Institute of Biotechnology, RWTH Aachen University, Aachen, Germany.
Fraunhofer Institute of Applied Information Technology FIT, Sankt Augustin, Germany.
PLoS One. 2020 Jul 23;15(7):e0231918. doi: 10.1371/journal.pone.0231918. eCollection 2020.
Determining the concentration of nucleic acids in biological samples precisely and reliably still is a challenge. In particular when only very small sample quantities are available for analysis, the established fluorescence-based methods give insufficient results. Photobleaching is seen as the main reason for this. In this paper we present a method to correct for the photobleaching effect. Using confocal microscopy with single molecule sensitivity, we derived calibration curves from DNA solutions with defined fragment length. We analyzed dilution series over a wide range of concentrations (1 pg/μl-1000 pg/μl) and measured their specific diffusion coefficients employing fluorescence correlation spectroscopy. Using this information, we corrected the measured fluorescence intensity of the calibration solutions for photobleaching effects. We evaluated our method by analyzing a series of DNA mixtures of varying composition. For fragments smaller than 1000 bp, our method allows to determine sample concentrations with high precision in very small sample quantities (< 2 μl with concentrations < 20 pg/μl). Once the technical parameters are determined and remain stable in an established process, our improved calibration method will make measuring molecular biological samples of unknown sequence composition more efficient, accurate and sample-saving than previous methods.
准确可靠地确定生物样本中的核酸浓度仍然是一个挑战。特别是当只有非常少量的样品可供分析时,现有的基于荧光的方法给出的结果并不充分。光漂白被认为是主要原因。在本文中,我们提出了一种校正光漂白效应的方法。我们使用具有单分子灵敏度的共焦显微镜,从具有定义片段长度的 DNA 溶液中得出校准曲线。我们分析了广泛浓度范围内的稀释系列(1 pg/μl-1000 pg/μl),并使用荧光相关光谱法测量它们的特定扩散系数。利用这些信息,我们校正了校准溶液的测量荧光强度的光漂白效应。我们通过分析一系列不同组成的 DNA 混合物来评估我们的方法。对于小于 1000 bp 的片段,我们的方法允许在非常小的样品量(<2 μl,浓度<20 pg/μl)下高精度地确定样品浓度。一旦确定了技术参数,并且在既定过程中保持稳定,我们改进的校准方法将使测量未知序列组成的分子生物学样本比以前的方法更高效、更准确、更节省样本。