Fig. 6.
Fig. 6. US2 targets HFE for proteasome-mediated degradation. / 293/HFE and 293/HFE/US2 cells were untreated or treated with the proteasome inhibitor MG132 followed by metabolic labeling with35[S]methionine for 30 minutes, chase for 50 minutes, and immunoprecipitation. Cell lysates were treated with N-glycanase (0.2 units) as indicated, and immunoprecipitated with mAb 2F5 (anti-HFE/β2m, A) followed by anti-HFE CT (anti-HFE heavy chains, B). Immunoprecipitates were separated on 8% SDS-PAGE. Short (A,B) and long exposure of the boxed area (C) are presented. * indicates a nonspecific band.

US2 targets HFE for proteasome-mediated degradation.

293/HFE and 293/HFE/US2 cells were untreated or treated with the proteasome inhibitor MG132 followed by metabolic labeling with35[S]methionine for 30 minutes, chase for 50 minutes, and immunoprecipitation. Cell lysates were treated with N-glycanase (0.2 units) as indicated, and immunoprecipitated with mAb 2F5 (anti-HFE/β2m, A) followed by anti-HFE CT (anti-HFE heavy chains, B). Immunoprecipitates were separated on 8% SDS-PAGE. Short (A,B) and long exposure of the boxed area (C) are presented. * indicates a nonspecific band.

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