Synthesis, characterization, conformation and self-assembly behavior of polypeptide-based brush with oligo (ethylene glycol) side chains

被引:8
|
作者
Huang, Yugang [1 ]
Luo, Weiang [2 ]
Ye, Guodong [1 ]
机构
[1] Guangzhou Med Univ, Sch Pharmaceut Sci, Dept Chem, Guangzhou 510182, Guangdong, Peoples R China
[2] Xiamen Univ, Coll Mat, Xiamen 361005, Peoples R China
基金
中国国家自然科学基金;
关键词
Conformation; Polypeptide; Self-assembly; alpha-Helix; CIRCULAR-DICHROISM; MOLECULAR BRUSHES; BLOCK-COPOLYMERS; INFRARED-SPECTRA; DIBLOCK;
D O I
10.1016/j.molstruc.2014.10.045
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A new polypeptide-based copolymer brush composed of poly (gamma-propargyl-L-glutamate)-block-poly (propylene oxide)-block-poly (gamma-propargyl-L-glutamate) backbone (PPLG-b-PPO-b-PPLG) and oligo (ethylene glycol) (PEG) side-chain was synthesized by combination of N-carboxyanhydride ring-opening polymerization and click chemistry. Nearly 100% grafting efficiency was achieved by copper-catalyzed azidealkyne Huisgen 1,3-dipolar cycloaddition (CuAAc) reaction. The alpha-helical conformation adopted by the grafted polypeptide blocks in water was relatively stable and showed a reversible change in a heatingcooling circle from 5 to 70 degrees C. It displayed weak stability against elevated temperature but still reversible changes in the presence of 0.47 M NaCl. The brushes were amphiphilic and could self-assemble into thermo-sensitive micelles in water. Big micelles could break into small micelles upon heating due to the improved solubility. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:274 / 280
页数:7
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