Highly Efficient Fluorescent Probe to Visualize Protein Interactions at the Superresolution
Author:
Affiliation:
1. Graduate School of Arts and Sciences, The University of Tokyo, Tokyo 153-8902, Japan
2. Kanagawa Institute of Industrial Science and Technology, Kanagawa 243-0435, Japan
Funder
Japan Society for the Promotion of Science
Kanagawa Institute of Industrial Science and Technology
Publisher
American Chemical Society (ACS)
Link
https://pubs.acs.org/doi/pdf/10.1021/acschembio.4c00075
Reference24 articles.
1. Imaging Intracellular Fluorescent Proteins at Nanometer Resolution
2. Nanometer resolution imaging and tracking of fluorescent molecules with minimal photon fluxes
3. Super-resolution imaging and tracking of protein–protein interactions in sub-diffraction cellular space
4. Photoactivated Localization Microscopy with Bimolecular Fluorescence Complementation (BiFC-PALM) for Nanoscale Imaging of Protein-Protein Interactions in Cells
5. Three-Fragment Fluorescence Complementation Coupled with Photoactivated Localization Microscopy for Nanoscale Imaging of Ternary Complexes
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