Unifying Perspective of the Ultrafast ...
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Article dans une revue scientifique: Article original
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Title :
Unifying Perspective of the Ultrafast Photodynamics of Orange Carotenoid Proteins from <i>Synechocystis</i>: Peril of High-Power Excitation, Existence of Different S* States, and Influence of Tagging.
Author(s) :
Niziński, Stanislaw [Auteur]
Uniwersytet im. Adama Mickiewicza w Poznaniu = Adam Mickiewicz University in Poznań [UAM]
Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement - UMR 8516 [LASIRE]
Wilson, Adjéle [Auteur]
Institut de Biologie Intégrative de la Cellule [I2BC]
Uriarte, Lucas M. [Auteur]
Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement - UMR 8516 [LASIRE]
Ruckebusch, Cyril [Auteur]
Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement (LASIRE) - UMR 8516
Andreeva, Elena A. [Auteur]
Institut de biologie structurale [IBS - UMR 5075]
Schlichting, I. [Auteur]
Colletier, Jacques-Philippe [Auteur]
Institut de biologie structurale [IBS - UMR 5075]
Kirilovsky, Diana [Auteur]
Institut de Biologie Intégrative de la Cellule [I2BC]
Burdzinski, G. [Auteur]
Sliwa, Michel [Auteur]
Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement (LASIRE) - UMR 8516
Uniwersytet im. Adama Mickiewicza w Poznaniu = Adam Mickiewicz University in Poznań [UAM]
Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement - UMR 8516 [LASIRE]
Wilson, Adjéle [Auteur]
Institut de Biologie Intégrative de la Cellule [I2BC]
Uriarte, Lucas M. [Auteur]
Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement - UMR 8516 [LASIRE]
Ruckebusch, Cyril [Auteur]

Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement (LASIRE) - UMR 8516
Andreeva, Elena A. [Auteur]
Institut de biologie structurale [IBS - UMR 5075]
Schlichting, I. [Auteur]
Colletier, Jacques-Philippe [Auteur]
Institut de biologie structurale [IBS - UMR 5075]
Kirilovsky, Diana [Auteur]
Institut de Biologie Intégrative de la Cellule [I2BC]
Burdzinski, G. [Auteur]
Sliwa, Michel [Auteur]

Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement (LASIRE) - UMR 8516
Journal title :
JACS Au
Abbreviated title :
JACS Au
Volume number :
2
Pages :
1084-1095
Publication date :
2022-06-03
ISSN :
2691-3704
English keyword(s) :
orange carotenoid protein
photodynamics
ultrafast spectroscopy
multiphoton absorption
cation radical
echinenone
quantum yield
His-tag
photodynamics
ultrafast spectroscopy
multiphoton absorption
cation radical
echinenone
quantum yield
His-tag
HAL domain(s) :
Sciences du Vivant [q-bio]/Biochimie, Biologie Moléculaire/Biologie structurale [q-bio.BM]
English abstract : [en]
A substantial number of Orange Carotenoid Protein (OCP) studies have aimed to describe the evolution of singlet excited states leading to the formation of a photoactivated form, OCPR. The most recent one suggests that 3 ...
Show more >A substantial number of Orange Carotenoid Protein (OCP) studies have aimed to describe the evolution of singlet excited states leading to the formation of a photoactivated form, OCPR. The most recent one suggests that 3 ps-lived excited states are formed after the sub-100 fs decay of the initial S2 state. The S* state, which has the longest reported lifetime of a few to tens of picoseconds, is considered to be the precursor of the first red photoproduct P1. Here, we report the ultrafast photodynamics of the OCP from Synechocystis PCC 6803 carried out using visible–near infrared femtosecond time-resolved absorption spectroscopy as a function of the excitation pulse power and wavelength. We found that a carotenoid radical cation can form even at relatively low excitation power, obscuring the determination of photoactivation yields for P1. Moreover, the comparison of green (540 nm) and blue (470 nm) excitations revealed the existence of an hitherto uncharacterized excited state, denoted as S∼, living a few tens of picoseconds and formed only upon 470 nm excitation. Because neither the P1 quantum yield nor the photoactivation speed over hundreds of seconds vary under green and blue continuous irradiation, this S∼ species is unlikely to be involved in the photoactivation mechanism leading to OCPR. We also addressed the effect of His-tagging at the N- or C-termini on the excited-state photophysical properties. Differences in spectral signatures and lifetimes of the different excited states were observed at a variance with the usual assumption that His-tagging hardly influences protein dynamics and function. Altogether our results advocate for the careful consideration of the excitation power and His-tag position when comparing the photoactivation of different OCP variants and beg to revisit the notion that S* is the precursor of photoactivated OCPR.Show less >
Show more >A substantial number of Orange Carotenoid Protein (OCP) studies have aimed to describe the evolution of singlet excited states leading to the formation of a photoactivated form, OCPR. The most recent one suggests that 3 ps-lived excited states are formed after the sub-100 fs decay of the initial S2 state. The S* state, which has the longest reported lifetime of a few to tens of picoseconds, is considered to be the precursor of the first red photoproduct P1. Here, we report the ultrafast photodynamics of the OCP from Synechocystis PCC 6803 carried out using visible–near infrared femtosecond time-resolved absorption spectroscopy as a function of the excitation pulse power and wavelength. We found that a carotenoid radical cation can form even at relatively low excitation power, obscuring the determination of photoactivation yields for P1. Moreover, the comparison of green (540 nm) and blue (470 nm) excitations revealed the existence of an hitherto uncharacterized excited state, denoted as S∼, living a few tens of picoseconds and formed only upon 470 nm excitation. Because neither the P1 quantum yield nor the photoactivation speed over hundreds of seconds vary under green and blue continuous irradiation, this S∼ species is unlikely to be involved in the photoactivation mechanism leading to OCPR. We also addressed the effect of His-tagging at the N- or C-termini on the excited-state photophysical properties. Differences in spectral signatures and lifetimes of the different excited states were observed at a variance with the usual assumption that His-tagging hardly influences protein dynamics and function. Altogether our results advocate for the careful consideration of the excitation power and His-tag position when comparing the photoactivation of different OCP variants and beg to revisit the notion that S* is the precursor of photoactivated OCPR.Show less >
Language :
Anglais
Peer reviewed article :
Oui
Audience :
Internationale
Popular science :
Non
Administrative institution(s) :
Université de Lille
CNRS
CNRS
Collections :
Submission date :
2024-02-28T22:26:39Z
2024-03-19T09:37:28Z
2024-03-19T09:37:28Z
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