Chemically-Rich Structure and Dynamics in the Active Site of Tryptophan Synthase

色氨酸合酶活性位点的化学丰富结构和动力学

• 批准号: 8087430
• 负责人: Leonard J Mueller
• 金额: $ 28.54万
• 依托单位: UNIVERSITY OF CALIFORNIA RIVERSIDE
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-09-30 至 2016-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8087430
• 关键词: Active Sites; Adopted; Animals; Bacteria; Biochemistry; Boxing; Catalysis; Catalytic Domain; Charge; Chemical Structure; Chemicals; Chemistry; Coenzymes; Communicable Diseases; Complex; Data; Development; Diamines; Drug Design; Electrostatics; Environment; Enzymes; Equilibrium; Goals; Herbicides; Homologous Gene; Housing; Human; Hydroxyl Radical; Indoles; Kinetics; Label; Ligands; Location; Measures; Methodology; Modeling; Molds; Nuclear Magnetic Resonance; Organic Chemistry; Pathway interactions; Plants; Positioning Attribute; Process; Proteins; Protons; Pyridoxal Phosphate; Reaction; Resolution; Roentgen Rays; Salmonella typhimurium; Scanning; Scheme; Schiff Bases; Side; Site; Solutions; Specific qualifier value; Spin Labels; Staging; Structure; System; Tryptophan Synthase; Vitamin B6; Water; Work; X-Ray Crystallography; Yeasts; analog; base; computational chemistry; electronic structure; enzyme mechanism; indoline; insight; molecular mechanics; nanomachine; novel; protonation; serine containing aminolipid; solid state nuclear magnetic resonance; success; three dimensional structure

DESCRIPTION (provided by applicant): The goal of this proposal is to provide the chemical level details necessary to understand the enzymatic mechanism in tryptophan synthase at atomic resolution. Enzymes have evolved to achieve remarkably efficient and specific chemical transformations that enable a diverse biochemistry. Yet atomic level details of enzyme mechanisms remain elusive; the intermediates are transient and the chemistry that drives the transformation, such as changes in hyrbridizaton and protonation states, is difficult to characterize in functioning enzyme systems. The pyridoxal-phosphate (vitamin-B6)-dependent tryptophan synthase 1222 bienzyme complex catalyses the last two steps in the synthesis of L-Trp, consecutive processes that require channeling of the common metabolite, indole, between the 1- and 2-subunits. Tryptophan synthase homologues are found in bacteria, yeasts, molds, plants, and some protozoans. The absence of a synthetic pathway for L-Trp in higher animals and in humans makes the tryptophan synthase nanomachine a potential target both for the development of herbicides, and for the design of drugs to treat infectious disease. Consequently, understanding the catalytic mechanism could provide useful insights for developing tryptophan synthase as an important target for drug design, or for the development of herbicides. Recent X-ray structure determinations of complexes with substrates, intermediates, and substrate analogues have resulted in a significant breakthrough concerning identification of the linkages between the bienzyme complex structure and catalysis. This effort combined organic synthetic work and solution kinetic/spectroscopic studies with X-ray crystal structure determinations of 10-15 different ligand complexes with tryptophan synthase at 1.7 to 2.4 A resolution. Despite these successes, significant chemical questions remain as the resolution of these structures does not allow for a detailed chemical mechanism to be established for the substrate transformation. Yet chemical level details such as protonation and hybridization states are critical for understanding enzymatic mechanism and function. Even under moderately high resolution, these are difficult to determine from X-ray crystallography alone. The chemical shift in nuclear magnetic resonance (NMR), however, is an extremely sensitive probe of chemical environment, making solid- state NMR and X-ray crystallography a powerful combination for defining chemically-detailed three dimensional structures. Here we adopt a combined X-ray crystallography/solid state NMR/ab initio calculation approach to determine the chemically-rich crystal structures of several key intermediates in the multistep transformation of substrate to product in the 2-subunit of tryptophan synthase. Models of the active site are developed using a synergistic approach in which the structure of this reactive substrate/analogue is freely optimized using computational chemistry in the presence of side chain residues fixed at their crystallographically determined coordinates. Various models of charge and protonation state for the substrate and nearby catalytic residues can be uniquely distinguished by their calculated effect on the chemical shifts, measured at specifically 13C and 15N-labeled positions on substrates/analogues, coenzyme and site catalytic residues. This treatment provides an accurate chemically-detailed starting point for dynamics and reaction coordinate scans that have already provided unique insight into the connection between chemical structure and the resulting local electrostatic fields that help drive and direct the next step in the catalysis. PUBLIC HEALTH RELEVANCE: The vitamin-B6-dependent tryptophan synthase complex catalyses the last two steps in the synthesis of L-Trp. Tryptophan synthase homologues are found in bacteria, yeasts, molds, plants, and some protozoans. The absence of a synthetic pathway for L-Trp in higher animals and in humans makes the tryptophan synthase nanomachine a potential target both for the development of herbicides, and for the design of drugs to treat infectious disease. Consequently, understanding the catalytic mechanism could provide useful insights for developing tryptophan synthase as an important target for drug design, or for the development of herbicides.

描述(由申请人提供)：本提案的目标是提供在原子分辨率下理解色氨酸合成酶的酶机制所需的化学水平的详细信息。酶的进化实现了非常有效和特定的化学转化，从而实现了多样化的生物化学。然而，酶机制的原子水平细节仍然难以捉摸；中间体是暂时的，驱动转化的化学物质，如氢化和质子化状态的变化，很难在起作用的酶系统中表征。依赖于磷酸吡哆醛(维生素B6)的色氨酸合成酶1222双酶复合体催化合成L-色氨酸的最后两步，这是一个连续的过程，需要共同的代谢物吲哚在1-和2-亚基之间输送。色氨酸合成酶同源物存在于细菌、酵母菌、霉菌、植物和一些原生动物中。L-色氨酸在高等动物和人类中缺乏合成途径，这使得色氨酸合成酶纳米机器成为除草剂开发和治疗传染病药物设计的潜在靶点。因此，了解色氨酸合成酶的催化机理可以为开发色氨酸合成酶作为药物设计或除草剂开发的重要靶点提供有用的见解。最近对具有底物、中间体和底物类似物的络合物的X射线结构测定在鉴定双酶络合物结构和催化之间的联系方面取得了重大突破。这项工作将有机合成工作和溶液动力学/光谱研究与10-15个不同配体与色氨酸合成酶配合物的X射线晶体结构测定结合在一起，分辨率为1.7至2.4A。尽管取得了这些成功，但重大的化学问题仍然存在，因为这些结构的解析不允许为底物转化建立详细的化学机制。然而，质子化和杂交状态等化学水平的细节对于理解酶的机制和功能至关重要。即使在中等高分辨率下，仅从X射线结晶学也很难确定它们的存在。然而，核磁共振中的化学位移是化学环境的一个极其敏感的探针，使固态核磁共振和X射线结晶学成为定义化学细节三维结构的强大组合。在这里，我们采用X射线结晶学/固体核磁共振/从头计算相结合的方法来确定色氨酸合成酶2-亚基中底物到产物的多步转化过程中几个关键中间体的富含化学成分的晶体结构。活性中心的模型是用协同方法建立的，其中这种反应底物/类似物的结构是在存在固定在结晶学确定的坐标上的侧链残基的情况下使用计算化学自由优化的。底物和附近催化残基的各种电荷和质子化状态模型可以通过计算它们对化学位移的影响来唯一地区分，这些效应是在底物/类似物、辅酶和位置催化残基上特别是13C和15N标记的位置测量的。这种处理为动力学和反应坐标扫描提供了准确的化学细节起点，这些扫描已经提供了对化学结构和产生的局部静电场之间的联系的独特见解，这些电场有助于推动和指导催化中的下一步。 与公共健康相关：依赖维生素B6的色氨酸合成酶复合体催化合成L-色氨酸的最后两步。色氨酸合成酶同源物存在于细菌、酵母菌、霉菌、植物和一些原生动物中。L-色氨酸在高等动物和人类中缺乏合成途径，这使得色氨酸合成酶纳米机器成为除草剂开发和治疗传染病药物设计的潜在靶点。因此，了解色氨酸合成酶的催化机理可以为开发色氨酸合成酶作为药物设计或除草剂开发的重要靶点提供有用的见解。