首页> 外文期刊>Molecular and Biochemical Parasitology >Molecular characterization of a calcium binding translationally controlled tumor protein homologue from the filarial parasites Brugia malayi and Wuchereria bancrofti.
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Molecular characterization of a calcium binding translationally controlled tumor protein homologue from the filarial parasites Brugia malayi and Wuchereria bancrofti.

机译:钙结合的翻译控制的来自丝状寄生虫的马来亚黑麦草和黑麦草的肿瘤蛋白的分子特征。

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We have cloned homologues of the mammalian translationally controlled tumor protein (TCTP) from the human filarial parasites Wuchereria bancrofti and Brugia malayi. TCTP genes from B. malayi and W. bancrofti were expressed in a T7 promoter vector as histidine tagged fusion proteins. Both the recombinant B. malayi TCTP (rBm-TCTP) and recombinant W. bancrofti TCTP (rWb-TCTP) have a molecular mass of approximately 28 kDa with the histidine tag. Sequence analyses showed that there is a 98% similarity between the two filarial TCTPs at amino acid levels and are immunologically cross-reactive. Analysis of soluble proteins from various lifecycle stages of B. malayi suggested that the expression of Bm-TCTP might be differentially regulated and occurs in multimeric form. Recombinant TCTP were found to form multimers in solution under non-reducing conditions. The tendency for filarial TCTPs to become multimers was predicted by the presence of the Lupas coiled coil structure in their sequence. Despite the absence of a signal sequence, Bm-TCTP is present abundantly in the excretory/secretions (ES) of microfilariae. Characterization studies showed that both Bm- and Wb-TCTPs are calcium-binding proteins and have histamine-releasing function in vitro. When injected intraperitoneally both the filarial TCTPs induced inflammatory infiltration of eosinophils into the peritoneal cavity of mice suggesting that the filarial TCTPs may have a role in the allergic inflammatory responses associated with filarial infections.
机译:我们已经从人类丝虫寄生物Wuchereria bancrofti和Brugia malayi克隆了哺乳动物翻译控制肿瘤蛋白(TCTP)的同源物。来自马来西亚芽孢杆菌和班氏酵母的TCTP基因在T7启动子载体中表达为组氨酸标记的融合蛋白。重组的马来西亚马来酸TCTP(rBm-TCTP)和重组的班氏罗非鱼TCTP(rWb-TCTP)均具有带有组氨酸标签的约28kDa的分子量。序列分析表明,两个丝状TCTP在氨基酸水平上有98%的相似性,并且在免疫学上具有交叉反应性。对来自马来西亚芽孢杆菌各个生命周期阶段的可溶性蛋白的分析表明,Bm-TCTP的表达可能受到差异调节,并以多聚体形式出现。发现重组TCTP在非还原条件下在溶液中形成多聚体。丝状TCTP变成多聚体的趋势是通过Lupas卷曲螺旋结构的顺序来预测的。尽管没有信号序列,但Bm-TCTP大量存在于微丝aria的排泄/分泌物中。表征研究表明,Bm和Wb-TCTP都是钙结合蛋白,在体外具有组胺释放功能。当腹膜内注射时,两个丝状TCTP都诱导嗜酸性粒细胞炎性浸润到小鼠腹膜腔中,提示丝状TCTP可能在与丝状感染相关的变应性炎症反应中起作用。

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