Decarboxylation via a Higher Electronic Excited State Drives LSSmOrange Photoconversion

LSSmOrange is a fluorescent protein that exhibits slow photoconversion and is used as an imaging tool to highlight specific subpopulations of molecules. While photoconversion in LSSmOrange is known to involve Kolbe decarboxylation of the E215 side chain, its structural dynamics remain unexplored. We addressed the excited state dynamics of LSSmOrange by using serial femtosecond crystallography (SFX) with an X-ray free electron laser. SFX enabled us to determine the crystal structure of unconverted LSSmOrange without detectable X-ray damage, facilitating a femtosecond optical pump─X-ray probe experiment to track time-resolved structural changes. A decrease in electron density at E215 was observed 250 ps after strong pump laser illumination (mean fluence of 0.31 J/cm2), consistent with photoconversion by decarboxylation. Extrapolated structures suggested the appearance of an alternative E215 conformation in addition to illumination-induced decarboxylation. Since the photoinduced decarboxylation occurred despite the extremely low single-photon photoconversion quantum yield of LSSmOrange (8.5 × 10–6), we hypothesized that the photoconversion proceeds via a multiphoton process. Power titration using transient absorption spectroscopy revealed that photoconversion was linked to optical nonlinearity under a high pump laser energy. We propose that LSSmOrange photoconversion involves a higher-lying electronic excited state triggered by multiphoton absorption, as supported by quantum-chemical calculations. Photoconversion via a multiphoton process enables spatially confined highlighting on a microscope.

Authors

Institutions

Publication Details

Journal
ACS Physical Chemistry Au
Published
2026-04-12
DOI
https://doi.org/10.1021/acsphyschemau.6c00009
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
OCT
article

Decarboxylation via a Higher Electronic Excited State Drives LSSmOrange Photoconversion

Eriko Nango, Kunio Hirata, Tomoyuki Tanaka, Luc Van Meervelt et al.
ACS Physical Chemistry Au
Advanced Fluorescence Microscopy Techniques
article

Decarboxylation via a Higher Electronic Excited State Drives LSSmOrange Photoconversion

Eriko Nango, Kunio Hirata, Tomoyuki Tanaka, Luc Van Meervelt, Fangjia Luo, Kazuya Hasegawa, Hiroki Noguchi, Neil R. McFarlane, Jacques‐Philippe Colletier, Eduard Fron, Jeremy Noel Harvey, Kensuke Tono, Rie Tanaka, Nipawan Nuemket, Martin H. Weik, Hideaki Mizuno, Tetsunari Kimura, Thi Yen Hang Bui, Elke De Zitter, Tsuyoshi Araya, Janko Čivić, Toshi Arima, So Iwata, Leonie De Vrieze, Savannah Van Bel, Michiel Postelmans, Shigeki Owada, Hyang Sook Seol
article en

Abstract

LSSmOrange is a fluorescent protein that exhibits slow photoconversion and is used as an imaging tool to highlight specific subpopulations of molecules. While photoconversion in LSSmOrange is known to involve Kolbe decarboxylation of the E215 side chain, its structural dynamics remain unexplored. We addressed the excited state dynamics of LSSmOrange by using serial femtosecond crystallography (SFX) with an X-ray free electron laser. SFX enabled us to determine the crystal structure of unconverted LSSmOrange without detectable X-ray damage, facilitating a femtosecond optical pump─X-ray probe experiment to track time-resolved structural changes. A decrease in electron density at E215 was observed 250 ps after strong pump laser illumination (mean fluence of 0.31 J/cm2), consistent with photoconversion by decarboxylation. Extrapolated structures suggested the appearance of an alternative E215 conformation in addition to illumination-induced decarboxylation. Since the photoinduced decarboxylation occurred despite the extremely low single-photon photoconversion quantum yield of LSSmOrange (8.5 × 10–6), we hypothesized that the photoconversion proceeds via a multiphoton process. Power titration using transient absorption spectroscopy revealed that photoconversion was linked to optical nonlinearity under a high pump laser energy. We propose that LSSmOrange photoconversion involves a higher-lying electronic excited state triggered by multiphoton absorption, as supported by quantum-chemical calculations. Photoconversion via a multiphoton process enables spatially confined highlighting on a microscope.

ACS Physical Chemistry Au
Centre National de la Recherche Scientifique (FR), Tohoku University (JP), Kyoto University (JP), Commissariat à l'Énergie Atomique et aux Énergies Alternatives (FR), CEA Grenoble (FR), SPring-8 (JP), Japan Synchrotron Radiation Research Institute (JP), Institut de Biologie Structurale (FR), Kobe University (JP), Université Grenoble Alpes (FR), KU Leuven (BE)
Japan Agency for Medical Research and Development, Fonds Wetenschappelijk Onderzoek, KU Leuven, Japan Society for the Promotion of Science
Openalex Percentile: Top 18%
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.