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基于白细胞介素-1受体拮抗剂序列寻找白细胞介素-1抑制剂。

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

作者信息

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

机构信息

Institute of Immunology and Experimental Therapy, Wroclaw.

出版信息

Biomed Pept Proteins Nucleic Acids. 1996;2(4):123-9.

PMID:9575352
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.

摘要

为了找到低分子量白细胞介素-1(IL-1)抑制剂,我们合成了一系列肽段,这些肽段源自白细胞介素-1受体拮抗剂(IL-1ra)的三个区域:N端(第5至9位氨基酸残基)、中间(第90至98位氨基酸残基)和C端(第143至148位氨基酸残基)。该决定基于对IL-1蛋白结构和功能特性的深入分析,以及IL-1ra的一些片段与知名免疫调节剂(如胸腺五肽和促吞噬素)的相似性。我们通过在LBRM/CTLL细胞系系统中抑制IL-1诱导的IL-2产生,来测定我们合成的肽段与IL-1之间的竞争作用。所有肽段都表现出一定活性,不过(考虑到活性范围和剂量依赖性)最有趣的结果是促吞噬素和来自IL-1ra C端部分的肽段VTKFYF所呈现的。

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