One Molecule Detection by Laser Induced Fluorescence of Levitated Microdroplets

W. Whitten, J. Ramsey, K. Ng, S. Arnold
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Abstract

The extreme sensitivity of fluorescence spectrophotometry results from the fact that a molecule can undergo many excitation-emission cycles before destruction by photochemical degradation. For example, Rhodamine 6G (R6G) can emit in excess of 105 photons before photolysis takes place1. The fraction of emitted photons collected and converted to countable pulses can be as high as 10-3, although 10-4 is more readily attainable. Therefore, sufficient signal exists for single molecules to be detectable. Detection limits for molecules in solution have been limited by background signal from solvent Raman scattering and fluorescence. This background signal adds noise to the measurement and has effectively restricted the detectable concentration to about 10-13 M. Over the past decade, advances in detection of fewer molecules have all been made by reducing the measurement volume and/or increasing the measuring time. Given the above concentration detection limit a reduction of the measurement volume to 1 pL leads to a minimum observable quantity of ≈1 molecule. The ability to detect a single molecule in condensed phase could have many important applications in addition to being an interesting problem. The obvious application of this approach is to situations where small quantities of material are available for analysis. The capability to reliably detect a single fluorophore might also allow the screening and/or sorting of a collection of molecules. Such abilities would have application to many biological problems such as DNA sequencing and detection of DNA adducts.
悬浮微滴激光诱导荧光单分子检测
荧光分光光度法的极高灵敏度是由于一个分子在被光化学降解破坏之前可以经历多次激发-发射循环。例如,罗丹明6G (R6G)在光解发生之前可以发射超过105个光子。收集并转换为可计数脉冲的发射光子的比例可高达10-3,尽管10-4更容易实现。因此,存在足够的信号来检测单个分子。溶液中分子的检测限受溶剂拉曼散射和荧光的背景信号的限制。该背景信号给测量增加了噪声,并有效地将可检测浓度限制在10-13 m左右。在过去的十年中,通过减小测量体积和/或增加测量时间,在检测较少分子方面取得了进展。在上述浓度检测限下,将测量体积减小到1 pL,可获得≈1个分子的最小可观察量。检测凝聚态单个分子的能力除了是一个有趣的问题外,还可以有许多重要的应用。这种方法的明显应用是在可用于分析的少量材料的情况下。可靠地检测单个荧光团的能力也可能使分子集合的筛选和/或分类成为可能。这种能力将应用于许多生物学问题,如DNA测序和DNA加合物的检测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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