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Liquid-phase-based separation systems for depletion prefractionation and enrichment of proteins in biological fluids and matrices for in-depth proteomics analysis – An update covering the period 2011-2014

机译:基于液相的分离系统用于生物液和基质中蛋白质的消耗预分馏和富集用于深入的蛋白质组学分析– 2011-2014年的更新

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摘要

This review article expands on the previous one (S. Selvaraju and Z. El Rassi, Electrophoresis 2012, 33, 74-88) by reviewing pertinent literature in the period extending from early 2011 to present. As the previous review article, the present one is concerned with proteomic sample preparation (e.g., depletion of high abundance proteins, reduction of the protein dynamic concentration range, enrichment of a particular sub-proteome), and the subsequent chromatographic and/or electrophoretic pre-fractionation prior to peptide separation and identification by LC-MS/MS. This review article is distinguished from its second version published in Electrophoresis 2012, 33, 74-88 by expanding on capturing/enriching sub-phosphoproteomes by immobilized metal affinity chromatography and metal oxide affinity chromatography. Seventy-seven papers published in the period extending from mid 2011 to the present have been reviewed. By no means this review article is exhaustive, given the fact that its aim is to give a concise treatment of the latest developments in the field.
机译:这篇评论文章通过回顾从2011年初到现在的相关文献,对上一篇文章(S. Selvaraju和Z. El Rassi,Electrophoresis 2012,33,74-88)进行了扩展。如前一篇评论文章所述,本人关注蛋白质组学样品的制备(例如,高丰度蛋白质的消耗,蛋白质动态浓度范围的减小,特定子蛋白质组的富集)以及随后的色谱和/或电泳前处理肽分离和通过LC-MS / MS鉴定之前的分离。这篇综述文章与第二版发表在《电泳》(Electrophoresis)2012,33,74-88上,其区别在于通过固定化金属亲和色谱和金属氧化物亲和色谱来捕获/富集亚磷酸化蛋白质组。从2011年年中至今,共发表了77篇论文。鉴于这篇文章的目的是对本领域的最新进展进行简明扼要的论述,因此它绝不是详尽无遗的。

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