In vitro expressed GPCR inserted in polymersome membranes for ligand-binding studies
The dopamine receptor D2 (DRD2), a G-protein coupled receptor is expressed into PBd22-PEO13 and PMOXA20-PDMS54-PMOXA20 block copolymer vesicles (see scheme). The conformational integrity of the receptor is confirmed by antibody- and ligand-binding assays. Replacement of bound dopamine is demonstrate...
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sg-ntu-dr.10356-1023652020-06-01T10:13:45Z In vitro expressed GPCR inserted in polymersome membranes for ligand-binding studies Low, Ying Xiu De Hoog, Hans-Peter M. May, Sylvia Andreasson-Ochsner, Mirjam Fu, Zhikang Tan, Darren Ritz, Sandra Nallani, Madhavan Sinner, Eva-Kathrin School of Materials Science & Engineering DRNTU::Engineering::Materials::Biomaterials The dopamine receptor D2 (DRD2), a G-protein coupled receptor is expressed into PBd22-PEO13 and PMOXA20-PDMS54-PMOXA20 block copolymer vesicles (see scheme). The conformational integrity of the receptor is confirmed by antibody- and ligand-binding assays. Replacement of bound dopamine is demonstrated on surface-immobilized polymersomes, thus making this a promising platform for drug screening. 2014-03-27T09:06:11Z 2019-12-06T20:53:58Z 2014-03-27T09:06:11Z 2019-12-06T20:53:58Z 2013 2013 Journal Article May, S., Andreasson-Ochsner, M., Fu, Z., Low , Y. X., Tan, D., de Hoog, H.-P. M., et al. (2013). In vitro expressed GPCR inserted in polymersome membranes for ligand-binding studies. Angewandte Chemie International Edition, 52(2), 749-753. 1433-7851 https://hdl.handle.net/10356/102365 http://hdl.handle.net/10220/19016 10.1002/anie.201204645 en Angewandte chemie international edition © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. |
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DRNTU::Engineering::Materials::Biomaterials Low, Ying Xiu De Hoog, Hans-Peter M. May, Sylvia Andreasson-Ochsner, Mirjam Fu, Zhikang Tan, Darren Ritz, Sandra Nallani, Madhavan Sinner, Eva-Kathrin In vitro expressed GPCR inserted in polymersome membranes for ligand-binding studies |
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The dopamine receptor D2 (DRD2), a G-protein coupled receptor is expressed into PBd22-PEO13 and PMOXA20-PDMS54-PMOXA20 block copolymer vesicles (see scheme). The conformational integrity of the receptor is confirmed by antibody- and ligand-binding assays. Replacement of bound dopamine is demonstrated on surface-immobilized polymersomes, thus making this a promising platform for drug screening. |
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School of Materials Science & Engineering |
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School of Materials Science & Engineering Low, Ying Xiu De Hoog, Hans-Peter M. May, Sylvia Andreasson-Ochsner, Mirjam Fu, Zhikang Tan, Darren Ritz, Sandra Nallani, Madhavan Sinner, Eva-Kathrin |
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Article |
author |
Low, Ying Xiu De Hoog, Hans-Peter M. May, Sylvia Andreasson-Ochsner, Mirjam Fu, Zhikang Tan, Darren Ritz, Sandra Nallani, Madhavan Sinner, Eva-Kathrin |
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Low, Ying Xiu |
title |
In vitro expressed GPCR inserted in polymersome membranes for ligand-binding studies |
title_short |
In vitro expressed GPCR inserted in polymersome membranes for ligand-binding studies |
title_full |
In vitro expressed GPCR inserted in polymersome membranes for ligand-binding studies |
title_fullStr |
In vitro expressed GPCR inserted in polymersome membranes for ligand-binding studies |
title_full_unstemmed |
In vitro expressed GPCR inserted in polymersome membranes for ligand-binding studies |
title_sort |
in vitro expressed gpcr inserted in polymersome membranes for ligand-binding studies |
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2014 |
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https://hdl.handle.net/10356/102365 http://hdl.handle.net/10220/19016 |
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1681056537784614912 |