» Articles » PMID: 27869189

Species-Specific Standard Redox Potential of Thiol-Disulfide Systems: A Key Parameter to Develop Agents Against Oxidative Stress

Overview
Journal Sci Rep
Specialty Science
Date 2016 Nov 22
PMID 27869189
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

Microscopic standard redox potential, a new physico-chemical parameter was introduced and determined to quantify thiol-disulfide equilibria of biological significance. The highly composite, codependent acid-base and redox equilibria of thiols could so far be converted into pH-dependent, apparent redox potentials (E'°) only. Since the formation of stable metal-thiolate complexes precludes the direct thiol-disulfide redox potential measurements by usual electrochemical techniques, an indirect method had to be elaborated. In this work, the species-specific, pH-independent standard redox potentials of glutathione were determined primarily by comparing it to 1-methylnicotinamide, the simplest NAD analogue. Secondarily, the species-specific standard redox potentials of the two-electron redox transitions of cysteamine, cysteine, homocysteine, penicillamine, and ovothiol were determined using their microscopic redox equilibrium constants with glutathione. The 30 different, microscopic standard redox potential values show close correlation with the respective thiolate basicities and provide sound means for the development of potent agents against oxidative stress.

Citing Articles

Sub-organellar mitochondrial hydrogen peroxide observed using a SNAP tag targeted coumarin-based fluorescent reporter.

Eaglesfield R, Fernandez-Vizarra E, Lacko E, Caldwell S, Sloan N, Siciarz D Redox Biol. 2025; 80:103502.

PMID: 39864323 PMC: 11802384. DOI: 10.1016/j.redox.2025.103502.


Prediction of Antioxidant Capacity of Thiolate-Disulfide Systems Using Species-Specific Basicity Values.

Palla T, Noszal B, Mirzahosseini A Antioxidants (Basel). 2024; 13(9).

PMID: 39334712 PMC: 11428801. DOI: 10.3390/antiox13091053.


Simple and Cost-Effective Quantum Dot Chemodosimeter for Visual Detection of Biothiols in Human Blood Serum.

Ramachandran Nair V, Sandeep K, Shanthil M, Dhanya S, Archana A, Vibin M ACS Omega. 2024; 9(6):6588-6594.

PMID: 38371793 PMC: 10870302. DOI: 10.1021/acsomega.3c07518.


Properties of Selenolate-Diselenide Redox Equilibria in View of Their Thiolate-Disulfide Counterparts.

Palla T, Mirzahosseini A, Noszal B Antioxidants (Basel). 2023; 12(4).

PMID: 37107197 PMC: 10134987. DOI: 10.3390/antiox12040822.


Close correlation between thiolate basicity and certain NMR parameters in cysteine and cystine microspecies.

Ferreira de Santana J, Mirzahosseini A, Mandity B, Bogdan D, Mandity I, Noszal B PLoS One. 2022; 17(3):e0264866.

PMID: 35275940 PMC: 8916652. DOI: 10.1371/journal.pone.0264866.


References
1.
Inoue T, Kirchhoff J . Electrochemical detection of thiols with a coenzyme pyrroloquinoline quinone modified electrode. Anal Chem. 2000; 72(23):5755-60. DOI: 10.1021/ac000716c. View

2.
Szakacs Z, Kraszni M, Noszal B . Determination of microscopic acid-base parameters from NMR-pH titrations. Anal Bioanal Chem. 2004; 378(6):1428-48. DOI: 10.1007/s00216-003-2390-3. View

3.
Kosower N, Kosower E . The glutathione status of cells. Int Rev Cytol. 1978; 54:109-60. DOI: 10.1016/s0074-7696(08)60166-7. View

4.
Orgovan G, Noszal B . Electrodeless, accurate pH determination in highly basic media using a new set of (1)H NMR pH indicators. J Pharm Biomed Anal. 2010; 54(5):958-64. DOI: 10.1016/j.jpba.2010.11.022. View

5.
Mirzahosseini A, Noszal B . The species- and site-specific acid-base properties of biological thiols and their homodisulfides. J Pharm Biomed Anal. 2014; 95:184-92. DOI: 10.1016/j.jpba.2014.02.023. View