DNA-PAINT MINFLUX nanoscopy

被引:53
作者
Ostersehlt, Lynn M. [1 ]
Jans, Daniel C. [1 ,2 ]
Wittek, Anna [1 ,2 ]
Keller-Findeisen, Jan [1 ]
Inamdar, Kaushik [1 ,2 ]
Sahl, Steffen J. [1 ]
Hell, Stefan W. [1 ,3 ,4 ]
Jakobs, Stefan [1 ,2 ,4 ,5 ]
机构
[1] Max Planck Inst Multidisciplinary Sci, Dept NanoBiophoton, Gottingen, Germany
[2] Univ Med Ctr Gottingen, Dept Neurol, Gottingen, Germany
[3] Max Planck Inst Med Res, Dept Opt Nanoscopy, Heidelberg, Germany
[4] Univ Gottingen, Cluster Excellence Multiscale Bioimaging Mol Mach, Gottingen, Germany
[5] Fraunhofer Inst Translat Med & Pharmacol ITMP, Translat Neuroinflammat & Automated Microscopy, Gottingen, Germany
关键词
MICROSCOPY; RESOLUTION; BINDING;
D O I
10.1038/s41592-022-01577-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
MINimal fluorescence photon FLUXes (MINFLUX) nanoscopy, providing photon-efficient fluorophore localizations, has brought about three-dimensional resolution at nanometer scales. However, by using an intrinsic on-off switching process for single fluorophore separation, initial MINFLUX implementations have been limited to two color channels. Here we show that MINFLUX can be effectively combined with sequentially multiplexed DNA-based labeling (DNA-PAINT), expanding MINFLUX nanoscopy to multiple molecular targets. Our method is exemplified with three-color recordings of mitochondria in human cells. A systematic exploration of MINFLUX nanoscopy with DNA-PAINT labeling leads to improved nanoscopy in fixed cells and MINFLUX imaging with increased multiplexing, as exemplified by three-color imaging of mitochondria in mammalian cells.
引用
收藏
页码:1072 / +
页数:13
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