The interaction between lipid derivatives of colchicine and tubulin: Consequences of the interaction of the alkaloid with lipid membranes
Stéphane Mons
1
,
Françoise Veretout
2
,
Marie-France Carlier
2
,
Inge Erk
3
,
Jean Lepault
3
,
Eric Trudel
4
,
Christian Salesse
4
,
Pierre Ducray
1
,
CHARLES MIOSKOWSKI
1
,
Luc Lebeau
1
1
Laboratoire de Synthèse Bioorganique associé au CNRS, Université Louis Pasteur de Strasbourg, 67401 Illkirch, France
|
2
Laboratoire d’Enzymologie et Biochimie Structurales du CNRS, 91198 Gif-sur-Yvette, France
|
3
Centre de Génétique Moléculaire du CNRS, 91198 Gif-sur- Yvette, France
|
Publication type: Journal Article
Publication date: 2000-09-01
scimago Q1
wos Q3
SJR: 0.812
CiteScore: 6.8
Impact factor: 2.5
ISSN: 00052736, 18792642
PubMed ID:
11018681
Biochemistry
Cell Biology
Biophysics
Abstract
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.
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MLA
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GOST
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Mons S. et al. The interaction between lipid derivatives of colchicine and tubulin: Consequences of the interaction of the alkaloid with lipid membranes // Biochimica et Biophysica Acta - Biomembranes. 2000. Vol. 1468. No. 1-2. pp. 381-395.
GOST all authors (up to 50)
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Mons S., Veretout F., Carlier M., Erk I., Lepault J., Trudel E., Salesse C., Ducray P., MIOSKOWSKI C., Lebeau L. The interaction between lipid derivatives of colchicine and tubulin: Consequences of the interaction of the alkaloid with lipid membranes // Biochimica et Biophysica Acta - Biomembranes. 2000. Vol. 1468. No. 1-2. pp. 381-395.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1016/S0005-2736(00)00279-0
UR - https://doi.org/10.1016/S0005-2736(00)00279-0
TI - The interaction between lipid derivatives of colchicine and tubulin: Consequences of the interaction of the alkaloid with lipid membranes
T2 - Biochimica et Biophysica Acta - Biomembranes
AU - Mons, Stéphane
AU - Veretout, Françoise
AU - Carlier, Marie-France
AU - Erk, Inge
AU - Lepault, Jean
AU - Trudel, Eric
AU - Salesse, Christian
AU - Ducray, Pierre
AU - MIOSKOWSKI, CHARLES
AU - Lebeau, Luc
PY - 2000
DA - 2000/09/01
PB - Elsevier
SP - 381-395
IS - 1-2
VL - 1468
PMID - 11018681
SN - 0005-2736
SN - 1879-2642
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2000_Mons,
author = {Stéphane Mons and Françoise Veretout and Marie-France Carlier and Inge Erk and Jean Lepault and Eric Trudel and Christian Salesse and Pierre Ducray and CHARLES MIOSKOWSKI and Luc Lebeau},
title = {The interaction between lipid derivatives of colchicine and tubulin: Consequences of the interaction of the alkaloid with lipid membranes},
journal = {Biochimica et Biophysica Acta - Biomembranes},
year = {2000},
volume = {1468},
publisher = {Elsevier},
month = {sep},
url = {https://doi.org/10.1016/S0005-2736(00)00279-0},
number = {1-2},
pages = {381--395},
doi = {10.1016/S0005-2736(00)00279-0}
}
Cite this
MLA
Copy
Mons, Stéphane, et al. “The interaction between lipid derivatives of colchicine and tubulin: Consequences of the interaction of the alkaloid with lipid membranes.” Biochimica et Biophysica Acta - Biomembranes, vol. 1468, no. 1-2, Sep. 2000, pp. 381-395. https://doi.org/10.1016/S0005-2736(00)00279-0.