Lancaster Jack R
Department of Pharmacology & Chemical Biology, University of Pittsburgh School of Medicine, United States; Department of Medicine, University of Pittsburgh School of Medicine, United States; Department of Surgery, University of Pittsburgh School of Medicine, United States.
Arch Biochem Biophys. 2017 Mar 1;617:137-144. doi: 10.1016/j.abb.2016.10.015. Epub 2016 Oct 26.
The biological mechanisms of de novo formation of cellular nitrosothiols (as opposed to transnitrosation) are reviewed. The approach is to introduce chemical foundations for each mechanism, followed by evidence in biological systems. The general categories include mechanisms involving nitrous acid, NO autoxidation and oxidant stress, redox active and inactive metal ions, and sulfide/persulfide. Important conclusions/speculations are that de novo cellular thiol nitrosation (1) is an oxidative process, and so should be considered within the family of other thiol oxidative modifications, (2) may not involve a single dominant process but depends on the specific conditions, (3) does not involve O under at least some conditions, and (4) may serve to provide a "substrate pool" of protein cysteine nitrosothiol which could, through subsequent enzymatic transnitrosation/denitrosation, be "rearranged" to accomplish the specificity and regulatory control required for effective post-translational signaling.
本文综述了细胞内亚硝基硫醇从头合成的生物学机制(与转亚硝化作用相对)。方法是先介绍每种机制的化学基础,再给出生物系统中的证据。一般类别包括涉及亚硝酸、NO自氧化和氧化应激、氧化还原活性和非活性金属离子以及硫化物/过硫化物的机制。重要结论/推测如下:细胞内硫醇亚硝化从头合成(1)是一个氧化过程,因此应在其他硫醇氧化修饰类别中考虑;(2)可能不涉及单一主导过程,而是取决于特定条件;(3)至少在某些条件下不涉及O;(4)可能用于提供蛋白质半胱氨酸亚硝基硫醇的“底物池”,该底物池可通过随后的酶促转亚硝化/脱亚硝化作用“重新排列”,以实现有效翻译后信号传导所需的特异性和调节控制。