4.1 Article

Self-Assembly and Responsiveness of Polypeptide-Based Block Copolymers: How Smart Behavior and Topological Complexity Yield Unique Assembly in Aqueous Media

Journal

JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS
Volume 51, Issue 7, Pages 508-523

Publisher

WILEY
DOI: 10.1002/polb.23259

Keywords

amphiphiles; biomimetic; block copolymers; self-assembly

Funding

  1. National Science Foundation [CHE-1213840]
  2. USM startup funds
  3. National Science Foundation GK-12 program through the University of Southern Mississippi [0947944]
  4. Division Of Chemistry
  5. Direct For Mathematical & Physical Scien [1213840] Funding Source: National Science Foundation

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Polypeptide-based amphiphilic block copolymers are an attractive class of materials given their ability to form well-defined aqueous nanoassemblies that respond to external stimulus through secondary structure transitions. This report will highlight recent literature in the area of polypeptide-based block copolymer self-assembly, with the major focus being on how the responsive nature and structural complexity of the polypeptide blocks can be incorporated into systems with complex topologies such as ABA/BAB/ABC triblock copolymers, AB(2) and A(2)B star copolymers, and miktoarml-ABC star terpolymers. In particular, the role of interfacial curvature changes and how they result in morphology transitions will be discussed. The 'smart' assembly properties of peptides in complex block copolymer topologies can lead to enhanced responsiveness, morphological complexity, and unique morphological transitions with varying solution conditions. (C) 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2013, 51, 508-523

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