Analysis of unsaturated lipids by ozone-induced dissociation

Recent developments in analytical technologies have driven significant advances in lipid science. The sensitivity and selectivity of modern mass spectrometers can now provide for the detection and even quantification of many hundreds of lipids in a single analysis. In parallel, increasing evidence f...

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Published inBiochimica et biophysica acta Vol. 1811; no. 11; pp. 807 - 817
Main Authors Brown, Simon H.J., Mitchell, Todd W., Blanksby, Stephen J.
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.11.2011
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Summary:Recent developments in analytical technologies have driven significant advances in lipid science. The sensitivity and selectivity of modern mass spectrometers can now provide for the detection and even quantification of many hundreds of lipids in a single analysis. In parallel, increasing evidence from structural biology suggests that a detailed knowledge of lipid molecular structure including carbon–carbon double bond position, stereochemistry and acyl chain regiochemistry is required to fully appreciate the biochemical role(s) of individual lipids. Here we review the capabilities and limitations of tandem mass spectrometry to provide this level of structural specificity in the analysis of lipids present in complex biological extracts. In particular, we focus on the capabilities of a novel technology termed ozone-induced dissociation to identify the position(s) of double bonds in unsaturated lipids and discuss its possible role in efforts to develop workflows that provide for complete structure elucidation of lipids by mass spectrometry alone: so-called top-down lipidomics. This article is part of a Special Issue entitled: Lipodomics and Imaging Mass Spectrom. ► The importance of molecular structure in understanding lipid biochemistry ► The strengths and limitations of contemporary mass spectrometry ► The capabilities of ozone induced dissociation
Bibliography:http://dx.doi.org/10.1016/j.bbalip.2011.04.015
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ISSN:1388-1981
0006-3002
1879-2618
DOI:10.1016/j.bbalip.2011.04.015