Chao Shu-Yi, Ho Yi-Ping, Bailey Vasudev J, Wang Tza-Huei
Department of Mechanical Engineering, The Johns Hopkins University, Baltimore, MD 21218, USA.
J Fluoresc. 2007 Nov;17(6):767-74. doi: 10.1007/s10895-007-0194-0. Epub 2007 Jul 27.
We present a novel method for quantifying low concentrations of DNA based on single molecule detection (SMD) for molecular counting and flow measurements inside a microchannel. A custom confocal fluorescence spectroscopic system is implemented to detect fluorescent bursts emitted from stained DNA molecules. Measurements are made one molecule at a time as they flow through a femtoliter-sized laser focal probe. Durations of single molecule fluorescent bursts, which are found to be strongly related to the molecular transit times through the detection region, are statistically analyzed to determine the in situ flow speed and subsequently the sample volume flowing through the focal probe. Therefore, the absolute concentration of a DNA sample can be quantified based on the single molecule fluorescent counts from the DNA molecules and the associated probe volume for a measured time course. To validate this method for quantifying low concentrations of biomolecules, we tested samples of pBR322 DNA ranging from 1 pM to 10 fM ( approximately 3 ng/ml to 30 pg/ml). Besides molecular quantification, we also demonstrate this method to be a precise and non-invasive way for flow profiling within a microchannel.
我们提出了一种基于单分子检测(SMD)的新型方法,用于在微通道内对低浓度DNA进行分子计数和流量测量的定量分析。我们实施了一个定制的共聚焦荧光光谱系统,以检测染色DNA分子发出的荧光猝发。当分子流经飞升级大小的激光聚焦探针时,一次对一个分子进行测量。对单分子荧光猝发的持续时间进行统计分析,发现其与分子通过检测区域的传输时间密切相关,从而确定原位流速,进而确定流经聚焦探针的样品体积。因此,DNA样品的绝对浓度可以基于DNA分子的单分子荧光计数以及测量时间过程中的相关探针体积来进行定量分析。为了验证这种用于定量低浓度生物分子的方法,我们测试了浓度范围从1 pM到10 fM(约3 ng/ml至30 pg/ml)的pBR322 DNA样品。除了分子定量分析外,我们还证明了该方法是一种用于微通道内流量分析的精确且非侵入性的方法。