Evidence map›Paper›PMID 28705698›Full record

ArticleBiochemical pharmacology2017

Receptor activity-modifying protein dependent and independent activation mechanisms in the coupling of calcitonin gene-related peptide and adrenomedullin receptors to Gs.

Michael J Woolley, Christopher A Reynolds, John Simms, Christopher S Walker, Juan Carlos Mobarec, Michael L Garelja, Alex C Conner, David R Poyner, Debbie L Hay

Open access · hybridAbstract read
In one paragraph

Article in Biochemical pharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.9field-weighted citation impact, top 15% of its field
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

22 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. PACAP Induces Light Aversion in Mice by an Inheritable Mechanism Independent of CGRP.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  14. Article
  15. Structure and Dynamics of Adrenomedullin Receptors AMACS pharmacology & translational science · 2020
    Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article
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

9 authors at 4 institutions in 2 countries.

Michael J WoolleyInstitute of Clinical Sciences, University of Birmingham, Edgbaston, Birmingham, UK.
Christopher A ReynoldsSchool of Biological Sciences, University of Essex, Wivenhoe Park, Colchester CO4 3SQ, UK.
John SimmsSchool of Life and Health Sciences, Aston University, Aston Triangle, Birmingham, UK.
Christopher S WalkerSchool of Biological Sciences, University of Auckland, Auckland, New Zealand.
Juan Carlos MobarecSchool of Biological Sciences, University of Essex, Wivenhoe Park, Colchester CO4 3SQ, UK.
Michael L GareljaSchool of Biological Sciences, University of Auckland, Auckland, New Zealand.
Alex C ConnerInstitute of Clinical Sciences, University of Birmingham, Edgbaston, Birmingham, UK.
David R PoynerSchool of Life and Health Sciences, Aston University, Aston Triangle, Birmingham, UK. Electronic address: d.r.poyner@aston.ac.uk.
Debbie L HaySchool of Biological Sciences, University of Auckland, Auckland, New Zealand. Electronic address: dl.hay@auckland.ac.nz.
University of Auckland · NZAston University · GBUniversity of Birmingham · GBUniversity of Essex · GB

Funding

Biotechnology and Biological Sciences Research Council BB/M000176/1Biotechnology and Biological Sciences Research Council BB/M006883/1British Heart Foundation PG/12/59/29795
6 · The paper itself

Abstract

Calcitonin gene-related peptide (CGRP) or adrenomedullin (AM) receptors are heteromers of the calcitonin receptor-like receptor (CLR), a class B G protein-coupled receptor, and one of three receptor activity-modifying proteins (RAMPs). How CGRP and AM activate CLR and how this process is modulated by RAMPs is unclear. We have defined how CGRP and AM induce Gs-coupling in CLR-RAMP heteromers by measuring the effect of targeted mutagenesis in the CLR transmembrane domain on cAMP production, modeling the active state conformations of CGRP and AM receptors in complex with the Gs C-terminus and conducting molecular dynamics simulations in an explicitly hydrated lipidic bilayer. The largest effects on receptor signaling were seen with H295A

Indexed as

AnimalsCalcitonin Gene-Related PeptideCalcitonin Receptor-Like ProteinChlorocebus aethiopsCOS CellsCyclic AMPGTP-Binding Protein alpha Subunits, GsHumansHydrophobic and Hydrophilic InteractionsMolecular Dynamics SimulationMutationProtein BindingRadioligand AssayReceptor Activity-Modifying ProteinsReceptors, AdrenomedullinRecombinant Fusion ProteinsCalcitonin Gene-Related PeptideCalcitonin Receptor-Like ProteinCyclic AMPGTP-Binding Protein alpha Subunits, GsReceptor Activity-Modifying ProteinsReceptors, AdrenomedullinRecombinant Fusion ProteinsAdrenomedullinAdrenomedullin (PubChem CID: 56841671)Calcitonin gene-related peptideCalcitonin gene-related peptide (PubChem CID: 56841902)cAMP (PubChem CID: 6076)GPCRMolecular dynamicsMolecular modelingReceptor activity-modifying protein

Identifiers

PMID28705698
PMCPMC5609567
OpenAlexW2735517537

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.