Author
Listed:
- Rebecca L. Miller
(University of Copenhagen
University of Liverpool
University of Oxford, Old Road Campus Research Building)
- Scott E. Guimond
(University of Liverpool
Keele University)
- Ralf Schwörer
(Ferrier Research Institute, Victoria University of Wellington, 69 Gracefield Road, Gracefield)
- Olga V. Zubkova
(Ferrier Research Institute, Victoria University of Wellington, 69 Gracefield Road, Gracefield)
- Peter C. Tyler
(Ferrier Research Institute, Victoria University of Wellington, 69 Gracefield Road, Gracefield)
- Yongmei Xu
(University of North Carolina)
- Jian Liu
(University of North Carolina)
- Pradeep Chopra
(University of Georgia)
- Geert-Jan Boons
(University of Georgia
Utrecht University)
- Márkó Grabarics
(Freie Universitaet Berlin, Institute of Chemistry and Biochemistry
Fritz Haber Institute of the Max Planck Society)
- Christian Manz
(Freie Universitaet Berlin, Institute of Chemistry and Biochemistry
Fritz Haber Institute of the Max Planck Society)
- Johanna Hofmann
(Freie Universitaet Berlin, Institute of Chemistry and Biochemistry
Fritz Haber Institute of the Max Planck Society)
- Niclas G. Karlsson
(University of Gothenburg)
- Jeremy E. Turnbull
(University of Copenhagen
University of Liverpool)
- Weston B. Struwe
(University of Oxford)
- Kevin Pagel
(Freie Universitaet Berlin, Institute of Chemistry and Biochemistry
Fritz Haber Institute of the Max Planck Society)
Abstract
Despite evident regulatory roles of heparan sulfate (HS) saccharides in numerous biological processes, definitive information on the bioactive sequences of these polymers is lacking, with only a handful of natural structures sequenced to date. Here, we develop a “Shotgun” Ion Mobility Mass Spectrometry Sequencing (SIMMS2) method in which intact HS saccharides are dissociated in an ion mobility mass spectrometer and collision cross section values of fragments measured. Matching of data for intact and fragment ions against known values for 36 fully defined HS saccharide structures (from di- to decasaccharides) permits unambiguous sequence determination of validated standards and unknown natural saccharides, notably including variants with 3O-sulfate groups. SIMMS2 analysis of two fibroblast growth factor-inhibiting hexasaccharides identified from a HS oligosaccharide library screen demonstrates that the approach allows elucidation of structure-activity relationships. SIMMS2 thus overcomes the bottleneck for decoding the informational content of functional HS motifs which is crucial for their future biomedical exploitation.
Suggested Citation
Rebecca L. Miller & Scott E. Guimond & Ralf Schwörer & Olga V. Zubkova & Peter C. Tyler & Yongmei Xu & Jian Liu & Pradeep Chopra & Geert-Jan Boons & Márkó Grabarics & Christian Manz & Johanna Hofmann , 2020.
"Shotgun ion mobility mass spectrometry sequencing of heparan sulfate saccharides,"
Nature Communications, Nature, vol. 11(1), pages 1-12, December.
Handle:
RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-15284-y
DOI: 10.1038/s41467-020-15284-y
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