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Título

Understanding the nitrolipidome: From chemistry to mass spectrometry and biological significance of modified complex lipids

AutorNeves, Bruna; Pérez-Sala, Dolores CSIC ORCID ; Ferreira, Elena Beatriz; Guerra, Inês M. S.; Moreira, Ana S. P.; Domingues, P.; Domingues, M. Rosário; Melo, Tania
Palabras claveEpilipids
Lipidomics
Nitration
Nitroxidation
Reactive nitrogen species
Fecha de publicación27-may-2022
EditorElsevier
CitaciónProgress in Lipid Research 101176 (2022)
ResumenComplex lipids, phospholipids (PLs) and triacylglycerides (TAGs), are prone to modifications induced by reactive nitrated species and reactive oxygen species, generating a range of nitrated, nitrosated or nitroxidized derivatives, as nitro PLs and nitro TAGs. These modified lipids (epilipids) have been reported in vitro and in vivo using lipidomics approaches. However, their detection in living systems remains a challenge hampered by its complexity, high structural diversity, and low abundance. The advances in high-resolution mass spectrometry combined with the higher sensitivity of the instruments like Orbitrap-based mass spectrometers opened new opportunities for the detection of these modified complex lipids. This review summarizes the challenges and findings behind the identification of nitrated, nitrosated and nitroxidized PLs and TAGs fragmentation fingerprints based on collision-induced dissociation (CID) and higher energy CID (HCD) MS/MS approaches. Following what has already been reported for nitrated fatty acids, these complex lipids are found to act as endogenous mediators with potential electrophilic properties and can express bioactivities such as anti-inflammatory and antioxidant actions. This information can be used to design untargeted and targeted lipidomics strategies for these modified complex lipids in biological samples as well as in pathological, food and industrial settings, further unveiling their biological and signalling roles.
Descripción58 p.-16 fig.-5 tab.
Versión del editorhttps://doi.org/10.1016/j.plipres.2022.101176
URIhttp://hdl.handle.net/10261/271791
DOI10.1016/j.plipres.2022.101176
E-ISSN0163-7827
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