Institute for Systems Biology, Seattle, Washington 98109, United States.
J Proteome Res. 2024 Nov 1;23(11):5143-5152. doi: 10.1021/acs.jproteome.4c00663. Epub 2024 Oct 23.
Covalent protein adducts formed by drugs or their reactive metabolites are risk factors for adverse reactions, and inactivation of cytochrome P450 (CYP) enzymes. Characterization of drug-protein adducts is limited due to lack of methods identifying and quantifying covalent adducts in complex matrices. This study presents a workflow that combines data-dependent and data-independent acquisition (DDA and DIA) based liquid chromatography with tandem mass spectrometry (LC-MS/MS) to detect very low abundance adducts resulting from CYP mediated drug metabolism in human liver microsomes (HLMs). HLMs were incubated with raloxifene as a model compound and adducts were detected in 78 proteins, including CYP3A and CYP2C family enzymes. Experiments with recombinant CYP3A and CYP2C enzymes confirmed adduct formation in all CYPs tested, including CYPs not subject to time-dependent inhibition by raloxifene. These data suggest adducts can be benign. DIA analysis showed variable adduct abundance in many peptides between livers, but no concomitant decrease of unadducted peptides. This study sets a new standard for adduct detection in complex samples, offering insights into the human adductome resulting from reactive metabolite exposure. The methodology presented will aid mechanistic studies to identify, quantify and differentiate between adducts that result in adverse drug reactions and those that are benign.
共价蛋白质加合物是由药物或其反应性代谢物形成的,是不良反应和细胞色素 P450(CYP)酶失活的风险因素。由于缺乏识别和定量复杂基质中共价加合物的方法,药物-蛋白质加合物的特征描述受到限制。本研究提出了一种工作流程,该流程结合了基于数据依赖和独立采集(DDA 和 DIA)的液相色谱与串联质谱(LC-MS/MS),以检测人肝微粒体(HLM)中 CYP 介导的药物代谢产生的非常低丰度的加合物。用雷洛昔芬作为模型化合物孵育 HLMs,并在 78 种蛋白质中检测到加合物,包括 CYP3A 和 CYP2C 家族酶。用重组 CYP3A 和 CYP2C 酶进行的实验证实了所有测试的 CYP 中都形成了加合物,包括不受雷洛昔芬时间依赖性抑制的 CYP。这些数据表明加合物可能是良性的。DIA 分析显示,在肝脏中许多肽之间的加合物丰度存在差异,但未修饰的肽没有相应减少。本研究为复杂样品中的加合物检测设定了新标准,为反应性代谢物暴露导致的人类加合物组提供了深入了解。所提出的方法将有助于识别、定量和区分导致不良反应和良性的加合物的机制研究。