bioRxiv (Cold Spring Harbor Laboratory) · 2019 · 19 citations · 39 references
Natural SciencesBiophysicsPhysicsBiomedical OpticsBiophotonicsNanotechnologyFluorescence ImagingFluorescence MicroscopyFluorescence SpectroscopySingle-molecule Fluorescence MicroscopySingle-molecule ImagingSingle-molecule MeasurementsExcitationFluorescent DyesFluorescent ProbesMolecule LocalizationSingle-molecule Fluorescence ImagingSingle-molecule Localization MicroscopySingle-molecule Localization Precision
Abstract Strategies have been developed in LIDAR to perform distance measurements for non-coherent emission in sparse samples based on excitation modulation. Super-resolution fluorescence microscopy is also striving to perform axial localization but through entirely different approaches. Here we revisit the amplitude modulated LIDAR approach to reach nanometric localization precision and we successfully adapt it to bring distinct advantages to super-resolution microscopy. The excitation pattern is performed by interference enabling the decoupling between spatial and time modulation. The localization of a single emitter is performed by measuring the relative phase of its linear fluorescent response to the known shifting excitation field. Taking advantage of a tilted interfering configuration, we obtain a typical axial localization precision of 7.5 nm over the entire field of view and the axial capture range, without compromising on the acquisition time, the emitter density or the lateral localization precision. The interfering pattern being robust to optical aberrations, this modulated localization (ModLoc) strategy is particularly well suited for observations deep in the samples. Images performed on various biological samples show that the localization precision remains nearly constant up to several micrometers.
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