Multifunctional Coating Improves Cell Adhesion on Titanium by using Cooperatively Acting Peptides

被引:63
作者
Pagel, Mareen [1 ]
Hassert, Rayk [1 ,5 ]
John, Torsten [2 ,3 ]
Braun, Klaus [4 ]
Wiessler, Manfred [4 ]
Abel, Bernd [2 ,3 ]
Beck-Sickinger, Annette G. [1 ]
机构
[1] Univ Leipzig, Inst Biochem, Bruderstr 34, D-04103 Leipzig, Germany
[2] Univ Leipzig, Leibniz Inst Oberflachenmodifizierung IOM, D-04103 Leipzig, Germany
[3] Univ Leipzig, Wilhelm Ostwald Inst Phys & Theoret Chem, D-04103 Leipzig, Germany
[4] Deutsch Krebsforschungszentrum, Dept Med Phys Radiol, Neuenheimer Feld 280, D-69120 Heidelberg, Germany
[5] Univ Leipzig, Inst Bioanalyt Chem, Deutsch Pl 5, D-04103 Leipzig, Germany
关键词
cell adhesion; click chemistry; DOPA; peptides; surface chemistry; CYCLIC RGD PEPTIDES; FOCAL ADHESIONS; STEM-CELLS; SURFACES; BINDING; BIOMATERIALS; OSTEOBLASTS; ATTACHMENT; CHEMISTRY; POLYMERS;
D O I
10.1002/anie.201511781
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Promotion of cell adhesion on biomaterials is crucial for the long-term success of a titanium implant. Herein a novel concept is highlighted combining very stable and affine titanium surface adhesive properties with specific cell binding moieties in one molecule. A peptide containing l-3,4-dihydroxyphenylalanine was synthesized and affinity to titanium was investigated. Modification with a cyclic RGD peptide and a heparin binding peptide (HBP) was realized by an efficient on-resin combination of Diels-Alder reaction with inverse electron demand and Cu-I catalyzed azide-alkyne cycloaddition. The peptide was fluorescently labeled by thiol Michael addition. Conjugating the cyclic RGD and HBP in one peptide gave improved spreading, proliferation, viability, and the formation of well-developed actin cytoskeleton and focal contacts of osteoblast-like cells.
引用
收藏
页码:4826 / 4830
页数:5
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