Polysomes & Subunits: Structure-Function Relationships

多核糖体

• 批准号: 8450936
• 负责人: ALBERT E DAHLBERG
• 金额: $ 63.43万
• 依托单位: BROWN UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 1975
• 资助国家: 美国
• 起止时间: 1975-09-01 至 2015-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8450936
• 关键词: Address; Amino Acyl Transfer RNA; Antibiotic Resistance; Antibiotics; Anticodon; Applications Grants; Area; Bacteria; Biochemical; Biochemistry; Biological Models; Chemicals; Codon Nucleotides; Complex; Crystallization; Dependence; Development; Drug Design; EEF1A1 gene; Enzymatic Biochemistry; Genetic; Goals; Guanosine Triphosphate; Guanosine Triphosphate Phosphohydrolases; Hydrolysis; Kinetics; Laboratories; Lead; Life; Medical; Messenger RNA; Methods; Modification; Molecular; Molecular Conformation; Mutation; Pathway interactions; Polyribosomes; Process; Protein Biosynthesis; Proteins; Research; Resistance; Resolution; Ribosomes; Series; Signal Pathway; Signal Transduction; Streptomycin; Structure; Structure-Activity Relationship; Thermus thermophilus; Time; Transfer RNA; X-Ray Crystallography; antimicrobial drug; base; clinically relevant; conformational conversion; design; fighting; genetic analysis; genetic manipulation; insight; interdisciplinary approach; microbial; microorganism; mutant; novel; pathogen; protein complex; public health relevance; research study; resistance mutation; ribosomal protein S12; stereochemistry; structural biology; success; thermophilic bacteria; working group

DESCRIPTION (provided by applicant): ABSTRACT: The long-term goal of this grant proposal is to understand at an atomic level how the ribosome functions during protein synthesis. We will take a multidisciplinary approach utilizing genetic, biochemical and structural methods to study the bacterial ribosome. Our first aim is to examine ribosome structural dynamics during decoding of mRNA and its inhibition by antibiotics. We will use X-ray crystallography to obtain high-resolution structures of mutant Thermus thermophilus 30S subunits that reveal new conformational states. We will examine the effects of the mutations on the accuracy and kinetics of decoding. Our second aim is to probe a pathway by which codon recognition is signaled via ribosomal protein S12 and aminoacyl-tRNA to EF-Tu to activate GTP hydrolysis, a key step in the tRNA selection process. These experiments are designed to provide fundamental insights into ribosome structure and function, including new conformational states of the ribosome, to aid in understanding the decoding process. The ability to solve structures of ribosomes with antibiotic-resistance mutations will aid in understanding the mechanisms of antibiotic action and resistance, and has particular clinical relevance for the rational design of drugs to fight resistant microbial pathogens.

摘要：本课题的长期目标是在原子水平上了解核糖体在蛋白质合成过程中的功能。我们将采取多学科的方法，利用遗传，生化和结构的方法来研究细菌核糖体。我们的第一个目的是研究核糖体在mRNA解码过程中的结构动力学及其抗生素的抑制作用。我们将使用x射线晶体学来获得突变的Thermus thermoophilus 30S亚基的高分辨率结构，揭示新的构象状态。我们将研究突变对解码的准确性和动力学的影响。我们的第二个目标是探索通过核糖体蛋白S12和氨基酰基tRNA向EF-Tu发出密码子识别信号以激活GTP水解的途径，这是tRNA选择过程中的关键步骤。这些实验旨在提供对核糖体结构和功能的基本见解，包括核糖体的新构象状态，以帮助理解解码过程。解决具有抗生素抗性突变的核糖体结构的能力将有助于理解抗生素作用和耐药性的机制，并对合理设计药物以对抗耐药微生物病原体具有特殊的临床意义。