ミカミ アカネ
三上 あかね 所属 医療保健学部 臨床検査学科 職種 専任講師 |
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言語種別 | 英語 |
発行・発表の年月 | 2020/02 |
形態種別 | 学術論文 |
査読 | 査読あり |
標題 | A novel biofunctionalizing peptide for metallic alloy |
執筆形態 | 共著 |
掲載誌名 | Biotechnology letter |
掲載区分 | 国外 |
出版社・発行元 | Springer |
巻・号・頁 | 42,pp.747-756 |
総ページ数 | 10 |
著者・共著者 | Akane Sakaguchi-Mikami, Kazuhiro Fujimoto, Tetsushi Taguchi, Isao Karube,Tomohiko Yamazaki |
概要 | Objectives
Improving biocompatibility of metallic alloy biomaterials has been of great interest to prevent implant associated-diseases, such as stent thrombosis. Herein a simple and efficient procedure was designed to biofunctionalize a biomaterial surface by isolating a SUS316L stainless steel binding peptide. Results After three rounds of phage panning procedure, 12 mer peptide (SBP-A; VQHNTKYSVVIR) was identified as SUS316L-binding peptide. The SBP-A peptide formed a stable bond to a SUS316L modified surface and was not toxic to HUVECs. The SBP-A was then used for anti-ICAM antibody modification on SUS316L to construct a vascular endothelial cell-selective surface. The constructed surface dominantly immobilized vascular endothelial cells to smooth muscle cells, demonstrating that the SBP-A enabled simple immobilization of biomolecules without disturbing their active biological function. Conclusions The SUS316L surface was successfully biofunctionalized using the novel isolated peptide SBP-A, showing its potential as an ideal interface molecule for stent modification. This is the first report of material binding peptide-based optimal surface functionalization to promote endothelialisation. This simple and efficient biofunctionalization procedure is expected to contribute to the development of biocompatible materials. |