4.8 Article

Super-resolution spectroscopic microscopy via photon localization

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NATURE COMMUNICATIONS
卷 7, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/ncomms12290

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资金

  1. National Institutes of Health [T32GM008152, T32HL076139, R01EY019951, R24EY022883, R01CA165309]
  2. National Science Foundation [DBI-1353952, CBET-1055379, CBET-1066776, EFRI-1240416, EEC-1530734]
  3. Northwestern McCormick School of Engineering
  4. Emerging Frontiers & Multidisciplinary Activities
  5. Directorate For Engineering [1240416] Funding Source: National Science Foundation

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Traditional photon localization microscopy analyses only the spatial distributions of photons emitted by individual molecules to reconstruct super-resolution optical images. Unfortunately, however, the highly valuable spectroscopic information from these photons have been overlooked. Here we report a spectroscopic photon localization microscopy that is capable of capturing the inherent spectroscopic signatures of photons from individual stochastic radiation events. Spectroscopic photon localization microscopy achieved higher spatial resolution than traditional photon localization microscopy through spectral discrimination to identify the photons emitted from individual molecules. As a result, we resolved two fluorescent molecules, which were 15 nm apart, with the corresponding spatial resolution of 10 nm-a four-fold improvement over photon localization microscopy. Using spectroscopic photon localization microscopy, we further demonstrated simultaneous multi-colour super-resolution imaging of microtubules and mitochondria in COS-7 cells and showed that background autofluorescence can be identified through its distinct emission spectra.

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