A versatile approach to high-throughput microarrays using thiol-ene chemistry

Nat Chem. 2010 Feb;2(2):138-45. doi: 10.1038/nchem.478. Epub 2009 Dec 20.

Abstract

Microarray technology has become extremely useful in expediting the investigation of large libraries of materials in a variety of biomedical applications, such as in DNA chips, protein and cellular microarrays. In the development of cellular microarrays, traditional high-throughput printing strategies on stiff, glass substrates and non-covalent attachment methods are limiting. We have developed a facile strategy to fabricate multifunctional high-throughput microarrays embedded at the surface of a hydrogel substrate using thiol-ene chemistry. This user-friendly method provides a platform for the immobilization of a combination of bioactive and diagnostic molecules, such as peptides and dyes, at the surface of poly(ethylene glycol)-based hydrogels. The robust and orthogonal nature of thiol-ene chemistry allows for a range of covalent attachment strategies in a fast and reliable manner, and two complementary strategies for the attachment of active molecules are demonstrated.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Alkenes / chemistry*
  • Amino Acid Sequence
  • Animals
  • Biomimetic Materials / chemistry
  • Cell Adhesion
  • Hydrogels / chemistry
  • Mice
  • Microarray Analysis*
  • Microtechnology / methods*
  • NIH 3T3 Cells
  • Peptides / chemistry
  • Peptides / metabolism
  • Printing
  • Sulfhydryl Compounds / chemistry*

Substances

  • Alkenes
  • Hydrogels
  • Peptides
  • Sulfhydryl Compounds

Associated data

  • PubChem-Substance/85752838
  • PubChem-Substance/85752839
  • PubChem-Substance/85752840
  • PubChem-Substance/85752841
  • PubChem-Substance/85752842
  • PubChem-Substance/85752843
  • PubChem-Substance/85752844
  • PubChem-Substance/85752845
  • PubChem-Substance/85752846
  • PubChem-Substance/85752847