Nanodomain-induced chain folding in poly(γ-benzyl-L-glutamate)-b-polyglycine diblock copolymers

P. Papadopoulos, G. Floudas*, I. Schnell, T. Aliferis, H. Iatrou, N. Hadjichristidis

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

61 Scopus citations


We report on the self-assembly mechanism and dynamics in a series of poly(γ-benzyl-L-glutamate)-b-poly(glycine) (PBLG-b-PGly) diblock copolymers within the composition range 0.67 ≤ fPBLG ≤ 0.97 and the temperature (T) range 303 < T < 433 K. Small- and wide-angle X-ray scattering, 13C NMR, and differential scanning calorimetry are used for the structure investigation coupled with dielectric spectroscopy for both the peptide secondary structure and the associated dynamics. These techniques provide not only the nanophase morphology but also the type and persistence of peptide secondary structures. The thermodynamic confinement of the blocks within the nanodomains and the disparity in their packing efficiency results in multiple chain folding of the PGly secondary structure that effectively stabilize a lamellar morphology for high fPBLG. Nanoscale confinement proves to be important in controlling the persistence length of secondary peptide motifs.

Original languageEnglish (US)
Pages (from-to)2352-2361
Number of pages10
Issue number4
StatePublished - Jul 2005
Externally publishedYes

ASJC Scopus subject areas

  • Bioengineering
  • Biomaterials
  • Polymers and Plastics
  • Materials Chemistry


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