Iodomycin and iodipine, a structural analogue of azidopine, bind to a common domain in hamster P-glycoprotein. |
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Authors: | A Demmer S Andreae H Thole B Tümmler |
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Affiliation: | Klinische Forschergruppe, Zentrum Biochemie, Medizinische Hochschule, Hannover, Germany. Demmer.annette@MH-Hannover.de |
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Abstract: | Both the overexpression of P-glycoprotein and the broad range of substrates of this ATP-binding cassette (ABC) transporter induce the phenomenon of multidrug resistance, one major cause of the failure of cancer chemotherapy in humans. This study reports that [125I]iodipine, a structural analogue of the 1,4-dihydropyridine azidopine, shares a common binding site with iodomycin, a Bolton-Hunter derivative of the anthracycline daunomycin. This binding site is different from that described for iodoarylazidoprazosin, which is presumed to share a common binding site with azidopine. Edman sequencing revealed that [125I]iodipine had photolabelled the same peptide as iodomycin and spans the primary sequence of hamster isoform pgp1 from amino acid 230 to amino acid 312. |
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