Evidence map›Paper›PMID 38275046›Full record

ArticleCurrent protein & peptide science2024

CTXP, The Major Cobra Toxin Peptide from

Mohammad Hosseininejad Chafi, Mohsen Eslamnezhad-Namin, Mansoureh Shahbazi Dastjerdeh, Mohammad Reza Zareinejad, Akbar Oghalaie, Kamran Pooshang Bagheri, Fatemeh Kazemi-Lomedasht, Gholamreza Karimi, Mehdi Razzaghi-Abyaneh, Sima Sadat Seyedjavadi and 1 more

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Article in Current protein & peptide science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

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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

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0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

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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

11 authors at 1 institution in 1 country.

Mohammad Hosseininejad ChafiVenom and Biotherapeutics Molecules Laboratory, Medical Biotechnology Department, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.ORCID 0000-0002-1851-9287
Mohsen Eslamnezhad-NaminVenom and Biotherapeutics Molecules Laboratory, Medical Biotechnology Department, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.ORCID 0009-0003-9597-566X
Mansoureh Shahbazi DastjerdehVenom and Biotherapeutics Molecules Laboratory, Medical Biotechnology Department, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.ORCID 0000-0003-1211-6193
Mohammad Reza ZareinejadVenom and Biotherapeutics Molecules Laboratory, Medical Biotechnology Department, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.ORCID 0009-0007-7340-7732
Akbar OghalaieVenom and Biotherapeutics Molecules Laboratory, Medical Biotechnology Department, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.ORCID 0000-0003-2135-8143
Kamran Pooshang BagheriVenom and Biotherapeutics Molecules Laboratory, Medical Biotechnology Department, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.ORCID 0000-0003-0125-3918
Fatemeh Kazemi-LomedashtVenom and Biotherapeutics Molecules Laboratory, Medical Biotechnology Department, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.ORCID 0000-0002-5832-1822
Gholamreza KarimiMedical Toxicology Research Center and Pharmacy School, Mashhad University of Medical Sciences, Mashhad, Iran.ORCID 0000-0002-1273-5448
Mehdi Razzaghi-AbyanehDepartment of Mycology, Pasteur Institute of Iran, Tehran, Iran.ORCID 0000-0001-8217-399X
Sima Sadat SeyedjavadiDepartment of Mycology, Pasteur Institute of Iran, Tehran, Iran.ORCID 0000-0002-5896-5636
Mahdi BehdaniVenom and Biotherapeutics Molecules Laboratory, Medical Biotechnology Department, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.ORCID 0000-0002-4839-5123
Pasteur Institute of Iran · IR

Funding

Pasteur Institute of Iran, Tehran, Iran 1695
6 · The paper itself

Abstract

BACKGROUND AND

objectiveSnakebite envenoming is a serious public health issue causing more than 135,000 annual deaths worldwide.

methodsVenom proteomic profiling was performed using gel filtration (GF), reversed-phase (RP) chromatography, and intact mass spectrometry. The toxicity of GF-, and RP-eluted fractions was analyzed in BALB/c mice. The rabbit polyclonal antisera were produced against crude venom, GF fraction V (FV), and RP peak 1 (CTXP) and applied in neutralization assays.

resultsToxicity studies in BALB/c identified FV as the major toxic fraction of venom. Subsequently, RP separation of FV resulted in eight peaks, of which peak 1, referred to as "CTXP" (cobra toxin peptide), was identified as the major lethal protein. In vivo neutralization assays using rabbit antisera showed that polyclonal antibodies raised against FV and CTXP are capable of neutralizing at least 2-LD50s of crude venom, FV, and CTXP in all tested mice.

conclusionSurprisingly, the Anti-CTXP antibody could neutralize 8-LD50 of the CTXP peptide. These results identified CTXP (a 7 kDa peptide) as a potential target for the development of novel efficient antivenom agents.

Indexed as

AntiveninsElapid VenomsNaja najaAnimalsLethal Dose 50MiceMice, Inbred BALB CPeptidesProteomicsRabbitsAntiveninsElapid VenomsPeptidesantivenomCTXP (Cobra toxin peptide)gel filtration.lethal proteinNaja naja oxianavenom

Identifiers

PMID38275046
OpenAlexW4391219915

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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.