UV photochemistry of the L-cystine disulfide bridge in aqueous solution investigated by femtosecond X-ray absorption spectroscopy

Miguel Ochmann, Jessica Harich, Rory Ma, Antonia Freibert (), Yujin Kim, Madhusudana Gopannagari, Da Hye Hong, Daewoong Nam, Sangsoo Kim, Minseok Kim, Intae Eom, Jae Hyuk Lee, Briony A. Yorke, Tae Kyu Kim () and Nils Huse ()
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Miguel Ochmann: University of Hamburg and Center for Free-Electron Laser Science
Jessica Harich: University of Hamburg and Center for Free-Electron Laser Science
Rory Ma: POSTECH
Antonia Freibert: University of Hamburg and Center for Free-Electron Laser Science
Yujin Kim: POSTECH
Madhusudana Gopannagari: Korea Advanced Institute of Science and Technology (KAIST)
Da Hye Hong: Korea Advanced Institute of Science and Technology (KAIST)
Daewoong Nam: POSTECH
Sangsoo Kim: POSTECH
Minseok Kim: POSTECH
Intae Eom: POSTECH
Jae Hyuk Lee: POSTECH
Briony A. Yorke: University of Leeds
Tae Kyu Kim: Korea Advanced Institute of Science and Technology (KAIST)
Nils Huse: University of Hamburg and Center for Free-Electron Laser Science

Nature Communications, 2024, vol. 15, issue 1, 1-8

Abstract: Abstract The photolysis of disulfide bonds is implicated in denaturation of proteins exposed to ultraviolet light. Despite this biological relevance in stabilizing the structure of many proteins, the mechanisms of disulfide photolysis are still contested after decades of research. Herein, we report new insight into the photochemistry of L-cystine in aqueous solution by femtosecond X-ray absorption spectroscopy at the sulfur K-edge. We observe homolytic bond cleavage upon ultraviolet irradiation and the formation of thiyl radicals as the single primary photoproduct. Ultrafast thiyl decay due to geminate recombination proceeds at a quantum yield of >80 % within 20 ps. These dynamics coincide with the emergence of a secondary product, attributed to the generation of perthiyl radicals. From these findings, we suggest a mechanism of perthiyl radical generation from a vibrationally excited parent molecule that asymmetrically fragments along a carbon-sulfur bond. Our results point toward a dynamic photostability of the disulfide bridge in condensed-phase.

Date: 2024
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DOI: 10.1038/s41467-024-52748-x

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