Abstract
Genetically-encoded fluorescence-based sensors have emerged as an essential tool for measuring the abundance of heme, revealing its trafficking pathways, and probing its signalling and regulatory role in cells. A number of different sensor designs have been described in the literature, and these typically report on the abundance of exchangeable heme via an intensity modulation of the emission from fluorescent-protein reporters. Here, we show that multi-photon fluorescence-lifetime imaging microscopy (MP-FLIM) can be used to monitor the response of heme sensors in transfected-HEK293 cells. The adoption of a multi-photon approach could extend heme quantification further to deep-tissue imaging in the future, where it could also reduce phototoxicity as the non-linear excitation of fluorescent reporters is confined to the focal volume.
| Original language | English |
|---|---|
| Article number | 113082 |
| Pages (from-to) | 1-9 |
| Number of pages | 9 |
| Journal | Journal of Inorganic Biochemistry |
| Volume | 274 |
| Early online date | 27 Sept 2025 |
| DOIs | |
| Publication status | Published - 1 Jan 2026 |
Bibliographical note
Publisher Copyright:© 2025 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY license. http://creativecommons.org/licenses/by/4.0/
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