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dc.contributor.author
Sapra, K.T.
dc.contributor.author
Spoerri, Patrizia M.
dc.contributor.author
Engel, Andreas
dc.contributor.author
Alsteens, David
dc.contributor.author
Müller, Daniel J.
dc.date.accessioned
2018-11-30T09:34:52Z
dc.date.available
2018-11-20T05:20:36Z
dc.date.available
2018-11-30T09:34:52Z
dc.date.issued
2019-04
dc.identifier.issn
0955-0674
dc.identifier.issn
1879-0410
dc.identifier.other
10.1016/j.ceb.2018.10.006
en_US
dc.identifier.uri
http://hdl.handle.net/20.500.11850/304712
dc.identifier.doi
10.3929/ethz-b-000304712
dc.description.abstract
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.
en_US
dc.format
application/pdf
en_US
dc.language.iso
en
en_US
dc.publisher
Elsevier
en_US
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.title
Seeing and sensing single G protein-coupled receptors by atomic force microscopy
en_US
dc.type
Review Article
dc.rights.license
Creative Commons Attribution 4.0 International
dc.date.published
2018-11-06
ethz.journal.title
Current Opinion in Cell Biology
ethz.journal.volume
57
en_US
ethz.journal.abbreviated
Curr. Opin. Cell Biol.
ethz.pages.start
25
en_US
ethz.pages.end
32
en_US
ethz.version.deposit
publishedVersion
en_US
ethz.grant
Gleichzeitiges hochauflösendes Abbilden von Membranproteinen und dreidimensionales Kartieren der Wechselwirkungskräfte und Energielandschaften mit Liganden
en_US
ethz.identifier.wos
ethz.identifier.scopus
ethz.publication.place
Kidlington
en_US
ethz.publication.status
published
en_US
ethz.leitzahl
ETH Zürich::00002 - ETH Zürich::00012 - Lehre und Forschung::00007 - Departemente::02060 - Dep. Biosysteme / Dep. of Biosystems Science and Eng.::03870 - Müller, Daniel J. / Müller, Daniel J.
ethz.leitzahl.certified
ETH Zürich::00002 - ETH Zürich::00012 - Lehre und Forschung::00007 - Departemente::02060 - Dep. Biosysteme / Dep. of Biosystems Science and Eng.::03870 - Müller, Daniel J. / Müller, Daniel J.
ethz.grant.agreementno
160199
ethz.grant.fundername
SNF
ethz.grant.funderDoi
10.13039/501100001711
ethz.grant.program
Projekte MINT
ethz.date.deposited
2018-11-20T05:21:09Z
ethz.source
SCOPUS
ethz.eth
yes
en_US
ethz.availability
Open access
en_US
ethz.rosetta.installDate
2018-11-30T09:35:13Z
ethz.rosetta.lastUpdated
2022-03-28T21:50:51Z
ethz.rosetta.versionExported
true
ethz.COinS
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