Trudinger M, Chua K Y, Thomas W R
Western Australia Research Institute for Child Health, Princess Margaret Hospital, Perth.
Clin Exp Allergy. 1991 Jan;21(1):33-7. doi: 10.1111/j.1365-2222.1991.tb00801.x.
cDNA encoding the major house dust mite allergen Der f II from Dermatophagoides farinae was amplified using the polymerase chain reaction and cloned into E. coli. It encoded a 129-residue protein with a calculated molecular weight of 14,021 D and had the expected high homology (88%) with Der p II including the absence of N-glycosylation sites and conserved cysteine residues. These results are consistent with the high degree of antibody crossreactivity and may help identify the differences in T-cell epitopes revealed for these molecules so far.
利用聚合酶链反应扩增编码来自粉尘螨的主要屋尘螨变应原Der f II的cDNA,并将其克隆到大肠杆菌中。它编码一种由129个氨基酸残基组成的蛋白质,计算分子量为14,021 D,与Der p II具有预期的高度同源性(88%),包括不存在N-糖基化位点和保守的半胱氨酸残基。这些结果与高度的抗体交叉反应性一致,可能有助于识别到目前为止这些分子所显示的T细胞表位的差异。