AI Article Synopsis

  • Carbohydrates like oligosaccharides and polysaccharides are important biopolymers involved in various biological processes and often studied after being isolated from natural sources.
  • Pure compounds with well-defined structures, obtained via chemical or enzymatic synthesis, are necessary for accurate analysis, and new synthetic techniques have made it easier to access larger polysaccharides.
  • The study uses advanced MALDI FT-ICR mass spectrometry to analyze synthetic carbohydrates of different sizes, revealing details about their monosaccharide content and linkage types through the identification of fragment ions, enhancing our understanding of their composition and structures.

Article Abstract

Carbohydrates, such as oligo- and polysaccharides, are highly abundant biopolymers that are involved in numerous processes. The study of their structure and functions is commonly based on a material that is isolated from complex natural sources. However, a more precise analysis requires pure compounds with well-defined structures that can be obtained from chemical or enzymatic syntheses. Novel synthetic strategies have increased the accessibility of larger monodisperse polysaccharides, posing a challenge to the analytical methods used for their molecular characterization. Here, we present wide mass range ultrahigh-resolution matrix-assisted laser desorption/ionization (MALDI) Fourier transform ion cyclotron resonance (FT-ICR) mass spectrometry (MS) as a powerful platform for the analysis of synthetic oligo- and polysaccharides. Synthetic carbohydrates 16-, 64-, 100-, and 151-mers were mass analyzed and characterized by MALDI in-source decay FT-ICR MS. Detection of fragment ions generated from glycosidic bond cleavage (or cross-ring cleavage) provided information of the monosaccharide content and the linkage type, allowing for the corroboration of the carbohydrate compositions and structures.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8034773PMC
http://dx.doi.org/10.1021/acs.analchem.1c00239DOI Listing

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