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Carborane-beta-cyclodextrin complexes as a supramolecular connector for bioactive surfaces

Year: 2015

Journal: JOURNAL OF MATERIALS CHEMISTRY B, 2015,3, 539-545, 20150430

Authors: Neirynck, P.; Schimer, J.; Jonkheijm, P.; Milroy, L. -G.; Cigler, P.; Brunsveld, L.

Organizations: Eindhoven Univ Technol, Biol Chem Lab, NL-5612 AZ Eindhoven, Netherlands; Eindhoven Univ Technol, Inst Complex Mol Syst, Dept Biomed Engn, NL-5612 AZ Eindhoven, Netherlands; Acad Sci Czech Republic, Inst Organ Chem & Biochem, Vvi, CR-16610 Prague 6, Czech Republic; Univ Twente, MESA Inst Nanotechnol, Dept Sci & Technol, Mol Nanofabricat Grp, NL-7500 AE Enschede, Netherlands

Supramolecular chemistry provides an attractive entry to generate dynamic and well-controlled bioactive surfaces. Novel host-guest systems are urgently needed to provide a broader affinity and applicability portfolio. A synthetic strategy to carborane-peptide bioconjugates was therefore developed to provide an entry to monovalent supramolecular functionalization of beta-cyclodextrin coated surfaces. The beta-cyclodextrin carborane-cRGD surfaces are formed efficiently and with high affinity as demonstrated by IR-RAS, WCA, and QCM-D, compare favourable to existing bio-active host-guest surface assemblies, and display an efficient bioactivity, as illustrated by a strong functional effect of the supramolecular system on the cell adhesion and spreading properties. Cells seeded on the supramolecular surface displaying bioactive peptide epitopes exhibited a more elongated morphology, focal adhesions, and stronger cell adhesion compared to control surfaces. This highlights the macroscopic functionality of the novel supramolecular immobilization strategy.