Selective Cell Adhesion and Biosensing Applications of Bio-Active Block Copolymers Prepared by CuAAC/Thiol-ene Double Click Reactions

Macromol Biosci. 2015 Sep;15(9):1233-41. doi: 10.1002/mabi.201500099. Epub 2015 May 13.

Abstract

N-Acetyl-l-cysteine (NAC)-capped poly(methyl methacrylate)-b-polycaprolactone block copolymer (PMMA-b-PCL-NAC) was prepared using the previously described one-pot photoinduced sequential CuAAC/thiol-ene double click procedure. PMMA-b-PCL-NAC had previously shown good applicability as a matrix for cell adhesion of cells from the Vero cell line (African green monkey kidney epithelial). Here, in this work, PMMA-b-PCL-NAC served as an excellent immobilization matrix for biomolecule conjugation. Covalent binding of RGD (R: arginine, G: glycine, and D: aspartic acid) peptide sequence onto the PMMA-b-PCL-NAC-coated surface was performed via EDC chemistry. RGD-modified PMMA-b-PCL-NAC (PMMA-b-PCL-NAC-RGD) as a non-toxic cell proliferation platform was used for selective "integrin αvβ3-mediated cell adhesion and biosensing studies. Both optical and electrochemical techniques were used to monitor the adhesion differences between "integrin αvβ3" receptor positive and negative cell lines on to the designed biofunctional surfaces.

Keywords: cell adhesion; cell sensing; electrochemical biosensor; selective surfaces.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biosensing Techniques*
  • Cell Adhesion*
  • Cell Line, Tumor
  • Click Chemistry
  • Humans
  • Keratinocytes / physiology
  • Methylmethacrylates / chemistry*
  • Oligopeptides / metabolism*
  • Polyesters / chemistry*
  • Protein Binding
  • Surface Properties
  • Tissue Scaffolds*

Substances

  • Methylmethacrylates
  • Oligopeptides
  • Polyesters
  • poly(methyl methacrylate)-b-polycaprolactone-N-acetylcysteine
  • arginyl-glycyl-aspartic acid