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饱和Förster 共振能量转移显微镜与受激辐射耗散光束:远场生物成像中单分子分辨率的途径。

Saturated Förster resonance energy transfer microscopy with a stimulated emission depletion beam: a pathway toward single-molecule resolution in far-field bioimaging.

机构信息

Laboratory of Physical Biology, Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai 201800, China.

出版信息

Opt Lett. 2010 Dec 1;35(23):3862-4. doi: 10.1364/OL.35.003862.

Abstract

We theoretically demonstrate that the spatial resolution of stimulated emission depletion (STED) microscopy can be substantially enhanced without increasing the intensity of the STED beam. In our scheme, tiny nanobeads codoped with donor and acceptor molecules are used as fluorescent probes, in which Förster resonance energy transfer (FRET) can occur with an ~100% efficiency between the donors and acceptors. Enhancement of the depletion of acceptors in the nanobeads with the doughnut-shaped depletion beam can lead to an increase of FRET efficiency in the outer area of the excitation spot, which itself is used for deexciting donor molecules and, consequently, enhancing the optical resolution.

摘要

我们从理论上证明,在不增加 STED 光束强度的情况下,可大幅提高受激发射损耗(STED)显微镜的空间分辨率。在我们的方案中,使用同时掺杂给体和受体分子的微小纳米珠作为荧光探针,其中供体和受体之间的Förster 共振能量转移(FRET)可达到~100%的效率。利用环形损耗光束对纳米珠中的受体进行损耗增强,可以提高激发光斑外区的 FRET 效率,而激发光斑本身用于去激发供体分子,从而提高光学分辨率。

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