Glycoprotein Biosynthesis in Peripheral Nervous System Myelin: Effect of Tunicamycin

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Abstract
The effect of an inhibitor of N-glycosylation of glycoproteins, tunicamycin, on synthesis of PNS [peripheral nervous system] myelin proteins was investigated in vitro by using chopped sciatic nerves or spinal roots of 21-day-old Wistar rats. Tunicamycin when incubated with these nerves in the presence of 3H-labeled fucose, mannose or glucosamine inhibited the uptake of radioactivity into myelin proteins including some high MW proteins, P0, 23K [kilodalton] protein, and 19K protein by amounts ranging from 42-79%. Uptake of 14C amino acid mixture was inhibited much less by tunicamycin, but a new radioactive protein peak appeared when the protein mixtures had been separated by electrophoresis on polyacrylamide gels in the presence of sodium dodecyl sulfate. This protein ran directly in front of the P0 peak, did not correspond to any bands stained by Fast green, and was not labeled by fucose. This peak appeared in increasing larger proportions with progressive time of incubation of nerves with 3H amino acids in the presence of tunicamycin. The new protein, which cross-reacts with P0 antiserum, was tentatively identified as a nonglycosylated P0 protein that seems almost as well incorporated as P0 into the subcellular fraction containing myelin. At this time it is not possible to determine whether the unglycosylated P0 is actually assembled into a site and configuration like that of P0.