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Formation of 2-nitrophenol from salicylaldehyde as a suitable test for low peroxynitrite fluxes

Formation of 2-nitrophenol from salicylaldehyde as a suitable test for low peroxynitrite fluxes

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Prüfsumme: MD5:b08d17f15c0624a4be5d506f16dcb81d

MIKHED, Yuliya, Kai BRUNS, Stefan SCHILDKNECHT, Michael JÖRG, Mobin DIB, Matthias OELZE, Karl J. LACKNER, Thomas MÜNZEL, Volker ULLRICH, Andreas DAIBER, 2016. Formation of 2-nitrophenol from salicylaldehyde as a suitable test for low peroxynitrite fluxes. In: Redox Biology. 7, pp. 39-47. ISSN 2213-2317

@article{Mikhed2016Forma-33516, title={Formation of 2-nitrophenol from salicylaldehyde as a suitable test for low peroxynitrite fluxes}, year={2016}, doi={10.1016/j.redox.2015.11.008}, volume={7}, issn={2213-2317}, journal={Redox Biology}, pages={39--47}, author={Mikhed, Yuliya and Bruns, Kai and Schildknecht, Stefan and Jörg, Michael and Dib, Mobin and Oelze, Matthias and Lackner, Karl J. and Münzel, Thomas and Ullrich, Volker and Daiber, Andreas} }

Lackner, Karl J. Bruns, Kai Daiber, Andreas There has been some dispute regarding reaction products formed at physiological peroxynitrite fluxes in the nanomolar range with phenolic molecules, when used to predict the behavior of protein-bound aromatic amino acids like tyrosine. Previous data showed that at nanomolar fluxes of peroxynitrite, nitration of these phenolic compounds was outcompeted by dimerization (e.g. biphenols or dityrosine). Using 3-morpholino sydnonimine (Sin-1), we created low fluxes of peroxynitrite in our reaction set-up to demonstrate that salicylaldehyde displays unique features in the detection of physiological fluxes of peroxynitrite, yielding detectable nitration but only minor dimerization products.<br />By means of HPLC analysis and detection at 380 nm we could identify the expected nitration products 3- and 5-nitrosalicylaldehyde, but also novel nitrated products. Using mass spectrometry, we also identified 2-nitrophenol and a not fully characterized nitrated dimerization product. The formation of 2-nitrophenol could proceed either by primary generation of a phenoxy radical, followed by addition of the NO<sub>2</sub>-radical to the various resonance structures, or by addition of the peroxynitrite anion to the polarized carbonyl group with subsequent fragmentation of the adduct (as seen with carbon dioxide). Interestingly, we observed almost no 3- and 5-nitrosalicylic acid products and only minor dimerization reaction.<br />Our results disagree with the previous general assumption that nitration of low molecular weight phenolic compounds is always outcompeted by dimerization at nanomolar peroxynitrite fluxes and highlight unique features of salicylaldehyde as a probe for physiological concentrations of peroxynitrite. Jörg, Michael Oelze, Matthias 2016 eng Lackner, Karl J. 2016-03-31T08:45:40Z 2016-03-31T08:45:40Z Schildknecht, Stefan Dib, Mobin Oelze, Matthias Jörg, Michael Münzel, Thomas Bruns, Kai Formation of 2-nitrophenol from salicylaldehyde as a suitable test for low peroxynitrite fluxes Ullrich, Volker Mikhed, Yuliya Dib, Mobin Ullrich, Volker Mikhed, Yuliya Schildknecht, Stefan Daiber, Andreas Münzel, Thomas

Dateiabrufe seit 31.03.2016 (Informationen über die Zugriffsstatistik)

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