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青霉属特异青霉主要过敏原Pen n 13的特性分析

Characterization of Pen n 13, a major allergen from the mold Penicillium notatum.

作者信息

Chow L P, Chiou S H, Hsiao M C, Yu C J, Chiang B L

机构信息

Institute of Biochemistry, National Taiwan University, Taipei, Taiwan 100, Republic of China.

出版信息

Biochem Biophys Res Commun. 2000 Mar 5;269(1):14-20. doi: 10.1006/bbrc.2000.2253.

Abstract

Penicillium notatum is a well-known indoor aeroallergen and is frequently included in skin test panels for allergic diagnosis. On two-dimensional immunoblotting using patients' sera containing IgE and monoclonal antibody D7B8 specific for Pen c 1 of P. citrinum, two allergens with a molecular mass of 33 kDa but different isoelectric points were identified. A novel cDNA coding for Pen n 13 was cloned and sequenced. The nucleotide sequence codes for a protein 397 amino acids including a putative signal peptide of 25 amino acids and a propeptide of 90 amino acids. The allergen is an alkaline serine protease that shares more than 39% identical residues with other kinds of mold allergens. The coding cDNA of Pen n 13 was cloned into vector pQE-30 and expressed in E. coli M15 as a His-tag fusion protein and purified to homogeneity. The fusion protein reacted with monoclonal antibodies of Pen c 1 and with IgE from Penicillium-allergic patients. Furthermore, it also cross-reacted strongly with IgE specific for the natural Pen c 1, indicating that similar IgE binding epitopes may exist in the allergens of P. notatum and P. citrinum. Antigenicity index plots indicated that there are several similar epitope regions of high antigenic indices in Pen c 1 and Pen n 13, corroborating that mold allergens belonging to the alkaline serine protease family possess similar protein structure and strong antigenic cross-reactivity.

摘要

橘青霉是一种著名的室内空气变应原,常用于过敏性诊断的皮肤试验组合中。使用含有IgE的患者血清和对橘青霉Pen c 1具有特异性的单克隆抗体D7B8进行二维免疫印迹分析时,鉴定出两种分子量为33 kDa但等电点不同的变应原。克隆并测序了编码Pen n 13的新cDNA。核苷酸序列编码一种包含397个氨基酸的蛋白质,其中包括一个25个氨基酸的推定信号肽和一个90个氨基酸的前肽。该变应原是一种碱性丝氨酸蛋白酶,与其他种类的霉菌变应原具有超过39%的相同残基。将Pen n 13的编码cDNA克隆到载体pQE - 30中,并在大肠杆菌M15中作为His标签融合蛋白表达,然后纯化至同质。该融合蛋白与Pen c 1的单克隆抗体以及来自对青霉过敏患者的IgE发生反应。此外,它还与天然Pen c 1特异性的IgE发生强烈交叉反应,表明在点青霉和橘青霉的变应原中可能存在相似的IgE结合表位。抗原性指数图表明,Pen c 1和Pen n 13中有几个具有高抗原性指数的相似表位区域,证实属于碱性丝氨酸蛋白酶家族的霉菌变应原具有相似的蛋白质结构和强烈的抗原交叉反应性。

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