School of Physics and Astronomy, University of Minnesota, 116 Church St., SE, Minneapolis, MN 55455, USA.
Eur Biophys J. 2012 Mar;41(3):341-52. doi: 10.1007/s00249-012-0792-x. Epub 2012 Feb 4.
Fluorescence studies of cellular protein-protein interactions commonly employ transient cotransfection to express two proteins carrying distinct fluorescent labels. Because transiently transfected cells differ significantly in their expression level, the concentration ratio of the two expressed proteins varies, which in turn influences the measured fluorescence signal. Knowledge of the statistics of protein expression ratios is of considerable interest both from a fundamental point of view and for cellular fluorescence studies. Despite the perceived randomness of transient transfection, we were able to develop a quantitative model that describes the average and distribution of the protein expression ratio from a cell population. We show that the expression ratio is proportional to the molar plasmid ratio and relate the distribution to the finite number of active plasmids in the cell. The process of cationic lipid-mediated transfection is explored in more detail. Specifically, the influence of lipoplexes on the statistics of the expression ratio is examined. We further demonstrate that the transfection model provides a quantitative description of fluorescence fluctuation experiments, where only a fraction of the proteins are labeled.
细胞内蛋白质相互作用的荧光研究通常采用瞬时共转染来表达携带不同荧光标签的两种蛋白质。由于瞬时转染的细胞在表达水平上有很大差异,因此两种表达蛋白的浓度比会发生变化,从而影响测量的荧光信号。从基础理论和细胞荧光研究两个方面来看,了解蛋白质表达比的统计信息都具有重要意义。尽管瞬时转染看起来是随机的,但我们还是能够开发出一种定量模型,可以描述细胞群体中蛋白质表达比的平均值和分布。我们发现,表达比与摩尔质粒比成正比,并将分布与细胞中有效的质粒数量联系起来。我们更详细地探讨了阳离子脂质介导的转染过程。具体来说,我们研究了脂质体复合物对表达比统计的影响。我们进一步证明,转染模型可以定量描述荧光波动实验,其中只有一部分蛋白质被标记。