4.5 Article

Simultaneous quantification of sialyloligosaccharides from human milk by capillary electrophoresis

Journal

ANALYTICAL BIOCHEMISTRY
Volume 370, Issue 2, Pages 206-214

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ab.2007.07.004

Keywords

human milk oligosaccharides; sialyloligosaccharides; capillary electrophoresis

Funding

  1. NICHD NIH HHS [HD12437, P01 HD013021-260013, HD13021, R37 HD012437, P01 HD013021-269007, P01 HD013021, R37 HD012437-27] Funding Source: Medline
  2. NIDDK NIH HHS [DK40561, P30 DK040561, P30 DK040561-129004] Funding Source: Medline

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The acidic oligosaccharides of human milk are predominantly sialyloligosaccharides. Pathogens that bind sialic acid-containing glycans on their host mucosal surfaces may be inhibited by human milk sialyloligosaccharides, but testing this hypothesis requires their reliable quantification in milk. Sialyloligosaccharides have been quantified by anion exchange high-performance liquid chromatography (HPLC), reverse- or normal-phase HPLC, and capillary clectrophoresis (CE) of fluorescent derivatives; in milk, these oligosaccha rides have been analyzed by high pH anion exchange chromatography with pulsed amperometric detection and, in our laboratory, by CE with detection at 205 nm. The novel method described here uses a running buffer of aqueous 200 mM NaH2PO4 (pH 7.05) containing 100 mM sodium dodecyl sulfate (SDS) mixed with 45% (v/v) methanol to baseline resolve 5 oligosaccharides and separate all 12. This allows automated simultaneous quantification of the 12 major sialyloligosaccharides of human milk in a single 35-min run. This method revealed differences in sialyloligosaccharide concentrations between less and more mature milk from the same donors. Individual donors also varied in expression of sialyl oligo saccha rides in their milk. Thus, the facile quantification of sialyloligosaccharides by this method is suitable for measuring variation in expression of specific sialyloligosaccharides in milk and their relationship to decreased risk of specific diseases in infants. (c) 2007 Elsevier Inc. All rights reserved.

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