Publication | Closed Access
ATP‐binding properties of P glycoprotein from multidrug‐resistant KB cells
207
Citations
14
References
1987
Year
Proteinlipid InteractionCellular PhysiologyMolecular PharmacologyMembrane TransportCell SignalingGlycosylationBiochemistryMm AdpProtein TransportDrug TransportP GlycoproteinPharmacologyCell BiologyProtein PhosphorylationSignal TransductionNatural SciencesIntracellular TraffickingCellular BiochemistryMedicine
The photoaffinity reagent 8-azido-alpha-[32P]ATP was used to label a protein of 170 kDa in membrane vesicle preparations from a highly multidrug-resistant cell line, KB-V1, but not from the drug-sensitive parental cell line KB-3-1. The 170-kDa labeled protein was immunoprecipitated with a monoclonal antibody (MRK-16) to P glycoprotein. Both ATP and GTP inhibited labeling by 8-azido-alpha-[32P]ATP. Labeling of P170 was not inhibited by 5 mM ADP, 5 mM ribose-5-phosphate, or 100 microM vinblastine. These data directly demonstrate that P glycoprotein has a nucleotide-binding site that could supply energy for drug transport.
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