Functional Dynamics and Activation Mechanisms in Enzymes

酶的样品状态被引导以结合底物，形成米氏中间体，采用促进化学步骤的构象异构体，沿着整个反应坐标途径以原子分辨率描述所有构象异构体。*虽然可以研究许多酶，但我们专注于氟乙酸脱卤酶（FAcD）作为模型酶，即因为它是同二聚体（蛋白质中最常见的基序），因此引发了关于分子内和分子间变构的问题，这是蛋白质功能的核心。功能状态的动态平衡。我们将确定关键的功能状态，确定系综自由能景观，重点是状态间动力学和解决至少一个激发态的结构（准备基板捕获），其中没有晶体结构。2.变构网络和机制。甲基（TROSY）和19F NMR将提供跨二聚体的化学位移网络。协方差分析的化学位移作为一个功能的抑制剂，底物类似物，和D2O将产生一个变构网络和地址的氢键沃茨作为变构开关的关键作用。3.酶动力学和催化。将通过主链和侧链松弛实验评估整个二聚体的动力学。我们将研究催化效率和分子动力学之间的联系。4.底物抑制。我们将研究二聚体中的变构底物口袋如何有助于高浓度下的抑制和低浓度下的有效催化。5. 19F NMR分配结晶学。我们将改进DFT和局部MD模拟的使用，作为19F NMR分配诱变的替代方法。6.二聚体的蛋白质折叠。同时使用变性剂和压力，以原子级的分辨率来研究这种二聚体的复杂折叠过程。第七章蛋白质突变与进化。将通过单细胞（FACS）方法制备和研究大量变体。将测试变构网络&酶将朝着更高的催化效率或底物混杂的方向进化。** 结果将从系综的角度极大地推进对结构和动力学在催化中的作用的理解，同时解决关于原型二聚体中的变构和水网络的几个范式转变问题。

Enzymes sample states primed to bind substrates, form Michaelis intermediates, adopt conformers facilitating chemical steps, describe all conformers with atomic resolution along the entire reaction coordinate pathway.******While many enzymes could be studied, we focus on fluoroacetate dehalogenase (FAcD) as a model enzyme namely because it is a homodimer (the most common motif among proteins) thus inviting questions regarding intra- and intermolecular allostery, which is at the heart of protein function FacD also detoxifies a fluorinated poison We will address:******1. The dynamic equilibrium of functional states. We will identify key functional states, determine the ensemble free energy landscape with a focus on interstate dynamics & solve a structure of at least one excited state (poised for substrate capture) for which there is no crystal structure. ******2. Allosteric networks & mechanisms. Methyl (TROSY) & 19F NMR will provide a network of chemical shifts across the dimer. Covariance analysis of chemical shifts as a function of inhibitor, substrate analogue, & D2O will generate an allosteric network & address the critical role of hydrogen-bonded waters as allosteric switches. ******3. Enzyme dynamics & catalysis. Dynamics will be assessed across the dimer via backbone & side chain relaxation experiments. We will study the connection between catalytic efficiency & molecular dynamics. ******4. Substrate inhibition. We will study how an allosteric substrate pocket in the dimer contributes to inhibition at high concentrations & efficient catalysis at low concentrations. ******5. 19F NMR assignments crystallography. We will improve the use of DFT & local MD simulations as an alternative to mutagenesis for 19F NMR assignments.******6. Protein folding of a dimer. Both denaturant & pressure will be used to study the complex folding process of this dimer with atomic resolution. ******7. Protein mutagenesis & evolution. High numbers of variants will be made & studied via single cell (FACS) methods. Allosteric networks will be tested & the enzyme will be evolved toward greater catalytic efficiency or substrate promiscuity. ******Results will greatly advance understanding of the role of structure & dynamics in catalysis from the perspective of an ensemble, while addressing several paradigm shifting questions regarding allostery & water networks in a prototypical dimer.