Authors: G. Kim, L. Jiang, P.K. Rathod, C.T. Campbell, A. Nishimoto and V. Casasanta
Affilation: University of Washington, United States
Pages: 381 - 384
Keywords: immunoassay, spr, protein microarray, biosensor
The use of Surface Plasmon Resonance (SPR) for the detection of biomolecular binding events at the nanometer scale is of great utility when expanded into microarray density formats. Protein microarray analysis is particularly well suited for such methodology. In this work we demonstrate a high-throughput, quantitative immunoassay by employing microarray techniques in combination with SPR microscopy. Antibody microarrays with various immunoglobulin proteins, including human immunoglobulin subclasses were printed on functionalized gold-coated glass slides. Gold-coated glass slides presenting amine reactive moieties were prepared by traditional silation reactions to facilitate protein microarray printing. Antigen microarrays were also printed with various allergens including human serum albumin as well as bovine serum albumin in similar fashion. A spot density of up to 240 120-µm spots was generated using conventional robotic microspotting. Application of antibody/antigen microarrays with SPR microscopy allows for the simultaneous monitoring of immunoglobulin protein binding kinetics over the whole array (allergens or antibodies), at a time resolution of one second. The ability of microarray based SPR to quantitatively monitor (in “real-time”) antigen-antibody binding kinetics allows it to become a complementary tool in support of the multi-step and labor-intensive ELISA method (with a sensitivity of 1.2 ng/cm2 for most proteins).