Volume 11 Issue 3
Jun.  2018
Turn off MathJax
Article Contents
ZHANG Zhi-min, KUANG Cui-fang, WANG Zi-ang, ZHU Da-zhao, CHEN You-hua, LI Chuan-kang, LIU Wen-jie, LIU Xu. Dual-color fluorescence emission difference super-resolution microscopy[J]. Chinese Optics, 2018, 11(3): 329-336. doi: 10.3788/CO.20181103.0329
Citation: ZHANG Zhi-min, KUANG Cui-fang, WANG Zi-ang, ZHU Da-zhao, CHEN You-hua, LI Chuan-kang, LIU Wen-jie, LIU Xu. Dual-color fluorescence emission difference super-resolution microscopy[J]. Chinese Optics, 2018, 11(3): 329-336. doi: 10.3788/CO.20181103.0329

Dual-color fluorescence emission difference super-resolution microscopy

Funds:

National Key Scientific Instrument and Equipment Development Projects of China No.2016YFF0101401

More Information
  • Corresponding author: KUANG Cui-fang, E-mail:cfkuang@zju.edu.cn
  • Received Date: 11 Jan 2018
  • Rev Recd Date: 05 Mar 2018
  • Publish Date: 01 Jun 2018
  • To perform super-resolution imaging of different tissue structures of biological samples using fluorescence radiation differential microscopy simultaneously, a dual-color FED microscopy system is studied in this paper. The basic principle of the FED is to remove the confocal microscopy image obtained by scanning the solid spot from the confocal microscopy image obtained by scanning the hollow spot to obtain a super-resolution microscopy image. Based on the study of the monochromatic FED microscopy system, a feasible dual-color FED microscopy imaging system is proposed and imaging experiments are performed on fluorescent particles in this paper. The experimental results indicate that under excitation light of 488nm and 640nm, the system realizes spatial resolution of 135 nm and 160 nm of the fluorescent particles respectively. In addition, this system can also perform multi-color super-resolution microscopy imaging simultaneously on different tissues of biological samples, which meets the requirements of practical applications.

     

  • loading
  • [1]
    李帅, 匡翠方, 丁志华, 等.受激发射损耗显微术(STED)的机理及进展研究[J].激光生物学报, 2013, 2:103-113. doi: 10.3969/j.issn.1007-7146.2013.02.002

    LI SH, KUANG C F, DING ZH H, et al.. A review on concept and development of stimulated emission depletion microscopy(STED)[J]. Acta Laser Biology Sinica, 2013, 2:103-113.(in Chinese) doi: 10.3969/j.issn.1007-7146.2013.02.002
    [2]
    HUANG B, BATES M, ZHUANG X. Super-resolution fluorescence microscopy[J]. Annual Review of Biochemistry, 2009, 78:993-1016. doi: 10.1146/annurev.biochem.77.061906.092014
    [3]
    HELL S W, WICHMANN J. Breaking the diffraction resolution limit by stimulated emission:stimulated-emission-depletion fluorescence microscopy[J]. Optics Letters, 1994, 19(11):780-782. doi: 10.1364/OL.19.000780
    [4]
    KLAR T A, JAKOBS S, DYBA M, et al.. Fluorescence microscopy with diffraction resolution barrier broken by stimulated emission[J]. Proceedings of the National Academy of Sciences, 2000, 97(15):8206-8210. doi: 10.1073/pnas.97.15.8206
    [5]
    KUANG C, LI S, LIU W, et al.. Breaking the diffraction barrier using fluorescence emission difference microscopy[J]. Scientific Reports, 2013, 3:1441. doi: 10.1038/srep01441
    [6]
    李帅. 超分辨荧光显微方法与系统研究[D]. 杭州: 浙江大学, 2014. http://cdmd.cnki.com.cn/Article/CDMD-10335-1014269194.htm

    LI SH. Research on super-resolution fluorescence microscopy method and system[D]. Huangzhou: Zhejiang University, 2014. (in Chinese) http://cdmd.cnki.com.cn/Article/CDMD-10335-1014269194.htm
    [7]
    MEYER L, WILDANGER D, MEDDA R, et al.. Dual-color STED microscopy at 30-nm focal-plane resolution[J]. Small, 2008, 4(8):1095-1100. doi: 10.1002/smll.v4:8
    [8]
    LI S, KUANG C, HAO X, et al.. Enhancing the performance of fluorescence emission difference microscopy using beam modulation[J]. Journal of Optics, 2013, 15(12):125708. doi: 10.1088/2040-8978/15/12/125708
    [9]
    YOU S, KUANG C, RONG Z, et al.. Eliminating deformations in fluorescence emission difference microscopy[J]. Optics Express, 2014, 22(21):26375-26385. doi: 10.1364/OE.22.026375
    [10]
    RONG Z, LI S, KUANG C, et al.. Real-time super-resolution imaging by high-speed fluorescence emission difference microscopy[J]. Journal of Modern Optics, 2014, 61(16):1364-1371. doi: 10.1080/09500340.2014.933272
    [11]
    HAO X, KUANG C F, WANG T T, et al.. Effects of polarization on the de-excitation dark focal spot in STED microscopy[J]. Journal of Optics, 010, 12(11):115707. http://cn.bing.com/academic/profile?id=076fc5db3c528172e3bafe865a738aff&encoded=0&v=paper_preview&mkt=zh-cn
    [12]
    WILSON T. Resolution and optical sectioning in the confocal microscope[J]. Journal of Microscopy, 2011, 244(2):113-121. doi: 10.1111/jmi.2011.244.issue-2
    [13]
    BINGEN P, REUSS M, ENGELHARDT J, et al.. Parallelized STED fluorescence nanoscopy[J]. Optics Express, 2011, 19(24):23716-23726. doi: 10.1364/OE.19.023716
    [14]
    RANKIN B R, KELLNER R R, HELL S W. Stimulated-emission-depletion microscopy with a multicolor stimulated-Raman-scattering light source[J]. Optics Letters, 2008, 33(21):2491-2493. doi: 10.1364/OL.33.002491
    [15]
    STAUDT T M. Strategies to reduce photobleaching, dark state transitions and phototoxicity in subdiffraction optical microscopy[D]. Ruperto-Carola University of Heidelberg, Germany, 2009. https://www.researchgate.net/publication/33429512_Strategies_to_reduce_photobleaching_dark_state_transitions_and_phototoxicity_in_subdiffraction_optical_microscopy
    [16]
    HAO X, ALLGEYER E S, BOOTH M J, et al.. Point-spread function optimization in isoSTED nanoscopy[J]. Optics Letters, 2015, 40(15):3627-3630. doi: 10.1364/OL.40.003627
    [17]
    HIGDON P D, T R K P, WILSON T. Imaging properties of high aperture multiphoton fluorescence scanning optical microscopes[J]. Journal of Microscopy, 1999, 193(2):127-141. doi: 10.1046/j.1365-2818.1999.00448.x
    [18]
    RUST M J, BATES M, ZHUANG X. Sub-diffraction-limit imaging by stochastic optical reconstruction microscopy(STORM)[J]. Nature Methods, 2006, 3(10):793. doi: 10.1038/nmeth929
    [19]
    BRODEHL A, HEDDE P N, DIEDING M, et al.. Dual color photoactivation localization microscopy of cardiomyopathy-associated desmin mutants[J]. Journal of Biological Chemistry, 2012, 287(19):16047-16057. doi: 10.1074/jbc.M111.313841
    [20]
    CARRINGTON W A, LYNCH R M, MOORE E D, et al.. Superresolution three-dimensional images of fluorescence in cells with minimal light exposure[J]. Science, 1995, 268(5216):1483-1487. doi: 10.1126/science.7770772
  • 加载中

Catalog

    通讯作者: 陈斌, bchen63@163.com
    • 1. 

      沈阳化工大学材料科学与工程学院 沈阳 110142

    1. 本站搜索
    2. 百度学术搜索
    3. 万方数据库搜索
    4. CNKI搜索

    Figures(7)

    Article views(2380) PDF downloads(184) Cited by()
    Proportional views
    Related

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return