Evidence map›Paper›PMID 38760596›Full record

ArticleThe protein journal2024

Expression of Recombinant Stonustoxin Alpha Subunit and Preparation of polyclonal antiserum for Stonustoxin Neutralization Studies.

Amir Sajjad Hojjati-Razgi, Shahram Nazarian, Hossein Samiei-Abianeh, Amir Vazirizadeh, Emad Kordbacheh, Seyed Mojtaba Aghaie

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

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1 · What the graph read from it

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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

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Amir Sajjad Hojjati-RazgiDepartment of Biology, Faculty of Basic Sciences, Imam Hossein University, Tehran, Iran.
Shahram NazarianDepartment of Biology, Faculty of Basic Sciences, Imam Hossein University, Tehran, Iran. nazarian@ihu.ac.ir.
Hossein Samiei-AbianehDepartment of Biology, Faculty of Basic Sciences, Imam Hossein University, Tehran, Iran.
Amir VazirizadehDepartment of Marine Biotechnology, The Persian Gulf Research and Studies Center, The Persian Gulf University, Bushehr, Iran.
Emad KordbachehDepartment of Biology, Faculty of Basic Sciences, Imam Hossein University, Tehran, Iran.
Seyed Mojtaba AghaieDepartment of Biology, Faculty of Basic Sciences, Imam Hossein University, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stonustoxin (SNTX) is a lethal protein found in stonefish venom, responsible for many of the symptoms associated with stonefish envenomation. To counter stonefish venom challenges, antivenom is a well-established and effective solution. In this study, we aimed to produce the recombinant alpha subunit protein of Stonustoxin from Synanceia horrida and prepare antibodies against it The SNTXα gene sequence was optimized for E. coli BL21 (DE3) expression and cloned into the pET17b vector. Following purification, the recombinant protein was subcutaneously injected into rabbits, and antibodies were extracted from rabbit´s serum using a G protein column As a result of codon optimization, the codon adaptation index for the SNTXα cassette increased to 0.94. SDS-PAGE analysis validated the expression of SNTXα, with a band observed at 73.5 kDa with a yield of 60 mg/l. ELISA results demonstrated rabbits antibody titers were detectable up to a 1:256,000 dilution. The isolated antibody from rabbit´s serum exhibited a concentration of 1.5 mg/ml, and its sensitivity allowed the detection of a minimum protein concentration of 9.7 ng. In the neutralization assay the purified antibody against SNTXα protected mice challenged with 2 LD50. In conclusion, our study successfully expressed the alpha subunit of Stonustoxin in a prokaryotic host, enabling the production of antibodies for potential use in developing stonefish antivenom.

Indexed as

AntiveninsRecombinant ProteinsAnimalsEscherichia coliFish VenomsGene ExpressionImmune SeraMiceRabbitsAntiveninsFish VenomsImmune SeraRecombinant ProteinsstonustoxinPolyclonal AntiserumRecombinant proteinScorpaenidaeStonefish VenomStonustoxinStonustoxin Alpha Subunit

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Registered trials

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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 Socratic graph.