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Inostamycin an Inhibitor of P‐Glycoprotein Function Interacts Specifically with Phosphatidylethanolamine

机译:Inostamycin是P-糖蛋白功能的抑制剂与磷脂酰乙醇胺特别相互作用

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摘要

The mechanism of inostamycin action was further studied. When multidrug‐resistant KB‐C4 cells were preincubated with inostamycin for 30 min, the accumulation of [3H]vinblastine was increased for as long as 48 h thereafter. Inostamycin inhibited azidopine binding to P‐glycoprotein, even after KB plasma membranes had been preincubated with inostamycin and washed. Carbon 14‐labeled inostamycin bound to KB plasma membranes irreversibly, but the binding capacity did not parallel the amount of P‐glycoprotein in three KB cell lines. Inostamycin was found to interact specifically with purified phosphatidylethanolamine. These results suggest that inostamycin can inhibit P‐glycoprotein irreversibly by binding to plasma membranes irreversibly through phosphatidylethanolamine.
机译:进一步研究了稻瘟霉素的作用机理。将具有多重耐药性的KB‐C4细胞与ostostyycin预先孵育30分钟后,[ 3 H]长春碱的积累长达48小时。即使将KB质膜与Inostamycin预先孵育并洗涤后,Inostamycin仍可抑制azidopine与P-糖蛋白的结合。碳14标记的ostostyycin不可逆地与KB质膜结合,但结合能力与三种KB细胞系中P-糖蛋白的量不平行。发现Inostamycin与纯化的磷脂酰乙醇胺特异性相互作用。这些结果表明,ostostyycin可以通过磷脂酰乙醇胺不可逆地与质膜结合,从而不可逆地抑制P-糖蛋白。

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