Strategies exploiting functions and self-assembly properties of bioconjugates for polymer and materials sciences

被引：168

作者：

Boerner, Hans G. ^{[1
]}

机构：

[1] Max Planck Inst Colloids & Interfaces MPI KGF Gol, Colloid Dept, D-14424 Potsdam, Germany

来源：

PROGRESS IN POLYMER SCIENCE | 2009年 / 34卷 / 09期

关键词：

Peptide-polymer conjugates; Peptides; Proteins; Bioinspired; Biomimetic; Nanostructured; LIVING RADICAL POLYMERIZATION; HYBRID BLOCK-COPOLYMERS; SIDE-CHAIN POLYMERS; CROSS-LINKED POLYSTYRENES; PHASE PEPTIDE-SYNTHESIS; CLICK CHEMISTRY; BETA-SHEET; AMINO-ACIDS; RAFT POLYMERIZATION; CELL-ADHESION;

D O I：

10.1016/j.progpolymsci.2009.05.001

中图分类号：

O63 [高分子化学（高聚物）];

学科分类号：

070305 ; 080501 ; 081704 ;

摘要：

Controlling interactions in synthetic polymers as precisely as in proteins would have a strong impact on polymer science. Advanced structural and functional control can lead to rational design of integrated nano- and microstructures. To achieve this, properties of monomer sequence-defined peptides were exploited. Through their incorporation as monodisperse segments into synthetic polymers we learned in recent years how to program the structure formation of polymers, to adjust and exploit interactions in such polymers, to control inorganic-organic interfaces in fiber composites and induce structure in biomacromolecules like DNA for biomedical applications. (C) 2009 Elsevier Ltd. All rights reserved.

引用

页码：811 / 851

页数：41

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