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人α-8干扰素及其受体复合物的同源模型

Homology model of human interferon-alpha 8 and its receptor complex.

作者信息

Seto M H, Harkins R N, Adler M, Whitlow M, Church W B, Croze E

机构信息

Biosym Technologies, Inc., San Jose, California 95129, USA.

出版信息

Protein Sci. 1995 Apr;4(4):655-70. doi: 10.1002/pro.5560040406.

Abstract

Human interferon-alpha 8 (HuIFN alpha 8), a type I interferon (IFN), is a cytokine belonging to the hematopoietic super-family that includes human growth hormone (HGH). Recent data identified two human type I IFN receptor components. One component (p40) was purified from human urine by its ability to bind to immobilized type I IFN. A second receptor component (IFNAR), consisting of two cytokine receptor-like domains (D200 and D200'), was identified by expression cloning. Murine cells transfected with a gene encoding this protein were able to produce an antiviral response to human IFN alpha 8. Both of these receptor proteins have been identified as members of the immunoglobulin superfamily of which HGH receptor is a member. The cytokine receptor-like structural motifs present in p40 and IFNAR were modeled based on the HGH receptor X-ray structure. Models of the complexes of HuIFN alpha 8 with the receptor subunits were built by superpositioning the conserved C alpha backbone of the HuIFN alpha 8 and receptor subunit models with HGH and its receptor complex. The HuIFN alpha 8 model was constructed from the C alpha coordinates of murine interferon-beta crystal structure. Electrostatic potentials and hydrophobic interactions appear to favor the model of HuIFN alpha 8 interacting with p40 at site 1 and the D200' domain of IFNAR at site 2 because there are regions of complementary electrostatic potential and hydrophobic interactions at both of the proposed binding interfaces. Some of the predicted receptor binding residues within HuIFN alpha 8 correspond to functionally important residues determined previously for human IFN alpha 1, IFN alpha 2, and IFN alpha 4 subtypes by site-directed mutagenesis studies. The models predict regions of interaction between HuIFN alpha 8 and each of the receptor proteins, and provide insights into interactions between other type I IFNs (IFN-alpha subtypes and IFN-beta) and their respective receptor components.

摘要

人α-8干扰素(HuIFNα8)是一种I型干扰素(IFN),属于造血超家族的细胞因子,该家族还包括人生长激素(HGH)。最近的数据鉴定出了两种人I型干扰素受体成分。一种成分(p40)通过其与固定化I型干扰素结合的能力从人尿中纯化得到。通过表达克隆鉴定出了第二种受体成分(IFNAR),它由两个细胞因子受体样结构域(D200和D200')组成。用编码该蛋白的基因转染的鼠细胞能够对人α-8干扰素产生抗病毒反应。这两种受体蛋白均已被鉴定为免疫球蛋白超家族的成员,人生长激素受体也是该家族的成员。基于人生长激素受体的X射线结构,对p40和IFNAR中存在的细胞因子受体样结构基序进行了建模。通过将HuIFNα8和受体亚基模型的保守Cα主链与HGH及其受体复合物进行叠加,构建了HuIFNα8与受体亚基复合物的模型。HuIFNα8模型是根据鼠β-干扰素晶体结构的Cα坐标构建的。静电势和疏水相互作用似乎有利于HuIFNα8在位点1与p40相互作用以及在位点2与IFNAR的D200'结构域相互作用的模型,因为在两个拟议的结合界面处都存在互补的静电势和疏水相互作用区域。HuIFNα8内一些预测的受体结合残基与先前通过定点诱变研究确定的人α-1干扰素、α-2干扰素和α-4干扰素亚型的功能重要残基相对应。这些模型预测了HuIFNα8与每种受体蛋白之间的相互作用区域,并为其他I型干扰素(α-干扰素亚型和β-干扰素)与其各自受体成分之间的相互作用提供了见解。

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