A new rapid and micro-scale hydrolysis, using triethylamine citrate, for lipopolysaccharide characterization by mass spectrometry

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DOIResolve DOI: http://doi.org/10.1002/rcm.5084
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TypeArticle
Journal titleRapid Communications in Mass Spectrometry
ISSN0951-4198
Volume25
Issue14
Pages20432048; # of pages: 6
Subjectcitric acid; ethylamine; lipopolysaccharide; triethylamine; Actinobacillus pleuropneumoniae; article; chemistry; Escherichia coli; hydrolysis; isolation and purification; mass spectrometry; methodology; Salmonella enterica; thin layer chromatography; Actinobacillus pleuropneumoniae; Chromatography, Thin Layer; Citrates; Escherichia coli; Ethylamines; Hydrolysis; Lipopolysaccharides; Salmonella enterica; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
AbstractEndotoxin (lipopolysaccharide, LPS) is, in general, composed of two moieties: a hydrophilic polysaccharide linked to a hydrophobic lipid A terminal unit and forms a major surface component of Gram-negative bacteria. The structural features of LPS moieties play a role in pathogenesis and also involve immunogenicity and diagnostic serology. The major toxic factor of LPS resides in the lipid A moiety, anchored in the outer layer of the bacterium, and its relative biological activity is critically related to fine structural features within the molecule. In establishing relationships between structural features and biological activities of LPS it is of the utmost importance to develop new analytical methods that can be applied to the complete unambiguous characterization of a specific LPS molecule. Herein is presented a practical rapid and sensitive analytical procedure for the mass spectral screening of LPS using triethylamine citrate as an agent for both disaggregation and mild hydrolysis of LPS. It provides improved matrix-assisted laser desorption/ionization (MALDI) mass spectra and, in particular, affords the identification of fragments retaining labile substituents present in the native macromolecular LPS structures. The methods were developed and applied using purified LPS of Escherichia coli and Salmonella enterica, as well as more complex LPS of Actnobacillus pleuropneumoniae. Copyright © 2011 John Wiley & Sons, Ltd.
Publication date
LanguageEnglish
AffiliationNational Research Council Canada (NRC-CNRC); NRC Institute for Biological Sciences (IBS-ISB)
Peer reviewedYes
NPARC number21271121
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Record identifier6ad8723c-3142-4196-b07d-7417cf32d427
Record created2014-03-24
Record modified2016-05-09
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