Quantification of cellular protein and redox imbalance using SILAC-iodoTMT methodology
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
31154163
PubMed Central
PMC6545335
DOI
10.1016/j.redox.2019.101227
PII: S2213-2317(19)30131-4
Knihovny.cz E-zdroje
- Klíčová slova
- Cysteine, Liquid chromatography/mass spectrometry, Peroxiredoxin, Proteome, Redoxome, SILAC-iodoTMT labeling,
- MeSH
- chromatografie kapalinová MeSH
- cystein metabolismus MeSH
- oxidace-redukce * MeSH
- oxidační stres MeSH
- peroxid vodíku metabolismus MeSH
- peroxiredoxiny metabolismus MeSH
- proteom * MeSH
- proteomika * metody MeSH
- tandemová hmotnostní spektrometrie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- cystein MeSH
- peroxid vodíku MeSH
- peroxiredoxiny MeSH
- proteom * MeSH
Under normal conditions, the cellular redox status is maintained in a steady state by reduction and oxidation processes. These redox alterations in the cell are mainly sensed by protein thiol residues of cysteines thus regulating protein function. The imbalance in redox homeostasis may therefore regulate protein turnover either directly by redox modulating of transcription factors or indirectly by the degradation of damaged proteins due to oxidation. A new analytical method capable of simultaneously assessing cellular protein expression and cysteine oxidation would provide a valuable tool for the field of cysteine-targeted biology. Here, we show a workflow based on protein quantification using metabolic labeling and determination of cysteine oxidation using reporter ion quantification. We applied this approach to determine protein and redox changes in cells after 5-min, 60-min and 32-h exposure to H2O2, respectively. Based on the functional analysis of our data, we confirmed a biological relevance of this approach and its applicability for parallel mapping of cellular proteomes and redoxomes under diverse conditions. In addition, we revealed a specific pattern of redox changes in peroxiredoxins in a short time-interval cell exposure to H2O2. Overall, our present study offers an innovative, versatile experimental approach to the multifaceted assessment of cellular proteome and its redox status, with broad implications for biomedical research towards a better understanding of organismal physiology and diverse disease conditions.
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