Influence of assembling pH on the stability of poly(l-glutamic acid) and poly(l-lysine) multilayers against urea treatment

Jie Zhou, Bo Wang, Weijun Tong, Elena Maltseva, Gang Zhang, Rumen Krastev, Changyou Gao, Helmuth Möhwald, Jiacong Shen

Research output: Contribution to journalArticlepeer-review

22 Scopus citations

Abstract

Polyelectrolyte multilayers of poly(l-glutamic acid) (PGA) and poly(l-lysine) (PLL) were built up using the layer-by-layer (LbL) technique in low pH (3.6, PM3.6) and in neutral pH (7.4, PM7.4) solutions. The multilayers were then treated with a concentrated urea (one kind of denaturant for proteins and polypeptides) solution (8 M) and rinsed with corresponding buffer. The buildup and treatment processes were investigated by ultraviolet visible spectroscopy and ellipsometry. The surface morphology was observed by scanning force microscopy (SFM). The inner structures were determined by X-ray reflectometry and circular dichroism spectroscopy (CD). An exponential growth of the optical mass and the layer thickness was observed for both PM3.6 and PM7.4. After urea treatment, a significant mass loss for PM3.6 was found, while no mass change was recorded for PM7.4. The dominant driving force for PM7.4 is electrostatic interaction, resulting in multilayers with an abundant β-sheet structure, which has higher stability against urea treatment. By contrast, the dominant driving force for PM3.6 is hydrogen bonding and hydrophobic interaction, which are sensitive to the urea treatment. The mechanism is substantiated by molecular mechanics calculation. This has offered a convenient pathway to mediate the multilayer properties, which is of great importance for potential applications.

Original languageEnglish (US)
Pages (from-to)250-257
Number of pages8
JournalColloids and Surfaces B: Biointerfaces
Volume62
Issue number2
DOIs
StatePublished - Apr 1 2008

All Science Journal Classification (ASJC) codes

  • Biotechnology
  • Surfaces and Interfaces
  • Physical and Theoretical Chemistry
  • Colloid and Surface Chemistry

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