| Literature DB >> 29564812 |
Jiandong Wu1, Juan Wei1, John D Hogan2, Pradeep Chopra3, Apoorva Joshi3,4, Weigang Lu3,4, Joshua Klein2, Geert-Jan Boons3,4,5, Cheng Lin1, Joseph Zaia6.
Abstract
Among dissociation methods, negative electron transfer dissociation (NETD) has been proven the most useful for glycosaminoglycan (GAG) sequencing because it produces informative fragmentation, a low degree of sulfate losses, high sensitivity, and translatability to multiple instrument types. The challenge, however, is to distinguish positional sulfation. In particular, NETD has been reported to fail to differentiate 4-O- versus 6-O-sulfation in chondroitin sulfate decasaccharide. This raised the concern of whether NETD is able to differentiate the rare 3-O-sulfation from predominant 6-O-sulfation in heparan sulfate (HS) oligosaccharides. Here, we report that NETD generates highly informative spectra that differentiate sites of O-sulfation on glucosamine residues, enabling structural characterizations of synthetic HS isomers containing 3-O-sulfation. Further, lyase-resistant 3-O-sulfated tetrasaccharides from natural sources were successfully sequenced. Notably, for all of the oligosaccharides in this study, the successful sequencing is based on NETD tandem mass spectra of commonly observed deprotonated precursor ions without derivatization or metal cation adduction, simplifying the experimental workflow and data interpretation. These results demonstrate the potential of NETD as a sensitive analytical tool for detailed, high-throughput structural analysis of highly sulfated GAGs. Graphical Abstract.Entities:
Keywords: Fourier transform ion cyclotron resonance mass spectrometry; Glycomics; Glycosaminoglycan; Heparan sulfate; Negative electron transfer dissociation; Sulfation
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Year: 2018 PMID: 29564812 PMCID: PMC6004244 DOI: 10.1007/s13361-018-1907-0
Source DB: PubMed Journal: J Am Soc Mass Spectrom ISSN: 1044-0305 Impact factor: 3.109