Abstract
To broaden the range of tools available for proteomic research, we generated a library of 16,368 unique full-length human ORFs that are expressible as N-terminal GST-His6 fusion proteins. Following expression in yeast, these proteins were then individually purified and used to construct a human proteome microarray. To demonstrate the usefulness of this reagent, we developed a streamlined strategy for the production of monospecific monoclonal antibodies that used immunization with live human cells and microarray-based analysis of antibody specificity as its central components. We showed that microarray-based analysis of antibody specificity can be performed efficiently using a two-dimensional pooling strategy. We also demonstrated that our immunization and selection strategies result in a large fraction of monospecific monoclonal antibodies that are both immunoblot and immunoprecipitation grade. Our data indicate that the pipeline provides a robust platform for the generation of monoclonal antibodies of exceptional specificity. © 2012 by The American Society for Biochemistry and Molecular Biology, Inc.
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CITATION STYLE
Jeong, J. S., Jiang, L., Albino, E., Marrero, J., Rho, H. S., Hu, J., … Blackshaw, S. (2012). Rapid identification of monospecific monoclonal antibodies using a human proteome microarray. Molecular and Cellular Proteomics, 11(6). https://doi.org/10.1074/mcp.O111.016253
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