We review signaling by reactive oxygen species, which is emerging as a major physiological process. However, among the reactive oxygen species, H2O2 best fulfills the requirements of being a second messenger. Its enzymatic production and degradation, along with the requirements for the oxidation of thiols by H2O2, provide the specificity for time and place that are required in signaling. Both thermodynamic and kinetic considerations suggest that among possible oxidation states of cysteine, formation of sulfenic acid derivatives or disulfides call be relevant as thiol redox switches in signaling. In this Work, the general constraints that are required for protein thiol oxidation by H2O2 to be fast enough to be relevant for signaling are discussed ill light of the mechanism of oxidation of the catalytic cysteine or selenceysteine in thiol peroxidases. While the nonenzymatle reaction between thiol and H2O2 is, in most cases, too slow to be relevant in signaling, the enzymatic catalysis of thiol oxidation by these peroxidases provides a potential mechanism for redox signaling.
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Oklahoma Med Res Fdn, Free Rad Biol & Aging Res Program, Oklahoma City, OK 73104 USAOklahoma Med Res Fdn, Free Rad Biol & Aging Res Program, Oklahoma City, OK 73104 USA
Hensley, K
Robinson, KA
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Oklahoma Med Res Fdn, Free Rad Biol & Aging Res Program, Oklahoma City, OK 73104 USAOklahoma Med Res Fdn, Free Rad Biol & Aging Res Program, Oklahoma City, OK 73104 USA
Robinson, KA
Gabbita, SP
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Oklahoma Med Res Fdn, Free Rad Biol & Aging Res Program, Oklahoma City, OK 73104 USAOklahoma Med Res Fdn, Free Rad Biol & Aging Res Program, Oklahoma City, OK 73104 USA
Gabbita, SP
Salsman, S
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Oklahoma Med Res Fdn, Free Rad Biol & Aging Res Program, Oklahoma City, OK 73104 USAOklahoma Med Res Fdn, Free Rad Biol & Aging Res Program, Oklahoma City, OK 73104 USA
Salsman, S
Floyd, RA
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Oklahoma Med Res Fdn, Free Rad Biol & Aging Res Program, Oklahoma City, OK 73104 USAOklahoma Med Res Fdn, Free Rad Biol & Aging Res Program, Oklahoma City, OK 73104 USA
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Kanazawa Univ, Grad Sch Med Sci, Dept Dis Control & Homeostasis, Ishikawa, Japan
Kanazawa Univ, Grad Sch Nat Sci Technol, Div Mat Engn, Kanazawa, Ishikawa 9201192, JapanKanazawa Univ, Grad Sch Med Sci, Dept Dis Control & Homeostasis, Ishikawa, Japan
Iwakami, Satoshi
Misu, Hirofumi
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Kanazawa Univ, Grad Sch Med Sci, Dept Dis Control & Homeostasis, Ishikawa, JapanKanazawa Univ, Grad Sch Med Sci, Dept Dis Control & Homeostasis, Ishikawa, Japan
Misu, Hirofumi
Sugimori, Makoto
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Kanazawa Univ, Grad Sch Med Sci, Dept Dis Control & Homeostasis, Ishikawa, JapanKanazawa Univ, Grad Sch Med Sci, Dept Dis Control & Homeostasis, Ishikawa, Japan
Sugimori, Makoto
Matsugo, Seiichi
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Kanazawa Univ, Sch Nat Syst Bioengn Course, Coll Sci & Engn, Kanazawa, Ishikawa 9201192, JapanKanazawa Univ, Grad Sch Med Sci, Dept Dis Control & Homeostasis, Ishikawa, Japan
Matsugo, Seiichi
Kaneko, Shuichi
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Kanazawa Univ, Grad Sch Med Sci, Dept Dis Control & Homeostasis, Ishikawa, JapanKanazawa Univ, Grad Sch Med Sci, Dept Dis Control & Homeostasis, Ishikawa, Japan
Kaneko, Shuichi
Takamura, Toshinari
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Kanazawa Univ, Grad Sch Med Sci, Dept Dis Control & Homeostasis, Ishikawa, JapanKanazawa Univ, Grad Sch Med Sci, Dept Dis Control & Homeostasis, Ishikawa, Japan
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Dept Med, Div Pulm & Crit Care Med, Chicago, IL USA
Northwestern Univ, Dept Cell & Mol Biol, Sch Med, Chicago, IL 60611 USADept Med, Div Pulm & Crit Care Med, Chicago, IL USA
Hamanaka, Robert B.
Chandel, Navdeep S.
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Dept Med, Div Pulm & Crit Care Med, Chicago, IL USA
Northwestern Univ, Dept Cell & Mol Biol, Sch Med, Chicago, IL 60611 USADept Med, Div Pulm & Crit Care Med, Chicago, IL USA
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Univ Michigan, Sch Med, Div Pulm & Crit Care Med, Dept Internal Med, Ann Arbor, MI 48109 USAUniv Michigan, Sch Med, Div Pulm & Crit Care Med, Dept Internal Med, Ann Arbor, MI 48109 USA