Evidence map›Paper›PMID 40878830›Full record

ArticleFEBS letters2025

Development of visible light-sensitive human neuropsin (OPN5) via single amino acid substitution.

Yusuke Sakai, Richard J McDowell, Robert J Lucas

Abstract read
In one paragraph

Article in FEBS letters, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Acute Ocular Effects of Violet and Red Light Exposure in Young Adults.Ophthalmic & physiological optics : the journal of the British College of Ophthalmic Opticians (Optometrists) · 2026
    Article
  2. A key spectral tuning site of UV-sensitive vertebrate non-visual opsin Opn5.Cellular and molecular life sciences : CMLS · 2025
    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

3 authors.

Yusuke SakaiDivision of Neuroscience and Centre for Biological Timing, School of Biological Sciences, Faculty of Biology Medicine and Health, University of Manchester, UK.ORCID https://orcid.org/0000-0002-7092-0094
Richard J McDowellDivision of Neuroscience and Centre for Biological Timing, School of Biological Sciences, Faculty of Biology Medicine and Health, University of Manchester, UK.ORCID https://orcid.org/0000-0002-6051-106X
Robert J LucasDivision of Neuroscience and Centre for Biological Timing, School of Biological Sciences, Faculty of Biology Medicine and Health, University of Manchester, UK.

Funding

European Research Council 951644-SOL
6 · The paper itself

Abstract

Neuropsin (Opn5), a UV-sensitive 'non-visual' opsin, has the potential to be used as optogenetic tools applicable to tissues outside of the eye because of its broad expression. However, its sensitivity to poorly tissue-penetrating UV light poses challenges for its application. In this study, we focused on human OPN5 (hOPN5) to identify amino acid(s) responsible for the UV sensitivity. Sequence alignment across UV-sensitive Opn5s identified a conserved lysine residue (Lys91) at a position implicated in spectral tuning in invertebrate opsins. Substitution of this residue with neutral or acidic amino acids caused substantial shifts in spectral sensitivity towards visible wavelengths. Our findings identify Lys91 as a key spectral tuning site in hOPN5 and provide visible-light-sensitive versions as a candidate for optogenetic applications. Impact statement A "non-visual" opsin, Opn5, is the only UV-sensitive opsin in human. In this study, we identified, for the first time, a key tuning site responsible for the UV sensitivity of hOPN5. In addition to its impact on the opsin molecular studies, this finding could pave the way for the development of novel visual-sensitive Opn5-based optogenetic tools.

Indexed as

Amino Acid SubstitutionLightOpsinsAmino Acid SequenceAnimalsHEK293 CellsHumansLysineOptogeneticsUltraviolet RaysLysineOpsinsGPCRneuropsinopsinoptogeneticsspectral tuning

Identifiers

PMID40878830
PMCPMC12457702

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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.