Evolution of enzyme structure and function viewed at atomic resolution

从原子分辨率观察酶结构和功能的演变

• 批准号: 8668075
• 负责人: Douglas Lowell Theobald
• 金额: $ 29.47万
• 依托单位: BRANDEIS UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-07-01 至 2016-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8668075
• 关键词: Active Sites; Address; Affect; Amino Acid Sequence; Amino Acid Substitution; Anthrax disease; Bacteria; Bacteroides; Biochemical; Biological Models; Characteristics; Citric Acid Cycle; Crystallization; Data; Distal; Drug Targeting; Engineering; Enzymes; Event; Evolution; Family; Gene Duplication; Genes; Genetic Epistasis; Glycolysis; Goals; Homo; Homologous Protein; Human; Ionic Strengths; Knowledge; Lactate Dehydrogenase; Life; Malaria; Malate Dehydrogenase; Malates; Measures; Methodology; Methods; Molecular; Molecular Biology; Molecular Conformation; Mutate; Mutation; Natural Selections; Organism; Oxaloacetates; Pathway interactions; Peptide Sequence Determination; Phylogenetic Analysis; Positioning Attribute; Proteins; Pseudomonas; Pyruvate; Recording of previous events; Research; Resolution; Series; Site; Specificity; Structure; Substrate Specificity; Synthetic Genes; Temperature; Testing; Thermodynamics; Time; Visual; X-Ray Crystallography; base; enzyme structure; fitness; gene synthesis; innovation; interest; lactate dehydrogenase 5; mutant; novel; pathogen; protein structure; theories

DESCRIPTION (provided by applicant): The goal of this research is to explore the dynamic structural mechanisms by which proteins have evolved novel functions in an important class of enzymes, the malate and lactate dehydrogenases (MDHs and LDHs, M/LDH family). We plan to resurrect entire evolutionary lineages of ancestral M/LDH enzymes, probe their biochemical functions, solve their structures by X-ray crystallography, and correlate the functional changes with structural changes observed along these evolutionary trajectories. Our model system is the malate and lactate dehydrogenase superfamily, which contains some of the most readily crystallizable proteins known. Both enzymes are widely distributed throughout life. MDH is found in the citric acid cycle and catalyzes the interconversion of malate to oxaloacetate, while LDH converts pyruvate, the final product of glycolysis, to lactate. The evolution of this family has been accompanied by many interesting and important functional innovations, including sharp changes in substrate specificity, acquisition of thermophilic and cryophilic stability, and gain of allosteric control by small effector molecules, and homo-multimerization via new protein- protein interfaces. The specific aims are to: 1) Investigate the evolutionary history of MDH and LDH proteins, reconstruct ancestral protein sequences along multiple trajectories, and resurrect them in the lab (using phylogenetic inference and artificial gene synthesis). Of exceptional interest are ancestral proteins bracketing significant evolutionary events, such as changes in specificity, catalytic rate, temperature stability, allostery, and oligomerization state. 2) Crystallize and determine the high-resolution structures of MDH and LDH lineages by X-ray crystallography. Analyze the evolution of observed structural changes. 3) Functionally characterize the resurrected proteins and correlate the functional changes along an evolutionary pathway with their concomitant structural perturbations. To determine which changes in the ancestors are functionally important, key residues will be mutated and biochemically characterized. By investigating these ancestral proteins and their mutants, we will empirically address many unanswered questions in molecular biology and in evolutionary theory. How do substitutions distal from the active site affect activity? Do historical amino acid substitutions have different effects on enzyme structure and function compared to the artificial mutations we engineer in modern enzymes? What is the importance of correlations among mutations (epistasis)? Does specificity increase during evolution? Was the common ancestor of MDH and LDH a promiscuous multifunctional protein? This study will provide the first dynamic, high-resolution picture of how novel biomolecular functions are generated during evolution by mutations and gene duplications. The resulting data will help answer several long-standing evolutionary questions and will bolster our knowledge of how enzymatic functions can be rationally engineered.

描述（由申请人提供）：本研究的目的是探索蛋白质在一类重要的酶——苹果酸脱氢酶和乳酸脱氢酶（MDHs和LDHs， M/LDH家族）中进化出新功能的动态结构机制。我们计划复活祖先M/LDH酶的整个进化谱系，探索它们的生化功能，通过x射线晶体学解决它们的结构，并将沿着这些进化轨迹观察到的功能变化与结构变化联系起来。我们的模型系统是苹果酸和乳酸脱氢酶超家族，它包含一些已知的最容易结晶的蛋白质。这两种酶在生命中广泛分布。MDH存在于柠檬酸循环中，催化苹果酸相互转化为草酰乙酸，而LDH将糖酵解的最终产物丙酮酸转化为乳酸。该家族的进化伴随着许多有趣和重要的功能创新，包括底物特异性的急剧变化，嗜热和嗜冷稳定性的获得，小效应分子变抗控制的获得，以及通过新的蛋白质-蛋白质界面的同质多聚。具体目标是：1)研究MDH和LDH蛋白的进化史，沿着多个轨迹重建祖先蛋白序列，并在实验室中复活它们（使用系统发育推断和人工基因合成）。特别令人感兴趣的是包含重要进化事件的祖先蛋白，如特异性、催化速率、温度稳定性、变构和寡聚化状态的变化。2)通过x射线晶体学结晶并确定MDH和LDH谱系的高分辨率结构。分析观察到的结构变化的演变。3)对复活蛋白进行功能表征，并将其在进化过程中的功能变化与其伴随的结构扰动联系起来。为了确定祖先中哪些变化在功能上是重要的，将对关键残基进行突变并进行生物化学表征。通过研究这些祖先蛋白及其突变体，我们将从经验上解决分子生物学和进化理论中许多悬而未决的问题。远离活性位点的取代如何影响活性？与我们在现代酶中设计的人工突变相比，历史上的氨基酸取代对酶的结构和功能有不同的影响吗？突变之间的相关性（上位性）的重要性是什么？在进化过程中特异性是否增加？MDH和LDH的共同祖先是混杂的多功能蛋白吗？这项研究将提供第一个动态的、高分辨率的图像，说明在突变和基因复制的进化过程中，新的生物分子功能是如何产生的。由此产生的数据将有助于回答几个长期存在的进化问题，并将加强我们对酶的功能如何被合理设计的认识。