Sugar-modified Foldamers as Conformationally Defined and Biologically Distinct Glycopeptide Mimics

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dc.contributor.author Siriwardena, Aloysius
dc.contributor.author Pulukuri, K K
dc.contributor.author Kandiyal, P S
dc.contributor.author Roy, Saumya
dc.contributor.author Bande, Omprakash
dc.contributor.author Ghosh, Subhash
dc.contributor.author Fernàndez, J M G
dc.contributor.author Martin, F A
dc.contributor.author Ghigo, Jean-Marc
dc.contributor.author Beloin, Christophe
dc.contributor.author Ito, Keigo
dc.contributor.author Woods, R J
dc.contributor.author Ampapathi, R S
dc.contributor.author Chakraborty, T K
dc.date.accessioned 2014-07-14T11:50:44Z
dc.date.available 2014-07-14T11:50:44Z
dc.date.issued 2013
dc.identifier.citation Angewandte Chemie International Edition, 2013, 52(39), 10221–10226 en
dc.identifier.uri http://hdl.handle.net/123456789/1307
dc.description.abstract To fold or not to fold?: That the conformational preferences of foldamer backbones might be modulated by appended sugars and also that such effects might inform on the roles of glycans on the preferred secondary structures adopted by their natural glycopeptide counterparts, is the intriguing question posed. We demonstrate in this study that attached sugars do indeed play a defining role in the conformations adopted by a pair of novel SAA-derived foldamers in water and that these differences are reflected in the contrasting interactions of these glycofoldamers with various biological targets. en
dc.format.extent 332670 bytes
dc.format.mimetype application/pdf
dc.language.iso en en
dc.relation.ispartofseries CSIR-CDRI Communication No. 8490 en
dc.subject Sugar Amino acid (SAA) en
dc.subject Glycofoldamers en
dc.subject Neoglycopeptides en
dc.subject Solution conformational preferences en
dc.subject Restrained molecular dynamics en
dc.subject Protein-carbohydrate interactions en
dc.title Sugar-modified Foldamers as Conformationally Defined and Biologically Distinct Glycopeptide Mimics en
dc.type Article en


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