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dc.contributor.author | Usachev K. | |
dc.contributor.author | Yamaguchi Y. | |
dc.contributor.author | Takamatsu M. | |
dc.contributor.author | Pavlova N. | |
dc.contributor.author | Klochkov V. | |
dc.contributor.author | Kurbangalieva A. | |
dc.contributor.author | Murase T. | |
dc.contributor.author | Shimoda T. | |
dc.contributor.author | Tanaka K. | |
dc.date.accessioned | 2018-04-05T07:08:50Z | |
dc.date.available | 2018-04-05T07:08:50Z | |
dc.date.issued | 2017 | |
dc.identifier.issn | 0003-2654 | |
dc.identifier.uri | http://dspace.kpfu.ru/xmlui/handle/net/129359 | |
dc.description.abstract | © The Royal Society of Chemistry 2017. In the present Communication, we propose a quite simple but previously overlooked approach for conveniently analyzing, assigning, and extracting sialic acid-containing N-glycan structures using high-resolution NMR spectroscopy without pre-installing metal chelators.Paramagnetic metals, such as Gd 3+ , appear to bind to the carboxyl groups of N-acetylneuraminic acid when introduced at room temperature, leading to the measurement of nonequivalent proton and carbon NMR spectral signals among otherwise "identical" glycan branched structures. | |
dc.relation.ispartofseries | Analyst | |
dc.title | Simple Gd<sup>3+</sup>-Neu5: N Ac complexation results in NMR chemical shift asymmetries of structurally equivalent complex-type N -glycan branches | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 16 | |
dc.relation.ispartofseries-volume | 142 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 2897 | |
dc.source.id | SCOPUS00032654-2017-142-16-SID85027044188 |