Self-assembly and bioactivity of a polymer/peptide conjugate containing the RGD cell adhesion motif and PEG

被引:22
作者
Castelletto, Valeria [1 ]
Gouveia, Ricardo J. [1 ]
Connon, Che J. [1 ]
Hamley, Ian W. [1 ]
机构
[1] Univ Reading, Sch Chem Pharm & Food Biosci, Reading RG6 6AD, Berks, England
基金
英国生物技术与生命科学研究理事会;
关键词
Peptide-polymer conjugates; Self-assembly; beta-sheet structures; PEG; RGD peptide; POLY(ETHYLENE GLYCOL); SYNTHETIC STRATEGIES; PEPTIDE AMPHIPHILE; BLOCK-COPOLYMERS; HYDROGELS; CRYSTALLIZATION; PROTEIN; DESIGN;
D O I
10.1016/j.eurpolymj.2013.02.016
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 self-assembly and bioactivity of the peptide-polymer conjugate DGRFFF-PEG3000 containing the RGD cell adhesion motif has been examined, in aqueous solution. The conjugate is designed to be amphiphilic by incorporation of three hydrophobic phenylalanine residues as well as the RGD unit and a short poly(ethylene glycol) (PEG) chain of molar mass 3000 kg mol(-1). Above a critical aggregation concentration, determined by fluorescence measurements, signals of p-sheet structure are revealed by spectroscopic measurements, as well as X-ray diffraction. At high concentration, a self-assembled fibril nanostructure is revealed by electron microscopy. The fibrils are observed despite PEG crystallization which occurs on drying. This suggests that DGRFFF has an aggregation tendency that is sufficiently strong not to be prevented by PEG crystallization. The adhesion, viability and proliferation of human corneal fibroblasts was examined for films of the conjugate on tissue culture plates (TCPs) as well as low attachment plates. On TCP, DGRFFF-PEG3000 films prepared at sufficiently low concentration are viable, and cell proliferation is observed: However, on low attachment surfaces, neither cell adhesion nor proliferation was observed, indicating that the RGD motif was not available to enhance cell adhesion. This was ascribed to the core-shell architecture of the self-assembled fibrils with a peptide core surrounded by a PEG shell which hinders access to the RGD unit. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2961 / 2967
页数:7
相关论文
共 64 条
[41]   Cell-responsive synthetic hydrogels [J].
Lutolf, MP ;
Raeber, GP ;
Zisch, AH ;
Tirelli, N ;
Hubbell, JA .
ADVANCED MATERIALS, 2003, 15 (11) :888-+
[42]   Modern trends in polymer bioconjugates design [J].
Lutz, Jean-Francois ;
Boerner, Hans G. .
PROGRESS IN POLYMER SCIENCE, 2008, 33 (01) :1-39
[43]   Combining ATRP and "click" chemistry:: a promising platform toward functional biocompatible polymers and polymer bioconjugates [J].
Lutz, Jean-Francois ;
Boerner, Hans G. ;
Weichenhan, Katja .
MACROMOLECULES, 2006, 39 (19) :6376-6383
[44]   Smooth muscle cell growth in photopolymerized hydrogels with cell adhesive and proteolytically degradable domains: synthetic ECM analogs for tissue engineering [J].
Mann, BK ;
Gobin, AS ;
Tsai, AT ;
Schmedlen, RH ;
West, JL .
BIOMATERIALS, 2001, 22 (22) :3045-3051
[45]   Polymer-Peptide Block Copolymers - An Overview and Assessment of Synthesis Methods [J].
Marsden, Hana Robson ;
Kros, Alexander .
MACROMOLECULAR BIOSCIENCE, 2009, 9 (10) :939-951
[46]   Living radical polymerization as a tool for the synthesis of polymer-protein/peptide bioconjugates [J].
Nicolas, Julien ;
Mantovani, Giuseppe ;
Haddleton, David M. .
MACROMOLECULAR RAPID COMMUNICATIONS, 2007, 28 (10) :1083-1111
[47]  
Nordén B, 2010, LINEAR DICHROISM AND CIRCULAR DICHROISM: A TEXTBOOK ON POLARIZED LIGHT SPECTROSCOPY, P1
[48]   Spectroscopic methods for analysis of protein secondary structure [J].
Pelton, JT ;
McLean, LR .
ANALYTICAL BIOCHEMISTRY, 2000, 277 (02) :167-176
[49]   CELL ATTACHMENT ACTIVITY OF FIBRONECTIN CAN BE DUPLICATED BY SMALL SYNTHETIC FRAGMENTS OF THE MOLECULE [J].
PIERSCHBACHER, MD ;
RUOSLAHTI, E .
NATURE, 1984, 309 (5963) :30-33
[50]   NEW PERSPECTIVES IN CELL-ADHESION - RGD AND INTEGRINS [J].
RUOSLAHTI, E ;
PIERSCHBACHER, MD .
SCIENCE, 1987, 238 (4826) :491-497