4.4 Article

Addition of CsCl reduces ion suppression effects in the matrix-assisted laser desorption/ionization mass spectra of triacylglycerol/phosphatidylcholine mixtures and adipose tissue extracts

Journal

RAPID COMMUNICATIONS IN MASS SPECTROMETRY
Volume 31, Issue 5, Pages 411-418

Publisher

WILEY
DOI: 10.1002/rcm.7806

Keywords

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Funding

  1. German Research Council [DFG Schi 476/12-2, DFG Schi 476/16-1, SFB 1052/B6/Z3]
  2. Bruker Daltonik GmbH (Bremen, Germany)
  3. Merck Millipore (Darmstadt, Germany)

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RATIONALE: Ion suppression is a known disadvantage in mixture analysis. Matrix-assisted laser desorption/ionization (MALDI) mass spectra of crude adipose tissue extracts are dominated by triacylglycerol (TAG) signals while less abundant phospholipids such as phosphatidylcholines (PC) and particularly phosphatidylethanolamines (PE) are suppressed. It is suggested that addition of an excess of cesium (Cs) ions helps to overcome this problem. METHODS: Selected lipid mixtures of known compositions and organic adipose tissue extracts were investigated by positive ion MALDI-time-of-flight mass spectrometry (TOF MS). 2,5-Dihydroxybenzoic acid (DHB) in methanol was used as the matrix. In selected cases the methanolic DHB solution was saturated by the addition of different solid alkali chlorides (such as NaCl, KCl, RbCl and CsCl). Studies on the solubilities of these salts in methanol and the interaction with DHB (by C-13 NMR) were also performed. RESULTS: Saturation of the DHB matrix with solid CsCl leads to tremendous intensity differences, i.e. the intensities of the TAG signals (which otherwise dominate the mass spectra) are significantly reduced. In contrast, the intensity of small signals of phospholipids increases considerably. Decrease in the TAG signal intensity is particularly caused by the considerable size of the Cs+ ion which prevents successful analyte ionization. CONCLUSIONS: The addition of CsCl improves the detectability of otherwise invisible or weak phospholipid ions. This is a simple approach to detect small amounts of phospholipids in the presence of an excess of TAG. No laborious and timeconsuming separation of the total lipid extract into the individual lipid classes is required. Copyright (c) 2016 John Wiley & Sons, Ltd.

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