Wan Qun, Bennett Brad C
Jiangsu Provincial Key Lab for Solid Organic Waste Utilization, Key Lab of Organic-Based Fertilizers of China, Jiangsu Collaborative Innovation Center for Solid Organic Wastes, Educational Ministry Engineering Center of Resource-Saving Fertilizers, Nanjing Agricultural University, Nanjing 210095, China.
Department of Biological and Environmental Sciences, Samford University, Birmingham, AL 35229, USA.
Biology (Basel). 2024 Oct 22;13(11):850. doi: 10.3390/biology13110850.
Hydrogen is the lightest atom and composes approximately half of the atomic content in macromolecules, yet their location can only be inferred or predicted in most macromolecular structures. This is because hydrogen can rarely be directly observed by the most common structure determination techniques (such as X-ray crystallography and electron cryomicroscopy). However, knowledge of hydrogen atom positions, especially for enzymes, can reveal protonation states of titratable active site residues, hydrogen bonding patterns, and the orientation of water molecules. Though we know they are present, this vital layer of information, which can inform a myriad of biological processes, is frustratingly invisible to us. The good news is that, even at modest resolution, neutron crystallography (NC) can reveal this layer and has emerged this century as a powerful tool to elucidate enzyme catalytic mechanisms. Due to its strong and coherent scattering of neutrons, incorporation of deuterium into the protein crystal amplifies the power of NC. This is especially true when solvation and the specific participation of key water molecules are crucial for catalysis. Neutron data allow the modeling of all three atoms in water molecules and have even revealed previously unobserved and unique species such as hydronium (DO) and deuteroxide (OD) ions as well as lone deuterons (D). Herein, we briefly review why neutrons are ideal probes for identifying catalytically important water molecules and these unique water-like species, limitations in interpretation, and four vignettes of enzyme success stories from disparate research groups. One of these groups was that of Dr. Chris G. Dealwis, who died unexpectedly in 2022. As a memorial appreciation of his scientific career, we will also highlight his interest and contributions to the neutron crystallography field. As both the authors were mentored by Chris, we feel we have a unique perspective on his love of molecular structure and admiration for neutrons as a tool to query those structures.
氢是最轻的原子,在大分子中约占原子总量的一半,但在大多数大分子结构中,其位置只能通过推断或预测得知。这是因为在最常用的结构测定技术(如X射线晶体学和电子冷冻显微镜)下,氢很少能被直接观测到。然而,了解氢原子的位置,尤其是对于酶而言,能够揭示可滴定活性位点残基的质子化状态、氢键模式以及水分子的取向。尽管我们知道它们存在,但这一至关重要的信息层,本可揭示无数生物过程,却令人沮丧地对我们不可见。好消息是,即使在中等分辨率下,中子晶体学(NC)也能揭示这一信息层,并且在本世纪已成为阐明酶催化机制的强大工具。由于中子具有强烈且相干的散射,将氘掺入蛋白质晶体可增强中子晶体学的能力。当溶剂化以及关键水分子的特定参与对催化作用至关重要时,情况尤其如此。中子数据允许对水分子中的所有三个原子进行建模,甚至还揭示了诸如水合氢离子(DO)、氘氧基(OD)离子以及孤立氘核(D)等先前未观察到的独特物种。在此,我们简要回顾为何中子是识别具有催化重要性的水分子和这些独特类水物种的理想探针、解释方面的局限性,以及来自不同研究团队的四个酶研究成功案例。其中一个团队是克里斯·G·迪尔威斯博士所在的团队,他于2022年意外离世。作为对他科学事业的纪念与赞赏,我们还将突出他对中子晶体学领域的兴趣和贡献。由于两位作者都曾受克里斯指导,我们觉得自己对他对分子结构的热爱以及对中子作为探究这些结构工具的钦佩有着独特的视角。