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采用红色增强型定制技术单光子雪崩二极管(SPAD)进行的单分子荧光共振能量转移实验。

Single-molecule FRET experiments with a red-enhanced custom technology SPAD.

作者信息

Panzeri Francesco, Ingargiola Antonino, Lin Ron R, Sarkhosh Niusha, Gulinatti Angelo, Rech Ivan, Ghioni Massimo, Cova Sergio, Weiss Shimon, Michalet Xavier

机构信息

Dipartimento di Elettronica e Informazione, Politecnico di Milano, 20133 Milan, Italy.

Department of Chemistry & Biochemistry, UCLA, Los Angeles, CA 90095, USA.

出版信息

Proc SPIE Int Soc Opt Eng. 2013 Feb 2;8590. doi: 10.1117/12.2003187.

Abstract

Single-molecule fluorescence spectroscopy of freely diffusing molecules in solution is a powerful tool used to investigate the properties of individual molecules. Single-Photon Avalanche Diodes (SPADs) are the detectors of choice for these applications. Recently a new type of SPAD detector was introduced, dubbed red-enhanced SPAD (RE-SPAD), with good sensitivity throughout the visible spectrum and with excellent timing performance. We report a characterization of this new detector for single-molecule fluorescence resonant energy transfer (smFRET) studies on freely diffusing molecules in a confocal geometry and alternating laser excitation (ALEX) scheme. We use a series of doubly-labeled DNA molecules with donor-to-acceptor distances covering the whole range of useful FRET values. Both intensity-based (μs-ALEX) and lifetime-based (ns-ALEX) measurements are presented and compared to identical measurements performed with standard thick SPADs. Our results demonstrate the great potential of this new detector for smFRET measurements and beyond.

摘要

溶液中自由扩散分子的单分子荧光光谱是用于研究单个分子性质的强大工具。单光子雪崩二极管(SPAD)是这些应用的首选探测器。最近推出了一种新型SPAD探测器,称为红色增强型SPAD(RE-SPAD),在整个可见光谱范围内具有良好的灵敏度和出色的定时性能。我们报告了这种新型探测器在共聚焦几何结构和交替激光激发(ALEX)方案下对自由扩散分子进行单分子荧光共振能量转移(smFRET)研究的特性。我们使用了一系列供体到受体距离涵盖有用FRET值整个范围的双标记DNA分子。给出了基于强度(μs-ALEX)和基于寿命(ns-ALEX)的测量结果,并与使用标准厚SPAD进行的相同测量进行了比较。我们的结果证明了这种新型探测器在smFRET测量及其他方面的巨大潜力。

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本文引用的文献

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8-spot smFRET analysis using two 8-pixel SPAD arrays.
Proc SPIE Int Soc Opt Eng. 2013 Feb 22;8590. doi: 10.1117/12.2003704.
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