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Kinetics and mechanisms of thiol-disulfide exchange covering direct substitution and thiol oxidation-mediated pathways

机译:硫醇-二硫键交换的动力学和机理,涵盖直接取代和硫醇氧化介导的途径

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摘要

Significance: Disulfides are important building blocks in the secondary and tertiary structures of proteins, serving as inter- and intra-subunit cross links. Disulfides are also the major products of thiol oxidation, a process that has primary roles in defense mechanisms against oxidative stress and in redox regulation of cell signaling. Although disulfides are relatively stable, their reduction, isomerisation, and interconversion as well as their production reactions are catalyzed by delicate enzyme machineries, providing a dynamic system in biology. Redox homeostasis, a thermodynamic parameter that determines which reactions can occur in cellular compartments, is also balanced by the thiol-disulfide pool. However, it is the kinetic properties of the reactions that best represent cell dynamics, because the partitioning of the possible reactions depends on kinetic parameters. Critical Issues: This review is focused on the kinetics and mechanisms of thiol-disulfide substitution and redox reactions. It summarizes the challenges and advances that are associated with kinetic investigations in small molecular and enzymatic systems from a rigorous chemical perspective using biological examples. The most important parameters that influence reaction rates are discussed in detail. Recent Advances and Future Directions: Kinetic studies of proteins are more challenging than small molecules, and quite often investigators are forced to sacrifice the rigor of the experimental approach to obtain the important kinetic and mechanistic information. However, recent technological advances allow a more comprehensive analysis of enzymatic systems via using the systematic kinetics apparatus that was developed for small molecule reactions, which is expected to provide further insight into the cell's machinery.
机译:启示:二硫键是蛋白质二级和三级结构的重要组成部分,可作为亚基间和亚基内的交联分子。二硫化物也是硫醇氧化的主要产物,该过程在防御氧化应激的防御机制和细胞信号的氧化还原调节中起主要作用。尽管二硫化物相对稳定,但是它们的还原,异构化和相互转化以及它们的生产反应是由精细的酶机制催化的,从而提供了生物学上的动态系统。氧化还原稳态是一种热力学参数,它决定哪些反应可以在细胞区室中发生,而硫醇-二硫键池也可以平衡该平衡。但是,最能代表细胞动力学的是反应的动力学性质,因为可能的反应的分配取决于动力学参数。关键问题:本文的重点是巯基-二硫键取代和氧化还原反应的动力学和机理。它使用生物学实例从严格的化学角度总结了与小分子和酶系统动力学研究相关的挑战和进展。详细讨论了影响反应速率的最重要参数。最新进展和未来方向:蛋白质的动力学研究比小分子的研究更具挑战性,很多时候研究人员被迫牺牲实验方法的严格性来获得重要的动力学和机理信息。但是,最近的技术进步允许通过使用针对小分子反应开发的系统动力学仪器对酶系统进行更全面的分析,从而有望进一步了解细胞的机制。

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