Literature DB >> 15103655

Alternative approaches for the detection of various phospholipid classes by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.

Rosendo Estrada1, M Cecilia Yappert.   

Abstract

The detection of phospholipids (PLs) by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry was demonstrated nearly a decade ago. However, its use as a conventional tool for PL analysis has been hindered by ambiguities in peak assignments caused by spectral overlaps and difficulties in the detection of some PL classes when analytes with positively charged head groups, such as sphingomyelins (SMs) and phosphatidylcholines (PCs) are present. In this work, either a strong cation-exchange resin or CsCl crystals were added directly to the PL samples to reduce spectral complexity and enhance sensitivity. The quantitative exchange resulted in virtually only protonated or Cs+ adducts. To alleviate difficulties in the detection and identification of PL classes with ionization efficiencies lower than those of SMs and PCs, improvements in the sensitivity of negative-ion mass spectra were sought. For this purpose, several neutral and basic matrices were tried. Among them, p-nitroaniline (PNA) proved to be an advantageous alternative to the use of 2,5-dihydroxybenzoic acid (DHB), the most commonly used matrix in PL analysis. Because of its lower acidity, PNA increased the relative amount of deprotonated species and improved the sensitivity of negative-ion mass spectra. It was possible to confirm peak assignments for PL classes that normally give weak signals when DHB is used. Noteworthy is the detection (in both positive and negative modes) and conclusive identification of species in natural mixtures of phosphatidylethanolamines (PEs) and PE plasmalogens (PEps). PNA allowed the identification of PEs and PEps even in mixtures containing SMs and PCs. Although some cations related to PCs and PEs overlapped in positive-ion spectra, these interferences were eliminated in the negative mode as only the deprotonated forms of PEs and PEps were detectable and those of SMs and PCs were absent owing to their neutrality. Copyright 2004 John Wiley & Sons, Ltd.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15103655     DOI: 10.1002/jms.603

Source DB:  PubMed          Journal:  J Mass Spectrom        ISSN: 1076-5174            Impact factor:   1.982


  28 in total

Review 1.  Brain tissue lipidomics: direct probing using matrix-assisted laser desorption/ionization mass spectrometry.

Authors:  Amina S Woods; Shelley N Jackson
Journal:  AAPS J       Date:  2006-06-02       Impact factor: 4.009

2.  A snapshot of tissue glycerolipids.

Authors:  Amina S Woods; Hay-Yan J Wang; Shelley N Jackson
Journal:  Curr Pharm Des       Date:  2007       Impact factor: 3.116

Review 3.  Mass spectrometry based cellular phosphoinositides profiling and phospholipid analysis: a brief review.

Authors:  Youngjun Kim; Selina Rahman Shanta; Li-Hua Zhou; Kwang Pyo Kim
Journal:  Exp Mol Med       Date:  2010-01-31       Impact factor: 8.718

4.  para-Nitroaniline is a promising matrix for MALDI-MS imaging on intermediate pressure MS systems.

Authors:  Rory T Steven; Alan M Race; Josephine Bunch
Journal:  J Am Soc Mass Spectrom       Date:  2013-03-02       Impact factor: 3.109

5.  Single embryo and oocyte lipid fingerprinting by mass spectrometry.

Authors:  Christina R Ferreira; Sergio A Saraiva; Rodrigo R Catharino; Jerusa S Garcia; Fabio C Gozzo; Gustavo B Sanvido; Luiz Fernando A Santos; Edson G Lo Turco; José Henrique F Pontes; Andréa C Basso; Ricardo P Bertolla; Roberto Sartori; Monique M Guardieiro; Felipe Perecin; Flávio V Meirelles; Juliano R Sangalli; Marcos N Eberlin
Journal:  J Lipid Res       Date:  2009-11-05       Impact factor: 5.922

6.  MALDI-Ion Mobility Mass Spectrometry of Lipids in Negative Ion Mode.

Authors:  Shelley N Jackson; Damon Barbacci; Thomas Egan; Ernest K Lewis; J Albert Schultz; Amina S Woods
Journal:  Anal Methods       Date:  2014-07-21       Impact factor: 2.896

7.  HOCl-mediated glycerophosphocholine and glycerophosphoethanolamine generation from plasmalogens in phospholipid mixtures.

Authors:  Jacqueline Lessig; Beate Fuchs
Journal:  Lipids       Date:  2009-11-25       Impact factor: 1.880

8.  Complementary precursor ion and neutral loss scan mode tandem mass spectrometry for the analysis of glycerophosphatidylethanolamine lipids from whole rat retina.

Authors:  Todd A Lydic; Julia V Busik; Walter J Esselman; Gavin E Reid
Journal:  Anal Bioanal Chem       Date:  2009-03-11       Impact factor: 4.142

9.  Matrix-assisted laser desorption/ionization time-of-flight mass spectrometric analysis of cellular glycerophospholipids enabled by multiplexed solvent dependent analyte-matrix interactions.

Authors:  Gang Sun; Kui Yang; Zhongdan Zhao; Shaoping Guan; Xianlin Han; Richard W Gross
Journal:  Anal Chem       Date:  2008-09-04       Impact factor: 6.986

Review 10.  Direct profiling of tissue lipids by MALDI-TOFMS.

Authors:  Shelley N Jackson; Amina S Woods
Journal:  J Chromatogr B Analyt Technol Biomed Life Sci       Date:  2008-11-28       Impact factor: 3.205

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.