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Isotropic three-dimensional dual-color super-resolution microscopy with metal-induced energy transfer

Over the past two decades, super-resolution microscopy has seen a tremendous development in speed and resolution, but for most of its methods, there exists a remarkable gap between lateral and axial resolution, which is by a factor of 2 to 3 worse. One recently developed method to close this gap is...

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Detalles Bibliográficos
Autores principales: Thiele, Jan Christoph, Jungblut, Marvin, Helmerich, Dominic A., Tsukanov, Roman, Chizhik, Anna, Chizhik, Alexey I., Schnermann, Martin J., Sauer, Markus, Nevskyi, Oleksii, Enderlein, Jörg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9176750/
https://www.ncbi.nlm.nih.gov/pubmed/35675401
http://dx.doi.org/10.1126/sciadv.abo2506
Descripción
Sumario:Over the past two decades, super-resolution microscopy has seen a tremendous development in speed and resolution, but for most of its methods, there exists a remarkable gap between lateral and axial resolution, which is by a factor of 2 to 3 worse. One recently developed method to close this gap is metal-induced energy transfer (MIET) imaging, which achieves an axial resolution down to nanometers. It exploits the distance-dependent quenching of fluorescence when a fluorescent molecule is brought close to a metal surface. In the present manuscript, we combine the extreme axial resolution of MIET imaging with the extraordinary lateral resolution of single-molecule localization microscopy, in particular with direct stochastic optical reconstruction microscopy (dSTORM). This combination allows us to achieve isotropic three-dimensional super-resolution imaging of subcellular structures. Moreover, we used spectral demixing for implementing dual-color MIET-dSTORM that allows us to image and colocalize, in three dimensions, two different cellular structures simultaneously.