亲缘关系
α-干扰素
效力
受体
EC50型
干扰素
结合亲和力
生物
阿尔法(金融)
生物活性
BETA(编程语言)
配体(生物化学)
体外
Ⅰ型干扰素
化学
立体化学
分子生物学
生物化学
遗传学
医学
结构效度
护理部
患者满意度
计算机科学
程序设计语言
作者
Thomas Lavoie,Eyal Kalie,Sara Crisafulli-Cabatu,Renne Abramovich,G. A. DiGioia,Karlene Moolchan,Sidney Pestka,Gideon Schreiber
出处
期刊:Cytokine
[Elsevier BV]
日期:2011-08-19
卷期号:56 (2): 282-289
被引量:181
标识
DOI:10.1016/j.cyto.2011.07.019
摘要
Vertebrates have multiple genes encoding Type I interferons (IFN), for reasons that are not fully understood. The Type I IFN appear to bind to the same heterodimeric receptor and the subtypes have been shown to have different potencies in various experimental systems. To put this concept on a quantitative basis, we have determined the binding affinities and rate constants of 12 human Alpha-IFN subtypes to isolated interferon receptor chains 1 and 2. Alpha-IFNs bind IFNAR1 and IFNAR2 at affinities of 0.5-5 μM and 0.4-5 nM respectively (except for IFN-alpha1 - 220 nM). Additionally we have examined the biological activity of these molecules in several antiviral and antiproliferative models. Particularly for antiproliferative potency, the binding affinity and activity correlate. However, the EC50 values differ significantly (1.5 nM versus 0.1 nM for IFN-alpha2 in WISH versus OVCAR cells). For antiviral potency, there are several instances where the relationship appears to be more complicated than simple binding. These results will serve as a point of reference for further understanding of this multiple ligand/receptor system.
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