Design of bioactive peptides based on immunoglobulin structure
    1.
    发明公开
    Design of bioactive peptides based on immunoglobulin structure 失效
    设计von bioaktiven Peptiden auf der Basis von immunglobulin Strukturen

    公开(公告)号:EP1310557A1

    公开(公告)日:2003-05-14

    申请号:EP02080338.3

    申请日:1991-09-13

    摘要: The present invention relates to a method for producing peptides which have biological activity comprising: (i) identifying a region of a protein of interest which is homologous to a member of the immunoglobulin superfamily of molecules; (ii) synthesizing a peptide which comprises amino acid sequence found in the region of homology; and (iii) modifying the synthetic peptide such that it assumes a three-dimensional conformation which is biologically active. The invention is based, in part, on the discovery that a cyclic peptide comprising amino acid sequences of a CDR derived from an antibody directed toward a viral receptor molecule can be used to effectively inhibit the binding of virus to its receptor. The invention is also based in part on the discovery that a cyclic peptide corresponding to a portion of human immunodeficiency virus (HIV) gp120 that is homologous to immunoglobulins may be used to generate an anti-HIV immune response.

    摘要翻译: 本发明涉及具有生物活性的肽的生产方法,包括:(i)鉴定与分子的免疫球蛋白超家族的成员同源的目的蛋白质的区域; (ii)合成包含在同源性区域中发现的氨基酸序列的肽; 和(iii)修饰合成肽,使其呈现生物活性的三维构象。 本发明部分基于以下发现:包含衍生自针对病毒受体分子的抗体的CDR的氨基酸序列的环肽可用于有效抑制病毒与其受体的结合。 本发明也部分地基于以下发现:对应于与免疫球蛋白同源的人免疫缺陷病毒(HIV)gp120的一部分的环肽可用于产生抗HIV免疫应答。