In VIVO biochemistry: quantifying ion and metabolite levels in individual cells or cultures of yeast

被引:29
作者
Bermejo, Clara [1 ]
Ewald, Jennifer C. [2 ]
Lanquar, Viviane [1 ]
Jones, Alexander M. [1 ]
Frommer, Wolf B. [1 ]
机构
[1] Carnegie Inst Sci, Dept Plant Biol, Stanford, CA 94305 USA
[2] ETH, Inst Mol Syst Biol, CH-8093 Zurich, Switzerland
关键词
imaging; metabolic signalling; metabolic pathway; sugar signalling; yeast; RESONANCE ENERGY-TRANSFER; GREEN FLUORESCENT PROTEIN; GENETICALLY ENCODED INDICATORS; SACCHAROMYCES-CEREVISIAE; ARABIDOPSIS-THALIANA; CALCIUM INDICATOR; LIVING CELLS; FRET SENSORS; INTRACELLULAR CALCIUM; SPECTROSCOPIC RULER;
D O I
10.1042/BJ20110428
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Over the past decade, we have learned that cellular processes, including signalling and metabolism, are highly compartmentalized, and that relevant changes in metabolic state can occur at sub-second timescales. Moreover, we have learned that individual cells in populations, or as part of a tissue, exist in different states. If we want to understand metabolic processes and signalling better, it will be necessary to measure biochemical and biophysical responses of individual cells with high temporal and spatial resolution. Fluorescence imaging has revolutionized all aspects of biology since it has the potential to provide information on the cellular and subcellular distribution of ions and metabolites with sub-second time resolution. In the present review we summarize recent progress in quantifying ions and metabolites in populations of yeast cells as well as in individual yeast cells with the help of quantitative fluorescent indicators, namely FRET metabolite sensors. We discuss the opportunities and potential pitfalls and the controls that help preclude misinterpretation.
引用
收藏
页码:1 / 10
页数:10
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