Biological Mechanisms of <i>S</i>-Nitrosothiol Formation and Degradation: How Is Specificity of <i>S</i>-Nitrosylation Achieved?

The modification of protein cysteine residues underlies some of the diverse biological functions of nitric oxide (NO) in physiology and disease. The formation of stable nitrosothiols occurs under biologically relevant conditions and time scales. However, the factors that determine the selective natu...

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Main Authors: Christopher M. Massa, Ziping Liu, Sheryse Taylor, Ashley P. Pettit, Marena N. Stakheyeva, Elena Korotkova, Valentina Popova, Elena N. Atochina-Vasserman, Andrew J. Gow
Format: Article
Language:English
Published: MDPI AG 2021-07-01
Series:Antioxidants
Subjects:
Online Access:https://www.mdpi.com/2076-3921/10/7/1111
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spelling doaj-aa1a2739dc5c4f30b08c5b13215336092021-07-23T13:28:48ZengMDPI AGAntioxidants2076-39212021-07-01101111111110.3390/antiox10071111Biological Mechanisms of <i>S</i>-Nitrosothiol Formation and Degradation: How Is Specificity of <i>S</i>-Nitrosylation Achieved?Christopher M. Massa0Ziping Liu1Sheryse Taylor2Ashley P. Pettit3Marena N. Stakheyeva4Elena Korotkova5Valentina Popova6Elena N. Atochina-Vasserman7Andrew J. Gow8Department of Pharmacology & Toxicology, Ernest Mario School of Pharmacy, Rutgers University, Piscataway, NJ 08848, USADepartment of Pharmacology & Toxicology, Ernest Mario School of Pharmacy, Rutgers University, Piscataway, NJ 08848, USADepartment of Pharmacology & Toxicology, Ernest Mario School of Pharmacy, Rutgers University, Piscataway, NJ 08848, USADepartment of Pharmacology & Toxicology, Ernest Mario School of Pharmacy, Rutgers University, Piscataway, NJ 08848, USARASA Center in Tomsk, Tomsk Polytechnic University, 634050 Tomsk, RussiaInstitute of Natural Resources, Tomsk Polytechnic University, Lenin Av. 30, 634050 Tomsk, RussiaInstitute of Natural Resources, Tomsk Polytechnic University, Lenin Av. 30, 634050 Tomsk, RussiaRASA Center in Tomsk, Tomsk Polytechnic University, 634050 Tomsk, RussiaDepartment of Pharmacology & Toxicology, Ernest Mario School of Pharmacy, Rutgers University, Piscataway, NJ 08848, USAThe modification of protein cysteine residues underlies some of the diverse biological functions of nitric oxide (NO) in physiology and disease. The formation of stable nitrosothiols occurs under biologically relevant conditions and time scales. However, the factors that determine the selective nature of this modification remain poorly understood, making it difficult to predict thiol targets and thus construct informatics networks. In this review, the biological chemistry of NO will be considered within the context of nitrosothiol formation and degradation whilst considering how specificity is achieved in this important post-translational modification. Since nitrosothiol formation requires a formal one-electron oxidation, a classification of reaction mechanisms is proposed regarding which species undergoes electron abstraction: NO, thiol or S-NO radical intermediate. Relevant kinetic, thermodynamic and mechanistic considerations will be examined and the impact of sources of NO and the chemical nature of potential reaction targets is also discussed.https://www.mdpi.com/2076-3921/10/7/1111nitrosothiolnitric oxidecysteinepost-translational modificationthiol
collection DOAJ
language English
format Article
sources DOAJ
author Christopher M. Massa
Ziping Liu
Sheryse Taylor
Ashley P. Pettit
Marena N. Stakheyeva
Elena Korotkova
Valentina Popova
Elena N. Atochina-Vasserman
Andrew J. Gow
spellingShingle Christopher M. Massa
Ziping Liu
Sheryse Taylor
Ashley P. Pettit
Marena N. Stakheyeva
Elena Korotkova
Valentina Popova
Elena N. Atochina-Vasserman
Andrew J. Gow
Biological Mechanisms of <i>S</i>-Nitrosothiol Formation and Degradation: How Is Specificity of <i>S</i>-Nitrosylation Achieved?
Antioxidants
nitrosothiol
nitric oxide
cysteine
post-translational modification
thiol
author_facet Christopher M. Massa
Ziping Liu
Sheryse Taylor
Ashley P. Pettit
Marena N. Stakheyeva
Elena Korotkova
Valentina Popova
Elena N. Atochina-Vasserman
Andrew J. Gow
author_sort Christopher M. Massa
title Biological Mechanisms of <i>S</i>-Nitrosothiol Formation and Degradation: How Is Specificity of <i>S</i>-Nitrosylation Achieved?
title_short Biological Mechanisms of <i>S</i>-Nitrosothiol Formation and Degradation: How Is Specificity of <i>S</i>-Nitrosylation Achieved?
title_full Biological Mechanisms of <i>S</i>-Nitrosothiol Formation and Degradation: How Is Specificity of <i>S</i>-Nitrosylation Achieved?
title_fullStr Biological Mechanisms of <i>S</i>-Nitrosothiol Formation and Degradation: How Is Specificity of <i>S</i>-Nitrosylation Achieved?
title_full_unstemmed Biological Mechanisms of <i>S</i>-Nitrosothiol Formation and Degradation: How Is Specificity of <i>S</i>-Nitrosylation Achieved?
title_sort biological mechanisms of <i>s</i>-nitrosothiol formation and degradation: how is specificity of <i>s</i>-nitrosylation achieved?
publisher MDPI AG
series Antioxidants
issn 2076-3921
publishDate 2021-07-01
description The modification of protein cysteine residues underlies some of the diverse biological functions of nitric oxide (NO) in physiology and disease. The formation of stable nitrosothiols occurs under biologically relevant conditions and time scales. However, the factors that determine the selective nature of this modification remain poorly understood, making it difficult to predict thiol targets and thus construct informatics networks. In this review, the biological chemistry of NO will be considered within the context of nitrosothiol formation and degradation whilst considering how specificity is achieved in this important post-translational modification. Since nitrosothiol formation requires a formal one-electron oxidation, a classification of reaction mechanisms is proposed regarding which species undergoes electron abstraction: NO, thiol or S-NO radical intermediate. Relevant kinetic, thermodynamic and mechanistic considerations will be examined and the impact of sources of NO and the chemical nature of potential reaction targets is also discussed.
topic nitrosothiol
nitric oxide
cysteine
post-translational modification
thiol
url https://www.mdpi.com/2076-3921/10/7/1111
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