Hybrid live cell–supported membrane interfaces for signaling studies
A wide range of cell–microenvironmental interactions are mediated by membrane-localized receptors that bind ligands present on another cell or the extracellular matrix. This situation introduces a number of physical effects including spatial organization of receptor–ligand complexes and development...
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sg-ntu-dr.10356-1046302020-06-01T10:13:43Z Hybrid live cell–supported membrane interfaces for signaling studies Biswas, Kabir H. Groves, Jay T. School of Materials Science & Engineering NTU Institute for Health Technologies Receptor Clustering Cell Adhesion Receptor Engineering::Materials A wide range of cell–microenvironmental interactions are mediated by membrane-localized receptors that bind ligands present on another cell or the extracellular matrix. This situation introduces a number of physical effects including spatial organization of receptor–ligand complexes and development of mechanical forces in cells. Unlike traditional experimental approaches, hybrid live cell–supported lipid bilayer (SLB) systems, wherein a live cell interacts with a synthetic substrate supported membrane, allow interrogation of these aspects of receptor signaling. The SLB system directly offers facile control over the identity, density, and mobility of ligands used for engaging cellular receptors. Further, application of various nano- and micropatterning techniques allows for spatial patterning of ligands. In this review, we describe the hybrid live cell–SLB system and its application in uncovering a range of spatial and mechanical aspects of receptor signaling. We highlight the T cell immunological synapse, junctions formed between EphA2- and ephrinA1-expressing cells, and adhesions formed by cadherin and integrin receptors. 2019-08-05T01:52:26Z 2019-12-06T21:36:32Z 2019-08-05T01:52:26Z 2019-12-06T21:36:32Z 2019 Journal Article Biswas, K. H., & Groves, J. T. (2019). Hybrid live cell–supported membrane interfaces for signaling studies. Annual Review of Biophysics, 48, 537-562. doi:10.1146/annurev-biophys-070317-033330 1936-122X https://hdl.handle.net/10356/104630 http://hdl.handle.net/10220/49522 10.1146/annurev-biophys-070317-033330 en Annual Review of Biophysics © 2019 Annual Reviews, Inc. All rights reserved. |
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Receptor Clustering Cell Adhesion Receptor Engineering::Materials Biswas, Kabir H. Groves, Jay T. Hybrid live cell–supported membrane interfaces for signaling studies |
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A wide range of cell–microenvironmental interactions are mediated by membrane-localized receptors that bind ligands present on another cell or the extracellular matrix. This situation introduces a number of physical effects including spatial organization of receptor–ligand complexes and development of mechanical forces in cells. Unlike traditional experimental approaches, hybrid live cell–supported lipid bilayer (SLB) systems, wherein a live cell interacts with a synthetic substrate supported membrane, allow interrogation of these aspects of receptor signaling. The SLB system directly offers facile control over the identity, density, and mobility of ligands used for engaging cellular receptors. Further, application of various nano- and micropatterning techniques allows for spatial patterning of ligands. In this review, we describe the hybrid live cell–SLB system and its application in uncovering a range of spatial and mechanical aspects of receptor signaling. We highlight the T cell immunological synapse, junctions formed between EphA2- and ephrinA1-expressing cells, and adhesions formed by cadherin and integrin receptors. |
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School of Materials Science & Engineering |
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School of Materials Science & Engineering Biswas, Kabir H. Groves, Jay T. |
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Article |
author |
Biswas, Kabir H. Groves, Jay T. |
author_sort |
Biswas, Kabir H. |
title |
Hybrid live cell–supported membrane interfaces for signaling studies |
title_short |
Hybrid live cell–supported membrane interfaces for signaling studies |
title_full |
Hybrid live cell–supported membrane interfaces for signaling studies |
title_fullStr |
Hybrid live cell–supported membrane interfaces for signaling studies |
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Hybrid live cell–supported membrane interfaces for signaling studies |
title_sort |
hybrid live cell–supported membrane interfaces for signaling studies |
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2019 |
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https://hdl.handle.net/10356/104630 http://hdl.handle.net/10220/49522 |
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1681056644852613120 |