Self-assembly of polypeptide-based block copolymer amphiphiles

被引:265
作者
Carlsen, Autumn [1 ,2 ]
Lecommandoux, Sebastein [1 ,2 ]
机构
[1] Univ Bordeaux, ENSCPB, F-33607 Pessac, France
[2] CNRS, Lab Chim Polymeres Organ, UMR5629, Pessac, France
关键词
Polypeptide; Copolymer; Self-assembly; Micelle; Vesicle; Amphiphile; POLYION COMPLEX MICELLES; POLY(GAMMA-BENZYL L-GLUTAMATE); TRIBLOCK COPOLYMERS; DIBLOCK COPOLYMERS; POLYMERIC MICELLES; AQUEOUS-MEDIUM; NANO-OBJECTS; VESICLES; MICELLIZATION; TEMPERATURE;
D O I
10.1016/j.cocis.2009.04.007
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
The past decade has seen growing interest in the investigation of self-assembling nanostructures, particularly in aqueous solution. In this context, polypeptide-based copolymers show considerable promise as building blocks that allow enhanced control over intra- and intermolecular interactions, in concert with stable, yet modifiable, secondary and tertiary structures. We will focus here on the most recent advances in the formation of micelles and vesicles from peptide-polymer conjugates or from copolypeptide systems, and on the capacity of these structures to manifest stimuli-driven variation in size and shape. We will also discuss a new generation of materials based on protein-like copolymers that offer precise control over molecular composition and structure along with predetermined biological functionality. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:329 / 339
页数:11
相关论文
共 75 条
[1]   Vesicles from Peptidic Side-Chain Polymers Synthesized by Atom Transfer Radical Polymerization [J].
Adams, Dave J. ;
Atkins, Derek ;
Cooper, Andrew I. ;
Furzeland, Steve ;
Trewin, Abbie ;
Young, Iain .
BIOMACROMOLECULES, 2008, 9 (11) :2997-3003
[2]   Thermoresponsive micelles from jeffamine-b-poly(L-glutamic acid) double hydrophilic block copolymers [J].
Agut, Willy ;
Brulet, Annie ;
Taton, Daniel ;
Lecommandoux, Sebastien .
LANGMUIR, 2007, 23 (23) :11526-11533
[3]   Vesicles and liposomes:: A self-assembly principle beyond lipids [J].
Antonietti, M ;
Förster, S .
ADVANCED MATERIALS, 2003, 15 (16) :1323-1333
[4]   Formation of core-shell type biodegradable polymeric micelles from amphiphilic poly(aspartic acid)-block-polylactide diblock copolymer [J].
Arimura, H ;
Ohya, Y ;
Ouchi, T .
BIOMACROMOLECULES, 2005, 6 (02) :720-725
[5]   Self-assembled nanostructures from peptide-synthetic hybrid block copolymers: Complex, stimuli-responsive rod-coil architectures [J].
Babin, J ;
Rodriguez-Hernandez, J ;
Lecommandoux, S ;
Klok, HA ;
Achard, MF .
FARADAY DISCUSSIONS, 2005, 128 :179-192
[6]   Block copolymers - Designer soft materials [J].
Bates, FS ;
Fredrickson, GH .
PHYSICS TODAY, 1999, 52 (02) :32-38
[7]   Stimuli-responsive polypeptide vesicles by conformation-specific assembly [J].
Bellomo, EG ;
Wyrsta, MD ;
Pakstis, L ;
Pochan, DJ ;
Deming, TJ .
NATURE MATERIALS, 2004, 3 (04) :244-248
[8]   Rheology of block copolypeptide solutions: Hydrogels with tunable properties [J].
Breedveld, V ;
Nowak, AP ;
Sato, J ;
Deming, TJ ;
Pine, DJ .
MACROMOLECULES, 2004, 37 (10) :3943-3953
[9]   Self-assembly behavior of pH- and thermosensitive amphiphilic triblock copolymers in solution: Experimental studies and self-consistent field theory simulations [J].
Cai, Chunhua ;
Zhang, Liangshun ;
Lin, Jiaping ;
Wang, Liquan .
JOURNAL OF PHYSICAL CHEMISTRY B, 2008, 112 (40) :12666-12673
[10]   GENETIC-ENGINEERING OF STRUCTURAL PROTEIN POLYMERS [J].
CAPPELLO, J ;
CRISSMAN, J ;
DORMAN, M ;
MIKOLAJCZAK, M ;
TEXTOR, G ;
MARQUET, M ;
FERRARI, F .
BIOTECHNOLOGY PROGRESS, 1990, 6 (03) :198-202