
==== Front
Light Sci Appl
Light Sci Appl
Light, Science & Applications
2095-5545
2047-7538
Nature Publishing Group UK London

39231953
1584
10.1038/s41377-024-01584-1
Author Correction
Author Correction: Visualization of cristae and mtDNA interactions via STED nanoscopy using a low saturation power probe
Ren Wei 1
Ge Xichuan 2
http://orcid.org/0000-0003-3586-176X
Li Meiqi 3
Sun Jing 2
Li Shiyi 2
Gao Shu 1
http://orcid.org/0000-0002-5532-2811
Shan Chunyan chunyanshan@pku.edu.cn

34
http://orcid.org/0000-0002-1981-144X
Gao Baoxiang bxgao@hbu.edu.cn

2
http://orcid.org/0000-0001-6626-4840
Xi Peng xipeng@pku.edu.cn

1
1 https://ror.org/02v51f717 grid.11135.37 0000 0001 2256 9319 Department of Biomedical Engineering, National Biomedical Imaging Center, College of Future Technology, Peking University, Beijing, 100871 China
2 https://ror.org/01p884a79 grid.256885.4 0000 0004 1791 4722 Key Laboratory of Analytical Science and Technology of Hebei Province, College of Chemistry and Material Science, Hebei University, Baoding, 071002 China
3 https://ror.org/02v51f717 grid.11135.37 0000 0001 2256 9319 School of Life Sciences, Peking University, Beijing, 100871 China
4 https://ror.org/02v51f717 grid.11135.37 0000 0001 2256 9319 National Center for Protein Sciences, Peking University, Beijing, 100871 China
5 9 2024
5 9 2024
2024
13 235© The Author(s) 2024
2024
https://creativecommons.org/licenses/by/4.0/ Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
Subject terms

Super-resolution microscopy
Biophotonics
issue-copyright-statement© Changchun Institute of Optics, Fine Mechanics and Physics (CIOMP), CAS 2024
==== Body
pmcCorrection to: Light: Science & Applications

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).

These authors contributed equally: Wei Ren, Xichuan Ge
==== Refs
Reference

1. Ren W Visualization of cristae and mtDNA interactions via STED nanoscopy using a low saturation power probe Light Sci. Appl. 2024 13 116 10.1038/s41377-024-01463-9 38782912
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).38782912 10.1038/s41377-024-01463-9
