Extended Self-Assembled Long Periodicity and Zig-Zag Domains from Helix-Helix Diblock Copolymer Poly(γ-benzyl-L-glutamate)-block-poly(O-benzyk-hydroxyproline)

被引:15
|
作者
Gkikas, Manos [1 ,2 ]
Haataja, Johannes S. [2 ]
Seitsonen, Jani [2 ,3 ]
Ruokolainen, Janne [2 ,3 ]
Ikkala, Olli [2 ]
Iatrou, Hermis [1 ]
Houbenov, Nikolay [2 ]
机构
[1] Univ Athens, Dept Chem, Athens 15771, Greece
[2] Aalto Univ, Sch Sci & Technol, Dept Appl Phys, FIN-00076 Espoo, Finland
[3] Aalto Univ, Sch Sci & Technol, Nanomicroscopy Ctr, FIN-00076 Espoo, Finland
基金
芬兰科学院;
关键词
POLY-L-HYDROXYPROLINE; BLOCK COPOLYPEPTIDES; ROD; POLYPEPTIDE; DYNAMICS; POLYMERIZATION; PROLINE; THERMODYNAMICS; ORGANIZATION; L-GLUTAMATE);
D O I
10.1021/bm5009734
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We describe the synthesis and self-assembly of particularly high periodicity of diblock copolymers composed of poly(benzyl-l-hydroxyproline) (PBLHyP) and poly(gamma-benzyl-l-glutamate) (PBLG), that is, two polypeptide blocks with dissimilar helical structures. The robust helicity of the PBLHyP block is driven by steric constraints of the repeat units, while PBLG forms alpha-helices driven by hydrogen bonding, allowing defects and deformations. Herein, high-molecular-weight diblock copolypeptides of PBLG-b-PBLHyP with three different volume fractions of the PBLHyP-blocks are discussed. For shorter PBLHyP blocks, hexagonal packing of PBLHyP helices is observed, while by increasing the length of the PBLHyP block, keeping at a similar PBLG block length, the packing is distorted. Zig-zag lamellar structures were obtained due to the mismatch in the packing periodicities of the PBLG and PBLHyP helices. The frustration that takes place at the interface leads the PBLHyP to tilt to match the PBLG periodicity. The zig-zag morphology is reported for the first time for high-molecular-weight helixhelix (rodrod) copolypeptides, and the self-assembled periodicity is uncommonly large.
引用
收藏
页码:3923 / 3930
页数:8
相关论文
empty
未找到相关数据