MDR1 (multidrug resistance 1)/P-glycoprotein is an ATP-driven transporter which excretes a wide variety of structurally unrelated hydrophobic compounds from cells. It is suggested that drugs bind to MDR1 directly from the lipid bilayer and that cholesterol in the bilayer also interacts with MDR1. However, the effects of cholesterol on drug–MDR1 interactions are still unclear. To examine these effects, human MDR1 was expressed in insect cells and purified. The purified MDR1 protein was reconstituted in proteoliposomes containing various concentrations of cholesterol and enzymatic parameters of drug-stimulated ATPase were compared. Cholesterol directly binds to purified MDR1 in a detergent soluble form and the effects of cholesterol on drug-stimulated ATPase activity differ from one drug to another. The effects of cholesterol on Km values of drug-stimulated ATPase activity were strongly correlated with the molecular mass of that drug. Cholesterol increases the binding affinity of small drugs (molecular mass <500 Da), but does not affect that of drugs with a molecular mass of between 800 and 900 Da, and suppresses that of valinomycin (molecular mass >1000 Da). Vmax values for rhodamine B and paclitaxel are also increased by cholesterol, suggesting that cholesterol affects turnover as well as drug binding. Paclitaxel-stimulated ATPase activity of MDR1 is enhanced in the presence of stigmasterol, sitosterol and campesterol, as well as cholesterol, but not ergosterol. These results suggest that the drug-binding site of MDR1 may best fit drugs with a molecular mass of between 800 and 900 Da, and that cholesterol may support the recognition of smaller drugs by adjusting the drug-binding site and play an important role in the function of MDR1.
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Research Article|
December 21 2006
Modulation of drug-stimulated ATPase activity of human MDR1/P-glycoprotein by cholesterol
Yasuhisa Kimura;
Yasuhisa Kimura
*Laboratory of Cellular Biochemistry, Division of Applied Life Sciences, Kyoto University Graduate School of Agriculture, Kyoto 606-8502, Japan
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Noriyuki Kioka;
Noriyuki Kioka
*Laboratory of Cellular Biochemistry, Division of Applied Life Sciences, Kyoto University Graduate School of Agriculture, Kyoto 606-8502, Japan
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Hiroaki Kato;
Hiroaki Kato
†Department of Structural Biology, Kyoto University Graduate School of Pharmaceutical Sciences, Kyoto 606-8501, Japan
‡RIKEN Harima Institute at Spring-8, Hyogo 679-5148, Japan
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Michinori Matsuo;
Michinori Matsuo
*Laboratory of Cellular Biochemistry, Division of Applied Life Sciences, Kyoto University Graduate School of Agriculture, Kyoto 606-8502, Japan
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Kazumitsu Ueda
Kazumitsu Ueda
1
*Laboratory of Cellular Biochemistry, Division of Applied Life Sciences, Kyoto University Graduate School of Agriculture, Kyoto 606-8502, Japan
1To whom correspondence should be addressed (email uedak@kais.kyoto-u.ac.jp).
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Publisher: Portland Press Ltd
Received:
April 27 2006
Revision Received:
October 03 2006
Accepted:
October 10 2006
Accepted Manuscript online:
October 10 2006
Online ISSN: 1470-8728
Print ISSN: 0264-6021
The Biochemical Society, London
2007
Biochem J (2007) 401 (2): 597–605.
Article history
Received:
April 27 2006
Revision Received:
October 03 2006
Accepted:
October 10 2006
Accepted Manuscript online:
October 10 2006
Citation
Yasuhisa Kimura, Noriyuki Kioka, Hiroaki Kato, Michinori Matsuo, Kazumitsu Ueda; Modulation of drug-stimulated ATPase activity of human MDR1/P-glycoprotein by cholesterol. Biochem J 15 January 2007; 401 (2): 597–605. doi: https://doi.org/10.1042/BJ20060632
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