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 |
|