Antibody discovery ex vivo accelerated by the LacO/LacI regulatory network

4Citations
Citations of this article
27Readers
Mendeley users who have this article in their library.

Abstract

Monoclonal antibodies (mAbs) can be potent and highly specific therapeutics, diagnostics and research reagents. Nonetheless, mAb discovery using current in vivo or in vitro approaches can be costly and time-consuming, with no guarantee of success. We have established a platform for rapid discovery and optimization of mAbs ex vivo. This DTLacO platform derives from a chicken B cell line that has been engineered to enable rapid selection and seamless maturation of high affinity mAbs. We have validated the DTLacO platform by generation of high affinity and specific mAbs to five cell surface targets, the receptor tyrosine kinases VEGFR2 and TIE2, the glycoprotein TROP2, the small TNF receptor family member FN14, and the G protein-coupled receptor FZD10. mAb discovery is rapid and humanization is straightforward, establishing the utility of the DTLacO platform for identification of mAbs for therapeutic and other applications. © 2012 Yabuki et al.

Cite

CITATION STYLE

APA

Yabuki, M., Cummings, W. J., Leppard, J. B., Immormino, R. M., Wood, C. L., Allison, D. S., … Maizels, N. (2012). Antibody discovery ex vivo accelerated by the LacO/LacI regulatory network. PLoS ONE, 7(4). https://doi.org/10.1371/journal.pone.0036032

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free