Figure 4From: Mouse-adapted scrapie strains 139A and ME7 overcome species barrier to induce experimental scrapie in hamsters and changed their pathogenic featuresAnalyses for PrPSc in brain homogenates with Western blots. (A) PrPSc in hamsters' brains of agent 263 K, 139A and ME7 detected with mAb 3 F4. (B) PrPSc in mice brains of agent 139A and ME7 detected with mAb 1E4. (C) Deglycosylated PrPSc in hamsters' brains of agent 263 K, 139A and ME7 detected with mAb 3 F4. (D) Immunoreactivities of PrPSc in hamsters' brains of agent 263 K, 139A and ME7 with a panel of PrP specific mAbs, including 1E4, 6D11, 3 F4, 6H4 and 8H4. Molecular weight standards are shown on the left and different mAbs are shown on the right. "+": with PK or PNGase F; "-": without PK The products of PK-digested PrPSc from the hamsters' brains infected by mouse-adapted agents 139A and ME7 were further exposed to glycosidase. One single PrP-specific bands were observed, which were at the exactly same position in SDS-PAGE as that in the preparation of 263 K PrPSc (Figure 4C). It implies that the newly-formed PrPSc in the hamsters' brains by infections of mouse-adapted scrapie agents have the same glycosylated profiles as the hamster-adapted scrapie strain 263 K.Back to article page