Fu Yi, Lakowicz Joseph R
Center for Fluorescence Spectroscopy, University of Maryland School of Medicine, 725 West Lombard Street, Baltimore, MD 21201, USA.
Anal Chem. 2006 Sep 1;78(17):6238-45. doi: 10.1021/ac060586t.
Methods that increase the total emission per fluorophore would provide increased sensitivity and a wider dynamic range for chemical analysis, medical diagnostics, and in vivo molecular imaging. The use of fluorophore-metal interactions has the potential to dramatically increase the detectability of single fluorophores for bioanalytical monitoring. The fabrication and single-molecule analysis of fluorophore-labeled DNA molecules tethered to silver island films are described in this article. The single-molecule spectroscopic method reveals some insightful information on the behaviors of single molecules, rather than an ensemble of molecules. Analysis of fluorescence images, intensity profiles, total emitted photons, and lifetime distributions reveals some of sample heterogeneities. Investigations of time-dependent emission characteristics of single molecules indicate that the total number of emitted photons on the silvered surface is more than 10 times greater than on free labeled DNA molecules on a glass substrate. In addition, time-correlated single-photon counting results reveal the reduced lifetimes of single molecules tethered to silver island films.
提高每个荧光团总发射量的方法将为化学分析、医学诊断和体内分子成像提供更高的灵敏度和更宽的动态范围。利用荧光团与金属的相互作用有可能显著提高用于生物分析监测的单个荧光团的可检测性。本文描述了连接到银岛膜上的荧光团标记DNA分子的制备和单分子分析。单分子光谱方法揭示了关于单分子行为而非分子集合的一些有深刻见解的信息。对荧光图像、强度分布、总发射光子数和寿命分布的分析揭示了样品的一些不均匀性。对单分子时间相关发射特性的研究表明,镀银表面发射的光子总数比玻璃基板上的游离标记DNA分子上的光子总数大10倍以上。此外,时间相关单光子计数结果揭示了连接到银岛膜上的单分子寿命的缩短。