Co–Cr–Mo alloy binding peptide as molecular glue for constructing biomedical surfaces
Source abstract
Abstract
The mechanical properties of Co–Cr–Mo (CCM) alloys are advantageous in various biomedical applications. However, because of their bioinert surface, CCM alloys exhibit poor endothelial cell attachment properties; thus, problems of biocompatibility remain. In this study, we aimed to improve the biocompatibility of the CCM alloy surface using solid-binding peptides. We selected peptides with high binding affinity for cast CCM alloy surfaces through in vitro evolution by the phage display method. The peptides were functionalized on the CCM alloy surfaces by simple immersion in the peptide solution. The peptide bound to both cast and 3D-printed CCMs with the same affinity. The peptides linked to the amino acid motif that promotes cell adhesion, and improved the attachment of endothelial cells on the 3D-printed CCM in serum and serum-free conditions. Hence, CCM-binding peptides are attractive tools for constructing a biofunctional surface on CCM-based biodevices.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Bone Tissue Engineering Materials · Polymer Surface Interaction Studies · Metal and Thin Film Mechanics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Graduate School of Science and Engineering, Yamagata University, Yamagata, Japan
Research Center for Functional Materials, National Institute for Materials Science (NIMS), Tsukuba, Ibaraki, Japan
AM Design Lab, NTT Data Engineering Systems Corporation, Minoh, Osaka, Japan
References (38)
Show source-provided references
1. 10.1016/j.corsci.2007.03.02310.1016/j.corsci.2007.03.023 ↗
2. Nasab MB · Trends Biomater Artif Organs · 2010 · 24 · 69
3. 10.1016/j.actamat.2006.10.00510.1016/j.actamat.2006.10.005 ↗
4. 10.1007/s11661-999-0052-610.1007/s11661-999-0052-6 ↗
5. 10.1016/j.jmbbm.2013.01.02110.1016/j.jmbbm.2013.01.021 ↗
6. 10.1049/bsbt.2018.004310.1049/bsbt.2018.0043 ↗
7. 10.4012/dmj.2017-15410.4012/dmj.2017-154 ↗
8. 10.22203/eCM.v021a2710.22203/eCM.v021a27 ↗
9. 10.1002/jbm.a.3598810.1002/jbm.a.35988 ↗
10. 10.1016/j.colsurfb.2014.12.05610.1016/j.colsurfb.2014.12.056 ↗
11. 10.1016/j.apsusc.2016.09.10710.1016/j.apsusc.2016.09.107 ↗
12. 10.1016/j.biomaterials.2012.12.03610.1016/j.biomaterials.2012.12.036 ↗
13. 10.1016/j.biomaterials.2011.08.01810.1016/j.biomaterials.2011.08.018 ↗
14. 10.1016/j.biomaterials.2005.05.01310.1016/j.biomaterials.2005.05.013 ↗
15. 10.1016/j.biomaterials.2008.11.03010.1016/j.biomaterials.2008.11.030 ↗
16. 10.1016/j.aca.2007.05.03310.1016/j.aca.2007.05.033 ↗
17. 10.1016/j.colsurfb.2010.03.03310.1016/j.colsurfb.2010.03.033 ↗
18. 10.1016/j.tibtech.2015.02.00510.1016/j.tibtech.2015.02.005 ↗
19. 10.1021/ja038414q10.1021/ja038414q ↗
20. 10.1007/s10856-009-3970-310.1007/s10856-009-3970-3 ↗
21. 10.1016/j.actbio.2010.06.00410.1016/j.actbio.2010.06.004 ↗
22. 10.1007/s10529-020-02832-110.1007/s10529-020-02832-1 ↗
23. 10.1007/s00170-018-2473-010.1007/s00170-018-2473-0 ↗
24. 10.3934/bioeng.2017.1.16210.3934/bioeng.2017.1.162 ↗
25. 10.5301/jabfm.500026010.5301/jabfm.5000260 ↗
26. 10.1006/jmbi.2000.368210.1006/jmbi.2000.3682 ↗
27. 10.1016/j.msec.2014.12.01710.1016/j.msec.2014.12.017 ↗
28. 10.4012/dmj.2015-06410.4012/dmj.2015-064 ↗
29. 10.1016/0092-8674(92)90115-S10.1016/0092-8674(92)90115-S ↗
30. 10.1021/acsami.9b0303010.1021/acsami.9b03030 ↗
31. 10.1002/mabi.20180036810.1002/mabi.201800368 ↗
32. 10.1016/j.biomaterials.2019.02.00110.1016/j.biomaterials.2019.02.001 ↗
33. 10.1016/S1357-2725(96)00110-010.1016/S1357-2725(96)00110-0 ↗
34. 10.1016/j.biomaterials.2012.05.06910.1016/j.biomaterials.2012.05.069 ↗
35. 10.1002/jbm.a.3687010.1002/jbm.a.36870 ↗
36. 10.3390/ijms2006142910.3390/ijms20061429 ↗
37. 10.1021/acs.bioconjchem.9b0057310.1021/acs.bioconjchem.9b00573 ↗
38. 10.1016/j.burns.2018.06.00810.1016/j.burns.2018.06.008 ↗