Li B L, Zhao X X, Liu X Y, Kim H S, Raska K, Ortaldo J R, Schwartz B, Pestka S
Department of Molecular Genetics, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, Piscataway 08854.
Cancer Res. 1990 Sep 1;50(17):5328-32.
Expression vectors for human alpha-interferon (Hu-IFN-alpha) J1, a site-specific mutant [Ser116]Hu-IFN-alpha J1, and Hu-IFN-alpha J/C or Hu-IFN-alpha C/J hybrids were constructed and expressed in Escherichia coli. These interferons and others were purified by immunoaffinity chromatography with a monoclonal antibody against human alpha-interferon. Their antiviral activity and ability to stimulate natural killer cell activity were determined in comparison to several other human interferons. These results provide some insight into structure-activity relationships for stimulating natural killer cells and confirm our previous conclusions that antiviral activity cannot be used to predict other activities for an individual IFN-alpha species. The observations suggest that the tertiary structure rather than any specific linear sequence of amino acids regulates the ability of the interferons to stimulate natural killer cell activity.
构建了人α-干扰素(Hu-IFN-α)J1、位点特异性突变体[Ser116]Hu-IFN-α J1以及Hu-IFN-α J/C或Hu-IFN-α C/J杂合体的表达载体,并在大肠杆菌中进行表达。这些干扰素及其他干扰素通过用抗人α-干扰素单克隆抗体进行免疫亲和层析来纯化。与其他几种人干扰素相比,测定了它们的抗病毒活性以及刺激自然杀伤细胞活性的能力。这些结果为刺激自然杀伤细胞的构效关系提供了一些见解,并证实了我们之前的结论,即抗病毒活性不能用于预测单个IFN-α种类的其他活性。这些观察结果表明,三级结构而非任何特定的氨基酸线性序列调节干扰素刺激自然杀伤细胞活性的能力。