Covalent Self-Assembly and One-Step Photocrosslinking of Tyrosine-Rich Oligopeptides to Form Diverse Nanostructures

  • Kyoung Ik Min
  • , Gyeongwon Yun
  • , Yoonjung Jang
  • , Kyung Rok Kim
  • , Young Ho Ko
  • , Hyung Seok Jang
  • , Yoon Sik Lee
  • , Kimoon Kim
  • , Dong Pyo Kim

Research output: Contribution to journalArticlepeer-review

51 Scopus citations

Abstract

We present covalently self-assembled peptide hollow nanocapsule and peptide lamella. These biomimetic dityrosine peptide nanostructures are synthesized by one-step photopolymerization of a tyrosine-rich short peptide without the aid of a template. This simple approach offers direct synthesis of fluorescent peptide nanocages and free-standing thin films. The simple crosslinked peptide lamella films provide robust mechanical properties with an elastic modulus of approximately 30 GPa and a hardness of 740 MPa. These nanostructures also allow for the design of peptidosomes. The approach taken here represents a rare example of covalent self-assembly of short peptides into nano-objects, which may be useful as microcompartments and separation membranes. Covalent self-assembly of peptides: Direct synthesis of fluorescent peptide nanocapsules and free-standing thin films by bioinspired one-step photopolymerization of peptides is reported. The crosslinked peptides showed superior mechanical strength compared to non-covalent peptides, and were used to design robust peptidosomes.

Original languageEnglish
Pages (from-to)6925-6928
Number of pages4
JournalAngewandte Chemie - International Edition
Volume55
Issue number24
DOIs
StatePublished - 6 Jun 2016

Keywords

  • covalent self-assembly
  • films
  • nanocapsules
  • peptides
  • tyrosine-tyrosine crosslinking

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