TY - JOUR
T1 - Isotropic three-dimensional dual-color super-resolution microscopy with metal-induced energy transfer
AU - Thiele, Jan Christoph
AU - Jungblut, Marvin
AU - Helmerich, Dominic A.
AU - Tsukanov, Roman
AU - Chizhik, Anna
AU - Chizhik, Alexey I.
AU - Schnermann, Martin J.
AU - Sauer, Markus
AU - Nevskyi, Oleksii
AU - Enderlein, Jörg
N1 - Publisher Copyright:
Copyright © 2022 The Authors, some rights reserved;
PY - 2022/6/1
Y1 - 2022/6/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85131771692&partnerID=8YFLogxK
U2 - 10.1126/sciadv.abo2506
DO - 10.1126/sciadv.abo2506
M3 - Article
C2 - 35675401
AN - SCOPUS:85131771692
SN - 2375-2548
VL - 8
JO - Science advances
JF - Science advances
IS - 23
M1 - eabo2506
ER -