Tyrosinase-catalyzed synthesis of a universal coil-chitosan bioconjugate for protein immobilization

被引:32
作者
Demolliens, Antoine [1 ]
Boucher, Cyril [1 ,2 ]
Durocher, Yves [2 ]
Jolicoeur, Mario [1 ]
Buschmann, Michael D. [1 ]
De Crescenzo, Gregory [1 ]
机构
[1] Ecole Polytech, Inst Biomed Engn, Dept Chem Engn, Montreal, PQ H3C 3A7, Canada
[2] Natl Res Council Canada, Biotechnol Res Inst, Anim Cell Technol Grp, Bioproc Sector, Montreal, PQ H4P 2R2, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
D O I
10.1021/bc800066b
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Chitosan has been reported as a promising material for gene and drug delivery as well as for tissue engineering and regenerative medicine. We report here the conjugation of a de novo designed coil peptide (Kcoil) to chitosan (M-n = 200 kDa) to achieve a universal Kcoil-chitosan scaffold for subsequent immobilization of proteins tagged with the Kcoil partner, i.e., the Ecoil peptide. Kcoil-chitosan conjugate was synthesized using a tyrosinase-catalyzed protocol. Extensive UV/vis and IR characterization demonstrated that Kcoil peptide was covalently grafted to amines of chitosan. The ability of Kcoil-chitosan conjugate to recruit Ecoil tagged epidermal growth factor (EGF) was assessed by surface plasmon resonance measurements (SPR). Despite nonspecific interactions between chitosan and EGF, the specific formation of an E/K coiled coil complex was observed at slightly acidic pH and high salt concentration conditions, demonstrating that grafting to chitosan did not negatively impact binding characteristics of Kcoil peptide. Finally, the benefits of such bioconjugates for biomedical applications are discussed.
引用
收藏
页码:1849 / 1854
页数:6
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