Adopting orthogonal dual-labeling strategies, a cell-permeable RNase A prodrug was designed for ROS-responsive targeted cancer therapy.
Abstract The authors have requested that this preprint be removed from Research Square.
A novel clustered nanobody–drug conjugate is constructed by a site-specific ligation of a nanobody to dendrimeric-lysine, which enhances drug efficacy and reduces side-effects.
The chemically modified redox-responsive RNase A–NSA could be selectively activated by up-regulated GSH in live cells for targeted cancer therapy.