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Radical Formation in the Gas‐Phase Ozonolysis of Deprotonated Cysteine
Author(s) -
Khairallah George N.,
Maccarone Alan T.,
Pham Huong T.,
Benton Timothy M.,
Ly Tony,
da Silva Gabriel,
Blanksby Stephen J.,
O'Hair Richard A. J.
Publication year - 2015
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.201506019
Subject(s) - chemistry , ozonolysis , deprotonation , radical , cysteine , reactivity (psychology) , photochemistry , thiol , organic chemistry , medicine , ion , alternative medicine , pathology , enzyme
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.

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