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

被引:21
作者
Mons, S
Veretout, F
Carlier, MF
Erk, I
Lepault, J
Trudel, E
Salesse, C
Ducray, P
Mioskowski, C
Lebeau, L [1 ]
机构
[1] Univ Louis Pasteur Strasbourg 1, Lab Synthese Bioorgan, CNRS, F-67401 Illkirch, France
[2] CNRS, Lab Enzymol & Biochim Struct, F-91198 Gif Sur Yvette, France
[3] CNRS, Ctr Mol Genet, F-91198 Gif Sur Yvette, France
[4] Univ Quebec, Ctr Rech Photobiophys, Trois Rivieres, PQ G9A 5H7, Canada
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2000年 / 1468卷 / 1-2期
基金
澳大利亚研究理事会;
关键词
colchicine derivative; photoisomerization; lipid membrane; fluorescence; tubulin immobilization; electron microscopy;
D O I
10.1016/S0005-2736(00)00279-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:381 / 395
页数:15
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