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Development of targeted hydrophilic interaction liquid chromatography-tandem mass spectrometry method for acyl-Coenzyme A covering short- to long-chain species in a single analytical run.
Singh, Madhulika; Kiyuna, Ligia Akemi; Odendaal, Christoff; Bakker, Barbara M; Harms, Amy C; Hankemeier, Thomas.
Afiliación
  • Singh M; Metabolomics and Analytics Centre, Leiden Academic Centre for Drug Research, Leiden University, The Netherlands.
  • Kiyuna LA; Laboratory of Paediatrics, University of Groningen, University Medical Centre Groningen, The Netherlands.
  • Odendaal C; Laboratory of Paediatrics, University of Groningen, University Medical Centre Groningen, The Netherlands.
  • Bakker BM; Laboratory of Paediatrics, University of Groningen, University Medical Centre Groningen, The Netherlands.
  • Harms AC; Metabolomics and Analytics Centre, Leiden Academic Centre for Drug Research, Leiden University, The Netherlands.
  • Hankemeier T; Metabolomics and Analytics Centre, Leiden Academic Centre for Drug Research, Leiden University, The Netherlands. Electronic address: hankemeier@lacdr.leidenuniv.nl.
J Chromatogr A ; 1714: 464524, 2024 Jan 11.
Article en En | MEDLINE | ID: mdl-38056390
ABSTRACT
Acyl-CoAs play a significant role in numerous physiological and metabolic processes making it important to assess their concentration levels for evaluating metabolic health. Considering the important role of acyl-CoAs, it is crucial to develop an analytical method that can analyze these compounds. Due to the structural variations of acyl-CoAs, multiple analytical methods are often required for comprehensive analysis of these compounds, which increases complexity and the analysis time. In this study, we have developed a method using a zwitterionic HILIC column that enables the coverage of free CoA and short- to long-chain acyl-CoA species in one analytical run. Initially, we developed the method using an LC-QTOF instrument for the identification of acyl-CoA species and optimizing their chromatography. Later, a targeted HILIC-MS/MS method was created in scheduled multiple reaction monitoring mode using a QTRAP MS detector. The performance of the method was evaluated based on various parameters such as linearity, precision, recovery and matrix effect. This method was applied to identify the difference in acyl-CoA profiles in HepG2 cells cultured in different conditions. Our findings revealed an increase in levels of acetyl-CoA, medium- and long-chain acyl-CoA while a decrease in the profiles of free CoA in the starved state, indicating a clear alteration in the fatty acid oxidation process.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Acilcoenzima A / Espectrometría de Masas en Tándem Idioma: En Revista: J Chromatogr A Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Acilcoenzima A / Espectrometría de Masas en Tándem Idioma: En Revista: J Chromatogr A Año: 2024 Tipo del documento: Article