Fluorescence nanoscopy with optical sectioning by two-photon induced molecular switching using continuous-wave lasers

被引:60
作者
Folling, Joenas [1 ]
Belov, Vladimir [1 ]
Riedel, D. [2 ]
Schoenle, Andreas [1 ]
Egner, Alexander [1 ]
Eggeling, Christian [1 ]
Bossi, Mariano [1 ]
Hell, Stefan W. [1 ]
机构
[1] Max Planck Inst Biophys Chem, Dept NanoBiophoton, D-37077 Gottingen, Germany
[2] Max Planck Inst Biophys Chem, Electron Microscopy Lab, D-37077 Gottingen, Germany
关键词
dyes/pigments; fluorescence microscopy; fluorescent probes; photochromism; photoswitching;
D O I
10.1002/cphc.200700655
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
During the lost decade for-field fluorescence microscopy methods have evolved that have resolution for below the wavelength of light. To outperform the limiting role of diffraction, all these methods, in one way or another, switch the ability of a molecule to emit fluorescence. Here we present a novel rhodamine amide that can be photoswitched from a nonfluorescent to a fluorescent state by absorption of one or two photons from a continuous-wave loser beam. This bright marker enables strict control of on/off switching and provides single-molecule localization precision down to 15 nm in the focal plane. Two-photon induced nonlinear photoswitching of this marker with continuous-wave illumination offers optical sectioning with simple loser equipment. Future synthesis of similar compounds holds great promise for cost-effective fluorescence nanoscopy with noninvasive optical sectioning.
引用
收藏
页码:321 / 326
页数:6
相关论文
共 37 条
[1]  
Abbe E., 1873, ARCH MIKROSK ANAT, V9, P413, DOI [10.1007/BF02956173, DOI 10.1007/BF02956173]
[2]   A maximum-likelihood formalism for sub-resolution axial localization of fluorescent nanoparticles [J].
Aguet, F ;
Van De Ville, D ;
Unser, M .
OPTICS EXPRESS, 2005, 13 (26) :10503-10522
[3]  
[Anonymous], 2007, ANGEW CHEM
[4]   Multicolor super-resolution imaging with photo-switchable fluorescent probes [J].
Bates, Mark ;
Huang, Bo ;
Dempsey, Graham T. ;
Zhuang, Xiaowei .
SCIENCE, 2007, 317 (5845) :1749-1753
[5]   PROPOSED METHOD FOR MOLECULAR OPTICAL IMAGING [J].
BETZIG, E .
OPTICS LETTERS, 1995, 20 (03) :237-239
[6]   Imaging intracellular fluorescent proteins at nanometer resolution [J].
Betzig, Eric ;
Patterson, George H. ;
Sougrat, Rachid ;
Lindwasser, O. Wolf ;
Olenych, Scott ;
Bonifacino, Juan S. ;
Davidson, Michael W. ;
Lippincott-Schwartz, Jennifer ;
Hess, Harald F. .
SCIENCE, 2006, 313 (5793) :1642-1645
[7]   POSITION MEASUREMENT WITH A RESOLUTION AND NOISE-LIMITED INSTRUMENT [J].
BOBROFF, N .
REVIEW OF SCIENTIFIC INSTRUMENTS, 1986, 57 (06) :1152-1157
[8]   Two-color far-field fluorescence nanoscopy based on photoswitchable emitters [J].
Bock, H. ;
Geisler, C. ;
Wurm, C. A. ;
Von Middendorff, C. ;
Jakobs, S. ;
Schoenle, A. ;
Egner, A. ;
Hell, S. W. ;
Eggeling, C. .
APPLIED PHYSICS B-LASERS AND OPTICS, 2007, 88 (02) :161-165
[9]  
Booth MJ, 1998, J MICROSC-OXFORD, V190, P298, DOI 10.1046/j.1365-2818.1998.00375.x
[10]   Breaking the diffraction resolution barrier in far-field microscopy by molecular optical bistability [J].
Bossi, Mariano ;
Foelling, Jonas ;
Dyba, Marcus ;
Westphal, Volker ;
Hell, Stefan W. .
NEW JOURNAL OF PHYSICS, 2006, 8