Department of Anatomy and Embryology, Leiden University Medical Center, ZC Leiden.
Cold Spring Harb Perspect Biol. 2012 Mar 1;4(3):a008177. doi: 10.1101/cshperspect.a008177.
Genomics methodologies have advanced to the extent that it is now possible to interrogate the gene expression in a single cell but proteomics has traditionally lagged behind and required much greater cellular input and was not quantitative. Coupling protein with gene expression data is essential for understanding how cell behavior is regulated. Advances primarily in mass spectrometry have, however, greatly improved the sensitivity of proteomics methods over the last decade and the outcome of proteomic analyses can now also be quantified. Nevertheless, it is still difficult to obtain sufficient tissue from staged mammalian embryos to combine proteomic and genomic analyses. Recent developments in pluripotent stem cell biology have in part addressed this issue by providing surrogate scalable cell systems in which early developmental events can be modeled. Here we present an overview of current proteomics methodologies and the kind of information this can provide on the biology of human and mouse pluripotent stem cells.
基因组学方法已经发展到现在可以在单个细胞中检测基因表达的程度,但蛋白质组学传统上落后,需要更大的细胞投入,并且不是定量的。将蛋白质与基因表达数据相结合对于理解细胞行为如何受到调控至关重要。然而,主要在质谱技术方面的进展在过去十年中大大提高了蛋白质组学方法的灵敏度,现在也可以对蛋白质组分析的结果进行定量。尽管如此,仍然很难从分期哺乳动物胚胎中获得足够的组织来结合蛋白质组学和基因组学分析。多能干细胞生物学的最新发展在一定程度上解决了这个问题,提供了可扩展的替代细胞系统,可以在其中模拟早期发育事件。在这里,我们概述了当前的蛋白质组学方法以及这些方法可以提供的关于人类和小鼠多能干细胞生物学的信息。