TY - JOUR
T1 - Reaction rates of glutathione and ascorbate with alkyl radicals are too slow for protection against protein peroxidation in vivo
AU - Nauser, Thomas
AU - Gebicki, Janusz M.
PY - 2017/11/1
Y1 - 2017/11/1
N2 - Reaction kinetics of amino acid and peptide alkyl radicals with GSH and ascorbate, the two most abundant endogenous antioxidants, were investigated by pulse radiolysis. Rate constants in the order of 106 M−1s−1 were found. Alkyl radicals react at almost diffusion controlled rates and irreversibly with oxygen to form peroxyl radicals, and competition with this reaction is the benchmark for efficient repair in vivo. We consider repair of protein radicals and assume comparable rate constants for the reactions of GSH/ascorbate with peptide alkyl radicals and with alkyl radicals on a protein surface. Given physiological concentrations of oxygen, GSH and ascorbate, protein peroxyl radicals will always be a major product of protein alkyl radicals in vivo. Therefore, if they are formed by oxidative stress, protein alkyl radicals are a probable cause for biological damage.
AB - Reaction kinetics of amino acid and peptide alkyl radicals with GSH and ascorbate, the two most abundant endogenous antioxidants, were investigated by pulse radiolysis. Rate constants in the order of 106 M−1s−1 were found. Alkyl radicals react at almost diffusion controlled rates and irreversibly with oxygen to form peroxyl radicals, and competition with this reaction is the benchmark for efficient repair in vivo. We consider repair of protein radicals and assume comparable rate constants for the reactions of GSH/ascorbate with peptide alkyl radicals and with alkyl radicals on a protein surface. Given physiological concentrations of oxygen, GSH and ascorbate, protein peroxyl radicals will always be a major product of protein alkyl radicals in vivo. Therefore, if they are formed by oxidative stress, protein alkyl radicals are a probable cause for biological damage.
UR - http://www.scopus.com/inward/record.url?scp=85029877788&partnerID=8YFLogxK
U2 - 10.1016/j.abb.2017.09.011
DO - 10.1016/j.abb.2017.09.011
M3 - Article
C2 - 28939102
AN - SCOPUS:85029877788
SN - 0003-9861
VL - 633
SP - 118
EP - 123
JO - Archives of Biochemistry and Biophysics
JF - Archives of Biochemistry and Biophysics
ER -