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The interaction between lipid derivatives of colchicine and tubulin: Consequences of the interaction of the alkaloid with lipid membranes

机译:秋水仙碱脂质衍生物与微管蛋白之间的相互作用:生物碱与脂质膜相互作用的后果

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摘要

Colchicine is a potent antimitotic poison which is well known to prevent microtubule assembly by binding tubulin very tightly. Colchicine also possesses anti-inflammatory properties which are not well understood yet. Here we show that colchicine tightly interacts with lipid layers. The physical and biological properties of three different lipid derivatives of colchicine are investigated parallel to those of membrane lipids in the presence of colchicine. Upon insertion in the fatty alkyl chains, colchicine rigidifies the lipid monolayers in a fluid phase and fluidifies rigid monolayers. Similarly X-ray diffraction data show that lecithin-water phases are destabilized by colchicine. In addition, an unexpectedly drastic enhancement of the photoisomerization rate of colchicine into lumicolchicine in the lipid environment is observed and further supports insertion of the alkaloid in membranes. Finally the interaction of colchicine with lipids makes the drug inaccessible to tubulin. The possible in vivo significance of these results is discussed.
机译:秋水仙碱是一种有力的抗有丝分裂药,众所周知,它通过紧密结合微管蛋白来防止微管组装。秋水仙碱还具有尚未被很好理解的抗炎特性。在这里,我们显示秋水仙碱与脂质层紧密相互作用。在秋水仙碱存在的情况下,平行于膜脂质研究了三种秋水仙碱脂质衍生物的物理和生物学特性。插入脂肪烷基链中后,秋水仙碱使脂质单分子层在液相中硬化,并使刚性单分子层流化。同样,X射线衍射数据表明卵磷脂水​​相被秋水仙碱不稳定。另外,在脂质环境中观察到秋水仙碱向光明秋水仙碱的光异构化速率出乎意料的急剧增加,并进一步支持生物碱在膜中的插入。最后,秋水仙碱与脂质的相互作用使微管蛋白难以接近该药物。讨论了这些结果的可能的体内意义。

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