Abstract

Mitochondria–lysosome interactions are essential for maintaining intracellular homeostasis. Although various fluorescent probes have been developed to visualize such interactions, they remain unable to label mitochondria and lysosomes simultaneously and dynamically track their interaction. Here, we introduce a cell-permeable, biocompatible, viscosity-responsive, small organic molecular probe, Coupa, to monitor the interaction of mitochondria and lysosomes in living cells. Through a functional fluorescence conversion, Coupa can simultaneously label mitochondria with blue fluorescence and lysosomes with red fluorescence, and the correlation between the red–blue fluorescence intensity indicates the progress of mitochondria–lysosome interplay during mitophagy. Moreover, because its fluorescence is sensitive to viscosity, Coupa allowed us to precisely localize sites of mitochondria–lysosome contact and reveal increases in local viscosity on mitochondria associated with mitochondria–lysosome contact. Thus, our probe represents an attractive tool for the localization and dynamic tracking of functional mitochondria–lysosome interactions in living cells.

Dynamic labeling and tracking of organelle–organelle contacts is essential to understand the formation and function of these interactions. Here the authors present a small molecule probe, Coupa, that labels mitochondria and lysosomes with blue and red fluorescence, respectively.

Details

Title
A dual-labeling probe to track functional mitochondria–lysosome interactions in live cells
Author
Chen, Qixin 1 ; Fang Hongbao 2 ; Shao Xintian 3 ; Tian Zhiqi 3 ; Geng Shanshan 4 ; Zhang, Yuming 4 ; Fan Huaxun 5   VIAFID ORCID Logo  ; Pan, Xiang 6 ; Zhang, Jie 7 ; Tian Xiaohe 6   VIAFID ORCID Logo  ; Zhang, Kai 5   VIAFID ORCID Logo  ; He Weijiang 4   VIAFID ORCID Logo  ; Guo Zijian 4 ; Diao Jiajie 3   VIAFID ORCID Logo 

 Nanjing University, State Key Laboratory of Coordination Chemistry, Coordination Chemistry Institute, School of Chemistry and Chemical Engineering, Nanjing, China (GRID:grid.41156.37) (ISNI:0000 0001 2314 964X); Shandong First Medical University & Shandong Academy of Medical Sciences, Institute of Materia Medica, Jinan, China (GRID:grid.410587.f); University of Cincinnati College of Medicine, Department of Cancer Biology, Cincinnati, USA (GRID:grid.24827.3b) (ISNI:0000 0001 2179 9593) 
 Nanjing University, State Key Laboratory of Coordination Chemistry, Coordination Chemistry Institute, School of Chemistry and Chemical Engineering, Nanjing, China (GRID:grid.41156.37) (ISNI:0000 0001 2314 964X); University of Cincinnati College of Medicine, Department of Cancer Biology, Cincinnati, USA (GRID:grid.24827.3b) (ISNI:0000 0001 2179 9593) 
 University of Cincinnati College of Medicine, Department of Cancer Biology, Cincinnati, USA (GRID:grid.24827.3b) (ISNI:0000 0001 2179 9593) 
 Nanjing University, State Key Laboratory of Coordination Chemistry, Coordination Chemistry Institute, School of Chemistry and Chemical Engineering, Nanjing, China (GRID:grid.41156.37) (ISNI:0000 0001 2314 964X) 
 University of Illinois at Urbana-Champaign, Department of Biochemistry, Urbana, USA (GRID:grid.35403.31) (ISNI:0000 0004 1936 9991) 
 Anhui University, Anhui Province Key Laboratory of Chemistry for Inorganic/Organic Hybrid Functionalized Materials, Hefei, China (GRID:grid.252245.6) (ISNI:0000 0001 0085 4987) 
 Shandong University, Advanced Medical Research Institute/Translational Medicine Core Facility of Advanced Medical Research Institute, Jinan, China (GRID:grid.27255.37) (ISNI:0000 0004 1761 1174) 
Publication year
2020
Publication date
2020
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2473293076
Copyright
© The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.