Peptide-directed self-assembly of hydrogels

被引：161
作者：
Kopecek, Jindrich [1 ]
Yang, Jiyuan
机构：
[1] Univ Utah, Dept Pharmaceut & Pharmaceut Chem, Salt Lake City, UT 84112 USA
来源：
ACTA BIOMATERIALIA | 2009年 / 5卷 / 03期
关键词：
Hydrogels; Self-assembly; Hybrid biomaterials; Peptides; Proteins; GENETICALLY-ENGINEERED PROTEIN; NONCANONICAL AMINO-ACIDS; CONTROLLED DRUG-DELIVERY; HYBRID BLOCK-COPOLYMERS; GLYCOL) STAR COPOLYMER; HELICAL COILED-COILS; CO-PEG NETWORKS; POLY(ETHYLENE GLYCOL); REVERSIBLE HYDROGELS; TRIBLOCK COPOLYMERS;
D O I：
10.1016/j.actbio.2008.10.001
中图分类号：
R318 [生物医学工程];
学科分类号：
0831 ;
摘要：
This review focuses on the self-assembly of macromolecules mediated by the biorecognition of peptide/protein domains. Structures forming a-helices and P-sheets have been used to mediate self-assembly into hydrogels of peptides, reactive copolymers and peptide motifs, block copolymers, and graft copolymers. Structural factors governing the self-assembly of these molecules into precisely defined three-dimensional structures (hydrogels) are reviewed. The incorporation of peptide motifs into hybrid systems, composed of synthetic and natural macromolecules, enhances design opportunities for new biomaterials when compared to individual components. (c) 2008 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码：805 / 816
页数：12
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