STRUCTURAL STUDIES OF THE LACTOSE REPRESSOR OF E COLI

大肠杆菌乳糖抑制剂的结构研究

• 批准号: 2520494
• 负责人: CHARLES E BELL
• 金额: $ 2.62万
• 依托单位: UNIVERSITY OF PENNSYLVANIA
• 依托单位国家: 美国
• 财政年份: 1998
• 资助国家: 美国
• 起止时间: 1998-07-23 至
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/2520494
• 关键词: Escherichia coli; X ray crystallography; bacterial genetics; bacterial proteins; gene induction /repression; lactose; microorganism culture; nucleic acid sequence; operon; protein structure function; transcription factor

Transcriptional gene regulation is an intense field of research in biology and in medicine. The lac operon of E. coli is the paradigm for transcriptional gene regulation. Its key component, the lac repressor (lacR), is one of the most intensely studied proteins both genetically and biochemically. Recent crystal structures of the uncomplexed tetrameric lacR, lacR bound to the inducer IPTG, and lacR bound to operator DNA have provided a framework for understanding how lacR functions as a genetic switch. The research in this proposal will extend our current structural understanding of lacR. Of paramount importance is extending the resolution of the structure of lacR bound to operator DNA. Since the structure was determined at only 4.8Angstrom units resolution, the current model for the operator-bound, repressed conformation of lacR does not include side chains. A major premise of this proposal is that a dimeric version of lacR, when complexed to operator DNA, will grow crystals which diffract to higher resolution than has so far been achieved for the tetramer of lacR. Dimeric lacR will also be used to achieve: (1) a structural comparison of lacR bound to both wild-type and symmetric operator sequences, (2) a structural basis for the action of allolactose, the natural inducer of lacR, and orthonitrophenylfucoside, an anti-inducer of lacR, and (3) a structural basis for single point mutations in lacR which lead to 100-fold increased affinity for operator.

转录基因调控是生物学研究的热点领域