The development of a catalytic monoclonal antibody (mAb) provides the means for not only binding, but also degrading cocaine, which offers a broad-based therapy for cocaine addition. Hapten design is the central element for programming antibody catalysis. The characteristics of the linker used in classic transition-state analog phosphonate haptens are shown to be important for obtaining mAbs that hydrolyze the benzoate ester of cocaine.
申请公布号
WO0246234(A1)
申请公布日期
2002.06.13
申请号
WO2001US47471
申请日期
2001.12.07
申请人
THE SCRIPPS RESEARCH INSTITUTE;JANDA, KIM, D.;WIRSCHING, PETER