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本文引用的文献

1
Superresolution by localization of quantum dots using blinking statistics.利用闪烁统计通过量子点定位实现超分辨率
Opt Express. 2005 Sep 5;13(18):7052-62. doi: 10.1364/opex.13.007052.
2
Beyond Rayleigh's criterion: a resolution measure with application to single-molecule microscopy.超越瑞利判据:一种应用于单分子显微镜的分辨率测量方法。
Proc Natl Acad Sci U S A. 2006 Mar 21;103(12):4457-62. doi: 10.1073/pnas.0508047103. Epub 2006 Mar 1.
3
Breaking the diffraction barrier in fluorescence microscopy at low light intensities by using reversibly photoswitchable proteins.通过使用可逆光开关蛋白在低光强度下突破荧光显微镜中的衍射极限。
Proc Natl Acad Sci U S A. 2005 Dec 6;102(49):17565-9. doi: 10.1073/pnas.0506010102. Epub 2005 Nov 28.
4
Nonlinear structured-illumination microscopy: wide-field fluorescence imaging with theoretically unlimited resolution.非线性结构光照显微镜:具有理论上无限分辨率的宽场荧光成像。
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Short-range spectroscopic ruler based on a single-molecule optical switch.基于单分子光开关的短程光谱尺。
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Carbocyanine dyes as efficient reversible single-molecule optical switch.作为高效可逆单分子光学开关的碳菁染料。
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Nanometer-localized multiple single-molecule fluorescence microscopy.纳米定位多单分子荧光显微镜术
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8
Single-molecule high-resolution imaging with photobleaching.基于光漂白的单分子高分辨率成像
Proc Natl Acad Sci U S A. 2004 Apr 27;101(17):6462-5. doi: 10.1073/pnas.0401638101. Epub 2004 Apr 19.
9
Nonlinear magic: multiphoton microscopy in the biosciences.非线性魔法:生物科学中的多光子显微镜术
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10
Toward fluorescence nanoscopy.迈向荧光纳米显微镜技术。
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基于随机光学重建显微镜(STORM)的亚衍射极限成像

Sub-diffraction-limit imaging by stochastic optical reconstruction microscopy (STORM).

作者信息

Rust Michael J, Bates Mark, Zhuang Xiaowei

机构信息

Department of Physics, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138, USA.

出版信息

Nat Methods. 2006 Oct;3(10):793-5. doi: 10.1038/nmeth929. Epub 2006 Aug 9.

DOI:10.1038/nmeth929
PMID:16896339
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2700296/
Abstract

We have developed a high-resolution fluorescence microscopy method based on high-accuracy localization of photoswitchable fluorophores. In each imaging cycle, only a fraction of the fluorophores were turned on, allowing their positions to be determined with nanometer accuracy. The fluorophore positions obtained from a series of imaging cycles were used to reconstruct the overall image. We demonstrated an imaging resolution of 20 nm. This technique can, in principle, reach molecular-scale resolution.

摘要

我们基于可光开关荧光团的高精度定位开发了一种高分辨率荧光显微镜方法。在每个成像周期中,只有一小部分荧光团被开启,从而能够以纳米精度确定它们的位置。从一系列成像周期中获得的荧光团位置被用于重建整体图像。我们展示了20纳米的成像分辨率。从原理上讲,这项技术可以达到分子尺度的分辨率。