Cold physical plasma-induced oxidation of cysteine yields reactive sulfur species (RSS)

dc.bibliographicCitation.firstPage100083eng
dc.bibliographicCitation.volume14eng
dc.contributor.authorBruno, Giuliana
dc.contributor.authorHeusler, Thea
dc.contributor.authorLackmann, Jan-Wilm
dc.contributor.authorWoedtke, Thomas von
dc.contributor.authorWeltmann, Klaus-Dieter
dc.contributor.authorWende, Kristian
dc.date.accessioned2021-10-19T09:01:10Z
dc.date.available2021-10-19T09:01:10Z
dc.date.issued2019
dc.description.abstractPurpose: Studying plasma liquid chemistry can reveal insights into their biomedical effects, i.e. to understand the direct and indirect processes triggered by the treatment in a model or clinical application. Due to the reactivity of the sulfur atom, thiols are potential targets for plasma- derived reactive species. Being crucial for protein function and redox signaling pathways, their controllable modification would allow expanding the application range. Additionally, models to control and standardize CAP sources are desired tools for plasma source design. Methods: Cysteine, a ubiquitous amino acid, was used as a tracer compound to scavenge the reactive species produced by an argon plasma jet (kINPen). The resulting product pattern was identified via high-resolution mass spectrometry. The Ellman´s assay was used to screen CAP derived thiol consumption, and long-lived species deposition (hydrogen peroxide, nitrite, nitrate) was monitored in relation to the presence of cysteine. Results: The intensity of cysteine oxidation increased with treatment time and availability of oxygen in the feed gas. A range of products from cysteine was identified, in part indicative for certain treatment conditions. Several non-stable products occur transiently during the plasma treatment. Bioactive reactive sulfur species (RSS) have been found for mild treatment conditions, such as cysteine sulfoxides and cysteine-S-sulfonate. Considering the number of cysteine molecules in the boundary layer and the achieved oxidation state, short-lived species dominate in cysteine conversion. In addition, a boundary layer depletion of the tracer was observed. Conclusion: Translating these data into the in-vivo application, strong direct oxidation of protein thiol groups with subsequent changes in protein biochemistry must be considered. Plasma-derived RSS may in part contribute to the observed biomedical effects of CAP. Care must be taken to control the discharge parameter tightly as chemical dynamics at or in the liquid are subject to change easily. © 2019eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/7039
dc.identifier.urihttps://doi.org/10.34657/6086
dc.language.isoengeng
dc.publisherAmsterdam [u.a.] : Elseviereng
dc.relation.doihttps://doi.org/10.1016/j.cpme.2019.100083
dc.relation.essn2212-8166
dc.relation.ispartofseriesClinical Plasma Medicine 14 (2019)eng
dc.rights.licenseCC BY-NC-ND 4.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/eng
dc.subjectCAPeng
dc.subjectCold physical plasmaeng
dc.subjectPlasma liquid chemistryeng
dc.subjectReactive sulfur specieseng
dc.subjectRedox signalingeng
dc.subject.ddc610eng
dc.titleCold physical plasma-induced oxidation of cysteine yields reactive sulfur species (RSS)eng
dc.typearticleeng
dc.typeTexteng
dcterms.bibliographicCitation.journalTitleClinical Plasma Medicineeng
tib.accessRightsopenAccesseng
wgl.contributorINPeng
wgl.subjectMedizin, Gesundheiteng
wgl.typeZeitschriftenartikeleng
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