Induction of Secondary Structure through Micellization of an Oppositely Charged Pair of Homochiral Block- and Homopolypeptides in an Aqueous Medium

Omer F. Mutaf, Akihiro Kishimura, Yuki Mochida, Ahram Kim, Kazunori Kataoka

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Abstract

Polyion complex (PIC) formation is an attractive method for obtaining molecular assemblies owing to their facile fabrication process in aqueous media, but more insights are required in order to control the higher-dimensional structures of polypeptide-based PICs. Herein, the PIC formation behavior of oppositely charged homochiral polypeptides, poly-l-lysine and poly(ethylene glycol)-b-poly(l-glutamate) (PEG-PLG), and their secondary structures are carefully studied in water. PIC formation takes place in a polymer concentration-dependent manner, and clear β-sheet formation is observed at polymer concentrations ≥0.3 mg mL-1. The results also confirm that multimolecular aggregation is a prerequisite for β-sheet formation, which indicates that the inner hydrophobic environment of PICs is favorable for β-sheet formation. Furthermore, the PEG weight fraction, stereoregularity of the polypeptide, and ionic strength of the solutions are found to be key factors for generating a secondary structure, presumably because these factors can contribute to the tuning of the inner environment of PICs. This method of producing water-soluble nanoassemblies from oppositely charged polypeptides may expedite self-assembly studies in biological systems and be incorporated into various molecular systems to exploit protein-mimicking features. Polyion complex formation behavior of oppositely charged polypeptides, poly-l-lysine and poly(ethylene glycol)-block-poly(l-glutamate), is carefully studied in water. It is shown that multimolecular aggregation is prerequisite for β-sheet formation. Besides, noncharged hydrophilic segment, stereoregularity of the polypeptide, and ionic strength of solutions are found to be key factors for generating a secondary structure.

Original languageEnglish
Pages (from-to)1958-1964
Number of pages7
JournalMacromolecular rapid communications
Volume36
Issue number22
DOIs
Publication statusPublished - Nov 1 2015

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All Science Journal Classification (ASJC) codes

  • Organic Chemistry
  • Polymers and Plastics
  • Materials Chemistry

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