Creating ultrathin nanoscopic collagen matrices for biological and biotechnological applications

被引:57
作者
Cisneros, David A. [1 ]
Friedrichs, Jens [1 ]
Taubenberger, Anna [1 ]
Franz, Clemens M. [1 ]
Muller, Daniel J. [1 ]
机构
[1] Tech Univ Dresden, BIOTEC, Inst Biol, D-01307 Dresden, Germany
关键词
atomic force microscopy; biofunctionalization; biomaterials; collagen; self-assembly; ATOMIC-FORCE MICROSCOPY; DIP-PEN NANOLITHOGRAPHY; SCANNING PROBE MICROSCOPY; CELL-ADHESION; I COLLAGEN; FIBRIL; INTEGRIN; PROTEIN; ORGANIZATION; RECOGNITION;
D O I
10.1002/smll.200600598
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The biofunctionalization of materials creates interfaces on which proteins, cells, or tissues can fulfill native or desired tasks. Here we report how to control the assembly of type I collagen into well-defined nanoscopic matrices of different patterns. Collagen fibrils in these ultrathin (approximate to 3 nm) matrices maintained their native structure as observed in vivo. This opens up the possibility to create programmable biofunctionalized matrices using collagen-binding proteins or proteins fused with collagen-binding domains. Applied to eukaryotic cells, these nanostructured matrices can direct cellular processes such as adhesion, orientation and migration.
引用
收藏
页码:956 / 963
页数:8
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