Grieco Alice, Quereda-Moraleda Isabel, Martin-Garcia Jose Manuel
Department of Crystallography and Structural Biology, Institute of Physical Chemistry Blas Cabrera, Spanish National Research Council (CSIC), 28006 Madrid, Spain.
J Pers Med. 2024 Aug 27;14(9):909. doi: 10.3390/jpm14090909.
Enzymes are crucial in metabolic processes, and their dysfunction can lead to severe metabolic disorders. Structural biology, particularly X-ray crystallography, has advanced our understanding of these diseases by providing 3D structures of pathological enzymes. However, traditional X-ray crystallography faces limitations, such as difficulties in obtaining suitable protein crystals and studying protein dynamics. X-ray free-electron lasers (XFELs) have revolutionized this field with their bright and brief X-ray pulses, providing high-resolution structures of radiation-sensitive and hard-to-crystallize proteins. XFELs also enable the study of protein dynamics through room temperature structures and time-resolved serial femtosecond crystallography, offering comprehensive insights into the molecular mechanisms of metabolic diseases. Understanding these dynamics is vital for developing effective therapies. This review highlights the contributions of protein dynamics studies using XFELs and synchrotrons to metabolic disorder research and their application in designing better therapies. It also discusses G protein-coupled receptors (GPCRs), which, though not enzymes, play key roles in regulating physiological systems and are implicated in many metabolic disorders.
酶在代谢过程中至关重要,其功能失调会导致严重的代谢紊乱。结构生物学,尤其是X射线晶体学,通过提供病理性酶的三维结构,加深了我们对这些疾病的理解。然而,传统的X射线晶体学面临着局限性,比如难以获得合适的蛋白质晶体以及研究蛋白质动力学。X射线自由电子激光(XFEL)凭借其明亮且短暂的X射线脉冲彻底改变了这一领域,提供了辐射敏感和难以结晶的蛋白质的高分辨率结构。XFEL还能够通过室温结构和时间分辨串联飞秒晶体学来研究蛋白质动力学,从而深入了解代谢疾病的分子机制。理解这些动力学对于开发有效的治疗方法至关重要。本综述强调了利用XFEL和同步加速器进行蛋白质动力学研究对代谢紊乱研究的贡献及其在设计更好治疗方法中的应用。它还讨论了G蛋白偶联受体(GPCR),尽管其不是酶,但在调节生理系统中起关键作用,并且与许多代谢紊乱有关。