Flow Chemistry System for Carbohydrate Analysis by Rapid Labeling of Saccharides after Glycan Hydrolysis

SLAS Technol. 2020 Aug;25(4):356-366. doi: 10.1177/2472630320924620. Epub 2020 Jun 19.

Abstract

This study demonstrates the utilization of a flow chemistry system for continuous glycan hydrolysis and saccharide labeling to assist with the existing methods in glycan structural analysis. Acidic hydrolysis of glycans could be accelerated in a flow system. Aldoses and α-ketoacid-type saccharides were effectively labeled with naphthalene-2,3-diamine (NADA) at 60 °C for 10 min to form the fluorescent naphthimidazole (NAIM) and quinoxalinone (QXO) derivatives, respectively. The NADA-labeled derivatives improved the structural determination and composition analysis for their parent saccharides by using matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF-MS), liquid chromatography mass spectrometry (LC-MS), and nuclear magnetic resonance (NMR). Furthermore, this protocol was applied to determine the SA-Gal-Glc sequence of GM3-sugar out of six possible permutations.

Keywords: DAB tagging; NADA tagging; carbohydrate analysis; flow chemistry; glycan hydrolysis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 2-Naphthylamine / analogs & derivatives
  • 2-Naphthylamine / chemistry
  • 2-Naphthylamine / metabolism
  • Glucose / chemistry
  • Glucose / metabolism
  • Glycomics / methods*
  • Hydrolysis
  • Imidazoles / chemistry
  • N-Acetylneuraminic Acid / chemistry
  • N-Acetylneuraminic Acid / metabolism
  • Polysaccharides / chemistry
  • Polysaccharides / metabolism*
  • Rheology*
  • Staining and Labeling*

Substances

  • Imidazoles
  • Polysaccharides
  • 2,3-diaminonaphthalene
  • 2-Naphthylamine
  • N-Acetylneuraminic Acid
  • Glucose