单克隆抗体
蛋白质组
生物
免疫沉淀
分子生物学
微阵列
蛋白质组学
计算生物学
抗体
蛋白质微阵列
基因
基因表达
生物信息学
生物化学
遗传学
作者
Jun Seop Jeong,Lizhi Jiang,Edisa Albino,Josean Marrero,Hee Sool Rho,Jianfei Hu,Shaohui Hu,Carlos Vera,Diane Bayron-Poueymiroy,Zully Ann Rivera-Pacheco,Leonardo Ramos,Cecil Torres-Castro,Jiang Qian,Joseph Bonaventura,Jef D. Boeke,W Y Yap,Ignacio Pino,Daniel Eichinger,Heng Zhu,Seth Blackshaw
标识
DOI:10.1074/mcp.o111.016253
摘要
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-His(6) 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.
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