Prester Andreas, Perbandt Markus, Galchenkova Marina, Oberthuer Dominik, Werner Nadine, Henkel Alessandra, Maracke Julia, Yefanov Oleksandr, Hakanpää Johanna, Pompidor Guillaume, Meyer Jan, Chapman Henry, Aepfelbacher Martin, Hinrichs Winfried, Rohde Holger, Betzel Christian
Institute of Medical Microbiology, Virology and Hygiene, University Medical Center Hamburg-Eppendorf UKE, Hamburg, Germany.
Institute of Biochemistry and Signal Transduction, University Medical Center Hamburg-Eppendorf UKE, Hamburg, Germany.
Commun Chem. 2024 Jul 5;7(1):152. doi: 10.1038/s42004-024-01236-w.
The emergence and spread of antibiotic resistance represent a growing threat to public health. Of particular concern is the appearance of β-lactamases, which are capable to hydrolyze and inactivate the most important class of antibiotics, the β-lactams. Effective β-lactamase inhibitors and mechanistic insights into their action are central in overcoming this type of resistance, and in this context boronate-based β-lactamase inhibitors were just recently approved to treat multidrug-resistant bacteria. Using boric acid as a simplified inhibitor model, time-resolved serial crystallography was employed to obtain mechanistic insights into binding to the active site serine of β-lactamase CTX-M-14, identifying a reaction time frame of 80-100 ms. In a next step, the subsequent 1,2-diol boric ester formation with glycerol in the active site was monitored proceeding in a time frame of 100-150 ms. Furthermore, the displacement of the crucial anion in the active site of the β-lactamase was verified as an essential part of the binding mechanism of substrates and inhibitors. In total, 22 datasets of β-lactamase intermediate complexes with high spatial resolution of 1.40-2.04 Å and high temporal resolution range of 50-10,000 ms were obtained, allowing a detailed analysis of the studied processes. Mechanistic details captured here contribute to the understanding of molecular processes and their time frames in enzymatic reactions. Moreover, we could demonstrate that time-resolved crystallography can serve as an additional tool for identifying and investigating enzymatic reactions.
抗生素耐药性的出现和传播对公众健康构成了日益严重的威胁。特别令人担忧的是β-内酰胺酶的出现,它能够水解并使最重要的一类抗生素——β-内酰胺失活。有效的β-内酰胺酶抑制剂及其作用机制的深入了解是克服这类耐药性的关键,在此背景下,基于硼酸盐的β-内酰胺酶抑制剂最近刚刚被批准用于治疗多重耐药细菌。以硼酸作为简化的抑制剂模型,采用时间分辨串行晶体学来深入了解与β-内酰胺酶CTX-M-14活性位点丝氨酸的结合机制,确定了80 - 100毫秒的反应时间框架。下一步,监测了在100 - 150毫秒时间框架内活性位点中与甘油随后形成1,2 -二醇硼酸酯的过程。此外,还证实了β-内酰胺酶活性位点中关键阴离子的置换是底物和抑制剂结合机制的重要组成部分。总共获得了22个β-内酰胺酶中间复合物数据集,其空间分辨率高达1.40 - 2.04埃,时间分辨率范围为50 - 10000毫秒,从而能够对所研究的过程进行详细分析。这里捕获的机制细节有助于理解酶促反应中的分子过程及其时间框架。此外,我们能够证明时间分辨晶体学可作为识别和研究酶促反应的额外工具。