2D Gel Electrophoresis to Address Biological Issues

D. Scumaci, G. Cuda
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引用次数: 1

Abstract

Two-dimensional (2D) gel electrophoresis is a high-resolution technique for the study of proteome. This chapter describes how it can be applied to characterize specific differences in the proteome profile of breast cancer cells following gene target interference. The proteome is the complete set of proteins encoded by a genome, and proteomic analysis consists in profiling the whole proteins expressed in a given cell, tissue, organ, or organism. Proteomic expression has the main purpose of qualitatively and quantitatively comparing proteins expressed under physiological and/or pathological conditions. Although it is not the unique approach used in modern proteomics, two-dimensional electrophoresis (2DE) is unrivaled allowing simultaneous separation of thousands of proteins and the detection of posttranslational modification, not predictable through genome analysis. 2DE combines two physical principles to separate complex protein mixtures: the isoelectric point and the molecular weight. The result is a gel map in which each protein isoform present in the sample can be visualized as a spot, analyzed, quantified, and identified by mass spectrometry analysis. Here we outline features and advantages of the 2DE-based proteomic approach and we describe how 2DE meets biochemistry and molecular biology to address specific issues. enhanced cisplatin cytotoxicity in tumor cells having both BRCA network and TP53 disruptions.
二维凝胶电泳解决生物学问题
二维凝胶电泳是研究蛋白质组学的一种高分辨率技术。本章描述了如何应用它来表征基因靶干扰后乳腺癌细胞蛋白质组谱的特定差异。蛋白质组是由基因组编码的蛋白质的完整集合,蛋白质组学分析包括在给定的细胞、组织、器官或有机体中表达的整个蛋白质的分析。蛋白质组学表达的主要目的是定性和定量地比较在生理和/或病理条件下表达的蛋白质。虽然它不是现代蛋白质组学中使用的唯一方法,但二维电泳(2DE)是无与伦比的,可以同时分离数千种蛋白质并检测翻译后修饰,这是通过基因组分析无法预测的。2DE结合了两个物理原理来分离复杂的蛋白质混合物:等电点和分子量。结果是凝胶图,其中样品中存在的每个蛋白质异构体可以可视化为一个点,分析,定量,并通过质谱分析鉴定。在这里,我们概述了基于2DE的蛋白质组学方法的特点和优势,并描述了2DE如何与生物化学和分子生物学相结合来解决具体问题。具有BRCA网络和TP53破坏的肿瘤细胞中顺铂的细胞毒性增强。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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