| Title | A versatile approach to high-throughput microarrays using thiol-ene chemistry |
| Publication Type | Journal Article |
| Year of Publication | 2010 |
| Authors | Gupta N, Lin BF, Campos LM, Dimitriou MD, Hikita ST, Treat ND, Tirrell MV, Clegg DO, Kramer EJ, Hawker CJ |
| Journal | Nature Chemistry |
| Volume | 2 |
| Issue | 2 |
| Pagination | 138-45 |
| Date Published | 2010 Feb |
| ISSN | 1755-4349 |
| Keywords | Alkenes, Amino Acid Sequence, Animals, Biomimetic Materials, Cell Adhesion, Hydrogels, Mice, Microarray Analysis, Microtechnology, NIH 3T3 Cells, Peptides, Printing, Sulfhydryl Compounds |
| 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. |
| DOI | 10.1038/nchem.478 |
| Alternate Journal | Nat Chem |
| PubMed ID | 21124405 |
