TY - JOUR
T1 - Speciation of reactive sulfur species and their reactions with alkylating agents
T2 - do we have any clue about what is present inside the cell?
AU - Bogdándi, Virág
AU - Ida, Tomoaki
AU - Sutton, Thomas R.
AU - Bianco, Christopher
AU - Ditrói, Tamás
AU - Koster, Grielof
AU - Henthorn, Hillary A.
AU - Minnion, Magda
AU - Toscano, John P.
AU - van der Vliet, Albert
AU - Pluth, Michael D.
AU - Feelisch, Martin
AU - Fukuto, Jon M.
AU - Akaike, Takaaki
AU - Nagy, Péter
N1 - Funding Information:
Financial support from the National Research, Development and Innovation Office (grant nos. KH17_126766 and K 109843) and the National Institutes of Health (grant no. R21AG055022-01) for P.N. is acknowledged. P.N. was a János Bolyai Research Scholar of the Hungarian Academy of Sciences. Financial supports from the National Science Foundation (grant nos. CHE-1454747 and CHE-1566065) to M.D.P and J.P.T are also acknowledged. This work was supported in part by Grants-in-Aid for Scientific Research (25253020 and 16K15208 to T.A.) and a Grant-in-Aid for Scientific Research on Innovative Areas (26111008, 26111001 and 15K21759 to T.A.) from the Ministry of Education, Sciences, Sports and Technology (MEXT), Japan. Dojindo Molecular Technologies Inc. is greatly acknowledged for their kind support of chemical supplies.
Publisher Copyright:
© 2018 The British Pharmacological Society
PY - 2019/2
Y1 - 2019/2
N2 - . Background and Purpose: Posttranslational modifications of cysteine residues represent a major aspect of redox biology, and their reliable detection is key in providing mechanistic insights. The metastable character of these modifications and cell lysis-induced artifactual oxidation render current state-of-the-art protocols to rely on alkylation-based stabilization of labile cysteine derivatives before cell/tissue rupture. An untested assumption in these procedures is that for all cysteine derivatives, alkylation rates are faster than their dynamic interchange. However, when the interconversion of cysteine derivatives is not rate limiting, electrophilic labelling is under Curtin–Hammett control; hence, the final alkylated mixture may not represent the speciation that prevailed before alkylation. Experimental Approach: Buffered aqueous solutions of inorganic, organic, cysteine, GSH and GAPDH polysulfide species were used. Additional experiments in human plasma and serum revealed that monobromobimane can extract sulfide from the endogenous sulfur pool by shifting speciation equilibria, suggesting caution should be exercised when interpreting experimental results using this tool. Key Results: In the majority of cases, the speciation of alkylated polysulfide/thiol derivatives depended on the experimental conditions. Alkylation perturbed sulfur speciation in both a concentration- and time-dependent manner and strong alkylating agents cleaved polysulfur chains. Moreover, the labelling of sulfenic acids with dimedone also affected cysteine speciation, suggesting that part of the endogenous pool of products previously believed to represent sulfenic acid species may represent polysulfides. Conclusions and Implications: We highlight methodological caveats potentially arising from these pitfalls and conclude that current derivatization strategies often fail to adequately capture physiological speciation of sulfur species. Linked Articles: This article is part of a themed section on Chemical Biology of Reactive Sulfur Species. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v176.4/issuetoc.
AB - . Background and Purpose: Posttranslational modifications of cysteine residues represent a major aspect of redox biology, and their reliable detection is key in providing mechanistic insights. The metastable character of these modifications and cell lysis-induced artifactual oxidation render current state-of-the-art protocols to rely on alkylation-based stabilization of labile cysteine derivatives before cell/tissue rupture. An untested assumption in these procedures is that for all cysteine derivatives, alkylation rates are faster than their dynamic interchange. However, when the interconversion of cysteine derivatives is not rate limiting, electrophilic labelling is under Curtin–Hammett control; hence, the final alkylated mixture may not represent the speciation that prevailed before alkylation. Experimental Approach: Buffered aqueous solutions of inorganic, organic, cysteine, GSH and GAPDH polysulfide species were used. Additional experiments in human plasma and serum revealed that monobromobimane can extract sulfide from the endogenous sulfur pool by shifting speciation equilibria, suggesting caution should be exercised when interpreting experimental results using this tool. Key Results: In the majority of cases, the speciation of alkylated polysulfide/thiol derivatives depended on the experimental conditions. Alkylation perturbed sulfur speciation in both a concentration- and time-dependent manner and strong alkylating agents cleaved polysulfur chains. Moreover, the labelling of sulfenic acids with dimedone also affected cysteine speciation, suggesting that part of the endogenous pool of products previously believed to represent sulfenic acid species may represent polysulfides. Conclusions and Implications: We highlight methodological caveats potentially arising from these pitfalls and conclude that current derivatization strategies often fail to adequately capture physiological speciation of sulfur species. Linked Articles: This article is part of a themed section on Chemical Biology of Reactive Sulfur Species. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v176.4/issuetoc.
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U2 - 10.1111/bph.14394
DO - 10.1111/bph.14394
M3 - Article
C2 - 29909607
AN - SCOPUS:85053206329
SN - 0007-1188
VL - 176
SP - 646
EP - 670
JO - British Journal of Pharmacology
JF - British Journal of Pharmacology
IS - 4
ER -