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Bioanalytical and Mass Spectrometric Methods for Aldehyde Profiling in Biological Fluids

机译:生物液中醛分析的生物分析和质谱方法

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Human exposure to aldehydes is implicated in multiple diseases including diabetes, cardiovascular diseases, neurodegenerative disorders (i.e., Alzheimer’s and Parkinson’s Diseases), and cancer. Because these compounds are strong electrophiles, they can react with nucleophilic sites in DNA and proteins to form reversible and irreversible modifications. These modifications, if not eliminated or repaired, can lead to alteration in cellular homeostasis, cell death and ultimately contribute to disease pathogenesis. This review provides an overview of the current knowledge of the methods and applications of aldehyde exposure measurements, with a particular focus on bioanalytical and mass spectrometric techniques, including recent advances in mass spectrometry (MS)-based profiling methods for identifying potential biomarkers of aldehyde exposure. We discuss the various derivatization reagents used to capture small polar aldehydes and methods to quantify these compounds in biological matrices. In addition, we present emerging mass spectrometry-based methods, which use high-resolution accurate mass (HR/AM) analysis for characterizing carbonyl compounds and their potential applications in molecular epidemiology studies. With the availability of diverse bioanalytical methods presented here including simple and rapid techniques allowing remote monitoring of aldehydes, real-time imaging of aldehydic load in cells, advances in MS instrumentation, high performance chromatographic separation, and improved bioinformatics tools, the data acquired enable increased sensitivity for identifying specific aldehydes and new biomarkers of aldehyde exposure. Finally, the combination of these techniques with exciting new methods for single cell analysis provides the potential for detection and profiling of aldehydes at a cellular level, opening up the opportunity to minutely dissect their roles and biological consequences in cellular metabolism and diseases pathogenesis.
机译:人体接触醛会导致多种疾病,包括糖尿病,心血管疾病,神经退行性疾病(即阿尔茨海默氏病和帕金森氏病)和癌症。因为这些化合物是强亲电试剂,所以它们可以与DNA和蛋白质中的亲核位点反应,形成可逆和不可逆的修饰。如果不消除或修复这些修饰,可能导致细胞稳态改变,细胞死亡,并最终导致疾病发病。这篇综述概述了醛暴露测量方法和应用的当前知识,特别着重于生物分析和质谱技术,包括基于质谱(MS)的轮廓分析方法的最新进展,用于鉴定醛暴露的潜在生物标志物。我们讨论了用于捕获小的极性醛的各种衍生试剂,以及在生物基质中定量这些化合物的方法。此外,我们提出了基于质谱的新兴方法,该方法使用高分辨率精确质量(HR / AM)分析来表征羰基化合物及其在分子流行病学研究中的潜在应用。借助此处介绍的多种生物分析方法的可用性,包括简单且快速的技术(可实现醛的远程监控),细胞中醛负载的实时成像,MS仪器的进步,高效色谱分离以及改进的生物信息学工具,所获得的数据得以实现识别特定醛的敏感性和醛暴露的新生物标记。最后,这些技术与令人振奋的单细胞分析新方法的结合为在细胞水平上检测和分析醛提供了潜力,从而为细化分析其在细胞代谢和疾病发病机理中的作用和生物学后果提供了机会。

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