Super-Resolution Optical Subtraction Microscopy Using Optical Scattering Imaging

被引:2
作者
Zhou Qian [1 ,2 ,3 ]
Yu Jian-Qiang [4 ]
Zhao Li-Bo [3 ]
Li De-Sheng [5 ]
Wu Kui [6 ]
Zhu Jian-Hua [1 ,2 ]
Yuan Jing-He [3 ]
Fang Xiao-Hong [3 ]
机构
[1] Sichuan Univ, Dept Phys, Chengdu 610064, Peoples R China
[2] Minist Educ, Key Lab High Energy Dens Phys & Technol, Chengdu 610064, Peoples R China
[3] Chinese Acad Sci, Inst Chem, Key Lab Mol Nanostruct & Nanotechnol, Beijing 100190, Peoples R China
[4] North China Univ Technol, Coll Sci, Beijing 100144, Peoples R China
[5] Chinese Acad Sci, Inst Chem, State Key Lab Polymer Phys & Chem, Beijing 100190, Peoples R China
[6] Chinese Acad Sci, Inst Chem, Key Lab Analyt Chem Living Biosyst, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
Super-resolution microscopy; Subtraction imaging; Non-fluorescence imaging; Optical scattering imaging; ELECTROMAGNETIC DIFFRACTION; CONFOCAL MICROSCOPY; STIMULATED-EMISSION; RESOLUTION; FIELD; SYSTEMS;
D O I
10.3866/PKU.WHXB201603234
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
The existing form of super-resolution microscopy based on specific fluorescent tagging is unable to obtain super-resolution images of non-fluorescent samples. Hence, we have developed optical subtraction microscopy for obtaining super-resolution imaging in such cases. This method is based on image subtraction between the two optical scattering images from general confocal excitation and doughnut-shaped excitation, respectively. Unlike super-resolution fluorescence microscopy, subtraction microscopy requires no preprocessing of the sample, and the excitation power can be kept low to avoid sample damage. The non-fluorescent imaging of gold nanobeads and polymer nanofibers has been realized to demonstrate the feasibility of super-resolution subtraction microscopy. The lateral resolution decreases to 215 nm (0.33 lambda, 1 lambda = 650 nm) in subtraction imaging, and greater imaging detail of the sample is achieved via optical scattering.
引用
收藏
页码:1123 / 1128
页数:6
相关论文
共 14 条
[1]   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
[2]   Resolution and contrast enhancement in laser scanning microscopy using dark beam imaging [J].
Dehez, Harold ;
Piche, Michel ;
De Koninck, Yves .
OPTICS EXPRESS, 2013, 21 (13) :15912-15925
[3]   Saturated structured confocal microscopy with theoretically unlimited resolution [J].
Haeberle, Olivier ;
Simon, Bertrand .
OPTICS COMMUNICATIONS, 2009, 282 (18) :3657-3664
[4]   Far-field optical nanoscopy [J].
Hell, Stefan W. .
SCIENCE, 2007, 316 (5828) :1153-1158
[5]  
Klar T. A., 2001, PHYS REV E, V64, DOI DOI 10.1103/PHYSREVE.64.066613
[6]   Fluorescence microscopy with diffraction resolution barrier broken by stimulated emission [J].
Klar, TA ;
Jakobs, S ;
Dyba, M ;
Egner, A ;
Hell, SW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (15) :8206-8210
[7]   Breaking the Diffraction Barrier Using Fluorescence Emission Difference Microscopy [J].
Kuang, Cuifang ;
Li, Shuai ;
Liu, Wei ;
Hao, Xiang ;
Gu, Zhaotai ;
Wang, Yifan ;
Ge, Jianhong ;
Li, Haifeng ;
Liu, Xu .
SCIENTIFIC REPORTS, 2013, 3
[8]   ELECTROMAGNETIC DIFFRACTION IN OPTICAL SYSTEMS .2. STRUCTURE OF THE IMAGE FIELD IN AN APLANATIC SYSTEM [J].
RICHARDS, B ;
WOLF, E .
PROCEEDINGS OF THE ROYAL SOCIETY OF LONDON SERIES A-MATHEMATICAL AND PHYSICAL SCIENCES, 1959, 253 (1274) :358-379
[9]   Sub-diffraction-limit imaging by stochastic optical reconstruction microscopy (STORM) [J].
Rust, Michael J. ;
Bates, Mark ;
Zhuang, Xiaowei .
NATURE METHODS, 2006, 3 (10) :793-795
[10]   Demonstration of subtraction imaging in confocal microscopy with vector beams [J].
Segawa, Susumu ;
Kozawa, Yuichi ;
Sato, Shunichi .
OPTICS LETTERS, 2014, 39 (15) :4529-4532