首页> 外文期刊>Toxicon: An International Journal Devoted to the Exchange of Knowledge on the Poisons Derived from Animals, Plants and Microorganisms >Molecular characterization of protective antibodies raised in mice by Tityus serrulatus scorpion venom toxins con ugated to bovine serum albumin
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Molecular characterization of protective antibodies raised in mice by Tityus serrulatus scorpion venom toxins con ugated to bovine serum albumin

机译:牛血清白蛋白蝎毒蛇毒素与小鼠血清白蛋白融合后在小鼠体内产生的保护性抗体的分子表征

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The possibility of raising a Immoral immune response capable of inducing in vivo protection against the lethal effects of Tityus serrulatus (Ts) scorpion venom was evaluated in the mouse model. An immunogen was prepared that consists of a toxic fraction (TstFG(50)) of the Tityus venom (this G(50) chromatography fraction represents most of the toxicity of the crude venom) conjugated to bovine serum albumin (BSA) with glutaraldehyde. TstFG(50) coupled to BSA yielded a thoroughly detoxified immunogen. BALB/c and C57BL/10 mice were immunized with this preparation and all developed an antibody response. In vivo protection assays one week after the last immunization showed that vaccinated mice could resist the challenge by twice the LD50 of the TstFG(50), a dose which killed all control non-immune mice. The protective effect persisted nine weeks after the end of the immunization protocol. To characterize epitopes of protective antibodies we used the Spot method of multiple peptide synthesis to prepare sets of immobilized 15 mer overlapping peptides, covering the complete amino acid sequences of the main Tityus toxins, TsII and TsVII (both beta-type toxins) and TsIV, an alpha-type toxin that is the major lethal component of the venom. Antibody binding to peptides, revealed one major antigenic region in the C-terminal part of the three toxins and another region in the helical part of TsII and TsIV toxins. It is likely that these epitopes correspond to neutralizing epitopes since they correspond to regions of the toxins that are known to be involved in the active site of the toxins. (C) 2004 Elsevier Ltd. All rights reserved.
机译:在小鼠模型中评估了产生不育免疫反应的可能性,该免疫反应能够诱导体内对抗拟南芥(Ts)蝎毒的致死作用。制备了一种免疫原,该免疫原由与戊二醛偶联的牛血清白蛋白(BSA)的Tityus毒液的毒性级分(TstFG(50))(此G(50)色谱级分代表粗毒液的大部分毒性)组成。 TstFG(50)耦合到BSA产生彻底解毒的免疫原。用该制剂免疫BALB / c和C57BL / 10小鼠,所有小鼠都产生抗体应答。上次免疫后一个星期的体内保护实验表明,接种疫苗的小鼠可以抵抗两倍于TstFG的LD50的攻击(50),该剂量杀死了所有非免疫小鼠。免疫方案结束后九周,保护作用持续存在。为了表征保护性抗体的表位,我们使用多肽合成的Spot方法制备了固定的15 mer重叠肽组,涵盖了主要Tityus毒素,TsII和TsVII(均为β型毒素)和TsIV的完整氨基酸序列,一种α型毒素,是毒液的主要致死成分。抗体与肽的结合揭示了三种毒素的C末端部分的一个主要抗原区域,以及TsII和TsIV毒素的螺旋部分的另一区域。这些表位可能对应于中和性表位,因为它们对应于已知与毒素的活性位点有关的毒素区域。 (C)2004 Elsevier Ltd.保留所有权利。

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