A novel method is proposed for the fabrication of protein microarrays using metal coordination chemistry and poly-histidine tagged protein molecules. The proposed method is aimed at microarrays with highly selective and facile linking chemistry, with uniform and controllable orientation of immobilized protein molecules, and with proteins in native states and easily accessible by targets in the solution. Preliminary experiments using 6x-His terminated green-fluorescence protein (GFP) demonstrated the feasibility and potential of the proposed approach. We will establish the advantage of an oriented protein microarray in protein-ligand interaction studies over randomly oriented arrays fabricated by existing methods. We also propose to explore protein immobilization without purification on the highly selective metal ion surface.

Proposed Commercial Applications

NOT AVAILABLE

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Small Business Innovation Research Grants (SBIR) - Phase I (R43)
Project #
1R43RR017130-01
Application #
6483666
Study Section
Special Emphasis Panel (ZRG1-SSS-2 (10))
Program Officer
Sheeley, Douglas
Project Start
2002-05-01
Project End
2003-03-31
Budget Start
2002-05-01
Budget End
2003-03-31
Support Year
1
Fiscal Year
2002
Total Cost
$100,000
Indirect Cost
Name
Microsurfaces, Inc.
Department
Type
DUNS #
City
Minneapolis
State
MN
Country
United States
Zip Code
Cha, Taewoon; Guo, Athena; Zhu, Xiao-Yang (2005) Enzymatic activity on a chip: the critical role of protein orientation. Proteomics 5:416-9
Cha, Taewoon; Guo, Athena; Jun, Yongseok et al. (2004) Immobilization of oriented protein molecules on poly(ethylene glycol)-coated Si(111). Proteomics 4:1965-76
Jun, Yongseok; Cha, Taewoon; Guo, Athena et al. (2004) Patterning protein molecules on poly(ethylene glycol) coated Si(111). Biomaterials 25:3503-9