Righetti Pier Giorgio
Politecnico di Milano, Department of Chemistry, Materials and Chemical Engineering "Giulio Natta", Via Mancinelli 7, Milano 20131, Italy.
J Proteomics. 2014 Jul 31;107:39-49. doi: 10.1016/j.jprot.2013.11.026. Epub 2013 Dec 6.
The review covers about fifty years of progress in "proteome" analysis, starting from primitive two-dimensional (2D) map attempts in the early sixties of last century. The polar star in 2D mapping arose in 1975 with the classic paper by O'Farrell in J Biol. Chem. It became the compass for all proteome navigators. Perfection came, though, only with the introduction of immobilized pH gradients, which fixed the polypeptide spots in the 2D plane. Great impetus in proteome analysis came with the introduction of informatic tools and creating databases, among which Swiss Prot remains the site of excellence. Towards the end of the nineties, 2D chromatography, epitomized by coupling strong cation exchangers with C18 resins, began to be a serious challenge to electrophoretic 2D mapping, although up to the present both techniques are still much in vogue and appear to give complementary results. Yet the migration of "proteomics" into the third millennium was made possible only by mass spectrometry (MS), which today represents the standard analytical tool in any lab dealing with proteomic analysis. Another major improvement has been the introduction of combinatorial peptide ligand libraries (CPLL), which, when properly used, enhance the visibility of low-abundance species by 3 to 4 orders of magnitude. Coupling MS to CPLLs permits the exploration of at least 8 orders of magnitude in dynamic range on any proteome.
The present review is a personal recollection highlighting the developments that led to present-day proteomics on a long march that lasted about 50years. It is meant to give to young scientists an overview on how science grows, which ones are the quantum jumps in science and which research is of particular significance in general and in the field of proteomics in particular. It also gives some real-life episodes of greater-than-life figures. As such, it can be viewed as a tutorial to stimulate the young generation to be creative (and use their imagination too!).This article is part of a Special Issue entitled: 20years of Proteomics in memory of Viatliano Pallini. Guest Editors: Luca Bini, Juan J. Calvete, Natacha Turck, Denis Hochstrasser and Jean-Charles Sanchez.
本综述涵盖了“蛋白质组”分析约五十年来的进展,始于上世纪六十年代初原始的二维(2D)图谱尝试。二维图谱的北极星出现在1975年,奥法雷尔发表于《生物化学杂志》的经典论文成为了所有蛋白质组导航者的指南针。然而,只有引入固定化pH梯度,使多肽斑点固定在二维平面上,才实现了完美。蛋白质组分析的巨大推动力来自信息工具的引入和数据库的创建,其中瑞士蛋白质数据库(Swiss Prot)仍然是卓越的数据库。到九十年代末,以强阳离子交换剂与C18树脂偶联为代表的二维色谱法开始对二维电泳图谱构成严峻挑战,尽管直到现在这两种技术仍然非常流行,并且似乎能提供互补的结果。然而,“蛋白质组学”进入第三个千年只有通过质谱(MS)才得以实现,如今质谱是任何从事蛋白质组分析的实验室的标准分析工具。另一项重大改进是引入了组合肽配体库(CPLL),如果使用得当,它能将低丰度物种的可见度提高3到4个数量级。将质谱与CPLL偶联可在任何蛋白质组的动态范围内探索至少8个数量级。
本综述是个人回忆,突出了在长达约50年的漫长历程中引领当今蛋白质组学发展的各项进展。旨在让年轻科学家了解科学是如何发展的,科学中的量子跃迁有哪些,以及哪些研究在总体上尤其是在蛋白质组学领域具有特别重要的意义。它还讲述了一些比真人还传奇的人物的真实故事。因此,它可被视为一篇教程,以激励年轻一代发挥创造力(并运用他们的想象力!)。本文是题为《纪念维亚利阿诺·帕利尼的蛋白质组学20年》特刊的一部分。客座编辑:卢卡·比尼、胡安·J·卡尔韦特、娜塔莎·图尔克、丹尼斯·霍赫施塔瑟和让 - 查尔斯·桑切斯。