Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/54739
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Type: Journal article
Title: Is ATP binding responsible for initiating drug translocation by the multidrug transporter ABCG2?
Author: McDevitt, C.
Crowley, E.
Hobbs, G.
Starr, K.
Kerr, I.
Callaghan, R.
Citation: FEBS Journal, 2008; 275(17):4354-4362
Publisher: Blackwell Publishing Ltd
Issue Date: 2008
ISSN: 1742-464X
1742-4658
Statement of
Responsibility: 
Christopher A. McDevitt, Emily Crowley, Gemma Hobbs, Kate J. Starr, Ian D. Kerr and Richard Callaghan
Abstract: ABCG2 confers resistance to cancer cells by mediating the ATP-dependent outward efflux of chemotherapeutic compounds. Recent studies have indicated that the protein contains a number of interconnected drug binding sites. The present investigation examines the coupling of drug binding to ATP hydrolysis. Initial drug binding to the protein requires a high-affinity interaction with the drug binding site, followed by transition and reorientation to the low-affinity state to enable dissociation at the extracellular face. [3H]Daunomycin binding to the ABCG2 R482G isoform was examined in the nucleotide-bound and post-hydrolytic conformations. Binding of [3H]daunomycin was displaced by ATP analogues, indicating transition to a low-affinity conformation prior to hydrolysis. The low-affinity state was observed to be retained immediately post-hydrolysis. Therefore, the dissociation of phosphate and/or ADP is likely to be responsible for resetting of the transporter. The data indicate that, like ABCB1 and ABCC1, the 'power stroke' for translocation in ABCG2 R482G is the binding of nucleotide.
Keywords: ABC transporter; chemotherapy; membrane protein; multidrug-resistance; power-stroke
RMID: 0020093480
DOI: 10.1111/j.1742-4658.2008.06578.x
Appears in Collections:Molecular and Biomedical Science publications

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