Publication | Open Access
Group translocation of the ribose moiety of inosine by vesicles of plasma membrane from T(3 cells transformed by Simian virus 40.
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References
1976
Year
Viral ReplicationMarker Enzyme AnalysisMolecular BiologyCytoskeletonViral Structural ProteinVirus StructureCellular PhysiologyProtein SynthesisMembrane FusionMembrane TransportBiochemistryRibose MoietySimian Virus 40VirologyMembrane BiologyProtein TransportCell BiologyGroup TranslocationPlasma Membrane VesiclesMolecular VirologyCellular EnzymologyNatural SciencesCellular BiochemistryMembrane VesiclesMedicine
Plasma membrane vesicles are isolated from Simian virus 40-transformed Balb/c mouse 3T3 (SV-3T3) cells. These membrane vesicles contain no significant contamination by mitochondria, endoplasmic reticulum, or lysosomes as determined by marker enzyme analysis. The use of [U-14C] inosine as a transport substrate results in the accumulation of labeled ribose-1P as transport product by the plasma membrane vesicles. This suggests the action of purine nucleoside phosphorylase (the enzyme which mediates the phosphorolysis of inosine to ribose-1-P and hypoxanthine0 before, during, or after the transport step. Neither inosine nor significant amounts of hypoxanthine are found intravesicularly. The Km for inosine, the substrate in this reaction which leads to the accumulation of ribose-1-P by the plasma membrane vesicles, is 35 to 45 muM while the Vmax for ribose-1-P accumulation is 100 to 120 pmol/min/mg of plasma membrane protein...
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