Functional polymer-bioconjugates as molecular LEGO® bricks

被引:52
作者
Boerner, Hans G. [1 ]
机构
[1] Max Planck Inst Colloids & Interfaces, Colloid Dept, D-14476 Potsdam, Golm, Germany
关键词
bioconjugates; peptide polymer conjugates; polymer microstructure; nanofibers; self-assembly; supramolecular structures;
D O I
10.1002/macp.200600559
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The controlled integration of sequence-defined oligopeptides into synthetic polymers leads to peptide-polymer conjugates with precisely defined, multifunctional peptide segments. These. bioconjugates allow for the direct realization of bio-inspired polymer science. Peptides combine self-assembly properties with the potential to actively interact with biological systems. Hence conjugates can be exploited to program microstructure formation processes in polymeric materials by controlling secondary interactions between the peptide segments. Moreover, the programmable functionalities of the peptides can be used to tune specific interactions, e.g., between drugs and polymeric drug carriers or between inorganic crystal surfaces and polymeric crystal-growth modifiers.
引用
收藏
页码:124 / 130
页数:7
相关论文
共 32 条
[1]   Elastin-based side-chain polymers synthesized by ATRP [J].
Ayres, L ;
Vos, MRJ ;
Adams, PJHM ;
Shklyarevskiy, IO ;
van Hest, JCM .
MACROMOLECULES, 2003, 36 (16) :5967-5973
[2]   Peptide-polymer bioconjugates:: hybrid block copolymers generated via living radical polymerizations from resin-supported peptides [J].
Becker, ML ;
Liu, JQ ;
Wooley, KL .
CHEMICAL COMMUNICATIONS, 2003, (02) :180-181
[3]  
Börner HG, 2002, MACROMOL SYMP, V177, P1, DOI 10.1002/1521-3900(200201)177:1<1::AID-MASY1>3.0.CO
[4]  
2-V
[5]   Synthesis of molecular brushes with block copolymer side chains using atom transfer radical polymerization [J].
Börner, HG ;
Beers, K ;
Matyjaszewski, K ;
Sheiko, SS ;
Möller, M .
MACROMOLECULES, 2001, 34 (13) :4375-4383
[6]  
BORNER HG, 2005, POLYM PREPR AM CHEM, V46, P744
[7]   Self-assembly of Aβ(10-35)-PEG block copolymer fibrils [J].
Burkoth, TS ;
Benzinger, TLS ;
Urban, V ;
Lynn, DG ;
Meredith, SC ;
Thiyagarajan, P .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (32) :7429-7430
[8]   Synthesis of 'difficult' peptide sequences:: application of a depsipeptide technique to the Jung-Redemann 10- and 26-mers and the amyloid peptide Aβ(1-42) [J].
Carpino, LA ;
Krause, E ;
Sferdean, CD ;
Schümann, M ;
Fabian, H ;
Bienert, M ;
Beyermann, M .
TETRAHEDRON LETTERS, 2004, 45 (40) :7519-7523
[9]   Depsipeptide methodology for solid-phase peptide synthesis:: Circumventing side reactions and development of an automated technique via depsidipeptide units [J].
Coin, Irene ;
Doelling, Rudolf ;
Krause, Eberhard ;
Bienert, Michael ;
Beyermann, Michael ;
Sferdean, Calin Dan ;
Carpino, Louis A. .
JOURNAL OF ORGANIC CHEMISTRY, 2006, 71 (16) :6171-6177
[10]  
DUNN AA, 2006, UNPUB