Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2145
Title: Design of Stable β-Hairpin Mimetics through Backbone Disulfide Bonds
Authors: Kumar, Mothukuri Ganesh
MALI, SACHITANAND M.
Raja, K. Muruga Poopathi
GOPI, HOSAHUDYA N.
Dept. of Chemistry
Keywords: Design of Stable β-Hairpin
Disulfide Bonds
Stable protein secondary structure
Antimicrobial peptides
2015
Issue Date: Jan-2015
Publisher: American Chemical Society
Citation: Organic Letters, 17 (2), 230-233.
Abstract: The synthesis and utilization of novel thiostatines (β-SH-substituted γ-amino acids) in the design of backbone-disulfide-stabilized β-hairpin mimetics, solution conformations of hybrid β-hairpins and Cys-disulfide-stabilized α-peptide analogue, their thiol exchange, and proteolytic stability are investigated. The results suggest that thiostatines can be used to design proteolytically stable water-soluble β-hairpin mimetics without deviating from overall β-hairpin conformation.
URI: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2145
https://doi.org/10.1021/ol503310r
ISSN: 1523-7060
1523-7052
Appears in Collections:JOURNAL ARTICLES

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