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用于检测人类DNA损伤的加合物组学方法的发展。

Development of the adductome approach to detect DNA damage in humans.

作者信息

Kanaly Robert A, Hanaoka Tomoyuki, Sugimura Haruhiko, Toda Hirokazu, Matsui Saburo, Matsuda Tomonari

机构信息

Department of Technology and Ecology, Graduate School of Global Environmental Studies, Kyoto University, Kyoto, Japan.

出版信息

Antioxid Redox Signal. 2006 May-Jun;8(5-6):993-1001. doi: 10.1089/ars.2006.8.993.

Abstract

The development of new strategies designed to detect DNA damage caused by oxidative stress and other means may advance our understanding of the roles of such types of damage in the etiology of cancers, in aging processes, and as biomarkers of exposure. A DNA adduct detection method that uses liquid chromatography coupled with electrospray ionization tandem mass spectrometry (LC/ESI-MS/MS) to detect multiple DNA adducts in human lung tissue is reported herein. This adductome analysis strategy is designed to detect the neutral loss of 2 -deoxyribose from positively ionized 2 -deoxynucleoside adducts in multiple reaction ion monitoring mode (MRM) transmitting the M + H > M + H - 116 transition over a total of 374 transitions in the mass range from m/z 228.8 to m/z 602.8. Data analysis is optimized and coupled with a comprehensive manual screening process designed to minimize the number of artifactual adducts appearing in the final analysis. In the final analysis, putative adducts were organized into an adductome map and unambiguous confirmation of selected oxidative adducts were made by stable isotope dilution and comparison to authentic standards. The future applications of this method are discussed.

摘要

旨在检测由氧化应激及其他因素引起的DNA损伤的新策略的发展,可能会增进我们对这类损伤在癌症病因、衰老过程以及作为暴露生物标志物方面所起作用的理解。本文报道了一种DNA加合物检测方法,该方法使用液相色谱与电喷雾电离串联质谱联用(LC/ESI-MS/MS)来检测人肺组织中的多种DNA加合物。这种加合物组分析策略旨在以多反应离子监测模式(MRM)检测正离子化的2-脱氧核苷加合物中2-脱氧核糖的中性丢失,传输M + H > M + H - 116跃迁,在m/z 228.8至m/z 602.8的质量范围内总共进行374次跃迁。数据分析经过优化,并结合了一个全面的手动筛选过程,旨在尽量减少最终分析中出现的人为加合物数量。在最终分析中,推定的加合物被整理成加合物组图谱,并通过稳定同位素稀释以及与真实标准品比较,对选定的氧化加合物进行明确确认。本文还讨论了该方法的未来应用。

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