Genetic Diagnosis Technology Unit, RIKEN Center for Integrative Medical Science, Yokohama, Kanagawa, Japan.
RIKEN Innovation Center, Wako, Saitama, Japan.
PLoS One. 2020 Dec 15;15(12):e0243319. doi: 10.1371/journal.pone.0243319. eCollection 2020.
Here, we report a rapid and ultra-sensitive detection technique for fluorescent molecules called scanning single molecular counting (SSMC). The method uses a fluorescence-based digital measurement system to count single molecules in a solution. In this technique, noise is reduced by conforming the signal shape to the intensity distribution of the excitation light via a circular scan of the confocal region. This simple technique allows the fluorescent molecules to freely diffuse into the solution through the confocal region and be counted one by one and does not require statistical analysis. Using this technique, 28 to 62 aM fluorescent dye was detected through measurement for 600 s. Furthermore, we achieved a good signal-to-noise ratio (S/N = 2326) under the condition of 100 pM target nucleic acid by only mixing a hybridization-sensitive fluorescent probe, called Eprobe, into the target oligonucleotide solution. Combination of SSMC and Eprobe provides a simple, rapid, amplification-free, and high-sensitive target nucleic acid detection system. This method is promising for future applications to detect particularly difficult to design primers for amplification as miRNAs and other short oligo nucleotide biomarkers by only hybridization with high sensitivity.
在这里,我们报告了一种快速超灵敏的荧光分子检测技术,称为扫描单分子计数(SSMC)。该方法使用基于荧光的数字测量系统来对溶液中的单分子进行计数。在该技术中,通过对共焦区域进行圆形扫描,使信号形状符合激发光的强度分布,从而减少噪声。这种简单的技术允许荧光分子自由扩散到溶液中通过共焦区域,并被逐个计数,而不需要进行统计分析。使用该技术,通过 600 秒的测量,可以检测到 28 到 62 aM 的荧光染料。此外,通过仅将一种称为 Eprobe 的杂交敏感荧光探针混合到目标寡核苷酸溶液中,在 100 pM 目标核酸的条件下,我们实现了良好的信噪比(S/N = 2326)。SSMC 和 Eprobe 的组合提供了一种简单、快速、无需扩增且高灵敏度的目标核酸检测系统。这种方法有望在未来的应用中通过仅与高灵敏度杂交来检测特别难以设计用于扩增的引物,如 miRNA 和其他短寡核苷酸生物标志物。