[1] 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.

[2] Klar T A, Jakobs S, Dyba M, et al. Fluorescence microscopy with diffraction resolution barrier broken by stimulated emission［C］. Proceedings of the National Academy of Sciences of the United States of America, 2000, 97(15): 8206-8210.

[3] D′Este E, Kamin D, Gttfert F, et al. STED nanoscopy reveals the ubiquity of subcortical cytoskeleton periodicity in living neurons［J］. Cell Reports, 2015, 10(8): 1246-1251.

[4] Gustafsson M G. Surpassing the lateral resolution limit by a factor of two using structured illumination microscopy［J］. Journal of Microscopy, 2000, 198(2): 82-87.

[5] Gustafsson M G. Nonlinear structured-illumination microscopy: wide-field fluorescence imaging with theoretically unlimited resolution［C］. Proceedings of the National Academy of Sciences of the United States of America, 2005, 102(37): 13081-13086.

[6] Betzig E, Patterson G H, Sougrat R, et al. Imaging intracellular fluorescent proteins at nanometer resolution［J］. Science, 2006, 313(5793): 1642-1645.

[7] Shtengel G, Galbraith J A, Galbraith C G, et al. Interferometric fluorescent super-resolution microscopy resolves 3D cellular ultrastructure［C］. Proceedings of the National Academy of Sciences of the United States of America, 2009, 106(9): 3125-3130.

[8] Shroff H, White H, Betzig E. Photoactivated localization microscopy (PALM) of adhesion complexes［J］. Current Protocols in Cell Biology, 2008, 4: 4-21.

[9] Rust M J, Bates M, Zhuang X. Sub-diffraction-limit imaging by stochastic optical reconstruction microscopy (STORM)［J］. Nature Methods, 2006, 3(10): 793-796.

[10] Heilemann M, van de Linde S, Schüttpelz M, et al. Subdiffraction-resolution fluorescence imaging with conventional fluorescent probes［J］. Angewandte Chemie (International Edition), 2008, 47(33): 6172-6176.

[11] Zhuang X. Nano-imaging with STORM［J］. Nature Photonics, 2009, 3(7): 365-367.

[12] Xu K, Shim S H, Zhuang X. Super-resolution imaging through stochastic switching and localization of single molecules: An overview［M］. Far-field Optical Nanoscopy, Berlin: Springer, 2015: 27-64.

[13] Yao Baoli, Lei Ming, Xue Bin, et al. Progress and applications of high-resolution and super-resolution optical imaging in space and biology［J］. Acta Photonica Sinica, 2011, 40(11): 1607-1618.

[14] Xia Peng, Dou Zhen, Yao Xuebiao. Progress of super-resolution microscopy［J］. Chemistry of Life, 2015, 35(3): 430-437.

[15] Li D, Shao L, Chen B C, et al. Advanced imaging. Extended-resolution structured illumination imaging of endocytic and cytoskeletal dynamics［J］. Science, 2015, 349(6251): aab3500.

[16] Bhme M A, Beis C, Reddy-Alla S, et al. Active zone scaffolds differentially accumulate Unc13 isoforms to tune Ca2+ channel-vesicle coupling［J］. Nature Neuroscience, 2016, 19(10): 1311-1320.

[17] French J B, Jones S A, Deng H, et al. Spatial colocalization and functional link of purinosomes with mitochondria［J］. Science, 2016, 351(6274): 733-737.

[18] Huang F, Sirinakis G, Allgeyer E S, et al. Ultra-high resolution 3D imaging of whole cells［J］. Cell, 2016, 166(4): 1028-1040.

[19] Xu K, Babcock H P, Zhuang X. Dual-objective STORM reveals three-dimensional filament organization in the actincytoskeleton［J］. Nature Methods, 2012, 9(2): 185-188.

[20] Betzig E. Proposed method for molecular optical imaging［J］. Optics Letters, 1995, 20(3): 237-239.

[21] Dickson R M, Cubitt A B, Tsien R Y, et al. On/off blinking and switching behaviour of single molecules of green fluorescent protein［J］. Nature, 1997, 388(6640): 355-358.

[22] Xu K, Zhong G, Zhuang X. Actin, spectrin, and associated proteins form a periodic cytoskeletal structure in axons［J］. Science, 2013, 339(6118): 452-456.

[23] Shroff H, Galbraith C G, Galbraith J A, et al. Dual-color superresolution imaging of genetically expressed probes within individual adhesion complexes［C］. Proceedings of the National Academy of Sciences of the United States of America, 2007, 104(51): 20308-20313.

[24] Subach F V, Patterson G H, Manley S, et al. Photoactivatable mCherry for high-resolution two-color fluorescence microscopy［J］. Nature Methods, 2009, 6(2): 153-159.

[25] Dempsey G T, Vaughan J C, Chen K H, et al. Evaluation of fluorophores for optimal performance in localization-based super-resolution imaging［J］. Nature Methods, 2011, 8(12): 1027-1036.

[26] Jones S A, Shim S H, He J, et al. Fast, three-dimensional super-resolution imaging of live cells［J］. Nature Methods, 2011, 8(6): 499-508.

[27] Leterrier C, Potier J, Caillol G, et al. Nanoscale architecture of the axon initial segment reveals an organized and robust scaffold［J］. Cell Reports, 2015, 13(12): 2781-2793.

[28] Lippincott-Schwartz J, Patterson G H. Photoactivatable fluorescent proteins for diffraction-limited and super-resolution imaging［J］. Trends in Cell Biology, 2009, 19(11): 555-565.

[29] Bates M, Huang B, Dempsey G T, et al. Multicolor super-resolution imaging with photo-switchable fluorescent probes［J］. Science, 2007, 317(5845): 1749-1753.

[30] Bates M, Dempsey G T, Chen K H, et al. Multicolor super-resolution fluorescence imaging via multi-parameter fluorophore detection［J］. Chem Phys Chem, 2012, 13(1): 99-107.

[31] Lubeck E, Cai L. Single-cell systems biology by super-resolution imaging and combinatorial labeling［J］. Nature Methods, 2012, 9(7): 743-748.

[32] Dani A, Huang B, Bergan J, et al. Superresolution imaging of chemical synapses in the brain［J］. Neuron, 2010, 68(5): 843-856.

[33] Tam J, Cordier G A, Borbely J S, et al. Cross-talk-free multi-color STORM imaging using a single fluorophore［J］. PLoS One, 2014, 9(7): e101772.

[34] Bossi M. Flling J, Belov V N, et al. Multicolor far-field fluorescence nanoscopy through isolated detection of distinct molecular species［J］. Nano Letters, 2008, 8(8): 2463-2468.

[35] Kim D, Curthoys N M, Parent M T, et al. Bleed-through correction for rendering and correlation analysis in multi-colour localization microscopy［J］. Journal of Optics, 2013, 15(9): 094011.

[36] Baddeley D, Crossman D, Rossberger S, et al. 4D super-resolution microscopy with conventional fluorophores and single wavelength excitation in optically thick cells and tissues［J］. PLoS One, 2011, 6(5): e20645.

[37] Lampe A, Haucke V, Sigrist S J, et al. Multi-colour direct STORM with red emitting carbocyanines［J］. Biology of the Cell, 2012, 104(4): 229-237.

[38] Gunewardene M S, Subach F V, Gould T J, et al. Superresolution imaging of multiple fluorescent proteins with highly overlapping emission spectra in living cells［J］. Biophysical Journal, 2011, 101(6): 1522-1528.

[39] Testa I, Wurm C A, Medda R, et al. Multicolor fluorescence nanoscopy in fixed and living cells by exciting conventional fluorophores with a single wavelength［J］. Biophysical Journal, 2010, 99(8): 2686-2694.

[40] Zhang Z, Kenny S J, Hauser M, et al. Ultrahigh-throughput single-molecule spectroscopy and spectrally resolved super-resolution microscopy［J］. Nature Methods, 2015, 12(10): 935-938.

[41] Mlodzianoski M J, Curthoys N M, Gunewardene M S, et al. Super-resolution imaging of molecular emission spectra and single molecule spectral fluctuations［J］. PLoS One, 2016, 11(3): e0147506.

[42] Dong B, Almassalha L, Urban B E, et al. Super-resolution spectroscopic microscopy via photon localization［J］. Nature Communications, 2016, 7: 12290.

[43] Shechtman Y, Weiss L E, Backer A S, et al. Multicolour localization microscopy by point-spread-function engineering［J］. Nature Photonics, 2016, 10: 590-595.

[44] Pavani S R P, Thompson M A, Biteen J S, et al. Three-dimensional, single-molecule fluorescence imaging beyond the diffraction limit by using a double-helix point spread function［C］. Proceedings of the National Academy of Sciences of the United States of America, 2009, 106(9): 2995-2999.

[45] Gahlmann A, Ptacin J L, Grover G, et al. Quantitative multicolor subdiffraction imaging of bacterial protein ultrastructures in three dimensions［J］. Nano Letters, 2013, 13(3): 987-993.

[46] Shechtman Y, Weiss L E, Backer A S, et al. Precise three-dimensional scan-free multiple-particle tracking over large axial ranges with tetrapod point spread functions［J］. Nano Letters, 2015, 15(6): 4194-4199.

[47] Allen J R, Ross S T, Davidson M W. Sample preparation for single molecule localization microscopy［J］. Physical Chemistry Chemical Physics, 2013, 15(43): 18771-18783.

[48] Whelan D R, Bell T D. Image artifacts in single molecule localization microscopy: why optimization of sample preparation protocols matters［J］. Scientific Reports, 2015, 5: 7924.