University of Nebraska Medical Center, Omaha, Nebraska.
Curr Protoc. 2023 Feb;3(2):e672. doi: 10.1002/cpz1.672.
Adductomics is epidemiology at the molecular level. Untargeted adductomics compares levels of chemical adducts on albumin, hemoglobin, and DNA between healthy and exposed individuals. The goal is to determine a cause-and-effect relationship between chemical exposure and illness. Chemical exposures are not necessarily due to synthetic chemicals but are often due to oxidation products of naturally occurring lipids, for example, 4-hydroxynonenal and acrolein produced by lipid peroxidation of arachidonic and linoleic acids. The preferred method used in adductomics is ultra-high pressure liquid chromatography coupled to with nanoelectrospray tandem mass spectrometry. The mass of the adduct indicates its structure and identifies the chemical. The advantages of molecular epidemiology include information about the many toxicants to which a person is exposed over a period of weeks or months and the relative exposure levels. The disadvantage is the absence of information about the mechanism of toxicity. Untargeted adductomics examines albumin and hemoglobin adducts, which serve as biomarkers of exposure but do not identify the proteins and genes responsible for the toxicity. Targeted adductomics is used when the origin of the toxicity is known. This can be either an adducted protein, such as the butyrylcholinesterase protein modified by nerve agents, or a toxicant, such as acetaminophen. Untargeted adductomics methods have identified potential protein adduct biomarkers of breast cancer, colorectal cancer, childhood leukemia, and lung cancer. Adductomics is a new research area that offers structural insights into chemical exposures and a platform for the discovery of disease biomarkers. © 2023 The Authors. Current Protocols published by Wiley Periodicals LLC.
加合物组学是分子水平上的流行病学。非靶向加合物组学比较健康个体和暴露个体之间白蛋白、血红蛋白和 DNA 上化学加合物的水平。目的是确定化学暴露与疾病之间的因果关系。化学暴露不一定是由于合成化学品引起的,而是经常由于天然存在的脂质的氧化产物引起的,例如,花生四烯酸和亚油酸的脂质过氧化产生的 4-羟基壬烯醛和丙烯醛。加合物组学中使用的首选方法是超高压液相色谱与纳升电喷雾串联质谱联用。加合物的质量表明其结构并识别化学物质。分子流行病学的优点包括有关一个人在数周或数月内接触的许多毒物的信息以及相对暴露水平。缺点是缺乏关于毒性机制的信息。非靶向加合物组学研究白蛋白和血红蛋白加合物,它们作为暴露的生物标志物,但不能识别导致毒性的蛋白质和基因。当毒性的起源已知时,使用靶向加合物组学。这可以是被神经毒剂修饰的丁酰胆碱酯酶蛋白等加合物蛋白,也可以是对乙酰氨基酚等毒物。非靶向加合物组学方法已经确定了乳腺癌、结直肠癌、儿童白血病和肺癌的潜在蛋白质加合物生物标志物。加合物组学是一个新的研究领域,它为化学暴露提供了结构见解,并为疾病生物标志物的发现提供了一个平台。© 2023 作者。Wiley Periodicals LLC 出版的《当代协议》。