TY - JOUR
T1 - Rapid identification of monospecific monoclonal antibodies using a human proteome microarray
AU - Jeong, Jun Seop
AU - Jiang, Lizhi
AU - Albino, Edisa
AU - Marrero, Josean
AU - Rho, Hee Sool
AU - Hu, Jianfei
AU - Hu, Shaohui
AU - Vera, Carlos
AU - Bayron-Poueymiroy, Diane
AU - Rivera-Pacheco, Zully Ann
AU - Ramos, Leonardo
AU - Torres-Castro, Cecil
AU - Qian, Jiang
AU - Bonaventura, Joseph
AU - Boeke, Jef D.
AU - Yap, Wendy Y.
AU - Pino, Ignacio
AU - Eichinger, Daniel J.
AU - Zhu, Heng
AU - Blackshaw, Seth
PY - 2012/6
Y1 - 2012/6
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=84862321638&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84862321638&partnerID=8YFLogxK
U2 - 10.1074/mcp.O111.016253
DO - 10.1074/mcp.O111.016253
M3 - Article
C2 - 22307071
AN - SCOPUS:84862321638
SN - 1535-9476
VL - 11
JO - Molecular and Cellular Proteomics
JF - Molecular and Cellular Proteomics
IS - 6
ER -