The development of peptide-based interfacial biomaterials for generating biological functionality on the surface of bioinert materials

被引:50
作者
Meyers, Steven R. [1 ,2 ]
Khoo, Xiaojuan [1 ,2 ]
Huang, Xin [3 ]
Walsh, Elisabeth B. [4 ]
Grinstaff, Mark W. [1 ,2 ]
Kenan, Daniel J. [5 ]
机构
[1] Boston Univ, Dept Biomed Engn, Boston, MA 02215 USA
[2] Boston Univ, Dept Chem, Boston, MA 02215 USA
[3] Duke Univ, Dept Biomed Engn, Durham, NC 27708 USA
[4] Duke Univ, Dept Chem, Durham, NC 27708 USA
[5] Duke Univ, Med Ctr, Dept Pathol, Durham, NC 27710 USA
基金
美国国家卫生研究院;
关键词
Biomaterial; Engineered peptides; Peptide coating; Bioactive surface; Interfacial biology; Surface modification; BACTERIAL BIOFILMS; PHAGE DISPLAY; CELL-SURVIVAL; IN-VIVO; FIBRONECTIN; ADHESION; RGD; APOPTOSIS; MATRIX; ANGIOGENESIS;
D O I
10.1016/j.biomaterials.2008.08.042
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Biomaterials used in implants have traditionally been selected based on their mechanical properties, chemical stability, and biocompatibility. However, the durability and clinical efficacy of implantable biomedical devices remain limited in part due to the absence of appropriate biological interactions at the implant interface and the lack of integration into adjacent tissues. Herein, we describe a robust peptide-based coating technology capable of modifying the surface of existing biomaterials and medical devices through the non-covalent binding of modular biofunctional peptides. These peptides contain at least one material binding sequence and at least one biologically active sequence and thus are termed, "Interfacial Biomaterials" (IFBMs). IFBMs can simultaneously bind the biomaterial surface while endowing it with desired biological functionalities at the interface between the material and biological realms. We demonstrate the capabilities of model IFBMs to convert native polystyrene, a bioinert surface, into a bioactive Surface that can support a range of cell activities. We further distinguish between simple cell attachment with insufficient integrin interactions, which in some cases can adversely impact downstream biology, versus biologically appropriate adhesion, cell spreading, and cell survival mediated by IFBMs. Moreover, we show that we can use the coating technology to create spatially resolved patterns of fluorophores and cells on substrates and that these patterns retain their borders in culture. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:277 / 286
页数:10
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