Evidence map›Paper›PMID 38379080›Full record

ArticleDoklady. Biochemistry and biophysics2023

Modular Nanotransporters Capable of Causing Intracellular Degradation of the N-Protein of the SARS-CoV-2 Virus in A549 Cells with Temporary Expression of This Protein Fused with a Fluorescent Protein mRuby3.

Y V Khramtsov, A V Ulasov, T N Lupanova, G P Georgiev, A S Sobolev

Abstract read
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Article in Doklady. Biochemistry and biophysics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

5 authors at 2 institutions in 1 country.

Y V KhramtsovInstitute of Gene Biology, Russian Academy of Sciences, Moscow, Russia.
A V UlasovInstitute of Gene Biology, Russian Academy of Sciences, Moscow, Russia.
T N LupanovaInstitute of Gene Biology, Russian Academy of Sciences, Moscow, Russia.
G P GeorgievInstitute of Gene Biology, Russian Academy of Sciences, Moscow, Russia.
A S SobolevInstitute of Gene Biology, Russian Academy of Sciences, Moscow, Russia. alsobolev@yandex.ru.
Institute of Gene Biology · RULomonosov Moscow State University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Modular nanotransporters (MNTs) containing an antibody-like molecule, monobody, to the N‑protein of the SARS-CoV-2 virus, as well as an amino acid sequence that recruits the Keap1 E3 ligase (E3BP) were created. This MNT also included a site for cleavage of the E3BP monobody from the MNT in acidic endocytic compartments. It was shown that this cleavage by the endosomal protease cathepsin B leads to a 2.7-fold increase in the affinity of the E3BP monobody for the N-protein. Using A549 cells with transient expression of the N-protein fused with the fluorescent protein mRuby3, it was shown that incubation with MNT leads to a significant decrease in mRuby3 fluorescence. It is assumed that the developed MNTs can serve as a basis for the creation of new antiviral drugs against the SARS-CoV-2 virus.

Indexed as

COVID-19SARS-CoV-2A549 CellsHumansKelch-Like ECH-Associated Protein 1NF-E2-Related Factor 2Kelch-Like ECH-Associated Protein 1NF-E2-Related Factor 2cathepsin BE3 ligaseflow cytometryKeap1nucleocapsid proteinSARS-CoV-2thermophoresis

Identifiers

PMID38379080
OpenAlexW4391951267

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.