Differential display and protein quantification.

EXS Pub Date : 2007-01-01 DOI:10.1007/978-3-7643-7439-6_6
Erich Brunner, Bertran Gerrits, Mike Scott, Bernd Roschitzki
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引用次数: 2

Abstract

High-throughput quantitation of proteins is of essential importance for all systems biology approaches and provides complementary information on steady-state gene expression and perturbation-induced systems responses. This information is necessary because it is, e.g., difficult to predict protein concentrations from the level of mRNAs, since regulatory processes at the posttranscriptional level adjust protein concentrations to prevailing conditions. Despite its importance, quantitative proteomics is still a challenging task because of the high dynamic range of protein concentrations in the cell and the variation in the physical properties of proteins. In this chapter we review the current status of, and options for, protein quantification in high-throughput experiments and discuss the suitability and limitations of different existing methods.

差异显示和蛋白质定量。
蛋白质的高通量定量对所有系统生物学方法至关重要,并为稳态基因表达和扰动诱导的系统反应提供补充信息。这些信息是必要的,因为很难从mrna水平预测蛋白质浓度,因为转录后水平的调节过程会根据普遍条件调整蛋白质浓度。尽管它很重要,但由于细胞中蛋白质浓度的高动态范围和蛋白质物理性质的变化,定量蛋白质组学仍然是一项具有挑战性的任务。在本章中,我们回顾了高通量实验中蛋白质定量的现状和选择,并讨论了不同现有方法的适用性和局限性。
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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EXS
EXS
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