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首页> 外文期刊>Molecular Biology Reports >Sequence analysis and expression of a cDNA clone encoding tropomysin in Sinonovacula constricta
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Sequence analysis and expression of a cDNA clone encoding tropomysin in Sinonovacula constricta

机译:中华Sino新变原菌编码cDNA克隆的序列分析与表达

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摘要

Shellfish can cause severe anaphylactic reactions. Tropomyosin has been assumed partly responsible for the cross-reactivity among shellfish and other invertebrates. In this study, cDNA of Sinonovacula constricta was amplified by RT-PCR and 3′-RACE from total RNA. The obtained tropomyosin cDNA included an open reading frame coding for 284 amino acids. The deduced amino acid sequence of the corresponding protein shared high identity with other allergenic tropomyosins. Expression of the recombinant tropomyosin was carried out in Escherichia coli BL21(DE3) using vector PET28a and the purification of the recombinant protein was performed via affinity chromatography. IgE reactivity of recombinant tropomyosin was investigated by immunoblot and the sensized precentage was 36% which indicated that tropomyosin was the minor allergens in S. constricta. Moreover, the character of the purified protein was analyzed by MALDI-TOF-MS.
机译:贝类会引起严重的过敏反应。认为原肌球蛋白部分负责贝类和其他无脊椎动物之间的交叉反应。通过RT-PCR和3'-RACE技术从总RNA中扩增出中华Sino虫的cDNA。获得的原肌球蛋白cDNA包括编码284个氨基酸的开放阅读框。推导的相应蛋白质的氨基酸序列与其他过敏原原肌球蛋白具有高度同一性。使用载体PET28a在大肠杆菌BL21(DE3)中进行重组原肌球蛋白的表达,并通过亲和色谱法纯化重组蛋白。用免疫印迹法检测了重组原肌球蛋白的IgE反应性,其阳性率为36%,表明原肌球蛋白是缩窄链球菌中的次要过敏原。此外,通过MALDI-TOF-MS分析纯化的蛋白质的特征。

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