Keith Alasdair D, Sawyer Elizabeth B, Choy Desmond C Y, Cole James L, Shang Cheng, Biggs George S, Klein Oskar James, Brear Paul D, Wales David J, Barker Paul D
Yusuf Hamied Department of Chemistry, University of Cambridge, Cambridge, UK.
Department of Biochemistry, Sanger Building, University of Cambridge, Cambridge, UK.
Protein Sci. 2025 Feb;34(2):e5243. doi: 10.1002/pro.5243.
We have recently demonstrated a novel anaerobic NADH-dependent haem breakdown reaction, which is carried out by a range of haemoproteins. The Yersinia enterocolitica protein, HemS, is the focus of further research presented in the current paper. Using conventional experimental methods, bioinformatics, and energy landscape theory (ELT), we provide new insight into the mechanism of the novel breakdown process. Of particular interest is the behavior of a double phenylalanine gate, which opens and closes according to the relative situations of haem and NADH within the protein pocket. This behavior suggests that the double phe-gate fulfills a regulatory role within the pocket, controlling the access of NADH to haem. Additionally, stopped-flow spectroscopy results provide kinetic comparisons between the wild-type and the selected mutants. We also present a fully resolved crystal structure for the F104AF199A HemS monomer, including its extensive loop, the first such structure to be completely resolved for HemS or any of its close homologues. The energy landscapes approach provided key information regarding the gating strategy employed by HemS, compensating for current limitations with conventional biophysical and molecular dynamics approaches. We propose that ELT become more widely used in the field, particularly in the investigation of the dynamics and interactions of weak-binding ligands, and for gating features, within protein cavities.
我们最近证明了一种新的厌氧NADH依赖性血红素分解反应,该反应由一系列血红素蛋白进行。小肠结肠炎耶尔森菌蛋白HemS是本文进一步研究的重点。我们使用传统实验方法、生物信息学和能量景观理论(ELT),对这种新的分解过程的机制提供了新的见解。特别令人感兴趣的是双苯丙氨酸门的行为,它根据蛋白口袋内血红素和NADH的相对情况打开和关闭。这种行为表明双苯丙氨酸门在口袋内起到调节作用,控制NADH与血红素的接触。此外,停流光谱结果提供了野生型和选定突变体之间的动力学比较。我们还展示了F104AF199A HemS单体的完全解析晶体结构,包括其广泛的环,这是第一个针对HemS或其任何紧密同源物完全解析的此类结构。能量景观方法提供了有关HemS采用的门控策略的关键信息,弥补了传统生物物理和分子动力学方法当前的局限性。我们建议ELT在该领域得到更广泛的应用,特别是在研究弱结合配体的动力学和相互作用以及蛋白腔内的门控特征方面。