Evidence map›Paper›PMID 35610225›Full record

ArticleNature communications2022

Functional expression of opioid receptors and other human GPCRs in yeast engineered to produce human sterols.

Björn D M Bean, Colleen J Mulvihill, Riddhiman K Garge, Daniel R Boutz, Olivier Rousseau, Brendan M Floyd, William Cheney, Elizabeth C Gardner, Andrew D Ellington, Edward M Marcotte and 3 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Do GPCRs constitute the target of 30% of newly approved drugs in Germany?Naunyn-Schmiedeberg's archives of pharmacology · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Cannabis and Paternal Epigenetic Inheritance.International journal of environmental research and public health · 2023
    Review
  9. Review
  10. Screening microbially produced ΔNature communications · 2022
    Article
  11. The Use of Yeast in Biosensing.Microorganisms · 2022
    Review
  12. Article
  13. 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

13 authors at 4 institutions in 2 countries.

Björn D M Bean *Department of Biology, Centre for Applied Synthetic Biology, Concordia University, Montréal, QC, H4B1R6, Canada.ORCID http://orcid.org/0000-0003-2409-3902
Colleen J Mulvihill *Department of Molecular Biosciences, Center for Systems and Synthetic Biology, The University of Texas at Austin, Austin, TX, 78712, USA.
Riddhiman K GargeDepartment of Molecular Biosciences, Center for Systems and Synthetic Biology, The University of Texas at Austin, Austin, TX, 78712, USA.ORCID http://orcid.org/0000-0002-6774-0172
Daniel R BoutzDepartment of Molecular Biosciences, Center for Systems and Synthetic Biology, The University of Texas at Austin, Austin, TX, 78712, USA.
Olivier RousseauDepartment of Biology, Centre for Applied Synthetic Biology, Concordia University, Montréal, QC, H4B1R6, Canada.ORCID http://orcid.org/0000-0002-8691-2048
Brendan M FloydDepartment of Molecular Biosciences, Center for Systems and Synthetic Biology, The University of Texas at Austin, Austin, TX, 78712, USA.
William CheneyDepartment of Biology, Centre for Applied Synthetic Biology, Concordia University, Montréal, QC, H4B1R6, Canada.ORCID http://orcid.org/0000-0002-4868-8145
Elizabeth C GardnerDepartment of Molecular Biosciences, Center for Systems and Synthetic Biology, The University of Texas at Austin, Austin, TX, 78712, USA.
Andrew D EllingtonDepartment of Molecular Biosciences, Center for Systems and Synthetic Biology, The University of Texas at Austin, Austin, TX, 78712, USA.ORCID http://orcid.org/0000-0001-6246-5338
Edward M MarcotteDepartment of Molecular Biosciences, Center for Systems and Synthetic Biology, The University of Texas at Austin, Austin, TX, 78712, USA.ORCID http://orcid.org/0000-0001-8808-180X
Jimmy D GolliharDepartment of Molecular Biosciences, Center for Systems and Synthetic Biology, The University of Texas at Austin, Austin, TX, 78712, USA. jgollihar2@houstonmethodist.org.
Malcolm WhitewayDepartment of Biology, Centre for Applied Synthetic Biology, Concordia University, Montréal, QC, H4B1R6, Canada.
Vincent J J MartinDepartment of Biology, Centre for Applied Synthetic Biology, Concordia University, Montréal, QC, H4B1R6, Canada. vincent.martin@concordia.ca.ORCID http://orcid.org/0000-0001-7511-115X
The University of Texas at Austin · USConcordia University · CADEVCOM Army Research Laboratory · USHouston Methodist · US

Funding

Proteomics and model organism humanization to decode human geneticsR35GM122480 · NIGMS · UNIVERSITY OF TEXAS AT AUSTIN · PI EDWARD M MARCOTTE · 2017 to 2026
$5.4M
Synthetic biology for the chemogenetic manipulation of pain pathwaysR21AT010777 · NCCIH · UNIVERSITY OF TEXAS AT AUSTIN · PI ELLINGTON, ANDREW D · 2019 to 2020
$424k
NCCIH NIH HHS R21 AT010777NIGMS NIH HHS R35 GM122480
6 · The paper itself

Abstract

The yeast Saccharomyces cerevisiae is powerful for studying human G protein-coupled receptors as they can be coupled to its mating pathway. However, some receptors, including the mu opioid receptor, are non-functional, which may be due to the presence of the fungal sterol ergosterol instead of cholesterol. Here we engineer yeast to produce cholesterol and introduce diverse mu, delta, and kappa opioid receptors to create sensitive opioid biosensors that recapitulate agonist binding profiles and antagonist inhibition. Additionally, human mu opioid receptor variants, including those with clinical relevance, largely display expected phenotypes. By testing mu opioid receptor-based biosensors with systematically adjusted cholesterol biosynthetic intermediates, we relate sterol profiles to biosensor sensitivity. Finally, we apply sterol-modified backgrounds to other human receptors revealing sterol influence in SSTR5, 5-HTR4, FPR1, and NPY1R signaling. This work provides a platform for generating human G protein-coupled receptor-based biosensors, facilitating receptor deorphanization and high-throughput screening of receptors and effectors.

Indexed as

PhytosterolsSaccharomyces cerevisiaeCholesterolHumansReceptors, OpioidReceptors, Opioid, kappaReceptors, Opioid, muSterolsCholesterolPhytosterolsReceptors, OpioidReceptors, Opioid, kappaReceptors, Opioid, muSterols

Identifiers

PMID35610225
PMCPMC9130329
OpenAlexW4281387249

What Socratic 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 Socratic graph.