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Updated: Dec 14, 2025

Formation of Ordered Biomolecular Structures by the Self-assembly of Short Peptides
Published on: November 21, 2013
Synthesis and self-assembly of dendritic-helical block copolypeptides
Kyoung Taek Kim1, Mitchell A Winnik1, Ian Manners2
1Department of Chemistry, University of Toronto, Toronto, Ontario M5S 3H6, Canada. mwinnik@chem.utoronto.ca.
Abstract:
Dendritic-helical diblock copolypeptides, dendritic poly(-lysine)--poly(γ-benzyl--glutamate) (PBLG-Lys) were synthesized up to 4th generation of dendritic poly(-lysine). PBLG was synthesized by conventional ring-opening polymerization of γ-benzyl--glutamate--carboxyanhydride with heptyl amine as an initiator. The -terminus of this PBLG was used for further coupling reactions with ,-bis(-butoxycarbonyl)--lysine pentafluorophenylester. These block copolypeptides possess well-defined 3-D structures in solution, and they self-assemble into a fibrous structure a nanoribbon mechanism in toluene. Amphiphilic block copolypeptides were obtained after deprotecting BOC groups at the periphery of the lysine dendrimer block. Due to the well-defined size and structure of the dendritic lysine block and well-defined α-helical conformation of the PBLG block, the block copolypeptides showed a generation-dependent self-assembly behavior in aqueous solution.
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