Labenski Matthew T, Fisher Ashley A, Lo Herng-Hsiang, Monks Terrence J, Lau Serrine S
Southwest Environmental Health Sciences Center, Department of Pharmacology and Toxicology, College of Pharmacy, University of Arizona Health Sciences Center, Tucson, AZ, USA.
Drug Metab Dispos. 2009 Jun;37(6):1211-8. doi: 10.1124/dmd.108.026211. Epub 2009 Feb 27.
Quinones represent an important class of endogenous compounds such as neurotransmitters and coenzyme Q10, electrophilic xenobiotics, and environmental toxicants that have known reactivity based on their ability to redox cycle and generate oxidative stress, as well as to alkylate target proteins. It is likely that topological, chemical, and physical features combine to determine which proteins become targets for chemical adduction. Chemical-induced post-translational modification of certain critical proteins causes a change in structure/function that contributes to the toxicological response to chemical exposure. In this study, we have identified a number of proteins that are modified by quinone-thioethers after administration of 2-(glutathion-S-yl)HQ. Parallel one-dimensional gel electrophoresis was performed, and the Coomassie-stained gel was aligned with the corresponding Western blot, which was probed for adductions. Immunopositive bands were then subjected to trypsin digestion and analyzed via liquid chromatography/tandem mass spectrometry. The proteins that were subsequently identified contained a higher than average (9.7 versus 5.5%) lysine content and numerous stretches of lysine run-ons, which is a presumed electrophile binding motif. Approximately 50% of these proteins have also been identified as targets for electrophilic adduction by a diverse group of chemicals by other investigators, implying overlapping electrophile adductomes. By identifying a motif targeted by electrophiles it becomes possible to make predictions of proteins that may be targeted for adduction and possible sites on these proteins that are adducted. An understanding of proteins targeted for adduction is essential to unraveling the toxicity produced by these electrophiles.
醌类代表了一类重要的内源性化合物,如神经递质和辅酶Q10、亲电外源性物质以及环境毒物,它们基于氧化还原循环和产生氧化应激以及烷基化靶蛋白的能力而具有已知的反应活性。拓扑学、化学和物理特征可能共同决定哪些蛋白质成为化学加合的靶标。化学诱导的某些关键蛋白质的翻译后修饰会导致结构/功能的改变,这有助于对化学暴露产生毒理学反应。在本研究中,我们已经鉴定出一些在给予2-(谷胱甘肽-S-基)氢醌后被醌硫醚修饰的蛋白质。进行了平行一维凝胶电泳,考马斯亮蓝染色的凝胶与相应的蛋白质印迹对齐,蛋白质印迹用于检测加合物。然后对免疫阳性条带进行胰蛋白酶消化,并通过液相色谱/串联质谱分析。随后鉴定出的蛋白质含有高于平均水平(9.7%对5.5%)的赖氨酸含量以及许多连续的赖氨酸片段,这是一种推测的亲电试剂结合基序。其他研究人员还发现,这些蛋白质中约50%也被多种化学物质鉴定为亲电加合的靶标,这意味着亲电加合物组存在重叠。通过鉴定亲电试剂靶向的基序,可以预测可能被加合的蛋白质以及这些蛋白质上可能被加合的位点。了解被加合的蛋白质对于阐明这些亲电试剂产生的毒性至关重要。