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Structural basis of α1A-adrenergic receptor activation and recognition by an extracellular nanobody

Abstract:

G protein-coupled receptors (GPCRs) represent the largest family of cell surface receptors targeted by therapeutics. Their diverse signalling capabilities lead to involvement in a wide range of physiological and disease responses. The vast majority of molecules currently available to target GPCRs are designed to act at the binding site (the orthosteric site) for endogenous ligands, either promoting receptor signalling as agonists, or inhibiting as antagonists. However, a continuing challenge ...

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Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1038/s41467-023-39310-x

Authors

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Role:
Author
ORCID:
0000-0002-2245-4666
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0002-3162-441X
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Role:
Author
ORCID:
0000-0001-8788-722X
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Role:
Author
ORCID:
0000-0002-7184-6818
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Role:
Author
ORCID:
0000-0002-0582-2105


Publisher:
Nature Research
Journal:
Nature Communications More from this journal
Volume:
14
Issue:
1
Pages:
3655-3655
Publication date:
2023-06-20
DOI:
EISSN:
2041-1723
ISSN:
2041-1723


Language:
English
Keywords:
Pubs id:
2364930
Local pid:
pubs:2364930
Source identifiers:
W4381433681
Deposit date:
2026-01-30
ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

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