Correction to: Light: Science & Applications
https://doi.org/10.1038/s41377-024-01463-9 published online 24 May 2024
After publication of this article1, it was brought to our attention that the unit of NaCl in the legend “NaCl (150 μM) + Liposome” in Fig. 1f was incorrect and should be “NaCl (150 mM) + Liposome”. The original publication has been corrected. The correct Fig. 1 is shown below:
Fig. 1: A lipid membrane light-up, highly photostable, lowly phototoxicity mitochondrial inner membrane probe. a Chemical structure of HBmito Crimson used for the specific labeling of the mitochondrial inner membrane. b The absorption and emission spectra of HBmito Crimson, which can be depleted using a 775-nm laser. c, d Absorption and fluorescence spectra of HBmito Crimson solution upon addition of different concentrations of NaCl (0–1000 mM). e, f Absorption and fluorescence spectra of HBmito Crimson solution in NaCl solution in the presence or absence of liposome. g The photostability of HBmito Crimson in different solutions and commercial Alexa Fluor 647 in water solution. h Photobleaching curve of HBmito Crimson, PK Mito Deep Red and Mito Tracker Deep Red in polymethyl methacrylate (PMMA). i Viability of HBmito Crimson, PK Mito Deep Red and Mito Tracker Deep Red-stained COS7 cells after Red light illumination (637 nm, 1.6 W/cm2).
Reference
Ren, W. et al. Visualization of cristae and mtDNA interactions via STED nanoscopy using a low saturation power probe. Light Sci. Appl. 13, 116 (2024).
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Ren, W., Ge, X., Li, M. et al. Author Correction: Visualization of cristae and mtDNA interactions via STED nanoscopy using a low saturation power probe. Light Sci Appl 13, 235 (2024). https://doi.org/10.1038/s41377-024-01584-1
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DOI: https://doi.org/10.1038/s41377-024-01584-1