Measurement of mass, density, and volume during the cell cycle of yeast

被引:206
作者
Bryan, Andrea K. [1 ,2 ]
Goranov, Alexi [2 ]
Amon, Angelika [2 ,3 ]
Manalis, Scott R. [1 ,2 ]
机构
[1] MIT, Dept Biol Engn, Cambridge, MA 02139 USA
[2] MIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
[3] MIT, Howard Hughes Med Inst, Cambridge, MA 02139 USA
基金
美国国家卫生研究院;
关键词
biosensor; cell growth; cell size; microfluidics; Saccharomyces; BUOYANT DENSITY; SACCHAROMYCES-CEREVISIAE; ESCHERICHIA-COLI; SCHIZOSACCHAROMYCES-POMBE; SYNCHRONOUS CULTURES; SINGLE CELLS; CONSTANCY; GROWTH; FLUCTUATION; RAPAMYCIN;
D O I
10.1073/pnas.0901851107
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cell growth comprises changes in both mass and volume-two processes that are distinct, yet coordinated through the cell cycle. Understanding this relationship requires a means for measuring each of the cell's three basic physical parameters: mass, volume, and the ratio of the two, density. The suspended microchannel resonator weighs single cells with a precision in mass of 0.1% for yeast. Here we use the suspended microchannel resonator with a Coulter counter to measure the mass, volume, and density of budding yeast cells through the cell cycle. We observe that cell density increases prior to bud formation at the G1/S transition, which is consistent with previous measurements using density gradient centrifugation. To investigate the origin of this density increase, we monitor relative density changes of growing yeast cells. We find that the density increase requires energy, function of the protein synthesis regulator target of rapamycin, passage through START (commitment to cell division), and an intact actin cytoskeleton. Although we focus on basic cell cycle questions in yeast, our techniques are suitable for most nonadherent cells and subcellular particles to characterize cell growth in a variety of applications.
引用
收藏
页码:999 / 1004
页数:6
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