Abstract
Recent advances in localization-based super-resolution microscopy have enabled researchers to visualize single molecular features down to individual molecular components (~5 nm), but do not yet allow manipulation of single-molecule targets in a user-prescribed, context-dependent manner. Here we report an ‘Action-PAINT’ (PAINT, point accumulation for imaging in nanoscale topography) strategy for super-resolution labelling upon visualization on single molecules. This approach monitors and localizes DNA binding events in real time with DNA-PAINT, and upon visualization of binding to a desired location, photo-crosslinks the DNA to affix the molecular label. We showed the efficiency of 3-cyanovinylcarbazole nucleoside photo-inducible crosslinking on single molecular targets and developed a software package for real-time super-resolution imaging and crosslinking control. We then benchmarked our super-resolution labelling method on synthetic DNA nanostructures and demonstrated targeted multipoint labelling on various complex patterns with 30 nm selectivity. Finally, we performed targeted in situ labelling on fixed microtubule samples with a 40 nm target size and custom-controlled, subdiffraction spacing.
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Data availability
Datasets generated during the study are available from the corresponding authors upon request.
Code availability
Custom computer programs used during the study are available from the corresponding authors upon request.
Change history
01 October 2019
In this Article originally published, the ORCID number for the author Mingjie Dai was missing; it should have been 0000-0002-8665-4966. This has now been corrected in all versions of the Article.
References
Sahl, S. J. & Moerner, W. Super-resolution fluorescence imaging with single molecules. Curr. Opin. Struc. Biol. 23, 778–787 (2013).
Sydor, A. M., Czymmek, K. J., Puchner, E. M. & Mennella, V. Super-resolution microscopy: from single molecules to supramolecular assemblies. Trends Cell Biol. 25, 730–748 (2015).
Eggeling, C., Willig, K. I., Sahl, S. J. & Hell, S. W. Lens-based fluorescence nanoscopy. Q. Rev. Biophys. 48, 178–243 (2015).
Sanders, D. P. Advances in patterning materials for 193 nm immersion lithography. Chem. Rev. 110, 321–360 (2010).
Cohen, A. E. Optogenetics: turning the microscope on its head. Biophys. J. 110, 997–1003 (2016).
Ando, T., Uchihashi, T. & Scheuring, S. Filming biomolecular processes by high-speed atomic force microscopy. Chem. Rev. 114, 3120–3188 (2014).
Rust, M. J., Bates, M. & Zhuang, X. Sub-diffraction-limit imaging by stochastic optical reconstruction microscopy (STORM). Nat. Methods 3, 793–795 (2006).
Heilemann, M. et al. Subdiffraction‐resolution fluorescence imaging with conventional fluorescent probes. Angew. Chem. Int. Ed. 47, 6172–6176 (2008).
Betzig, E. et al. Imaging intracellular fluorescent proteins at nanometer resolution. Science 313, 1642–1645 (2006).
Hess, S. T., Girirajan, T. & Mason, M. D. Ultra-high resolution imaging by fluorescence photoactivation localization microscopy. Biophys. J. 91, 4258–4272 (2006).
Sharonov, A. & Hochstrasser, R. M. Wide-field subdiffraction imaging by accumulated binding of diffusing probes. Proc. Natl Acad. Sci. USA 103, 18911–18916 (2006).
Jungmann, R. et al. Single-molecule kinetics and super-resolution microscopy by fluorescence imaging of transient binding on DNA origami. Nano Lett 10, 4756–4761 (2010).
Löschberger, A. et al. Super-resolution imaging visualizes the eightfold symmetry of gp210 proteins around the nuclear pore complex and resolves the central channel with nanometer resolution. J. Cell Sci. 125, 570–575 (2012).
Szymborska, A. et al. Nuclear pore scaffold structure analyzed by super-resolution microscopy and particle averaging. Science 341, 655–658 (2013).
Pertsinidis, A. et al. Ultrahigh-resolution imaging reveals formation of neuronal SNARE/Munc18 complexes in situ. Proc. Natl Acad. Sci. USA 110, E2812–E2820 (2013).
Huang, F. et al. Ultra-high resolution 3D imaging of whole cells. Cell 166, 1028–1040 (2016).
Kaplan, C. et al. Absolute arrangement of subunits in cytoskeletal septin filaments in cells measured by fluorescence microscopy. Nano Lett. 15, 3859–3864 (2015).
Mikhaylova, M. et al. Resolving bundled microtubules using anti-tubulin nanobodies. Nat. Commun. 6, 7933 (2015).
Dai, M., Jungmann, R. & Yin, P. Optical imaging of individual biomolecules in densely packed clusters. Nat. Nanotechnol. 11, 798–807 (2016).
Raab, M., Schmied, J. J., Jusuk, I., Forthmann, C. & Tinnefeld, P. Fluorescence microscopy with 6 nm resolution on DNA origami. Chemphyschem 15, 2431–2435 (2014).
Rittweger, E., Han, K., Irvine, S. E., Eggeling, C. & Hell, S. W. STED microscopy reveals crystal colour centres with nanometric resolution. Nat. Photon. 3, 144–147 (2009).
Giannone, G. et al. Dynamic superresolution imaging of endogenous proteins on living cells at ultra-high density. Biophys. J. 99, 1303–1310 (2010).
Schoen, I., Ries, J., Klotzsch, E., Ewers, H. & Vogel, V. Binding-activated localization microscopy of DNA structures. Nano Lett. 11, 4008–4011 (2011).
Kiuchi, T., Higuchi, M., Takamura, A., Maruoka, M. & Watanabe, N. Multitarget super-resolution microscopy with high-density labeling by exchangeable probes. Nat. Methods 12, 743–746 (2015).
Barish, R. & Yin, P. Methods and compositions relating to optical super-resolution patterning. US patent 10,041,108 (2018).
Yoshimura, Y. & Fujimoto, K. Ultrafast reversible photo-cross-linking reaction: toward in situ DNA manipulation. Org. Lett. 10, 3227–3230 (2008).
Vieregg, J. R., Nelson, H. M., Stoltz, B. M. & Pierce, N. A. Selective nucleic acid capture with shielded covalent probes. J. Am. Chem. Soc. 135, 9691–9699 (2013).
Jungmann, R. et al. Multiplexed 3D cellular super-resolution imaging with DNA-PAINT and Exchange-PAINT. Nat. Methods 11, 313–318 (2014).
Jungmann, R. et al. Quantitative super-resolution imaging with qPAINT. Nat. Methods 13, 439–442 (2016).
Rothemund, P. W. Folding DNA to create nanoscale shapes and patterns. Nature 440, 297–302 (2006).
Smith, C. S., Joseph, N., Rieger, B. & Lidke, K. A. Fast, single-molecule localization that achieves theoretically minimum uncertainty. Nat. Methods 7, 373–375 (2010).
Huang, B., Wang, W., Bates, M. & Zhuang, X. Three-dimensional super-resolution imaging by stochastic optical reconstruction microscopy. Science 319, 810–813 (2008).
Pavani et al. Three-dimensional, single-molecule fluorescence imaging beyond the diffraction limit by using a double-helix point spread function. Proc. Natl Acad. Sci. USA 106, 2995–2999 (2009).
Grotjohann, T. et al. Diffraction-unlimited all-optical imaging and writing with a photochromic GFP. Nature 478, 204–208 (2011).
Dorval, A. D. & White, J. A. Channel noise is essential for perithreshold oscillations in entorhinal stellate neurons. J. Neurosci. 25, 10025–10028 (2005).
Cao, Y.-Q. et al. Presynaptic Ca2+ channels compete for channel type-preferring slots in altered neurotransmission arising from Ca2+ channelopathy. Neuron 43, 387–400 (2004).
Huang, F. et al. Video-rate nanoscopy using sCMOS camera-specific single-molecule localization algorithms. Nat. Methods 10, 653–658 (2013).
Albrecht, D. et al. Nanoscopic compartmentalization of membrane protein motion at the axon initial segment. J. Cell Biol. 215, 37–46 (2016).
Rondelez, Y. et al. Microfabricated arrays of femtoliter chambers allow single molecule enzymology. Nat. Biotechnol. 23, 361–365 (2005).
Rhee, H.-W. et al. Proteomic mapping of mitochondria in living cells via spatially restricted enzymatic tagging. Science 339, 1328–1331 (2013).
Acknowledgements
The authors thank R. Barish, H. Soundarajan, S. Agasti, J. Woehrstein and R. Jungmann for preliminary work on aspects of earlier versions of the project and for helpful discussions, and W. Shih, H. Sasaki, B. Beliveau, E. Boyden and J. Paulsson for helpful discussions. This work was supported by a National Institutes of Health (NIH) Director’s New Innovator Award (1DP2OD007292), an NIH Transformative Research Award (1R01EB018659), an NIH Pioneer Award (1DP1GM133052), an NIH grant (5R21HD072481), an Office of Naval Research (ONR) Young Investigator Program Award (N000141110914), ONR grants (N000141010827, N000141310593 and N000141812549), a National Science Foundation (NSF) Faculty Early Career Development Award (CCF1054898), an NSF grant (CCF1162459) and the Molecular Robotics Initiative fund at the Wyss Institute for Biologically Engineering Faculty to P.Y. M.D. acknowledges support from a HHMI International Predoctoral Fellowship, Department Fellowship from Systems Biology Department at the Harvard Medical School, and a Technology Development Fellowship from the Wyss Institute at Harvard University. S.K.S. acknowledges support from a Human Frontier Science Program (HFSP) fellowship (LT000048/2016-L).
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M.D. and P.Y. conceived and designed the study, N.L. and M.D. designed and performed the experiments and analysed the data, M.D. developed the software, S.K.S. provided advice and assistance with the microtubule sample preparation. P.Y. supervised the study. All the authors wrote and approved the manuscript.
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A US patent (US App No. 15/104,570) has been filed that covers the concepts reported in this work (inventors, R. Barish and P.Y.). P.Y. is cofounder of Ultivue Inc. and NuProbe Global.
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Supplementary Materials 1, Supplementary Materials 2, Supplementary Methods 3, Supplementary Notes 4, Supplementary Figs. 1–15 and 5 and Supplementary Tables 1–4.
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Liu, N., Dai, M., Saka, S.K. et al. Super-resolution labelling with Action-PAINT. Nat. Chem. 11, 1001–1008 (2019). https://doi.org/10.1038/s41557-019-0325-7
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DOI: https://doi.org/10.1038/s41557-019-0325-7
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