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Deglycosylation of gM by PNGase F and endo H. Lysates of 35S-labeled infected cell membranes were immunoprecipitated with gMC antibody. Precipitates were treated with 0.8% SDS at 100 or 56°C and digested with 0 to 5 kU of PNGase F or 0 to 2 mU of endo H. The gM in the left lane of each panel was synthesized in an in vitro translation system programmed with the BHV-1 UL10 RNA transcript.
