重组石蒜毒素α亚基的表达和用于石蒜毒素中和研究的多克隆抗血清的制备。

The protein journal Pub Date : 2024-06-01 Epub Date: 2024-05-17 DOI:10.1007/s10930-024-10203-2
Amir Sajjad Hojjati-Razgi, Shahram Nazarian, Hossein Samiei-Abianeh, Amir Vazirizadeh, Emad Kordbacheh, Seyed Mojtaba Aghaie
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引用次数: 0

摘要

石首鱼毒素(SNTX)是一种存在于石首鱼毒液中的致命蛋白质,是造成许多与石首鱼中毒相关症状的原因。为应对石首鱼毒液的挑战,抗蛇毒血清是一种行之有效的解决方案。在这项研究中,我们的目标是生产石首鱼毒素的重组α亚基蛋白,并制备针对它的抗体。 SNTXα 基因序列经过优化,可在大肠杆菌 BL21 (DE3) 中表达,并克隆到 pET17b 载体中。纯化后,将重组蛋白注射到兔子皮下,用 G 蛋白柱从兔子血清中提取抗体。SDS-PAGE 分析验证了 SNTXα 的表达,观察到一条 73.5 kDa 的条带,产量为 60 mg/l。酶联免疫吸附试验(ELISA)结果表明,兔子的抗体滴度在 1:256,000 稀释度时仍可检测到。从兔血清中分离出的抗体浓度为 1.5 毫克/毫升,其灵敏度可检测到最小浓度为 9.7 纳克的蛋白质。在中和试验中,纯化的 SNTXα 抗体能保护受到 2 LD50 病毒挑战的小鼠。总之,我们的研究成功地在原核宿主中表达了石首毒蛋白的α亚基,从而能够生产抗体,用于开发石首鱼抗血清。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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.

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