Evidence map›Paper›PMID 33398811›Full record

ReviewAdvances in experimental medicine and biology2021

Optogenetic Potentials of Diverse Animal Opsins: Parapinopsin, Peropsin, LWS Bistable Opsin.

Mitsumasa Koyanagi, Tomoka Saito, Seiji Wada, Takashi Nagata, Emi Kawano-Yamashita, Akihisa Terakita

Abstract readReview
PubMed Publisher
In one paragraph

Review in Advances in experimental medicine and biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
9.9field-weighted citation impact, top 2% 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

9 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Engineering signalling pathways in mammalian cells.Nature biomedical engineering · 2024
    Review
  5. Article
  6. Fluorescence of the Retinal Chromophore in Microbial and Animal Rhodopsins.International journal of molecular sciences · 2023
    Review
  7. Article
  8. Article
  9. 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

6 authors at 1 institution in 1 country.

Mitsumasa KoyanagiDepartment of Biology and Geosciences, Graduate School of Science, Osaka City University, Osaka, Japan.
Tomoka SaitoDepartment of Biology and Geosciences, Graduate School of Science, Osaka City University, Osaka, Japan.
Seiji WadaDepartment of Biology and Geosciences, Graduate School of Science, Osaka City University, Osaka, Japan.
Takashi NagataDepartment of Biology and Geosciences, Graduate School of Science, Osaka City University, Osaka, Japan.
Emi Kawano-YamashitaDepartment of Biology and Geosciences, Graduate School of Science, Osaka City University, Osaka, Japan.
Akihisa TerakitaDepartment of Biology and Geosciences, Graduate School of Science, Osaka City University, Osaka, Japan. terakita@sci.osaka-cu.ac.jp.
Osaka City University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Animal opsin-based pigments are light-activated G-protein-coupled receptors (GPCRs), which drive signal transduction cascades via G-proteins. Thousands of animal opsins have been identified, and molecular phylogenetic and biochemical analyses have revealed the unexpected diversity in selectivity of G-protein activation and photochemical property. Here we discuss the optogenetic potentials of diverse animal opsins, particularly recently well-characterized three non-canonical opsins, parapinopsin, peropsin, and LWS bistable opsin. Unlike canonical opsins such as vertebrate visual opsins that have been conventionally used for optogenetic applications, these opsins are bistable; opsin-based pigments do not release the chromophore retinal after light absorption, and the stable photoproducts revert to their original dark states upon subsequent light absorption. Parapinopsins have a "complete photoregeneration ability," which allows a clear color-dependent regulation of signal transductions. On the other hand, peropsins serve as a "dark-active and light-inactivated" GPCR to regulate signal transductions in the opposite way compared with usual opsins. In addition, an LWS bistable opsin from a butterfly was revealed to be the longest wavelength-sensitive animal opsin with its absorption maximum at ~570 nm. The property-dependent optical regulations of signal transductions were demonstrated in mammalian cultured cells, showing potentials of new optogenetic tools.

Indexed as

OpsinsOptogeneticsAnimalsEvolution, MolecularVertebratesVision, OcularOpsinsAnimal rhodopsinBistable pigmentCultured cellsG-protein-coupled receptorOpsinOptogenetic potentialPhotoregenerationPhototransductionSecond messenger

Identifiers

PMID33398811
OpenAlexW3120355442

What OpenQuestion holds

Textmetadata
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.