Issue 24, 2016

Direct organelle thermometry with fluorescence lifetime imaging microscopy in single myotubes

Abstract

We describe organelle thermometry using an endoplasmic reticulum-targeting small molecule dye and cytosolic mCherry, whose fluorescence lifetimes reduce with increasing temperature and can be monitored by fluorescence lifetime imaging microscopy. The results show that heat production in single myotubes is highly localized and is coupled to a Ca2+ burst.

Graphical abstract: Direct organelle thermometry with fluorescence lifetime imaging microscopy in single myotubes

Supplementary files

Article information

Article type
Communication
Submitted
03 Dec 2015
Accepted
21 Jan 2016
First published
21 Jan 2016
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2016,52, 4458-4461

Author version available

Direct organelle thermometry with fluorescence lifetime imaging microscopy in single myotubes

H. Itoh, S. Arai, T. Sudhaharan, S. Lee, Y. Chang, S. Ishiwata, M. Suzuki and E. B. Lane, Chem. Commun., 2016, 52, 4458 DOI: 10.1039/C5CC09943A

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