Evidence map›Paper›PMID 34151984›Full record

ArticleThe Journal of experimental biology2021

Chimeric human opsins as optogenetic light sensitisers.

Doron G Hickey, Wayne I L Davies, Steven Hughes, Jessica Rodgers, Navamayooran Thavanesan, Robert E MacLaren, Mark W Hankins

Open access · hybridAbstract read
In one paragraph

Article in The Journal of experimental biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

10 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. A short story on how chromophore is hydrolyzed from rhodopsin for recycling.BioEssays : news and reviews in molecular, cellular and developmental biology · 2023
    Review
  9. Optogenetic Therapy for Visual Restoration.International journal of molecular sciences · 2022
    Review
  10. Review
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

7 authors at 3 institutions in 3 countries.

Doron G HickeyNuffield Laboratory of Ophthalmology, University of Oxford, Oxford, OX1 3QU, UK.ORCID 0000-0002-3711-5595
Wayne I L DaviesNuffield Laboratory of Ophthalmology, University of Oxford, Oxford, OX1 3QU, UK.ORCID 0000-0003-0232-1812
Steven HughesNuffield Laboratory of Ophthalmology, University of Oxford, Oxford, OX1 3QU, UK.
Jessica RodgersNuffield Laboratory of Ophthalmology, University of Oxford, Oxford, OX1 3QU, UK.
Navamayooran ThavanesanNuffield Laboratory of Ophthalmology, University of Oxford, Oxford, OX1 3QU, UK.
Robert E MacLarenNuffield Laboratory of Ophthalmology, University of Oxford, Oxford, OX1 3QU, UK.
Mark W HankinsNuffield Laboratory of Ophthalmology, University of Oxford, Oxford, OX1 3QU, UK.
University of Oxford · GBLa Trobe University · AUUniversity of Manchester · GB

Funding

Biotechnology and Biological Sciences Research CouncilDepartment of HealthMedical Research Council MR/S026266/1Wellcome Trust
6 · The paper itself

Abstract

Human opsin-based photopigments have great potential as light-sensitisers, but their requirement for phototransduction cascade-specific second messenger proteins may restrict their functionality in non-native cell types. In this study, eight chimeric human opsins were generated consisting of a backbone of either a rhodopsin (RHO) or long-wavelength-sensitive (LWS) opsin and intracellular domains from Gq/11-coupled human melanopsin. Rhodopsin/melanopsin chimeric opsins coupled to both Gi and Gq/11 pathways. Greater substitution of the intracellular surface with corresponding melanopsin domains generally showed greater Gq/11 activity with a decrease in Gi activation. Unlike melanopsin, rhodopsin and rhodopsin/melanopsin chimeras were dependent upon exogenous chromophore to function. By contrast, wild-type LWS opsin and LWS opsin/melanopsin chimeras showed only weak Gi activation in response to light, whilst Gq/11 pathway activation was not detected. Immunocytochemistry (ICC) demonstrated that chimeric opsins with more intracellular domains of melanopsin were less likely to be trafficked to the plasma membrane. This study demonstrates the importance of Gα coupling efficiency to the speed of cellular responses and created human opsins with a unique combination of properties to expand the range of customised optogenetic biotools for basic research and translational therapies.

Indexed as

OpsinsOptogeneticsChimeraHumansLightLight Signal TransductionRhodopsinRod OpsinsOpsinsRhodopsinRod OpsinsChimeraG proteinOpsinOptogeneticsPhototransductionRetina

Identifiers

PMID34151984
PMCPMC8325934
OpenAlexW3174454293

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.