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基于质谱的蛋白质组学——要么做大,要么回家?

Proteomics by mass spectrometry--go big or go home?

机构信息

University of Calgary, Department of Biochemistry and Molecular Biology, 3330 Hospital Drive NW, Calgary, Alberta T2N4N1, Canada.

出版信息

J Pharm Biomed Anal. 2011 Jun 25;55(4):832-41. doi: 10.1016/j.jpba.2011.02.012. Epub 2011 Feb 17.

Abstract

Mass spectrometry is an important technology for mapping composition and flux in whole proteomes. Over the last 5 years in particular, impressive gains in the depth of proteome coverage have been realized, particularly for model organisms. This review will provide an update on advancements in the key analytical techniques, methods and informatics directed towards whole proteome analysis by mass spectrometry. Practical issues involving sample requirements, analysis time and depth of coverage will be addressed, to gauge how useful data-driven approaches are for solving biological problems. Targeted mass spectrometric methods, based on selected reaction monitoring, are presented as a powerful alternative to data-driven methods. They offer robust, transferable protocols for hypothesis-directed monitoring of limited yet biologically significant tracts of any proteome.

摘要

质谱分析是一种用于绘制整个蛋白质组组成和通量的重要技术。特别是在过去的 5 年中,在蛋白质组覆盖深度方面取得了令人瞩目的进展,特别是对于模式生物。本综述将提供有关通过质谱进行整个蛋白质组分析的关键分析技术、方法和信息学的最新进展。将涉及涉及样品要求、分析时间和覆盖深度的实际问题,以评估数据驱动方法在解决生物学问题方面的有用程度。基于选择反应监测的靶向质谱方法被提出作为数据驱动方法的有力替代方法。它们为任何蛋白质组中有限但具有生物学意义的区域提供了稳健、可转移的协议,用于进行假设导向的监测。

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