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TitleExtracellular nanobody screening using conformationally stable GPCR variants.
Journal, issue, pagesProc Natl Acad Sci U S A, Vol. 122, Issue 45, Page e2508879122, Year 2025
Publish dateNov 11, 2025
AuthorsXin Zhang / Kaixuan Gao / Jia Nie / Hengyu Meng / Xiaoou Sun / Jiawei Zhao / Xiangyu Liu /
PubMed AbstractG protein-coupled receptors (GPCRs) are prominent drug targets that have attracted intensive efforts in drug screening. Binding-based screening methods for GPCR ligands often require conformationally ...G protein-coupled receptors (GPCRs) are prominent drug targets that have attracted intensive efforts in drug screening. Binding-based screening methods for GPCR ligands often require conformationally stable, purified receptors. However, obtaining large quantities of GPCRs in stable states, particularly with unoccupied extracellular ligand-binding pockets and especially in their active conformations, remains challenging due to the inherent dynamic nature of these receptors. To address this challenge, we propose a universal approach for stabilizing GPCRs in specific conformations. Using the M1 muscarinic acetylcholine receptor (M1R) as a model, we successfully stabilized M1R in its active conformation through de novo design of a fusion protein, and further demonstrated the generalizability of this strategy by applying it to other GPCRs. We screened a synthetic yeast display library of nanobodies against both the stabilized active-state and previously reported inactive-state M1R, identifying several nanobodies that specifically recognize each conformation. This method not only facilitates the stabilization of GPCRs in desired states but also provides valuable tools for developing more selective therapeutic agents, enhancing drug discovery efficiency and specificity.
External linksProc Natl Acad Sci U S A / PubMed:41187083 / PubMed Central
MethodsEM (single particle)
Resolution2.88 - 3.62 Å
Structure data

EMDB-63988, PDB-9uap:
cryo-EM structure of ligand-free active-state M1 muscarinic acetylcholine receptor with alpha5 helix of G11 protein complex
Method: EM (single particle) / Resolution: 3.62 Å

EMDB-63998, PDB-9uaz:
Cryo-EM structure of the M1 muscarinic acetylcholine receptor bound to atropine and nanobody NbA12
Method: EM (single particle) / Resolution: 3.29 Å

EMDB-64050, PDB-9ucp:
cryo-EM structure of M1 muscarinic acetylcholine receptor-alpha5 helix of G11 protein complex bound to iperoxo and nanobody Nb1B4
Method: EM (single particle) / Resolution: 2.88 Å

Chemicals

PDB-1ebt:
HEMOGLOBIN I FROM THE CLAM LUCINA PECTINATA BOUND WITH CYANIDE

ChemComp-IXO:
4-(4,5-dihydro-1,2-oxazol-3-yloxy)-N,N,N-trimethylbut-2-yn-1-aminium

Source
  • homo sapiens (human)
  • vicugna pacos (alpaca)
KeywordsMEMBRANE PROTEIN / GPCR / active-state / ligand-free / de novo protein / inactive-state / atropine / nanobody / MEMBRANE PROTEIN/IMMUNE SYSTEM / MEMBRANE PROTEIN-IMMUNE SYSTEM complex

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