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Two-photon Absorption and Photoionization of a Bacterial Phytochrome.

Authors :
Do TN
Menendez D
Bizhga D
Stojković EA
Kennis JTM
Source :
Journal of molecular biology [J Mol Biol] 2024 Mar 01; Vol. 436 (5), pp. 168357. Date of Electronic Publication: 2023 Nov 07.
Publication Year :
2024

Abstract

Phytochromes constitute a family of photosensory proteins that are utilized by various organisms to regulate several physiological processes. Phytochromes bind a bilin pigment that switches its isomeric state upon absorption of red or far-red photons, resulting in protein conformational changes that are sensed by the organism. Previously, the ultrafast dynamics in bacterial phytochrome was resolved to atomic resolution by time-resolved serial femtosecond X-ray diffraction (TR-SFX), showing extensive changes in its molecular conformation at 1 picosecond delay time. However, the large excitation fluence of mJ/mm <superscript>2</superscript> used in TR-SFX questions the validity of the observed dynamics. In this work, we present an excitation-dependent ultrafast transient absorption study to test the response of a related bacterial phytochrome to excitation fluence. We observe excitation power-dependent sub-picosecond dynamics, assigned to the population of high-lying excited state S <subscript>n</subscript> through resonantly enhanced two-photon absorption, followed by rapid internal conversion to the low-lying S <subscript>1</subscript> state. Inspection of the long-lived spectrum under high fluence shows that in addition to the primary intermediate Lumi-R, spectroscopic signatures of solvated electrons and ionized chromophore radicals are observed. Supported by numerical modelling, we propose that under excitation fluences of tens of μJ/mm <superscript>2</superscript> and higher, bacterial phytochrome partly undergoes photoionization from the S <subscript>n</subscript> state in competition with internal conversion to the S <subscript>1</subscript> state in 300 fs. We suggest that the extensive structural changes of related, shorter bacterial phytochrome, lacking the PHY domain, resolved from TR-SFX may have been affected by the ionized species. We propose approaches to minimize the two-photon absorption process by tuning the excitation spectrum away from the S <subscript>1</subscript> absorption or using phytochromes exhibiting minimized or shifted S <subscript>1</subscript> absorption.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2023 The Author(s). Published by Elsevier Ltd.. All rights reserved.)

Details

Language :
English
ISSN :
1089-8638
Volume :
436
Issue :
5
Database :
MEDLINE
Journal :
Journal of molecular biology
Publication Type :
Academic Journal
Accession number :
37944794
Full Text :
https://doi.org/10.1016/j.jmb.2023.168357