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通过IgE空斑免疫测定法分离编码主要螨过敏原Der p II的cDNA。

Isolation of cDNA coding for the major mite allergen Der p II by IgE plaque immunoassay.

作者信息

Chua K Y, Doyle C R, Simpson R J, Turner K J, Stewart G A, Thomas W R

机构信息

Clinical Immunology Research Unit, Princess Margaret Hospital for Children, Subiaco, Australia.

出版信息

Int Arch Allergy Appl Immunol. 1990;91(2):118-23. doi: 10.1159/000235101.

Abstract

A lambda gt11 library made with cDNA from the house dust mite Dermatophagoides pteronyssinus was screened with human allergic serum by IgE plaque radioimmunoassay. This resulted in the isolation of clones coding for the major allergen Der p II. The cDNA coded for a 129-residue protein of 14,131 daltons with no N-glycosylation sites. No sequence homology with other proteins was evident. The Der p II expressed in Escherichia coli reacted with IgE in 14 of 17 sera from mite-allergic patients giving clonal evidence for its designation as a major allergen. This, along with previous work, has resulted in the cloning of the two major mite allergens.

摘要

用人过敏性血清通过IgE空斑放射免疫测定法筛选了一个用来自屋尘螨变应原性螨(Dermatophagoides pteronyssinus)的cDNA构建的λgt11文库。这导致分离出编码主要变应原Der p II的克隆。该cDNA编码一个由129个氨基酸残基组成、分子量为14131道尔顿的蛋白质,且无N-糖基化位点。未发现与其他蛋白质有明显的序列同源性。在大肠杆菌中表达的Der p II与17例螨过敏患者血清中的14例血清中的IgE发生反应,为其被指定为主要变应原提供了克隆证据。这与先前的工作一起,实现了两种主要螨变应原的克隆。

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