MODIFIED NUCLEOSIDES AS TOOLS FOR MOLECULAR BIOLOGY

修饰核苷作为分子生物学的工具

• 批准号: 6180751
• 负责人: Donald E. BERGSTROM
• 金额: $ 28.32万
• 依托单位: PURDUE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 1996
• 资助国家: 美国
• 起止时间: 1996-04-01 至 2002-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6180751
• 关键词: DNA directed DNA polymerase; azoles; chemical models; chemical structure function; enzyme mechanism; enzyme substrate; intermolecular interaction; matrix assisted laser desorption ionization; nuclear magnetic resonance spectroscopy; nucleic acid biosynthesis; nucleic acid sequence; nucleic acid structure; nucleoside analog; nucleoside triphosphate; oligonucleotides; polymerase chain reaction; synthetic nucleotide

The long-range goal of this research is to develop modified nucleosides suitable for applications that require either the introduction or the recognition of nucleic acid sequence degeneracy. The results from the initial period of this project support the hypothesis that azole carboxamides are able to function as natural base mimics in DNA recognition. Furthermore, the azole nitrogen substitution pattern has a profound influence on the base pairing specificity. We have sufficient information to rationally design a second generation of azole carboxamide nucleosides. Specific aims include: 1) Synthesis of a series of azole carboxamide nucleosides to investigate the role of DNA polymerase-nucleobase interactions in template directed synthesis. 2) Construction of second generation azole nucleobase containing oligonucleotides for biophysical characterization. 3) Investigation of oligonucleotides containing first and second generation azole nucleobases as templates for Taq DNA polymerase and investigation of azole nucleoside triphosphates as alternative substrates in PCR. 4) Exploration of two strategies for using the azole nucleobases in directed evolution technology. The analogs described in this proposal present a broad diversity of electronic configurations within the steric confines of natural nucleobase structure, thereby providing a unique opportunity to explore enzyme recognition and function. The techniques described in this proposal have the potential to provide a thorough exploration of diversity space in short random walks from a starting gene sequence. Although this proposal centers primarily around DNA polymerase, the interaction of azole nucleobase containing oligonucleotides with other nucleic acid enzymes is an unexplored territory with the potential to lead to both fundamental understanding of nucleic acid-protein interactions as well as the development of new tools for protein engineering and directed evolution.

本研究的长期目标是开发适合于需要引入或识别核酸序列简并性的应用的修饰核苷。 该项目初期的结果支持了唑甲酰胺能够在DNA识别中充当天然碱基模拟物的假设。 此外，唑氮取代模式对碱基配对特异性有深远影响。 我们有足够的信息来合理设计第二代唑酰胺核苷。具体目标包括：1）合成了一系列唑酰胺核苷，以研究DNA聚合酶-核碱基相互作用在模板定向合成中的作用。 2)用于生物物理表征的含第二代唑核碱基的寡核苷酸的构建。3)研究含有第一代和第二代唑核碱基的寡核苷酸作为Taq DNA聚合酶的模板，并研究唑核苷三磷酸作为PCR中的替代底物。 4)唑类碱基在定向进化技术中应用的两种策略探讨。在该提案中描述的类似物在天然核碱基结构的空间范围内呈现出广泛多样的电子构型，从而提供了探索酶识别和功能的独特机会。 在这个建议中描述的技术有可能提供一个彻底的探索多样性空间在短随机游走从一个起始基因序列。 虽然这一建议主要围绕DNA聚合酶，唑核碱基含有寡核苷酸与其他核酸酶的相互作用是一个未开发的领域，有可能导致核酸-蛋白质相互作用的基本理解，以及蛋白质工程和定向进化的新工具的发展。