Studies of Riboswitch-Mediated Transcriptional Control Using Single-Molecule Fiel

利用单分子场进行核糖开关介导的转录控制的研究

• 批准号: 8860202
• 负责人: Ruben L Gonzalez
• 金额: $ 37.62万
• 依托单位: COLUMBIA UNIV NEW YORK MORNINGSIDE
• 依托单位国家: 美国
• 财政年份: 2014
• 资助国家: 美国
• 起止时间: 2014-06-04 至 2018-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8860202
• 关键词: 5' Untranslated Regions; Adenine; Antibiotics; Atomic Force Microscopy; Bacillus subtilis; Bacteria; Bacterial Genes; Binding; Biochemical; Biochemical Reaction; Biological Models; Carbon Nanotubes; Communicable Diseases; Complex; DNA Binding; DNA-Directed RNA Polymerase; Development; Devices; Diagnosis; Drug Targeting; Elements; Engineering; Enzymes; Escherichia coli; Event; Fluorescence Microscopy; Gene Expression; Genes; Genetic; Genetic Transcription; Health; Hereditary Disease; Holoenzymes; In Vitro; Investigation; Kinetics; Knowledge; Label; Length; Mediating; Messenger RNA; Methods; Motion; Organism; Process; Property; Protein Complex Subunit; RNA; RNA Splicing; Resolution; Series; Specificity; Staging; Structure; Synthetic Genes; System; Thermodynamics; Time; Transcriptional Regulation; Transistors; Translations; aptamer; base; biological systems; biophysical techniques; design; fluorophore; improved; new technology; next generation; particle; pathogen; prevent; research study; response; single molecule; synthetic biology; tool; transcription termination

DESCRIPTION (provided by applicant): Riboswitches are genetic control elements located within the 5' untranslated regions of messenger RNAs (mRNAs) that undergo metabolite-dependent structural rearrangements to regulate mRNA transcription, splicing, translation, or stability in response to the presence and concentration of specific metabolites. The ubiquity of riboswitch-mediated transcriptional control in bacteria and the specificity with which riboswitches control bacterial gene expression are fueling efforts to develop next-generation antibiotics that target bacterial riboswitches. In addition, riboswitches are quickly becoming powerful tools in the field of synthetic biology, where they can be engineered to artificially control gene expression. Fully exploiting riboswitches for these applications, however, requires a detailed understanding of the mechanism of riboswitch-mediated transcriptional control. Although single-molecule (sm) biophysical methods, including sm fluorescence microscopy and sm force microscopy, have established themselves as powerful tools for studying metabolite- dependent structural rearrangements of riboswitches and transcription by RNA polymerases (RNAPs), the mechanistic information available from these sm methods remains limited by technical obstacles such as: (i) difficulties in fluorophore labeling of biomolecules; (ii) the application of invasive artificial forces; (iii) limited time resolution; and (iv) limited total observation time. The higly multi-disciplinary effort described here will expand upon recent development of a carbon nanotube-based sm field effect transistor (smFET) as a new, label-free, non-invasive, high-time-resolution, extended-observation-time, sm method for in vitro studies of biomolecular binding kinetics and structural dynamics. This smFET-based experimental system will be further developed to overcome many of the limitations of established sm methods, enabling the Bacillus subtilis pbuE adenine-responsive riboswitch and the corresponding B. subtilis RNAP to be used as a model system for studying the mechanisms of metabolite- dependent riboswitch structural rearrangement (Aim 1), transcription (Aim 2), and real-time riboswitch- mediated transcriptional control (Aim 3) at unprecedented time resolutions and throughputs. These studies will enable characterization of some of the most poorly defined aspects of the mechanism of riboswitch-mediated transcriptional regulation and will provide the tools and knowledge necessary to drive the development of new antibiotic drugs that target bacterial riboswitches and the design of new riboswitches that can be used to regulate synthetic gene networks.

描述（由申请人提供）：核糖开关是位于信使RNA（mRNA）5 '非翻译区内的遗传控制元件，其经历代谢物依赖性结构重排以响应特定代谢物的存在和浓度来调节mRNA转录、剪接、翻译或稳定性。核糖开关介导的转录控制在细菌中的普遍性以及核糖开关的特异性 控制细菌基因表达的研究正在推动开发针对细菌核糖开关的下一代抗生素的努力。此外，核糖开关正迅速成为生物医学领域的有力工具。 合成生物学领域，在那里它们可以被工程化以人工控制基因表达。然而，充分利用核糖开关的这些应用，需要详细了解核糖开关介导的转录控制的机制。尽管单分子（sm）生物物理方法，包括sm荧光显微镜和sm力显微镜，已经确立了它们本身作为研究核糖开关的代谢物依赖性结构重排和RNA聚合酶（RNAP）转录的有力工具，但是从这些sm方法获得的机制信息仍然受到技术障碍的限制，例如：（i）生物分子的荧光团标记的困难;（二）侵入性 （iii）有限的时间分辨率;（iv）有限的总观测时间。 高度多学科的努力，这里描述的将扩大后，最近发展的碳纳米管为基础的sm场效应晶体管（smFET）作为一种新的，无标记，非侵入性，高时间分辨率，延长观察时间，sm方法在体外研究生物分子结合动力学和结构动力学。该基于smFET的实验系统将被进一步开发，以克服已建立的sm方法的许多局限性，使枯草芽孢杆菌pbuE腺嘌呤响应核糖开关和相应的B。枯草杆菌RNAP用作模型系统，用于以前所未有的时间分辨率和通量研究代谢物依赖性核糖开关结构重排（Aim 1）、转录（Aim 2）和实时核糖开关介导的转录控制（Aim 3）的机制。这些研究将能够表征核糖开关介导的转录调控机制的一些最不明确的方面，并将提供必要的工具和知识，以推动靶向细菌核糖开关的新抗生素药物的开发和可用于调节合成基因网络的新核糖开关的设计。