Single Molecule HIV-1 NC/Gad-DNA Interactions

单分子 HIV-1 NC/Gad-DNA 相互作用

• 批准号: 7480971
• 负责人: MARK C WILLIAMS
• 金额: $ 23.36万
• 依托单位: NORTHEASTERN UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2004
• 资助国家: 美国
• 起止时间: 2004-08-01 至 2010-05-05
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7480971
• 关键词: Base Pairing; Binding; Biological Assay; Characteristics; DNA; DNA Binding; DNA Packaging; DNA Structure; Development; Drug Delivery Systems; Elements; Fluorescence; Gagging; HIV-1; Helix (Snails); In Vitro; Institutes; Investigation; Libraries; Light; Malignant Neoplasms; Measurement; Modeling; Molecular Chaperones; Nucleic Acid Binding; Nucleic Acid Probes; Nucleic Acids; Nucleocapsid; Nucleocapsid Proteins; Pharmaceutical Preparations; Principal Investigator; Process; Protein Binding; Proteins; RNA; Rate; Regulation; Research; Retroviridae; Role; Signal Transduction; Spectrum Analysis; Stretching; Structure; System; Tars; Techniques; Testing; Time; Viral; Viral Physiology; Zinc Fingers; ear helix; gag Gene Products; in vivo; melting; mutant; novel; nucleic acid structure; programs; protein protein interaction; research study; self assembly; single molecule

DESCRIPTION (provided by applicant): The objective of this research is to investigate the role of HIV-1 and other retroviral Gag and nucleocapsid proteins (NC) in the regulation of processes involving nucleic acid structural transitions and viral self assembly in retroviral systems. Single molecule DNA stretching experiments can induce the DNA helix-coil transition. Investigation of the effects of retroviral NC proteins on this transition has shed light on the mechanism of nucleic acid chaperone activity. We will investigate these interactions by examining the effects of NC from HIV-1 and other retroviruses as well as HIV-1 Gag proteins on DNA packaging and the DNA helix-coil transition. We will use this novel technique to probe the effects of drugs on the capability of NC proteins to alter DNA melting, it has also been shown that specific structures of DNA and RNA can be probed using force spectroscopy. We will extend this technique to study the interactions of retroviral NC and Gag proteins with specific RNA structures that are important for retroviral replication. We will then develop a quantitative model for the interaction of retroviral NC and Gag proteins with nucleic acids, which will increase our understanding of nucleic acid chaperone activity and viral assembly. The 3 specific aims are: 1. To probe the nucleic acid chaperone activity of retroviral nucleocapsid proteins and the viral self-assembly of Gag proteins. 2. To probe the capabilities of NC binding drugs to alter NC's nucleic acid chaperone activity. 3. To probe the interaction of retroviral nucleocapsid and Gag proteins with HIV-1 RNA structures.

描述（由申请人提供）：本研究的目的是研究HIV-1和其他逆转录病毒Gag和核衣壳蛋白（NC）在逆转录病毒系统中涉及核酸结构转换和病毒自组装过程的调节中的作用。单分子DNA拉伸实验可以诱导DNA螺旋-卷曲转变。逆转录病毒NC蛋白对这种转变的影响的调查揭示了核酸伴侣活性的机制。我们将研究这些相互作用，通过检查NC从HIV-1和其他逆转录病毒，以及HIV-1 Gag蛋白的DNA包装和DNA螺旋-螺旋转换的影响。我们将使用这种新的技术来探测药物对NC蛋白改变DNA解链能力的影响，也已经表明可以使用力谱来探测DNA和RNA的特定结构。我们将扩展这种技术，研究逆转录病毒NC和Gag蛋白与逆转录病毒复制重要的特定RNA结构的相互作用。然后，我们将开发一个定量模型的逆转录病毒NC和Gag蛋白与核酸的相互作用，这将增加我们的核酸伴侣活性和病毒组装的理解。三个具体目标是：1。探讨逆转录病毒核衣壳蛋白的核酸伴侣活性和Gag蛋白的病毒自组装。2.探讨NC结合药物改变NC核酸伴侣活性的能力。3.探讨逆转录病毒核衣壳蛋白和Gag蛋白与HIV-1 RNA结构的相互作用。