NACE–ESI‐MS/MS method for separation and characterization of phosphorylation and acylation isomers of lipid A

Abstract: Lipid A represents a heterogeneous group of bacterial outer membrane phosphoglycolipids, which play a major role in the pathogenesis of Gram‐negative sepsis. The number and position of phosphoryl and acyl groups in lipid A molecules are key structural determinants in their bioactivities. In this study, a NACE–ESI‐MS/MS method was developed for the simultaneous analysis of lipid A isomers possessing a different degree of phosphorylation and acylation. Various C4’‐ and C1‐monophosphorylated lipid A isobars, as well as acylation isomers, were baseline separated within 43 min in a separation medium of methanol/dichloromethane/triethylamine/acetic acid 60:40:1.08:0.36 (v/v/v/v). Both normal and reverse CE polarities could be applied for proper detection of the analytes owing to the combination of a suction effect caused by the nebulizer gas at the outlet end of the capillary and external pressure applied on the inlet vial. The separated lipid A species could be identified unequivocally by their characteristic fragmentation patterns through CID performed in both negative‐ and positive‐ionization modes. The uniqueness of the NACE–ESI‐MS/MS method lies in its simplicity and reliability for proving the phosphorylation isomerism (C1 or C4’) and acylation pattern of native lipid A species or those designed for therapeutic applications.

Angaben zum Objekt

• Standort: Deutsche Nationalbibliothek Frankfurt am Main
• Umfang: Online-Ressource
• Sprache: Englisch

Verweise und Beziehungen

• Erschienen in: NACE–ESI‐MS/MS method for separation and characterization of phosphorylation and acylation isomers of lipid A ; volume:41 ; number:13-14 ; year:2020 ; pages:1178-1188 ; extent:11 ; Electrophoresis ; 41, Heft 13-14 (2020), 1178-1188 (gesamt 11)

Beteiligte, Orts- und Zeitangaben

• Urheber: Sándor, Viktor ; Berkics, Balázs Viktor ; Kilár, Anikó ; Kocsis, Béla ; Kilár, Ferenc ; Dörnyei, Ágnes

Weitere Informationen

• DOI: 10.1002/elps.201900251
• URN: urn:nbn:de:101:1-2022062811451171708530
• Rechteinformation: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
• Letzte Aktualisierung: 15.08.2025, 07:36 MESZ