Evidence map›Paper›PMID 42026038›Full record

ArticleNature communications2026

Molecular mechanisms of native ligand selectivity in catecholamine G protein-coupled receptors.

Nour Aldin Kahlous, Maiju K Rinne, Xin Zhang, Yanying Li, Yue Chen, Aikaterini Motso, Kaixuan Gao, Christina Bergqvist, Hongda Sheng, Yi Wang and 11 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

Nour Aldin Kahlous *Science for Life Laboratory, Department of Cell and Molecular Biology, Uppsala University, Uppsala, Sweden.ORCID 0000-0002-7744-1491
Maiju K Rinne *Department of Medical Cell Biology, Uppsala University, Uppsala, Sweden.ORCID 0000-0003-3218-2841
Xin Zhang *State Key Laboratory of Membrane Biology, Tsinghua-Peking Center for Life Sciences, Tsinghua University, Beijing, China.
Yanying LiDepartment of Medical Cell Biology, Uppsala University, Uppsala, Sweden.
Yue ChenScience for Life Laboratory, Department of Applied Physics, KTH Royal Institute of Technology, Stockholm, Sweden.
Aikaterini MotsoDepartment of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
Kaixuan GaoState Key Laboratory of Membrane Biology, Tsinghua-Peking Center for Life Sciences, Tsinghua University, Beijing, China.
Christina BergqvistDepartment of Medical Cell Biology, Uppsala University, Uppsala, Sweden.
Hongda ShengDepartment of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
Yi WangCollege of Pharmaceutical Sciences, Zhejiang University, Hangzhou, China.ORCID 0000-0002-3676-9183
Israel Cabeza de VacaScience for Life Laboratory, Department of Cell and Molecular Biology, Uppsala University, Uppsala, Sweden.ORCID 0000-0002-6208-1091
Alejandro Díaz-HolguínScience for Life Laboratory, Department of Cell and Molecular Biology, Uppsala University, Uppsala, Sweden.ORCID 0000-0002-3449-5086
Philip UllmannScience for Life Laboratory, Department of Cell and Molecular Biology, Uppsala University, Uppsala, Sweden.ORCID 0000-0003-2391-4609
Tore BengtssonDepartment of Molecular Biosciences, The Wenner-Gren Institute, Stockholm University, Stockholm, Sweden.ORCID 0000-0002-5396-030X
Volker M LauschkeDepartment of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0002-1140-6204
Jyrki P KukkonenDepartment of Pharmacology, Medicum, University of Helsinki, Helsinki, Finland.ORCID 0000-0002-6989-1564
Lucie DelemotteScience for Life Laboratory, Department of Applied Physics, KTH Royal Institute of Technology, Stockholm, Sweden.ORCID 0000-0002-0828-3899
Shane C WrightDepartment of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0002-7470-5068
Xiangyu LiuState Key Laboratory of Membrane Biology, Tsinghua-Peking Center for Life Sciences, Tsinghua University, Beijing, China. liu_xy@mail.tsinghua.edu.cn.ORCID 0000-0003-3178-9238
Dan LarhammarDepartment of Medical Cell Biology, Uppsala University, Uppsala, Sweden. dan.larhammar@uu.se.ORCID 0000-0002-6736-0663
Jens CarlssonScience for Life Laboratory, Department of Cell and Molecular Biology, Uppsala University, Uppsala, Sweden. jens.carlsson@icm.uu.se.ORCID 0000-0003-4623-2977

Funding

Knut och Alice Wallenbergs Stiftelse (Knut and Alice Wallenberg Foundation) 2019.0130
6 · The paper itself

Abstract

Activation of G protein-coupled receptors (GPCRs) by extracellular ligands is crucial for cellular communication and modulates numerous physiological processes. Despite sharing highly similar orthosteric binding sites, catecholamine GPCRs exhibit exquisite selectivity for their native agonists, even among nearly identical chemical messengers. However, the molecular basis and evolution of receptor selectivity remain poorly understood. To elucidate the structural mechanisms of GPCR selectivity, we focus on the prototypical human β

Indexed as

CatecholaminesReceptors, Adrenergic, beta-2Receptors, Dopamine D1Receptors, G-Protein-CoupledAmino Acid SequenceBinding SitesCryoelectron MicroscopyHumansLigandsModels, MolecularProtein BindingCatecholaminesLigandsReceptors, Adrenergic, beta-2Receptors, Dopamine D1Receptors, G-Protein-Coupled

Identifiers

PMID42026038
PMCPMC13150006

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.