Live cell imaging and systems biology

被引:24
|
作者
Sung, Myong-Hee [1 ]
McNally, James G. [1 ]
机构
[1] NCI, Lab Receptor Biol & Gene Express, NIH, Bethesda, MD 20892 USA
关键词
FLUORESCENCE CORRELATION SPECTROSCOPY; RESONANCE ENERGY-TRANSFER; SINGLE LIVING CELLS; GENE-EXPRESSION; DYNAMIC PROTEOMICS; FEEDBACK LOOP; IN-VIVO; PROTEIN; MICROSCOPY; CYCLE;
D O I
10.1002/wsbm.108
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Much of the experimental data used to construct mathematical models of molecular networks are derived from in vitro measurements. However, there is increasing evidence that in vitro measurements fail to capture both the complexity and the individuality found in single, living cells. These limitations can be overcome by live cell microscopy which is evolving to enable in vivo biochemistry. Here, we survey the current capabilities of live cell microscopy and illustrate how a number of different imaging approaches could be applied to analyze a specific molecular network. We argue that incorporation of such quantitative live-cell imaging methods is critical for the progress of systems biology. (C) 2010 John Wiley & Sons, Inc. WIREs Syst Biol Med 2011 3 167-182 DOI: 10.1002/wsbm.108
引用
收藏
页码:167 / 182
页数:16
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