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首页> 外文期刊>FEBS Letters >Cloning and expression in Escherichia coli of cDNA encoding house dust mite allergen Der f 3, serine protease from Dermatophagoides farinae
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Cloning and expression in Escherichia coli of cDNA encoding house dust mite allergen Der f 3, serine protease from Dermatophagoides farinae

机译:粉尘螨Der f 3,丝氨酸蛋白酶编码屋尘螨变应原Der f 3的cDNA的克隆及在大肠杆菌中的表达

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>Der f 3 is one of the allergens produced by house dust mite Dermatophagoides farinae showing serine protease activity. Based on its amino acid sequence, a cDNA clone encoding Der f 3 was isolated from a cDNA library of D. farinae. Sequencing analysis of the clone revealed the presence of an open reading frame of 780 bp, which encodes a mature protein of 232 amino acids with 27 amino acids of pre-pro sequence at the N-terminus. When proDer f 3 was produced in Escherichia coli as a fused protein with glutathione-S-transferase, the fused protein was accumulated as inclusion bodies. The protein purified with 8 M urea and glutathione-affinity column chromatography, however, did not show protease activity. When an arginine residue was introduced at the C-terminus of the pro-region in place of threonine, removal of the pro-region to produce an active mature protease was observed. The specificity and the activity of this recombinant protease were almost the same as those of native Der f 3.
机译:> Der f 3是由室内尘螨 Dermatophagoides farinae 产生的变应原之一,具有丝氨酸蛋白酶活性。根据其氨基酸序列,从 D的cDNA文库中分离出编码Der f 3的cDNA克隆。 farinae 。该克隆的测序分析显示,存在一个780 bp的开放阅读框,该框编码一个232个氨基酸的成熟蛋白,在N端带有pre-pro序列的27个氨基酸。当proDer f 3作为带有谷胱甘肽- S -转移酶的融合蛋白在大肠杆菌中产生时,融合蛋白作为包涵体积累。但是,用8 M尿素和谷胱甘肽亲和柱色谱纯化的蛋白质没有显示蛋白酶活性。当在前区的C末端取代苏氨酸引入精氨酸残基时,观察到前区的去除产生了活性的成熟蛋白酶。该重组蛋白酶的特异性和活性与天然Der f 3几乎相同。

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