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Reaction Mechanism of Covalent Modification of Phosphatidylethanolamine Lipids by Reactive Aldehydes 4-hydroxy-2-nonenal and 4-oxo-2-nonenal


Vazdar, Katarina; Vojta, Danijela; Margetić, Davor; Vazdar, Mario
Reaction Mechanism of Covalent Modification of Phosphatidylethanolamine Lipids by Reactive Aldehydes 4-hydroxy-2-nonenal and 4-oxo-2-nonenal // Chemical research in toxicology, 30 (2017), 3; 840-850 doi:10.1021/acs.chemrestox.6b00443 (međunarodna recenzija, članak, znanstveni)


Naslov
Reaction Mechanism of Covalent Modification of Phosphatidylethanolamine Lipids by Reactive Aldehydes 4-hydroxy-2-nonenal and 4-oxo-2-nonenal

Autori
Vazdar, Katarina ; Vojta, Danijela ; Margetić, Davor ; Vazdar, Mario

Izvornik
Chemical research in toxicology (0893-228X) 30 (2017), 3; 840-850

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
4-hydroxynonenal, 4-oxononenal, Phosphatidylethanolamine Lipids, Michael addition, Schiff base formation

Sažetak
4-hydroxy-2-nonenal (HNE) and 4-oxo-2- nonenal (ONE) are biologically important reactive aldehydes formed during oxidative stress in phospholipid bilayers. They are highly reactive species due to presence of several reaction centers and can react with amino acids in peptides and proteins, as well as phosphoethanolamine (PE) lipids, thus modifying their biological activity. The aim of this work is to study in a molecular detail the reactivity of HNE and ONE towards PE lipids in a simplified system containing only lipids and reactive aldehydes in dichloromethane as an inert solvent. We use a combination of quantum chemical calculations, 1H-NMR measurements, FT- IR spectroscopy and mass spectrometry experiments and show that for both reactive aldehydes two types of chemical reactions are possible – formation of Michael adducts and Schiff bases. In the case of HNE, an initially formed Michael adduct can also undergo an additional cyclization step to a hemiacetal derivative, whereas no cyclization occurs in the case of ONE and a Michael adduct is identified. A Schiff base product initially formed when HNE is added to PE lipid can also further cyclize to a pyrrole derivative in contrast to ONE, where only a Schiff base product is isolated. The suggested reaction mechanism by quantum-chemical calculations is in a qualitative agreement with experimental yields of isolated products and is also additionally investigated by 1H-NMR measurements, FT-IR spectroscopy and mass spectrometry experiments.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Projekt / tema
HRZZ-UIP-2014-09-6090 - Molekularni aspekti oksidativnih procesa u stanicama (Mario Vazdar, )

Ustanove
Institut "Ruđer Bošković", Zagreb

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


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