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ABCG2 transports anticancer drugs via a closed-to-open switch
by
Orlando, Benjamin J.
, Liao, Maofu
in
101/28
/ 13/31
/ 631/45/535/1258/1259
/ 631/67/1059/99
/ 82/83
/ ABC transporter
/ ABC transporters
/ Antibodies
/ Antineoplastic Agents - chemistry
/ Antineoplastic Agents - metabolism
/ Antineoplastic drugs
/ Antitumor agents
/ ATP Binding Cassette Transporter, Subfamily G, Member 2 - chemistry
/ ATP Binding Cassette Transporter, Subfamily G, Member 2 - metabolism
/ ATP Binding Cassette Transporter, Subfamily G, Member 2 - ultrastructure
/ Binding
/ Biological Transport
/ Cancer
/ Chemotherapy
/ Conformation
/ Disulfides - metabolism
/ HEK293 Cells
/ Humanities and Social Sciences
/ Humans
/ Imatinib
/ Imatinib Mesylate - metabolism
/ Inhibitor drugs
/ Ligands
/ Mitoxantrone - chemistry
/ Mitoxantrone - metabolism
/ Models, Biological
/ multidisciplinary
/ Protein Structure, Secondary
/ Science
/ Science (multidisciplinary)
/ Transport
2020
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ABCG2 transports anticancer drugs via a closed-to-open switch
by
Orlando, Benjamin J.
, Liao, Maofu
in
101/28
/ 13/31
/ 631/45/535/1258/1259
/ 631/67/1059/99
/ 82/83
/ ABC transporter
/ ABC transporters
/ Antibodies
/ Antineoplastic Agents - chemistry
/ Antineoplastic Agents - metabolism
/ Antineoplastic drugs
/ Antitumor agents
/ ATP Binding Cassette Transporter, Subfamily G, Member 2 - chemistry
/ ATP Binding Cassette Transporter, Subfamily G, Member 2 - metabolism
/ ATP Binding Cassette Transporter, Subfamily G, Member 2 - ultrastructure
/ Binding
/ Biological Transport
/ Cancer
/ Chemotherapy
/ Conformation
/ Disulfides - metabolism
/ HEK293 Cells
/ Humanities and Social Sciences
/ Humans
/ Imatinib
/ Imatinib Mesylate - metabolism
/ Inhibitor drugs
/ Ligands
/ Mitoxantrone - chemistry
/ Mitoxantrone - metabolism
/ Models, Biological
/ multidisciplinary
/ Protein Structure, Secondary
/ Science
/ Science (multidisciplinary)
/ Transport
2020
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ABCG2 transports anticancer drugs via a closed-to-open switch
by
Orlando, Benjamin J.
, Liao, Maofu
in
101/28
/ 13/31
/ 631/45/535/1258/1259
/ 631/67/1059/99
/ 82/83
/ ABC transporter
/ ABC transporters
/ Antibodies
/ Antineoplastic Agents - chemistry
/ Antineoplastic Agents - metabolism
/ Antineoplastic drugs
/ Antitumor agents
/ ATP Binding Cassette Transporter, Subfamily G, Member 2 - chemistry
/ ATP Binding Cassette Transporter, Subfamily G, Member 2 - metabolism
/ ATP Binding Cassette Transporter, Subfamily G, Member 2 - ultrastructure
/ Binding
/ Biological Transport
/ Cancer
/ Chemotherapy
/ Conformation
/ Disulfides - metabolism
/ HEK293 Cells
/ Humanities and Social Sciences
/ Humans
/ Imatinib
/ Imatinib Mesylate - metabolism
/ Inhibitor drugs
/ Ligands
/ Mitoxantrone - chemistry
/ Mitoxantrone - metabolism
/ Models, Biological
/ multidisciplinary
/ Protein Structure, Secondary
/ Science
/ Science (multidisciplinary)
/ Transport
2020
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ABCG2 transports anticancer drugs via a closed-to-open switch
Journal Article
ABCG2 transports anticancer drugs via a closed-to-open switch
2020
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Overview
ABCG2 is an ABC transporter that extrudes a variety of compounds from cells, and presents an obstacle in treating chemotherapy-resistant cancers. Despite recent structural insights, no anticancer drug bound to ABCG2 has been resolved, and the mechanisms of multidrug transport remain obscure. Such a gap of knowledge limits the development of novel compounds that block or evade this critical molecular pump. Here we present single-particle cryo-EM studies of ABCG2 in the apo state, and bound to the three structurally distinct chemotherapeutics. Without the binding of conformation-selective antibody fragments or inhibitors, the resting ABCG2 adopts a closed conformation. Our cryo-EM, biochemical, and functional analyses reveal the binding mode of three chemotherapeutic compounds, demonstrate how these molecules open the closed conformation of the transporter, and establish that imatinib is particularly effective in stabilizing the inward facing conformation of ABCG2. Together these studies reveal the previously unrecognized conformational cycle of ABCG2.
ABCG2 is a human ABC transporter that actively extrudes a wide variety of compounds from cells but the mechanisms of multidrug transport remain obscure. Here authors present cryo-EM structures of ABCG2 in the apo state, and bound to the three structurally distinct chemotherapeutics and demonstrate how these molecules open the closed conformation of the transporter.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
/ 13/31
/ 82/83
/ Antineoplastic Agents - chemistry
/ Antineoplastic Agents - metabolism
/ ATP Binding Cassette Transporter, Subfamily G, Member 2 - chemistry
/ ATP Binding Cassette Transporter, Subfamily G, Member 2 - metabolism
/ ATP Binding Cassette Transporter, Subfamily G, Member 2 - ultrastructure
/ Binding
/ Cancer
/ Humanities and Social Sciences
/ Humans
/ Imatinib
/ Imatinib Mesylate - metabolism
/ Ligands
/ Protein Structure, Secondary
/ Science
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