Structure and stability of 3-alpha vs alpha/beta folds

3-α 与 α/β 折叠的结构和稳定性

• 批准号: 7679474
• 负责人: JOHN ORBAN
• 金额: $ 15.9万
• 依托单位: UNIVERSITY OF MD BIOTECHNOLOGY INSTITUTE
• 依托单位国家: 美国
• 财政年份: 2002
• 资助国家: 美国
• 起止时间: 2002-03-01 至 2010-04-24
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7679474
• 关键词: Activities of Daily Living; Adopted; Amino Acid Sequence; Amino Acids; Area; Binding; Bioinformatics; Code; Development; Engineering; Evolution; Genetic; Goals; Health; Homologous Protein; Human; Immunoglobulin G; Ligands; Measures; Methods; Mutation; NMR Spectroscopy; Pathway interactions; Phage Display; Positioning Attribute; Protein Engineering; Proteins; Serum Albumin; Signal Transduction; Specific qualifier value; Structure; Subtilisins; Therapeutic; Thermodynamics; Work; base; design; improved; member; microcalorimetry; mutant; preference; protein folding; protein function; protein structure prediction; research study; success; three dimensional structure

DESCRIPTION (provided by applicant): The goal of this proposal is to give a genetic, thermodynamic and structural description of how one protein fold (and function) changes into another. This is based on our ability to: 1) Create highly homologous proteins with different folds (heteromorphic pairs); 2) Engineer dual functional capacity within each member of the heteromorphic pair such that one binding function is manifest in one fold and cryptic in the other fold; 3) Use the thermodynamic linkage between folding and binding to determine folding propensity; 4) Use NMR to determine structures of heteromorphic pairs. Our ability to parse the fold-specific folding code from the overall stability code allows us to study a code for conformational switching between two folds. The specific goals are as follows: 1. Determine an efficient evolutionary path from one fold and function to another; 2. Establish the minimum sequence gap separating two functional folds; 3. Generate heteromorphic pairs of maximum identity for structural and thermodynamic study. We will study how small sets of amino acids determine two different native folds. This will be done by completely examining the functional sequence space separating the two folds, measuring the effects of small numbers of mutations on folding propensity, and determining structures to assess how a limited set of interactions can determine fold. Understanding how a small set of mutations can cause a switch between two stable, monomeric folds and two different functions will have profound implications on our understanding of protein folding, bioinformatics and the natural evolution of new folds and functions. The aim of this proposal is to better understand how amino acid sequence specifies unique tertiary folds by reducing the folding problem to those amino acids that contain the most information toward specifying one fold versus another. This work has direct implications for understanding the protein folding code and the evolution of new folds and will greatly benefit the fields of protein engineering, protein structure prediction, and de novo protein design. Advances in these areas will be needed in the continuing development of new biomedically useful therapeutics to improve human health.

描述（由申请人提供）：本提案的目标是对一种蛋白质折叠（和功能）如何转变为另一种蛋白质进行遗传、热力学和结构描述。这是基于我们的能力：1）创建具有不同折叠的高度同源蛋白质（异形对）; 2）工程化异形对的每个成员内的双重功能能力，使得一种结合功能在一个折叠中是明显的，而在另一个折叠中是隐蔽的; 3）使用折叠和结合之间的热力学联系来确定折叠倾向; 4）利用NMR确定异晶对的结构。我们的能力，解析折叠特定的折叠代码的整体稳定性代码，使我们能够研究两个折叠之间的构象转换的代码。 具体目标如下：1.确定从一个折叠和功能到另一个的有效进化路径; 2.建立分离两个功能折叠的最小序列间隙; 3.生成最大同一性的异形对，用于结构和热力学研究。我们将研究氨基酸的小集合如何决定两种不同的天然折叠。这将通过完全检查分离两个折叠的功能序列空间，测量少量突变对折叠倾向的影响，并确定结构以评估有限的一组相互作用如何确定折叠来完成。了解一小部分突变如何导致两个稳定的单体折叠和两种不同功能之间的转换，将对我们理解蛋白质折叠，生物信息学以及新折叠和功能的自然进化产生深远的影响。这个建议的目的是更好地理解氨基酸序列如何通过将折叠问题减少到包含最多信息的那些氨基酸来指定独特的三级折叠。这项工作对于理解蛋白质折叠密码和新折叠的进化具有直接意义，并且将极大地有益于蛋白质工程、蛋白质结构预测和从头蛋白质设计领域。在继续开发新的生物医学有用的治疗方法以改善人类健康方面，需要在这些领域取得进展。