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High affinity type I interleukin 1 receptor antagonists discovered by screening recombinant peptide libraries.

机译:通过筛选重组肽库发现了高亲和力的I型白介素1受体拮抗剂。

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摘要

Two families of peptides that specifically bind the extracellular domain of the human type I interleukin I (IL-1) receptor were identified from recombinant peptide display libraries. Peptides from one of these families blocked binding of IL-lalpha to the type I IL-1 receptor with IC50 values of 45-140 microM. Affinity-selective screening of variants of these peptides produced ligands of much higher affinity (IC50 approximately 2 nM). These peptides block IL-1-driven responses in human and monkey cells; they do not bind the human type II IL-1 receptor or the murine type I IL-1 receptor. This is the first example (that we know of) of a high affinity peptide that binds to a cytokine receptor and acts as a cytokine antagonist.
机译:从重组肽展示文库中鉴定出了两个特异性结合人I型白介素I(IL-1)受体胞外域的肽家族。这些家族之一的肽以45-140 microM的IC50值阻断了IL-1α与I型IL-1受体的结合。这些肽的变体的亲和选择性筛选产生了具有更高亲和力的配体(IC50约为2 nM)。这些肽可阻断人和猴细胞中IL-1驱动的应答。它们不结合人类II型IL-1受体或鼠I型IL-1受体。这是(我们知道的)高亲和力肽的第一个例子,该肽与细胞因子受体结合并充当细胞因子拮抗剂。

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