Interaction of transported drugs with the lipid bilayer and P-glycoprotein through a solvation exchange mechanism

Hiroshi Omote, Marwan K. Al-Shawi

Research output: Contribution to journalArticle

70 Citations (Scopus)

Abstract

Broad substrate specificity of human P-glycoprotein (ABCB1) is an essential feature of multidrug resistance. Transport substrates of P-glycoprotein are mostly hydrophobic and many of them have net positive charge. These compounds partition into the membrane. Utilizing the energy of ATP hydrolysis, P-glycoprotein is thought to take up substrates from the cytoplasmic leaflet of the plasma membrane and to transport them to the outside of the cell. We examined this model by molecular dynamics simulation of the lipid bilayer, in the presence of transport substrates together with an atomic resolution structural model of P-glycoprotein. Taken together with previous electron paramagnetic resonance studies, the results suggest that most transported drugs are concentrated near the surface zone of the inner leaflet of the plasma membrane. Here the drugs can easily diffuse laterally into the drug-binding site of P-glycoprotein through an open cleft. It was concluded that the initial high-affinity drug-binding site was located in the interfacial surface area of P-glycoprotein in contact with the membrane interface. Based on these results and our recent kinetic studies, a "solvation exchange" drug transport mechanism of P-glycoprotein is discussed. A molecular basis for the improved colchicine transport efficiency by the much-studied colchicine-resistance G185V mutant human P-glycoprotein is also provided.

Original languageEnglish
Pages (from-to)4046-4059
Number of pages14
JournalBiophysical Journal
Volume90
Issue number11
DOIs
Publication statusPublished - Jun 2006

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Lipid Bilayers
P-Glycoprotein
Drug Interactions
Pharmaceutical Preparations
Colchicine
Binding Sites
Cell Membrane
Membranes
Structural Models
Electron Spin Resonance Spectroscopy
Multiple Drug Resistance
Molecular Dynamics Simulation
Substrate Specificity
Hydrolysis
Adenosine Triphosphate

ASJC Scopus subject areas

  • Biophysics

Cite this

Interaction of transported drugs with the lipid bilayer and P-glycoprotein through a solvation exchange mechanism. / Omote, Hiroshi; Al-Shawi, Marwan K.

In: Biophysical Journal, Vol. 90, No. 11, 06.2006, p. 4046-4059.

Research output: Contribution to journalArticle

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