Reversing the direction of drug transport mediated by the human multidrug transporter P-glycoprotein

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 117; no. 47; pp. 29609 - 29617
• Main Authors: Sajid, Andaleeb, Lusvarghi, Sabrina, Murakami, Megumi, Chufan, Eduardo E., Abel, Biebele, Gottesman, Michael M., Durell, Stewart R., Ambudkar, Suresh V.
• Format: Journal Article
• Language: English
• Published: United States National Academy of Sciences 24.11.2020
• Subjects: Adenosine triphosphate; Alanine; Amino Acid Substitution - physiology; Animals; ATP Binding Cassette Transporter, Subfamily B, Member 1 - metabolism; ATP-Binding Cassette Transporters - metabolism; Binding; Binding Sites - physiology; Biological Sciences; Biological Transport - physiology; Cancer; Cell Line; Cell Line, Tumor; Cell membranes; Chemotherapy; Domains; Drug resistance; Drug Resistance, Multiple - physiology; Drug Resistance, Neoplasm - physiology; Efflux; Glycoproteins; HeLa Cells; Helices; Homology; Humans; Insecta; Molecular Docking Simulation - methods; Mutagenesis; Mutants; Nucleotides; P-Glycoprotein; Paclitaxel; Pharmaceutical Preparations - metabolism; Residues; Rhodamine; Rhodamine 123 - metabolism; Substrate Specificity - physiology; Substrates; Taxol; Transmembrane domains; P-glycoprotein; drug transport; multidrug resistance; mechanism; ABC transporter

P-glycoprotein (P-gp), also known as ABCB1, is a cell membrane transporter that mediates the efflux of chemically dissimilar amphipathic drugs and confers resistance to chemotherapy in most cancers. Homologous transmembrane helices (TMHs) 6 and 12 of human P-gp connect the transmembrane domains with...