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Quantitative Fragmentation Model for Bottom-Up Shotgun Lipidomics.

MPS-Authors
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Schuhmann,  Kai
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

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Moon,  HongKee
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

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Thomas,  Henrik
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

/cone/persons/resource/persons219204

Groessl,  Michael
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

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Wagner,  Nicolai
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

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Henry,  Ian
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

/cone/persons/resource/persons219478

Nadler,  André
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

/cone/persons/resource/persons218972

Shevchenko,  Andrej
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

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引用

Schuhmann, K., Moon, H., Thomas, H., Ackerman, J. M., Groessl, M., Wagner, N., Kellmann, M., Henry, I., Nadler, A., & Shevchenko, A. (2019). Quantitative Fragmentation Model for Bottom-Up Shotgun Lipidomics. Analytical chemistry, 91(18), 12085-12093. doi:10.1021/acs.analchem.9b03270.


引用: https://hdl.handle.net/21.11116/0000-0006-7E1A-1
要旨
Quantitative bottom-up shotgun lipidomics relies on molecular species-specific "signature" fragments consistently detectable in tandem mass spectra of analytes and standards. Molecular species of glycerophospholipids are typically quantified using carboxylate fragments of their fatty acid moieties produced by higher-energy collisional dissociation of their molecular anions. However, employing standards whose fatty acids moieties are similar, yet not identical, to the target lipids could severely compromise their quantification. We developed a generic and portable fragmentation model implemented in the open-source LipidXte software that harmonizes the abundances of carboxylate anion fragments originating from fatty acid moieties having different sn-1/2 positions at the glycerol backbone, length of the hydrocarbon chain, and number and location of double bonds. The postacquisition adjustment enables unbiased absolute (molar) quantification of glycerophospholipid species independent of instrument settings, collision energy, and employed internal standards.