INCISIVE PROBING OF NUCLEIC ACID CONFORMATIONAL HETEROGENEITY

深入探究核酸构象异质性

• 批准号: 8170316
• 负责人: DANIEL HERSCHLAG
• 金额: $ 0.03万
• 依托单位: STANFORD UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-05-01 至 2011-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8170316
• 关键词: Complex; Computer Retrieval of Information on Scientific Projects Database; DNA; Functional RNA; Funding; Grant; HIV; Heterogeneity; Institution; Measures; Nucleic Acid Folding; Nucleic Acid Probes; Nucleic Acids; Probability; RNA; Research; Research Personnel; Resources; Source; Structure; Tars; Techniques; United States National Institutes of Health; base; flexibility; nucleic acid structure; protein structure

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. The conformational heterogeneity in nucleic acids is implied by the complex and rugged energy landscape of nucleic acids, which controls their folding and function. Moreover, there is increased evidence of heterogeneity in transient intermediates as well as the final folded state of proteins and structured RNAs. Despite the fundamental importance of conformational heterogeneity in nucleic acids, it has not been properly studied due to a lack of suitable experimental techniques. A newly developed Au-SAXS-based x-ray ruler provides the distance probability distribution of an ensemble of molecules. This technique provides a unique and powerful probe of macromolecular conformational heterogeneity. We propose to study the conformational flexibility and heterogeneity of modular DNA and RNA structures, including A-tract, bulges, single-stranded and double stranded junctions and simple functional RNA structure such as the HIV TAR RNA. We intend to measure the conformational distributions and heterogeneity in these nucleic acids structures and relate the distributions to nucleic acid folding and function.

这个子项目是许多研究子项目中利用 资源由NIH/NCRR资助的中心拨款提供。子项目和 调查员(PI)可能从NIH的另一个来源获得了主要资金， 并因此可以在其他清晰的条目中表示。列出的机构是 该中心不一定是调查人员的机构。 核酸复杂而崎岖的能量格局隐含着核酸的构象异质性，它控制着核酸的折叠和功能。此外，有越来越多的证据表明，瞬时中间产物以及蛋白质和结构RNA的最终折叠状态存在异质性。尽管核酸构象异质性具有重要的基础性意义，但由于缺乏合适的实验技术，这一问题一直没有得到很好的研究。一种新开发的基于Au-SAXS的X射线标尺提供了一组分子的距离概率分布。这一技术为研究大分子构象异质性提供了一种独特而有力的探针。我们建议研究模块化DNA和RNA结构的构象灵活性和异质性，包括A-道、凸起、单链和双链连接以及简单的功能RNA结构，如HIV TAR RNA。我们打算测量这些核酸结构中的构象分布和异质性，并将分布与核酸折叠和功能联系起来。