2020
DOI: 10.1002/ange.202005959
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A Multi‐responsive Fluorescent Probe Reveals Mitochondrial Nucleoprotein Dynamics with Reactive Oxygen Species Regulation through Super‐resolution Imaging

Abstract: Understanding the biomolecular interactions in a specific organelle has been a long‐standing challenge because it requires super‐resolution imaging to resolve the spatial locations and dynamic interactions of multiple biomacromolecules. Two key difficulties are the scarcity of suitable probes for super‐resolution nanoscopy and the complications that arise from the use of multiple probes. Herein, we report a quinolinium derivative probe that is selectively enriched in mitochondria and switches on in three diffe… Show more

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Cited by 7 publications
(2 citation statements)
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“…However, compounds 1 and 11 up to 100 μM displayed no significant toxicity with 95% cell survival, while entacapone without liver toxicity served as a negative control. The cell viability and mitochondria membrane potential is an indicator of cell viability 26 . Therefore, these data supported the idea that these novel non-nitrocatechol COMT inhibitors had the potential of being developed with a reduced risk of liver toxicity.…”
Section: Resultsmentioning
confidence: 99%
“…However, compounds 1 and 11 up to 100 μM displayed no significant toxicity with 95% cell survival, while entacapone without liver toxicity served as a negative control. The cell viability and mitochondria membrane potential is an indicator of cell viability 26 . Therefore, these data supported the idea that these novel non-nitrocatechol COMT inhibitors had the potential of being developed with a reduced risk of liver toxicity.…”
Section: Resultsmentioning
confidence: 99%
“…Several seminal reports have paved the ground for exploring the organization of mitochondria membranes and the co-localization of mitochondria proteins by super-resolution microscopy, at increased spatial sensitivity, partially bypassing the diffraction limits of visible light microscopy [28][29][30] and in live cells 30,31 . Thorough two-color 2D-STED analysis was applied to colocalize protein in the mitochondria membrane [32][33][34] , and the role of MIC26 and MIC27 in the stability and integration of the remaining MICOS subunits was studied by combining STED nanoscopy, and blue-native gel electrophoresis 35 .…”
Section: Discussionmentioning
confidence: 99%