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Seeing and sensing single G protein-coupled receptors by atomic force microscopy

G protein-coupled receptors (GPCRs) relay extracellular information across cell membranes through a continuum of conformations that are not always captured in structures. Hence, complementary approaches are required to quantify the physical and chemical properties of the dynamic conformations linkin...

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Autores principales: Sapra, K Tanuj, Spoerri, Patrizia M, Engel, Andreas, Alsteens, David, Müller, Daniel J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6472649/
https://www.ncbi.nlm.nih.gov/pubmed/30412846
http://dx.doi.org/10.1016/j.ceb.2018.10.006
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author Sapra, K Tanuj
Spoerri, Patrizia M
Engel, Andreas
Alsteens, David
Müller, Daniel J
author_facet Sapra, K Tanuj
Spoerri, Patrizia M
Engel, Andreas
Alsteens, David
Müller, Daniel J
author_sort Sapra, K Tanuj
collection PubMed
description G protein-coupled receptors (GPCRs) relay extracellular information across cell membranes through a continuum of conformations that are not always captured in structures. Hence, complementary approaches are required to quantify the physical and chemical properties of the dynamic conformations linking to GPCR function. Atomic force microscopy (AFM)-based high-resolution imaging and force spectroscopy are unique methods to scrutinize GPCRs and to sense their interactions. Here, we exemplify recent AFM-based applications to directly observe the supramolecular assembly of GPCRs in native membranes, to measure the ligand-binding free-energy landscape, and how interactions modulate the structural properties of GPCRs. Common trends in GPCR function are beginning to emerge. We envision that technical developments in combining AFM with superresolution fluorescence imaging will provide insights into how cellular states modulate GPCRs and vice versa.
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spelling pubmed-64726492019-04-19 Seeing and sensing single G protein-coupled receptors by atomic force microscopy Sapra, K Tanuj Spoerri, Patrizia M Engel, Andreas Alsteens, David Müller, Daniel J Curr Opin Cell Biol Article G protein-coupled receptors (GPCRs) relay extracellular information across cell membranes through a continuum of conformations that are not always captured in structures. Hence, complementary approaches are required to quantify the physical and chemical properties of the dynamic conformations linking to GPCR function. Atomic force microscopy (AFM)-based high-resolution imaging and force spectroscopy are unique methods to scrutinize GPCRs and to sense their interactions. Here, we exemplify recent AFM-based applications to directly observe the supramolecular assembly of GPCRs in native membranes, to measure the ligand-binding free-energy landscape, and how interactions modulate the structural properties of GPCRs. Common trends in GPCR function are beginning to emerge. We envision that technical developments in combining AFM with superresolution fluorescence imaging will provide insights into how cellular states modulate GPCRs and vice versa. Elsevier 2019-04 /pmc/articles/PMC6472649/ /pubmed/30412846 http://dx.doi.org/10.1016/j.ceb.2018.10.006 Text en © 2018 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sapra, K Tanuj
Spoerri, Patrizia M
Engel, Andreas
Alsteens, David
Müller, Daniel J
Seeing and sensing single G protein-coupled receptors by atomic force microscopy
title Seeing and sensing single G protein-coupled receptors by atomic force microscopy
title_full Seeing and sensing single G protein-coupled receptors by atomic force microscopy
title_fullStr Seeing and sensing single G protein-coupled receptors by atomic force microscopy
title_full_unstemmed Seeing and sensing single G protein-coupled receptors by atomic force microscopy
title_short Seeing and sensing single G protein-coupled receptors by atomic force microscopy
title_sort seeing and sensing single g protein-coupled receptors by atomic force microscopy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6472649/
https://www.ncbi.nlm.nih.gov/pubmed/30412846
http://dx.doi.org/10.1016/j.ceb.2018.10.006
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