4.8 Article

Multiplexed 3D cellular super-resolution imaging with DNA-PAINT and Exchange-PAINT

期刊

NATURE METHODS
卷 11, 期 3, 页码 313-U292

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/NMETH.2835

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资金

  1. US National Institutes of Health (NIH) Director's New Innovator Award [1DP2OD007292]
  2. NIH Transformative Research Award [1R01EB018659]
  3. NIH [5R21HD072481]
  4. Office of Naval Research (ONR) Young Investigator Program Award [N000141110914]
  5. ONR [N000141010827, N000141310593]
  6. US National Science Foundation (NSF) Faculty Early Career Development Award [CCF1054898]
  7. NSF [CCF1162459]
  8. Wyss Institute for Biologically Engineering Faculty Startup Fund
  9. NIH Director's New Innovator Award [1DP2OD004641]
  10. Wyss Institute for Biologically Inspired Engineering Faculty Award
  11. Alexander von Humboldt-Foundation through a Feodor-Lynen Fellowship
  12. Howard Hughes Medical Institute International Student Research Fellowships
  13. Direct For Computer & Info Scie & Enginr
  14. Division of Computing and Communication Foundations [1317694] Funding Source: National Science Foundation
  15. Division of Computing and Communication Foundations
  16. Direct For Computer & Info Scie & Enginr [1054898] Funding Source: National Science Foundation

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Super-resolution fluorescence microscopy is a powerful tool for biological research, but obtaining multiplexed images for a large number of distinct target species remains challenging. Here we use the transient binding of short fluorescently labeled oligonucleotides (DNA-PAINT, a variation of point accumulation for imaging in nanoscale topography) for simple and easy-to-implement multiplexed super-resolution imaging that achieves sub-10-nm spatial resolution in vitro on synthetic DNA structures. We also report a multiplexing approach (Exchange-PAINT) that allows sequential imaging of multiple targets using only a single dye and a single laser source. We experimentally demonstrate ten-color super-resolution imaging in vitro on synthetic DNA structures as well as four-color two-dimensional (2D) imaging and three-color 3D imaging of proteins in fixed cells.

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