Tagliabue A, Antoni G, Boraschi D
Sclavo Research Center, Siena, Italy.
Lymphokine Res. 1989 Fall;8(3):311-5.
The structure-function relationship in the human IL-1 beta protein has been analyzed by means of computer prediction, synthesis of peptides and use of monoclonal antibodies of predetermined specificity. A nine amino acid-long fragment (VQGEESNDK), corresponding to the human IL-1 beta sequence in position 163-171, was shown to possess only some of the IL-1 activities, i.e. those directed to the immune system, while being devoid of IL-1-like inflammatory effects. It is thus proposed that discrete domains within the IL-1 beta protein might be responsible for the different biological activities of the molecule and that the 163-171 fragment may represent one of the immunostimulatory sites of IL-1 beta.
通过计算机预测、肽合成以及使用具有预定特异性的单克隆抗体,对人白细胞介素-1β蛋白中的结构-功能关系进行了分析。一个对应于人白细胞介素-1β序列第163-171位的九氨基酸长片段(VQGEESNDK),被证明仅具有白细胞介素-1的部分活性,即那些针对免疫系统的活性,而没有白细胞介素-1样的炎症效应。因此有人提出,白细胞介素-1β蛋白内的离散结构域可能负责该分子的不同生物学活性,并且163-171片段可能代表白细胞介素-1β的免疫刺激位点之一。