2区 · 医学
Article
作者: van der Woning, Bas ; Bisharyan, Yelena ; Harriman, Rian ; Harriman, William ; Mariën, Lore ; Clark, Ted ; Abdiche, Yasmina ; Cassidy-Hanley, Donna ; Collarini, Ellen ; Colussi, Paul ; Pedersen, Darlene ; Bednenko, Janna ; Papoyan, Ashot ; Nguyen, Hai M. ; Cardarelli, Joanna ; Wulff, Heike ; de Haard, Hans ; Agrawal, Alka
Identifying monoclonal antibodies that block human voltage-gated ion channels (VGICs) is a challenging endeavor exacerbated by difficulties in producing recombinant ion channel proteins in amounts that support drug discovery programs. We have developed a general strategy to address this challenge by combining high-level expression of recombinant VGICs in Tetrahymena thermophila with immunization of phylogenetically diverse species and unique screening tools that allow deep-mining for antibodies that could potentially bind functionally important regions of the protein. Using this approach, we targeted human Kv1.3, a voltage-gated potassium channel widely recognized as a therapeutic target for the treatment of a variety of T-cell mediated autoimmune diseases. Recombinant Kv1.3 was used to generate and recover 69 full-length anti-Kv1.3 mAbs from immunized chickens and llamas, of which 10 were able to inhibit Kv1.3 current. Select antibodies were shown to be potent (IC50<10 nM) and specific for Kv1.3 over related Kv1 family members, hERG and hNav1.5.