Evidence map›Paper›PMID 39107369›Full record

ArticleCommunications biology2024

Optical inactivation of intracellular molecules by fast-maturating photosensitizing fluorescence protein, HyperNova.

Hisashi Shidara, Taku Shirai, Ryohei Ozaki-Noma, Susumu Jitsuki, Takeharu Nagai, Kiwamu Takemoto

Abstract read
In one paragraph

Article in Communications biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Differential elimination of marked sex chromosomes enables production of nontransgenic male mosquitoes in a single strain.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  3. 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

6 authors.

Hisashi ShidaraDepartment of Biochemistry, Mie University Graduate School of Medicine, Mie, 514-8507, Japan.
Taku ShiraiDepartment of Biochemistry, Mie University Graduate School of Medicine, Mie, 514-8507, Japan.
Ryohei Ozaki-NomaSANKEN, Osaka University, Ibaraki, Osaka, 567-0047, Japan.
Susumu JitsukiDepartment of Biochemistry, Mie University Graduate School of Medicine, Mie, 514-8507, Japan.
Takeharu NagaiSANKEN, Osaka University, Ibaraki, Osaka, 567-0047, Japan.ORCID 0000-0003-2650-9895
Kiwamu TakemotoDepartment of Biochemistry, Mie University Graduate School of Medicine, Mie, 514-8507, Japan. takemotk@med.mie-u.ac.jp.ORCID 0000-0002-3301-3268

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Photosensitizing fluorescence protein is a promising tool for chromophore-assisted light inactivation (CALI) that enables specific oxidation and inactivation of intracellular molecules. However, a commonly used monomeric photosensitizing fluorescent protein, SuperNova, shows a low CALI efficiency due to its insufficient maturation at 37 °C, thereby limiting the application of CALI to various molecules, especially in mammalian cells. Here, we present a photosensitizing fluorescence protein, HyperNova, with markedly improved maturation at 37 °C, leading to greatly enhanced CALI efficiency. Exploiting this quality, HyperNova enables the application of CALI to variety of molecules such as a mitotic kinase and transcriptional factors that were highly challenging with conventional SuperNova. To further demonstrate the utility of HyperNova, we have also succeeded in developing novel CALI techniques for MAP kinases by HyperNova. Our findings suggest that HyperNova has the potential to expand the molecular toolbox for manipulating biological events in living cells, providing new avenues for investigating cellular signaling pathways.

Indexed as

Luminescent ProteinsAnimalsChromophore-Assisted Light InactivationHeLa CellsHumansLightPhotosensitizing AgentsLuminescent ProteinsPhotosensitizing Agents

Identifiers

PMID39107369
PMCPMC11303530

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.