Multi-photon fluorescence-lifetime imaging of a genetically-encoded heme sensor

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.

Authors

Institutions

Publication Details

Journal
Journal of Inorganic Biochemistry
Published
2025-09-27
DOI
https://doi.org/10.1016/j.jinorgbio.2025.113082
Primary Topic
Biosensors and Analytical Detection
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Multi-photon fluorescence-lifetime imaging of a genetically-encoded heme sensor

Christiane Reick, Robert G Blore, Emma Lloyd Raven, Charalambos P. Kyriacou et al.
Journal of Inorganic Biochemistry
Biosensors and Analytical Detection
article

Multi-photon fluorescence-lifetime imaging of a genetically-encoded heme sensor

Christiane Reick, Robert G Blore, Emma Lloyd Raven, Charalambos P. Kyriacou, Ezio Rosato, Jaswir Basran, Andrea E. Gallio, Z Majewska, Andrew J. Hudson, Noa A. Marson, Michael J. James, Maryam Mohammad Qaed, Georgia A Ceeney, Kornelija Rimgailaite, Douha Ghrieb
article en

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.

Journal of Inorganic BiochemistryVol. 274
University of Leicester (GB), University of Bristol (GB)
Openalex Percentile: Top 73%
Biosensors and Analytical Detection
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.