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MINFLUX has achieved extraordinary resolution in superresolution imaging and single fluorophore tracking. It is based on localizing single fluorophores by rapid probing with a patterned beam that features a local intensity minimum. Current implementations, however, are complex and expensive and are limited in speed and robustness. Here, we show that a combination of an electro-optical modulator with a segmented birefringent element such as a spatial light modulator produces a variable phase plate for which the phase can be scanned on the MHz timescale. Bisected or top-hat phase patterns generate high-contrast compact excitation point-spread functions for MINFLUX localization in the x, y, and z-direction, respectively, which can be scanned across a fluorophore within a microsecond, switched within 60 microseconds and alternated among different excitation wavelengths. We discuss how to compensate for non-optimal performance of the components and present a robust 3D and multi-color MINFLUX excitation module, which we envision as an integral component of a high-performance and cost-effective open-source MINFLUX.
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http://dx.doi.org/10.1038/s41377-024-01487-1 | DOI Listing |
Nat Commun
July 2025
Department of NanoBiophotonics, Max Planck Institute for Multidisciplinary Sciences, RG Mitochondrial Structure and Dynamics, Göttingen, Germany.
Mitochondria contain their own DNA (mtDNA) and a dedicated gene expression machinery. As the mitochondrial dimensions are close to the diffraction limit of classical light microscopy, the spatial distribution of mitochondrial proteins and in particular of mitochondrial mRNAs remains underexplored. Here, we establish single-molecule fluorescence in situ hybridization (smFISH) combined with STED and MINFLUX super-resolution microscopy (nanoscopy) to visualize individual mitochondrial mRNA molecules and associated proteins.
View Article and Find Full Text PDFNat Commun
July 2025
Molecular Neurobiology Division, Biomedical Research Institute, UCA-CONICET, Buenos Aires, Argentina.
The diffusion and interaction dynamics of membrane proteins and lipids are key for cell function, but their disclosure is hampered by limited temporal and spatial resolution of conventional observation technologies. Here we exploit the capabilities of minimal fluorescence emission photon fluxes (MINFLUX) microscopy in single-molecule co-tracking experiments of an important membrane protein and cholesterol with enhanced spatiotemporal resolution. Specifically, we interrogate the 2D translational mobility of a ubiquitous cell-surface protein, the nicotinic acetylcholine receptor, in tandem with a fluorescent cholesterol analogue for minute-long periods, reaching nanometric precision and sub-millisecond time resolution.
View Article and Find Full Text PDFNat Photonics
March 2025
Max Perutz Labs, Vienna Biocenter Campus (VBC), Vienna, Austria.
Optical super-resolution microscopy is a key technology for structural biology that offers high imaging contrast and live-cell compatibility. Minimal (fluorescence) photon flux microscopy, or MINFLUX, is an emerging super-resolution technique that localizes single fluorophores with high spatiotemporal precision by targeted scanning of a patterned excitation beam featuring a minimum. MINFLUX offers super-resolution imaging with nanometre resolution.
View Article and Find Full Text PDFAnnu Rev Biophys
May 2025
Third Institute of Physics - Biophysics, Georg August University of Göttingen, Göttingen, Germany; email:
Over the last 30 years, fluorescence microscopy, renowned for its sensitivity and specificity, has undergone a revolution in resolving ever-smaller details. This advancement began with stimulated emission depletion (STED) microscopy and progressed with techniques such as photoactivatable localization microscopy and stochastic optical reconstruction microscopy (STORM). Single-molecule localization microscopy (SMLM), which encompasses methods like direct STORM, has significantly enhanced image resolution.
View Article and Find Full Text PDFLocalization microscopy enables imaging with resolutions that surpass the conventional optical diffraction limit. Notably, the Maximally INFormative LUminescence eXcitation (MINFLUX) method achieves super-resolution by shaping the excitation point spread function (PSF) to minimize the required photon flux for a given precision. Various beam shapes have recently been proposed to improve localization efficiency, yet their optimality remains an open question.
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