Modular design for the controlled production of polymeric nanotubes from polymer/peptide conjugates

被引:79
作者
Chapman, Robert [1 ]
Jolliffe, Katrina A. [1 ]
Perrier, Sebastien [1 ]
机构
[1] Univ Sydney, Sch Chem, Key Ctr Polymers & Colloids, Sydney, NSW 2006, Australia
关键词
FRAGMENTATION CHAIN TRANSFER; RADICAL POLYMERIZATION; CLICK CHEMISTRY; PEPTIDE; CYCLOADDITION; INITIATOR; ATRP; COPOLYMERS; STRATEGIES; EFFICIENT;
D O I
10.1039/c1py00202c
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 [高分子化学与物理];
摘要
We have established a new strategy to produce functional organic nanotubes of controlled structure from cyclic peptide/polymer conjugates. The structure guiding cyclic peptide motif was coupled to the polymeric chains via copper-catalyzed azide-alkyne click reaction, to yield very well-defined conjugates. The resulting conjugates were then self-assembled into nanotubes in solution. We were able to control to some extent the length of the nanotubes, by modifying the length of the polymer chain as well as by mixing conjugates of different molecular weights together. In a similar fashion we were able to prepare functional tubes from a range of polymers including poly(butyl acrylate), poly(dimethyl amino ethyl acrylate), poly(acrylic acid), poly(styrene) and poly(hydroxyl ethyl acrylate), as well as tubes with mixed functionality, by self-assembling a mixture of conjugates of differing polymer functionality. This modular approach is a powerful technique to generate a large number of nanotubes of varying size and functionality, in a controlled and rapid process. We believe this new approach will permit the design of a wide range of functional organic nanotubes of controlled structure, in a simple and efficient process.
引用
收藏
页码:1956 / 1963
页数:8
相关论文
共 49 条
[1]
Nanometre-size tubes of carbon [J].
Ajayan, PM ;
Ebbesen, TW .
REPORTS ON PROGRESS IN PHYSICS, 1997, 60 (10) :1025-1062
[2]
The future of reversible addition fragmentation chain transfer polymerization [J].
Barner-Kowollik, Christopher ;
Perrier, Sebastien .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2008, 46 (17) :5715-5723
[3]
Bioorthogonal click chemistry: Covalent labeling in living systems [J].
Baskin, Jeremy M. ;
Bertozzi, Carolyn R. .
QSAR & COMBINATORIAL SCIENCE, 2007, 26 (11-12) :1211-1219
[4]
Wrapping peptide tubes: Merging biological self-assembly and polymer synthesis [J].
Block, MAB ;
Hecht, S .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (43) :6986-6989
[5]
Strategies exploiting functions and self-assembly properties of bioconjugates for polymer and materials sciences [J].
Boerner, Hans G. .
PROGRESS IN POLYMER SCIENCE, 2009, 34 (09) :811-851
[6]
Bong DT, 2001, ANGEW CHEM INT EDIT, V40, P988, DOI 10.1002/1521-3773(20010316)40:6<988::AID-ANIE9880>3.3.CO
[7]
2-E
[8]
Towards functional bionanomaterials based on self-assembling cyclic peptide nanotubes [J].
Brea, Roberto J. ;
Reiriz, Cesar ;
Granja, Juan R. .
CHEMICAL SOCIETY REVIEWS, 2010, 39 (05) :1448-1456
[9]
Possibilities for 'smart' materials exploiting the self-assembly of polypeptides into fibrils [J].
Channon, Kevin ;
MacPhee, Cait E. .
SOFT MATTER, 2008, 4 (04) :647-652
[10]
Synthesis of Self-assembling Cyclic Peptide-polymer Conjugates using Click Chemistry [J].
Chapman, Robert ;
Jolliffe, Katrina A. ;
Perrier, Sebastien .
AUSTRALIAN JOURNAL OF CHEMISTRY, 2010, 63 (08) :1169-1172