作是基于X射线晶体学。我们一直在研究E。大肠杆菌DNA拓扑异构酶I和III多年来，并提出了一种催化机制。我们现在正在研究拓扑异构酶I与DNA的相互作用，以及突变蛋白质的结构，这可能会揭示反应的细节。1997年，我们使用SSRL收集的数据解决了鸡脑α-血影蛋白的两个重复序列的结构。我们现在正在研究含有三个连续重复的新晶体。第三个项目是关于RNase P的RNA组分的结构域I的结构。该结构域长154个碱基，晶体在同步加速器源下的反应速率为3.3。最后一个项目是关于ZntR的结构，ZntR是一种金属依赖的E.杆菌晶体很小，我们需要同步辐射MAD定相。