Secondary-Structure-Driven Self-Assembly of Reactive Polypept(o)ides: Controlling Size, Shape, and Function of Core Cross-Linked Nanostructures

Angew Chem Int Ed Engl. 2017 Aug 1;56(32):9608-9613. doi: 10.1002/anie.201702624. Epub 2017 Jul 6.

Abstract

Achieving precise control over the morphology and function of polymeric nanostructures during self-assembly remains a challenge in materials as well as biomedical science, especially when independent control over particle properties is desired. Herein, we report on nanostructures derived from amphiphilic block copolypept(o)ides by secondary-structure-directed self-assembly, presenting a strategy to adjust core polarity and function separately from particle preparation in a bioreversible manner. The peptide-inherent process of secondary-structure formation allows for the synthesis of spherical and worm-like core-cross-linked architectures from the same block copolymer, introducing a simple yet powerful approach to versatile peptide-based core-shell nanostructures.

Keywords: bioreversible cross-linking; micelles; reactive polypept(o)ides; secondary structure; self-assembly.

Publication types

  • Research Support, Non-U.S. Gov't