Figure 1.
Figure 1. Structure of the cAC10-vcMMAE system. Conjugates were prepared by controlled partial reduction of internal cAC10 disulfides with DTT, followed by addition of the maleimide-vc-linker-MMAE. Stable thioether-linked ADCs were formed with the addition of the free sulfhydryl groups on the mAbs to the maleimides present on the drugs. cAC10-vcMMAE and the cIgG-vcMMAE used in these studies contained approximately 8 drugs/mAb.

Structure of the cAC10-vcMMAE system. Conjugates were prepared by controlled partial reduction of internal cAC10 disulfides with DTT, followed by addition of the maleimide-vc-linker-MMAE. Stable thioether-linked ADCs were formed with the addition of the free sulfhydryl groups on the mAbs to the maleimides present on the drugs. cAC10-vcMMAE and the cIgG-vcMMAE used in these studies contained approximately 8 drugs/mAb.

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