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Structural identification of triacylglycerol isomers using electron impact excitation of ions from organics (EIEIO).


ABSTRACT: Electron-induced dissociation or electron impact excitation of ions from organics (EIEIO) was applied to triacylglycerols (TAGs) for in-depth molecular structure analysis using MS. In EIEIO, energetic electrons (?10 eV) fragmented TAG ions to allow for regioisomeric assignment of identified acyl groups at the sn-2 or sn-1/3 positions of the glycerol backbone. In addition, carbon-carbon double bond locations within the acyl chains could also be assigned by EIEIO. Beyond the analysis of lipid standards, this technique was applied to edible oils and natural lipid extracts to demonstrate the power of this method to provide in-depth structural elucidation of TAG molecular species.

SUBMITTER: Baba T 

PROVIDER: S-EPMC5087869 | biostudies-other | 2016 Nov

REPOSITORIES: biostudies-other

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Structural identification of triacylglycerol isomers using electron impact excitation of ions from organics (EIEIO).

Baba Takashi T   Campbell J Larry JL   Le Blanc J C Yves JC   Baker Paul R S PR  

Journal of lipid research 20160725 11


Electron-induced dissociation or electron impact excitation of ions from organics (EIEIO) was applied to triacylglycerols (TAGs) for in-depth molecular structure analysis using MS. In EIEIO, energetic electrons (∼10 eV) fragmented TAG ions to allow for regioisomeric assignment of identified acyl groups at the sn-2 or sn-1/3 positions of the glycerol backbone. In addition, carbon-carbon double bond locations within the acyl chains could also be assigned by EIEIO. Beyond the analysis of lipid stan  ...[more]

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