Bright monomeric fluorescent protein elite-niRFP704 for two-channel near-infrared STED nanoscopy

The near-infrared (NIR) spectral region is attractive for live-cell imaging, due to low autofluorescence and reduced phototoxicity. Some phytochrome-derived fluorescent proteins absorb and emit fluorescence in the NIR, but have short fluorescence lifetimes and relatively low quantum yields, requiring higher laser powers thus limiting their usefulness for live-cell superresolution microscopy. Using the bacterial phytochrome miRFP703 as a template, we screened for variants with longer fluorescence lifetimes, because the quantum yield and fluorescence lifetime are linked. We identified the bright monomeric fluorescent protein elite-niRFP704, which has a longer lifetime (1.12 ns) and a correspondingly higher quantum yield (0.21) than its template, absorbing and emitting completely in the NIR spectral region. elite-niRFP704 was used to tag proteins in living cells and facilitated extended stimulated emission depletion (STED) microscopy on cell lines stably expressing a fusion protein. Finally, elite-niRFP704 and miRFP703 could be separated based on their significantly different lifetimes, enabling two-channel NIR STED microscopy of living mammalian cells.

Authors

Institutions

Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2026-08-25
DOI
https://doi.org/10.1073/pnas.2533451123
Primary Topic
Advanced Fluorescence Microscopy Techniques
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
article

Bright monomeric fluorescent protein elite-niRFP704 for two-channel near-infrared STED nanoscopy

Kaushik Inamdar, Stefan Jakobs, Iman Esmaeil Zadeh, Jörg Enderlein et al.
Proceedings of the National Academy of Sciences
Advanced Fluorescence Microscopy Techniques
article

Bright monomeric fluorescent protein elite-niRFP704 for two-channel near-infrared STED nanoscopy

Kaushik Inamdar, Stefan Jakobs, Iman Esmaeil Zadeh, Jörg Enderlein, Daniel Stumpf, Marcel Leutenegger, Florian Habenstein, Jessie Qin-Dregely, Alexey I. Chizhik, Stefan W. Hell, Jin Chang, Andreas Fognini, Nickels Jensen, Laura L. Kirck
article en

Abstract

The near-infrared (NIR) spectral region is attractive for live-cell imaging, due to low autofluorescence and reduced phototoxicity. Some phytochrome-derived fluorescent proteins absorb and emit fluorescence in the NIR, but have short fluorescence lifetimes and relatively low quantum yields, requiring higher laser powers thus limiting their usefulness for live-cell superresolution microscopy. Using the bacterial phytochrome miRFP703 as a template, we screened for variants with longer fluorescence lifetimes, because the quantum yield and fluorescence lifetime are linked. We identified the bright monomeric fluorescent protein elite-niRFP704, which has a longer lifetime (1.12 ns) and a correspondingly higher quantum yield (0.21) than its template, absorbing and emitting completely in the NIR spectral region. elite-niRFP704 was used to tag proteins in living cells and facilitated extended stimulated emission depletion (STED) microscopy on cell lines stably expressing a fusion protein. Finally, elite-niRFP704 and miRFP703 could be separated based on their significantly different lifetimes, enabling two-channel NIR STED microscopy of living mammalian cells.

Proceedings of the National Academy of SciencesVol. 123(35)
Max Planck Institute for Medical Research (DE), Fraunhofer Institute for Translational Medicine and Pharmacology (DE), Universitätsmedizin Göttingen (DE), Max Planck Institute for Multidisciplinary Sciences, University of Göttingen (DE), Singer (United States) (US), Delft University of Technology (NL)
Deutsche Forschungsgemeinschaft, Bundesministerium für Bildung und Forschung, European Research Council, HORIZON EUROPE European Innovation Council
Openalex Percentile: Top 12%
Advanced Fluorescence Microscopy Techniques
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.