* Department of Medicinal Chemistry and.
Toxicol Sci. 2013 Oct;135(2):390-401. doi: 10.1093/toxsci/kft166. Epub 2013 Jul 28.
Many low molecular weight compounds undergo biotransformation to chemically reactive metabolites (CRMs) that covalently modify cellular proteins. However, the mechanisms by which this covalent binding leads to cytotoxicity are not understood. Prior analyses of lists of target proteins sorted by functional categories or hit frequency have not proven informative. In an attempt to move beyond covalent binding, we hypothesized that xenobiotic posttranslational modification of proteins might disrupt important protein-protein interactions (PPIs) and thereby direct cells from homeostasis into cell death pathways. To test this hypothesis, we analyzed a list of 302 proteins (66% rat, 26% mouse, 5% human) known to be targeted by 41 different cytotoxic CRMs. Human orthologs of rodent proteins were found by blast sequence alignment, and their interacting partners were found using the Human Protein Reference Database. The combined set of target orthologs and partners was sorted into KEGG pathways and Gene Ontology categories. Those most highly ranked based on sorting statistics and toxicological relevance were heavily involved with intracellular signaling pathways, protein folding, unfolded protein response, and regulation of apoptosis. Detailed examination revealed that many of the categories were flagged primarily by partner proteins rather than target proteins and that a majority of these partners interacted with just a small number of proteins in the CRM target set. A similar analysis performed without the partner proteins flagged very few categories as significant. These results support the hypothesis that disruption of important PPIs may be a major mechanism contributing to CRM-induced acute cytotoxicity.
许多低分子量化合物经历生物转化为化学活性代谢物(CRM),这些代谢物共价修饰细胞蛋白。然而,这种共价结合导致细胞毒性的机制尚不清楚。通过对按功能类别或命中频率排序的靶蛋白列表进行的先前分析并没有提供有价值的信息。为了超越共价结合,我们假设外源性蛋白质翻译后修饰可能会破坏重要的蛋白质-蛋白质相互作用(PPIs),从而使细胞从稳态进入细胞死亡途径。为了验证这一假设,我们分析了已知被 41 种不同细胞毒性 CRM 靶向的 302 种蛋白质(66%大鼠、26%小鼠、5%人)的列表。通过序列比对blast 找到了啮齿动物蛋白的人类同源物,并使用人类蛋白质参考数据库找到了它们的相互作用伙伴。将目标同源物和伙伴的组合集分类为 KEGG 途径和基因本体论类别。根据排序统计和毒理学相关性,排名最高的类别主要涉及细胞内信号通路、蛋白质折叠、未折叠蛋白反应和细胞凋亡的调节。详细检查发现,许多类别主要是由伙伴蛋白而不是靶蛋白标记的,而且这些伙伴蛋白中的大多数只与 CRM 靶集中的少数蛋白相互作用。没有标记伙伴蛋白的类似分析很少将类别标记为显著。这些结果支持这样一种假设,即重要的 PPI 破坏可能是 CRM 诱导的急性细胞毒性的主要机制。