Production of interferon
    14.
    发明授权
    Production of interferon 失效
    生产干扰素

    公开(公告)号:US5468609A

    公开(公告)日:1995-11-21

    申请号:US425933

    申请日:1982-09-28

    CPC classification number: C07K14/5412 C07K14/565

    Abstract: The present invention relates to a process to isolate genetic material (DNA) containing the nucleotide sequence coding for interferon in human fibroblastic cells which comprises cultivating cells producing interferon when exposed to an inducer of interferon, exposing same to such inducer, extracting messenger RNA from said induced cells, purifying the interferon messenger RNA, transcribing the messenger RNA into DNA and cloning the DNA in a suitable vector. Preferred cells are human diploid foreskin cells. The invention further relates to a process for engineering a bacterial strain to produce interferon polypeptide which comprises introducing a cloned interferon DNA into a suitable vector-carrier. A preferred vector-carrier is E. coli. The invention also relates to the mRNA of human interferon in highly purified form, to the mRNA of human interferon in .beta.1 highly purified form, to the mRNA of human interferon in .beta.2 highly purified form, to the DNA coding for a polypeptide having interferon activity, insertable in a vector, such as plasmid pBR322, and also to human interferon .beta.1 in highly purified form, and human interferon .beta.2 in highly purified form.

    Abstract translation: 本发明涉及一种分离含有人成纤维细胞中编码干扰素的核苷酸序列的遗传物质(DNA)的方法,其包括在暴露于干扰素诱导剂时培养产生干扰素的细胞,将其暴露于所述诱导物,从所述诱导物中提取信使RNA 诱导细胞,纯化干扰素信使RNA,将信使RNA转录成DNA,并将DNA克隆在合适的载体中。 优选的细胞是人二倍体包皮细胞。 本发明还涉及一种用于工程化细菌菌株以产生干扰素多肽的方法,其包括将克隆的干扰素DNA引入合适的载体载体中。 优选的载体载体是大肠杆菌。 本发明还涉及高度纯化形式的人干扰素的mRNA,β1高度纯化形式的人干扰素的mRNA与β2高度纯化形式的人干扰素的mRNA与编码具有干扰素的多肽的DNA 活性,可插入载体,如质粒pBR322,以及高度纯化形式的人干扰素β1和高度纯化形式的人干扰素β2。

    IFN receptor 1 binding proteins
    18.
    发明授权
    IFN receptor 1 binding proteins 失效
    IFN受体1结合蛋白

    公开(公告)号:US07524928B2

    公开(公告)日:2009-04-28

    申请号:US11350094

    申请日:2006-02-09

    Abstract: Novel proteins IR1B1 and IR1B4 have been isolated which bind to the type I IFN receptor IFNAR1 and function in the cellular response to IFNs. DNA encoding such proteins in either the sense or anti-sense orientation can be administered to either enhance or inhibit the cellular response to IFNs. Antibodies to the proteins can be used for isolation of the new protein or for immunodetection thereof.

    Abstract translation: 已经分离出新的蛋白质IR1B1和IR1B4,其结合I型IFN受体IFNAR1并在细胞对IFN的反应中起作用。 可以施用编码有义或反义方向的蛋白质的DNA,以增强或抑制对IFN的细胞应答。 蛋白质的抗体可用于分离新蛋白质或用于免疫检测。

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