| Literature DB >> 31932776 |
Klaus C Gwosch1, Jasmin K Pape1, Francisco Balzarotti1, Philipp Hoess2, Jan Ellenberg2, Jonas Ries2, Stefan W Hell3,4.
Abstract
The ultimate goal of biological super-resolution fluorescence microscopy is to provide three-dimensional resolution at the size scale of a fluorescent marker. Here we show that by localizing individual switchable fluorophores with a probing donut-shaped excitation beam, MINFLUX nanoscopy can provide resolutions in the range of 1 to 3 nm for structures in fixed and living cells. This progress has been facilitated by approaching each fluorophore iteratively with the probing-donut minimum, making the resolution essentially uniform and isotropic over scalable fields of view. MINFLUX imaging of nuclear pore complexes of a mammalian cell shows that this true nanometer-scale resolution is obtained in three dimensions and in two color channels. Relying on fewer detected photons than standard camera-based localization, MINFLUX nanoscopy is poised to open a new chapter in the imaging of protein complexes and distributions in fixed and living cells.Entities:
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Year: 2020 PMID: 31932776 DOI: 10.1038/s41592-019-0688-0
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 28.547