LOCAL AND GLOBAL CONFORMATIONS OF SUPERCOILED DNA
LOCAL AND GLOBAL CONFORMATIONS OF SUPERCOILED DNA
批准号:
6879001
负责人:
YURI L LYUBCHENKO
金额:
$24.62万
依托单位国家:
美国
项目类别:
财政年份:
2000
资助国家:
美国
项目状态:
已结题
起止时间:
2000-12-18 至 2008-03-31
关键词:
DNA binding proteinZ DNAatomic force microscopybinding siteschemical modelschemical structure functioncircular DNAcomputer simulationconformationfluorescence microscopyfluorescence resonance energy transfergenetic promoter elementgenetic regulationgenetic transcriptionintermolecular interactionmolecular dynamicsmolecular shapenucleic acid probesnucleic acid repetitive sequencenucleic acid sequencenucleic acid structureprotein bindingstructural biologytriple helixtwo dimensional gel electrophoresis
中文摘要
描述(由申请人提供):DNA超螺旋几乎涉及所有与DNA相关的生物化学过程,因此超螺旋DNA的物理化学和结构性质在过去二十年中一直是DNA生物物理学的重要领域。最近的实验研究和先进的理论分析表明,DNA的动态而不是静态的DNA结构在基因表达,DNA复制,重组和修复的控制中起着至关重要的作用。然而,由于缺乏适当的实验技术,在DNA生物物理学这一重要领域的实验研究进展一直很低。单分子研究的最新进展,允许观察单个分子的结构动力学,表明单分子方法可以提供关于生物分子的结构和动力学的独特信息。最近的研究表明,DNA的局部和整体构象处于动态平衡状态。不同的局部结构之间的竞争转换伴随着全球DNA构象的动态变化可能有深刻的作用,在各种DNA功能。利用单分子原子力显微镜和荧光显微镜的建议测试了一些关键的假设,并提供了一个现实的手段,在这个未开发的分子生物学领域的新突破。(1)十字形和H-DNA的形成可以限制影响远距离分离的DNA区域并置的整体DNA移动性的假设将被测试。(2)一种局部结构向另一种局部结构的转换是全局DNA结构和动力学的另一种分子开关机制的假设(3)将分析涉及远距离DNA区域相互作用的限制性内切酶SfiI的结合机制,并将验证局部结构的形成可以调节酶活性的假设。除了假设检验,新的DNA固定和标记技术的DNA动力学研究将被开发。总而言之,拟议的研究是第一次尝试在不同层次上研究DNA的动态,提供有关DNA基本和功能特性的空间和时间信息。样品制备技术的进步与相应的仪器开发相结合,将为追求单分子方法的结构生物学家提供新的应用工具,其影响远远超过本提案中概述的目标。
英文摘要
DESCRIPTION (provided by applicant): DNA supercoiling is involved with virtually all DNA-related biochemical processes, therefore physical chemical and structural properties of supercoiled DNA have been important areas of DNA biophysics over last two decades. Recent experimental studies and advanced theoretical analyses suggest that DNA dynamics rather than static DNA structure plays a critical role in the control of gene expression, DNA replication, recombination, and repair. However, progress in experimental studies in this important area of DNA biophysics has been very low due to the lack of appropriate experimental techniques. Recent advances in single molecule studies, allowing the observation of structural dynamics of individual molecules, showed that the single molecule approaches could provide unique information on the structure and dynamics of biological molecules. Recent studies showed that local and global DNA conformations are in a dynamic equilibrium. Competing transitions between different local structures accompanied by dynamic changes of global DNA conformations may have a profound role in various DNA functions. This proposal utilizing single molecule AFM and fluorescence microscopy tests a number of critical hypotheses and provides a realistic means for breaking new ground in this undeveloped area of molecular biology. (1) The hypothesis that the formation of cruciforms and H-DNA can limit global DNA mobility affecting the juxtaposition of distantly separated DNA regions will be tested. (2) The hypothesis that conversion of one local structure into another is an alternative molecular switch mechanism for the global DNA structure and dynamics (3) The mechanism of binding of the restriction enzyme SfiI involving the interaction of distant DNA regions will be analyzed and the hypothesis that the formation of local structures may regulate the enzyme activity will be tested. In addition to the hypotheses testing, novel DNA immobilization and labeling techniques for DNA dynamics studies will be developed. Altogether, the proposed studies are the first attempt to look at the dynamics of DNA at various levels providing spatial and temporal information about the fundamental and functional properties of DNA. Advances in sample preparation techniques combined with corresponding instrument development will provide structural biologists pursuing single molecule approaches with novel tools for applications, ramifications considerably wider than the objectives outlined in this proposal.
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