TY - JOUR
T1 - Chemical Biology of Reactive Sulfur Species
T2 - Hydrolysis-Driven Equilibrium of Polysulfides as a Determinant of Physiological Functions
AU - Sawa, Tomohiro
AU - Takata, Tsuyoshi
AU - Matsunaga, Tetsuro
AU - Ihara, Hideshi
AU - Motohashi, Hozumi
AU - Akaike, Takaaki
N1 - Funding Information:
This work was supported, in part, by Grants-in-Aid [for (S), (B), (C), Early-Career Scientists, Challenging Exploratory Research] from the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan, to Tetsuro Matsunaga (19K07554), Tsuyoshi Takata (20K15983), To-mohiro Sawa (21H02071), Hideshi Ihara (20K21256 and 21H02082), Hozumi Motohashi (20H04832), and Takaaki Akaike (18H05277 and 20K21496); the Japan Science and Technology Agency ( JST), CREST, Japan, to Takaaki Akaike ( JPMJCR2024); and the Japan Agency for Medical Research and Development (AMED), Japan, to Hozumi Motohashi ( JP21gm5010002).
Publisher Copyright:
© Tomohiro Sawa et al., 2022; Published by Mary Ann Liebert, Inc. 2022.
PY - 2022/2/1
Y1 - 2022/2/1
N2 - Significance: Polysulfide species (i.e., R-Sn-R′, n > 2; and R-Sn-H, n > 1) exist in many organisms. The highly nucleophilic nature of hydropersulfides and hydropolysulfides contributes to the potent antioxidant activities of polysulfide species that protect organisms against oxidative and electrophilic stresses. Recent Advances: Accumulating evidence suggests that organic polysulfides (R-Sn-R′) readily undergo alkaline hydrolysis, which results in formation of both nucleophilic hydrosulfide/polysulfide (R-Sn-1H) and electrophilic sulfenic acid (R′SOH) species. Polysulfides maintain a steady-state equilibrium that is driven by hydrolysis even in aqueous physiological milieus. This unique property makes polysulfide chemistry and biology more complex than previously believed. Critical Issues: The hydrolysis equilibrium of polysulfides shifts to the right when electrophiles are present. Strong electrophilic alkylating agents (e.g., monobromobimane) greatly enhance polysulfide hydrolysis, which leads to increased polysulfide degradation and artifactual formation of bis-S-bimane adducts in the absence of free hydrogen sulfide. The finding that hydroxyl group-containing substances such as tyrosine efficiently protected polysulfides from hydrolysis led to development of the new alkylating agent, N-iodoacetyl l-tyrosine methyl ester (TME-IAM). TME-IAM efficiently and specifically traps and stabilizes hydropolysulfides and protects polysulfide chains from hydrolysis, and, when used with mass spectrometry, TME-IAM allows speciation of the reactive sulfur metabolome. In addition, the polyethylene glycol-conjugated maleimide-labeling gel shift assay, which relies on unique hydrolysis equilibrium of polysulfides, will be a reliable technique for proteomics of polysulfide-containing proteins. Future Directions: Using precise methodologies to achieve a better understanding of the occurrence and metabolism of polysulfide species is necessary to gain insights into the undefined biology of polysulfide species. Antioxid. Redox Signal. 36, 327-336.
AB - Significance: Polysulfide species (i.e., R-Sn-R′, n > 2; and R-Sn-H, n > 1) exist in many organisms. The highly nucleophilic nature of hydropersulfides and hydropolysulfides contributes to the potent antioxidant activities of polysulfide species that protect organisms against oxidative and electrophilic stresses. Recent Advances: Accumulating evidence suggests that organic polysulfides (R-Sn-R′) readily undergo alkaline hydrolysis, which results in formation of both nucleophilic hydrosulfide/polysulfide (R-Sn-1H) and electrophilic sulfenic acid (R′SOH) species. Polysulfides maintain a steady-state equilibrium that is driven by hydrolysis even in aqueous physiological milieus. This unique property makes polysulfide chemistry and biology more complex than previously believed. Critical Issues: The hydrolysis equilibrium of polysulfides shifts to the right when electrophiles are present. Strong electrophilic alkylating agents (e.g., monobromobimane) greatly enhance polysulfide hydrolysis, which leads to increased polysulfide degradation and artifactual formation of bis-S-bimane adducts in the absence of free hydrogen sulfide. The finding that hydroxyl group-containing substances such as tyrosine efficiently protected polysulfides from hydrolysis led to development of the new alkylating agent, N-iodoacetyl l-tyrosine methyl ester (TME-IAM). TME-IAM efficiently and specifically traps and stabilizes hydropolysulfides and protects polysulfide chains from hydrolysis, and, when used with mass spectrometry, TME-IAM allows speciation of the reactive sulfur metabolome. In addition, the polyethylene glycol-conjugated maleimide-labeling gel shift assay, which relies on unique hydrolysis equilibrium of polysulfides, will be a reliable technique for proteomics of polysulfide-containing proteins. Future Directions: Using precise methodologies to achieve a better understanding of the occurrence and metabolism of polysulfide species is necessary to gain insights into the undefined biology of polysulfide species. Antioxid. Redox Signal. 36, 327-336.
KW - electrophile
KW - hydrolysis equilibrium
KW - nucleophile
KW - persulfide
KW - polysulfide
KW - reactive sulfur species
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U2 - 10.1089/ars.2021.0170
DO - 10.1089/ars.2021.0170
M3 - Review article
C2 - 34409860
AN - SCOPUS:85124435086
SN - 1523-0864
VL - 36
SP - 327
EP - 336
JO - Antioxidants and Redox Signaling
JF - Antioxidants and Redox Signaling
IS - 4-6
ER -