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从蛋白质到蛋白质组学。

From proteins to proteomics.

作者信息

Bradshaw Ralph A, Burlingame Alma L

机构信息

Department of Biochemistry, University of Cambridge, Cambridge, UK.

出版信息

IUBMB Life. 2005 Apr-May;57(4-5):267-72. doi: 10.1080/15216540500091536.

Abstract

During the second half of the 20th century, biochemistry and subsequently molecular biology blossomed into the core upon which all biological and biomedical sciences now depend. A major part of these closely related disciplines has been the study of the structure and function of proteins and the diverse biological functions that they perform. Early experimentation necessarily focused on individual entities, selected mainly for their activities, but as technology improved there developed a tendency to look at proteins as larger, interactive groups or clusters. Spurred by the recent exponential production of genomic sequence data for a rapidly increasing number of species, protein chemistry has now evolved into a new discipline, proteomics. In addition to embracing the methods and approaches that have served protein scientists well in the past, it includes, and is perhaps best defined by, high-throughput analyses based in large part on 2D gel electrophoresis, MALDI and ESI mass spectrometry and combinatorial arrays. Proteomic targets include the identification of all genome products and a mapping of their interactions and expression profiles. These hold great promise for the identification of disease markers and drug targets, but are not without their challenges and pitfalls.

摘要

在20世纪后半叶,生物化学以及随后的分子生物学蓬勃发展,成为如今所有生物和生物医学科学所依赖的核心。这些紧密相关学科的一个主要部分是对蛋白质的结构与功能以及它们所执行的多种生物学功能的研究。早期的实验必然聚焦于单个实体,主要因其活性而被挑选出来,但随着技术的进步,人们逐渐倾向于将蛋白质视为更大的、相互作用的群体或簇。受近期针对越来越多物种的基因组序列数据呈指数级增长的推动,蛋白质化学如今已演变成一门新学科——蛋白质组学。除了采用过去对蛋白质科学家很有帮助的方法和途径外,它还包括并且或许最好由很大程度上基于二维凝胶电泳、基质辅助激光解吸电离和电喷雾电离质谱以及组合阵列的高通量分析来定义。蛋白质组学的目标包括鉴定所有基因组产物以及绘制它们的相互作用和表达谱。这些对于疾病标志物和药物靶点的鉴定具有巨大潜力,但也并非没有挑战和陷阱。

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