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利用液相色谱-串联质谱分析在体外鉴定位点特异性化学蛋白质加合物。

Utilization of LC-MS/MS analyses to identify site-specific chemical protein adducts in vitro.

作者信息

Fisher Ashley A, Labenski Matthew T, Monks Terrence J, Lau Serrine S

机构信息

Department of Pharmacology and Toxicology, Southwest Environmental Health Sciences Center, Center for Toxicology, College of Pharmacy, University of Arizona, Tucson, AZ, USA.

出版信息

Methods Mol Biol. 2011;691:317-26. doi: 10.1007/978-1-60761-849-2_19.

Abstract

Biologically reactive intermediates are formed following metabolism of xenobiotics, and during normal oxidative metabolism. These reactive species are electrophilic in nature and are capable of forming stable adducts with target proteins. These covalent protein modifications can initiate processes that lead to acute tissue injury or chronic disease. Recent advancements in mass spectrometry techniques and data analysis has permitted a more detailed investigation of site-specific protein modifications by reactive electrophiles. Knowledge from such analyses will assist in providing a better understanding of how specific classes of electrophiles produce toxicity and disease progression via site-selective protein-specific covalent modification. Hydroquinone (HQ) is a known environmental toxicant, and its quinone-thioether metabolites, formed via the intermediate generation of 1,4-benzoquinone (1,4-BQ), elicit their toxic response via the covalent modification of target proteins and the generation of reactive oxygen species. We have utilized a model protein, cytochrome c, to guide us in identifying 1,4-BQ- and 1,4-BQ-thioether derived site-specific protein modifications. LC-MS/MS analyses reveals that these modifications occur selectively on lysine and glutamic acid residues of the target protein, and that these modifications occur within identifiable "electrophile binding motifs" within the protein. These motifs are found within lysine-rich regions of the protein and appear to be target sites of 1,4-BQ-thioether adduction. These residues also appear to dictate the nature of post-adduction chemistry and the final structure of the adduct. This model system will provide critical insight for in vivo adduct hunting following exposure to 1,4-BQ-thioethers, but the general approaches can also be extended to the identification of protein adducts derived from other classes of reactive electrophiles.

摘要

生物活性中间体在异源生物代谢过程中以及正常氧化代谢过程中形成。这些活性物质本质上是亲电的,能够与靶蛋白形成稳定的加合物。这些共价蛋白修饰可引发导致急性组织损伤或慢性疾病的过程。质谱技术和数据分析的最新进展使得能够更详细地研究反应性亲电试剂对位点特异性蛋白的修饰。此类分析所得的知识将有助于更好地理解特定类别的亲电试剂如何通过位点选择性蛋白特异性共价修饰产生毒性和疾病进展。对苯二酚(HQ)是一种已知的环境毒物,其通过1,4 - 苯醌(1,4 - BQ)的中间生成形成的醌硫醚代谢物,通过靶蛋白的共价修饰和活性氧的产生引发其毒性反应。我们利用一种模型蛋白细胞色素c来指导我们鉴定1,4 - BQ和1,4 - BQ硫醚衍生的位点特异性蛋白修饰。液相色谱 - 串联质谱分析表明,这些修饰选择性地发生在靶蛋白的赖氨酸和谷氨酸残基上,并且这些修饰发生在蛋白内可识别的“亲电试剂结合基序”内。这些基序存在于蛋白富含赖氨酸的区域,似乎是1,4 - BQ硫醚加合的靶位点。这些残基似乎也决定了加合后化学性质和加合物的最终结构。该模型系统将为暴露于1,4 - BQ硫醚后的体内加合物搜寻提供关键见解,但一般方法也可扩展到鉴定源自其他类反应性亲电试剂的蛋白加合物。

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