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编码主要屋尘螨变应原Der f I的cDNA序列分析

Sequence analysis of cDNA coding for a major house dust mite allergen, Der f I.

作者信息

Dilworth R J, Chua K Y, Thomas W R

机构信息

Western Australian Research Institute for Child Health, Princess Margaret Hospital for Children, Subiaco.

出版信息

Clin Exp Allergy. 1991 Jan;21(1):25-32. doi: 10.1111/j.1365-2222.1991.tb00800.x.

Abstract

A cDNA clone coding for Der f I, a major allergen from the house dust mite Dermatophagoides farinae has been isolated and sequenced. It codes for a putative 18-residue signal peptide, an 80-residue proenzyme region, and a 223-residue mature protein with a derived molecular weight of 25,191. The deduced amino-acid sequence shows significant homology to other cysteine proteases in the proregion as well as in the mature protein. Sequence alignment of the mature Der f I protein with the homologous allergen Der p I from the related mite D. pteronyssinus revealed a high degree of homology (81%) between the two proteins, as predicted by previous sequencing at the protein level. In particular, the residues comprising the active site of these enzymes and the cysteine residues were conserved. A potential N-glycosylation site was present at an equivalent position in both mite allergens. It is anticipated that the availability of recombinant Der f I will facilitate epitope mapping studies and studies of T-cell function in mite allergy by providing high levels of pure allergen.

摘要

编码来自屋尘螨粉尘螨主要变应原Der f I的一个cDNA克隆已被分离和测序。它编码一个推测的18个残基的信号肽、一个80个残基的酶原区域以及一个223个残基的成熟蛋白,其推导的分子量为25,191。推导的氨基酸序列在酶原区域以及成熟蛋白中与其他半胱氨酸蛋白酶显示出显著的同源性。成熟的Der f I蛋白与来自相关螨种柏氏禽刺螨的同源变应原Der p I的序列比对显示,这两种蛋白之间具有高度同源性(81%),这与之前在蛋白水平的测序结果一致。特别地,构成这些酶活性位点的残基以及半胱氨酸残基是保守的。在两种螨变应原的等效位置都存在一个潜在的N-糖基化位点。预计重组Der f I的可得性将通过提供高水平的纯变应原,促进表位作图研究以及螨过敏中T细胞功能的研究。

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