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Artykuł

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Tytuł

Sensitized photo-oxidation of plant cytokinin-specific binding protein - Does the environment of the thioether group influence the oxidation reaction? From primary intermediates to stable products

Autorzy

[ 1 ] Instytut Chemii Bioorganicznej Polskiej Akademii Nauk, Polska Akademia Nauk | [ P ] pracownik

Dyscyplina naukowa (Ustawa 2.0)

[7.5] Nauki biologiczne
[7.6] Nauki chemiczne

Rok publikacji

2021

Opublikowano w

Free Radical Biology and Medicine

Rocznik: 2021 | Tom: 165

Typ artykułu

artykuł naukowy

Język publikacji

angielski

Słowa kluczowe
EN
Streszczenie

EN The reactions of protein oxidation play a significant role in many biological processes, especially in diseases development. Therefore, it is important to understand, how the protein molecule behaves in the presence of oxidants. In the present work, photo-oxidation of phytohormone-binding plant protein (VrPhBP) was investigated using light and 3-carboxybenzophenone (3CB) as a sensitizer (one electron oxidant). The protein interacts with the sensitizer in the ground state forming a weak binding complex leading to the presence of bound and free 3CB in solution. The early events and transient species (such as radicals and radical ions) formed during irradiation were characterised by transient spectroscopy showing the formation of the sulphur radical cation Met>S center dot+ (stabilized by (SN)(+))and the tyrosyl radical TyrO(center dot) on VrPhBP. Thus the 3CB excited triplet state was quenched by the Met and Tyr residues and mostly by Met (based on the deconvoluted transient absorption spectra).The presence of a Tyr side chain in the vicinity of a Met residue results in intramolecular electron transfer from Tyr to the Met>S center dot+ radical cation, leading to regeneration of the thioether side chain and formation of TyrO(center dot). The presence of other side chains close to Met, such as Arg or Lys can induce the stabilization of Met>S center dot+ via the formation of two-centered three-electron bonded species (S therefore N)(+). The transient species were additionally confirmed by stable product analysis. Based on SDS-PAGE, chromatography and mass spectrometry, the formation of methionine sulphoxide and Met-3CB adduct was identified together with di-Tyr cross links. On the basis of the experimental results the overall mechanism of VrPhBP photo oxidation, from its early events to the formation of stable products, is described. In addition, a good correlation between the mechanisms of photooxidation of model compounds such as Met derivatives and peptides and those for real biological systems is emphasized.

Strony (od-do)

411 - 420

DOI

10.1016/j.freeradbiomed.2021.02.004

URL

https://doi.org/10.1016/j.freeradbiomed.2021.02.004

Typ licencji

CC BY-ND (uznanie autorstwa - bez utworów zależnych)

Wersja tekstu w otwartym dostępie

ostateczna wersja opublikowana

Data udostępnienia

02.2021

Czas udostępnienia publikacji w sposób otwarty

przed opublikowaniem

Punktacja Ministerstwa / czasopismo

140

Punktacja Ministerstwa / czasopismo w ewaluacji 2017-2021

140