124-Color Super-resolution Imaging by Engineering DNA-PAINT Blinking Kinetics

被引:88
作者
Wade, Orsolya K. [1 ,2 ,3 ]
Woehrstein, Johannes B. [1 ,2 ,3 ]
Nickels, Philipp C. [1 ,2 ,3 ]
Strauss, Sebastian [1 ,2 ,3 ]
Stehr, Florian [3 ]
Stein, Johannes [3 ]
Schueder, Florian [1 ,2 ,3 ]
Strauss, Maximilian T. [1 ,2 ,3 ]
Ganji, Mahipal [1 ,2 ,3 ]
Schnitzbauer, Joerg [1 ,2 ,3 ]
Grabmayr, Heinrich [1 ,2 ,3 ]
Yin, Peng [4 ,5 ]
Schwille, Petra [3 ]
Jungmann, Ralf [1 ,2 ,3 ]
机构
[1] Ludwig Maximilians Univ Munchen, Dept Phys, D-80539 Munich, Germany
[2] Ludwig Maximilians Univ Munchen, Ctr Nanosci, D-80539 Munich, Germany
[3] Max Planck Inst Biochem, D-82152 Martinsried, Germany
[4] Harvard Univ, Wyss Inst Biol Inspired Engn, Boston, MA 02115 USA
[5] Harvard Med Sch, Dept Syst Biol, Boston, MA 02115 USA
基金
欧洲研究理事会;
关键词
Super-resolution microscopy; DNA nanotechnology; DNA-PAINT; barcoding multiplexing; MICROSCOPY; MOLECULES;
D O I
10.1021/acs.nanolett.9b00508
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Optical super-resolution techniques reach unprecedented spatial resolution down to a few nanometers. However, efficient multiplexing strategies for the simultaneous detection of hundreds of molecular species are still elusive. Here, we introduce an entirely new approach to multiplexed super-resolution microscopy by designing the blinking behavior of targets with engineered binding frequency and duration in DNA-PAINT. We assay this kinetic barcoding approach in silico and in vitro using DNA origami structures, show the applicability for multiplexed RNA and protein detection in cells, and finally experimentally demonstrate 124-plex super-resolution imaging within minutes.
引用
收藏
页码:2641 / 2646
页数:6
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