| Literature DB >> 33047840 |
Javier Sastre Toraño1, Oier Aizpurua-Olaizola1,2, Na Wei3, Tiehai Li3, Luca Unione1, Gonzalo Jiménez-Osés4, Francisco Corzana5, Victor J Somovilla1, Juan M Falcon-Perez2, Geert-Jan Boons1,3.
Abstract
Glycans possess unparalleled structural complexity arising from chemically similar monosaccharide building blocks, configurations of anomeric linkages and different branching patterns, potentially giving rise to many isomers. This level of complexity is one of the main reasons that identification of exact glycan structures in biological samples still lags behind that of other biomolecules. Here, we introduce a methodology to identify isomeric N-glycans by determining gas phase conformer distributions (CDs) by measuring arrival time distributions (ATDs) using drift-tube ion mobility spectrometry-mass spectrometry. Key to the approach is the use of a range of well-defined synthetic glycans that made it possible to investigate conformer distributions in the gas phase of isomeric glycans in a systematic manner. In addition, we have computed CD fingerprints by molecular dynamics (MD) simulation, which compared well with experimentally determined CDs. It supports that ATDs resemble conformational populations in the gas phase and offer the prospect that such an approach can contribute to generating a library of CCS distributions (CCSDs) for structure identification.Entities:
Keywords: carbohydrates; chemo-enzymatic synthesis; conformations; ion mobility spectrometry; mass spectrometry; molecular dynamics
Year: 2021 PMID: 33047840 DOI: 10.1002/chem.202004522
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236