Literature DB >> 26480331

Radical Formation in the Gas-Phase Ozonolysis of Deprotonated Cysteine.

George N Khairallah1,2, Alan T Maccarone3, Huong T Pham3, Timothy M Benton1,2, Tony Ly3, Gabriel da Silva4, Stephen J Blanksby5,2, Richard A J O'Hair6,7.   

Abstract

Although the deleterious effects of ozone on the human respiratory system are well-known, many of the precise chemical mechanisms that both cause damage and afford protection in the pulmonary epithelial lining fluid are poorly understood. As a key first step to elucidating the intrinsic reactivity of ozone with proteins, its reactions with deprotonated cysteine [Cys-H](-) are examined in the gas phase. Reaction proceeds at near the collision limit to give a rich set of products including 1) sequential oxygen atom abstraction reactions to yield cysteine sulfenate, sulfinate and sulfonate anions, and significantly 2) sulfenate radical anions formed by ejection of a hydroperoxy radical. The free-radical pathway occurs only when both thiol and carboxylate moieties are available, implicating electron-transfer as a key step in this reaction. This novel and facile reaction is also observed in small cys-containing peptides indicating a possible role for this chemistry in protein ozonolysis.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Keywords:  cysteine; gas-phase reactions; mass spectrometry; ozone; radicals

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Year:  2015        PMID: 26480331     DOI: 10.1002/anie.201506019

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  1 in total

1.  Two-step reaction mechanism reveals new antioxidant capability of cysteine disulfides against hydroxyl radical attack.

Authors:  Sarju Adhikari; Ramon Crehuet; Josep M Anglada; Joseph S Francisco; Yu Xia
Journal:  Proc Natl Acad Sci U S A       Date:  2020-07-17       Impact factor: 11.205

  1 in total

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