Light-Induced Forward and Reverse Intersystem Crossing in Green Fluorescent Proteins at Cryogenic Temperatures
Author:
Affiliation:
1. Institut de Biologie Structurale, CNRS, Université Grenoble Alpes, CEA, IBS, 38044 Grenoble, France
Funder
Agence Nationale de la Recherche
Commissariat ? l'?nergie Atomique et aux ?nergies Alternatives
Publisher
American Chemical Society (ACS)
Subject
Materials Chemistry,Surfaces, Coatings and Films,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.jpcb.3c02971
Reference29 articles.
1. Cryo-fluorescence microscopy facilitates correlations between light and cryo-electron microscopy and reduces the rate of photobleaching
2. Photon Yield Enhancement of Red Fluorophores at Cryogenic Temperatures
3. Correlative cryo super-resolution light and electron microscopy on mammalian cells using fluorescent proteins
4. Correlative three-dimensional super-resolution and block-face electron microscopy of whole vitreously frozen cells
5. Photophysical studies at cryogenic temperature reveal a novel photoswitching mechanism of rsEGFP2
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4. Photophysical Studies at Cryogenic Temperature Reveal a Novel Photoswitching Mechanism of rsEGFP2;Journal of the American Chemical Society;2023-06-30
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