dc.contributor.author |
Yadav, Rohan |
en_US |
dc.contributor.author |
Ben Arye, Shani Leviatan |
en_US |
dc.contributor.author |
SUBRAMANI, BALAMURUGAN |
en_US |
dc.contributor.author |
Padler-Karavani, Vered |
en_US |
dc.contributor.author |
KIKKERI, RAGHAVENDRA |
en_US |
dc.date.accessioned |
2019-04-29T10:14:35Z |
|
dc.date.available |
2019-04-29T10:14:35Z |
|
dc.date.issued |
2016-09 |
en_US |
dc.identifier.citation |
Organic and Biomolecular Chemistry, 14(46), 10812-10815. |
en_US |
dc.identifier.issn |
1477-0520 |
en_US |
dc.identifier.issn |
1477-0539 |
en_US |
dc.identifier.uri |
http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2662 |
|
dc.identifier.uri |
https://doi.org/10.1039/C6OB01688J |
en_US |
dc.description.abstract |
Sialic acids (Sias) are important terminal sugars on cell surfaces involved in a wide range of protein–carbohydrate interactions. Hence, agents modulating sias-mediated protein interactions are promising inhibitors or vaccine candidates. Here, we report the synthesis of Neu5Acα(2–6)Gal structural analogs and their binding to a series of siglecs. The results showed distinct binding patterns with conserved siglecs (hCD22 and mCD22) compared to rapid evolving siglecs (Siglecs -3 & -10). |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
Royal Society of Chemistry |
en_US |
dc.subject |
Screening of Neu5Ac? |
en_US |
dc.subject |
Sialic acid microarray |
en_US |
dc.subject |
Glycoproteins |
en_US |
dc.subject |
Immune responses |
en_US |
dc.subject |
Tumorigenesis |
en_US |
dc.subject |
2016 |
en_US |
dc.title |
Screening of Neu5Acα(2–6)gal isomer preferences of siglecs with a sialic acid microarray |
en_US |
dc.type |
Article |
en_US |
dc.contributor.department |
Dept. of Chemistry |
en_US |
dc.identifier.sourcetitle |
Organic and Biomolecular Chemistry |
en_US |
dc.publication.originofpublisher |
Foreign |
en_US |