The search for inhibitors of interleukin-1 based on the sequence of interleukin-1 receptor antagonist.

Z Wieczorek, A Kluczyk, J J Slon-Usakiewicz, I Z Siemion
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Abstract

In order to find the low-molecular-weight interleukin-1 (IL-1) inhibitors, we synthesised a series of peptides, derived from three regions of interleukin-1 receptor antagonist (IL-1ra): N-terminal (residues 5-9), central (90-98) and C-terminal (143-148). The decision was based on the thorough analysis of structural and functional properties of IL-1 proteins and the resemblance of some fragments of IL-1ra to well-known immunomodulators, like thymopentin and tuftsin. The competition between our peptides and IL-1 were measured as the inhibition of IL-1 induced IL-2 production in LBRM/CTLL cell line system. All peptides presented some activity, although the most interesting results (when the range of activity and dose-dependence were taken into account) were obtained for tuftsin and peptide VTKFYF from the C-terminal part of IL-1ra.

基于白介素-1受体拮抗剂序列的白介素-1抑制剂的研究。
为了寻找低分子量的白介素-1 (IL-1)抑制剂,我们合成了一系列从白介素-1受体拮抗剂(IL-1ra)的三个区域衍生的肽:n端(残基5-9),中心(90-98)和c端(143-148)。这一决定是基于对IL-1蛋白的结构和功能特性的全面分析,以及IL-1ra的一些片段与众所周知的免疫调节剂(如胸腺喷素和簇毛素)的相似性。我们的肽和IL-1之间的竞争是通过抑制IL-1诱导的LBRM/CTLL细胞系系统中IL-2的产生来测量的。所有的肽都表现出一定的活性,尽管最有趣的结果(当活性范围和剂量依赖性被考虑在内时)是从IL-1ra的c端部分获得的tuftsin和肽VTKFYF。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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