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Anti-AIDS Peptides Inhibit the Interaction of Cell Receptors with HIV

机译:抗艾滋病肽抑制细胞受体与艾滋病毒的相互作用

摘要

The present invention provides a peptide that inhibits the interaction of CD4, a cellular receptor, and gp120, an outer membrane protein of human immunodeficiency virus type 1 (hereinafter abbreviated as "HIV-1"), its use, and the peptide. In particular, the screening method is composed of 12 amino acids, amino acid 4 amino acid from the proline (proline), amino acid 6 is phenylalanine (phenylalanine) and the rest of the amino acid peptide as a cell receptor CD4 and The peptide of the present invention, which inhibits the interaction with HIV-1 outer membrane protein gp120, is small enough to be chemically synthesized, yet has an existing acquired immunodeficiency syndrome (abbreviated as "AIDS"). It acts at the early stage of infection of HIV-1 virus, which is completely different from the stage of action of Since membrane specifically inhibiting the interaction of the protein gp120, as well as can be developed into a new AIDS treatment, a peptide that can effectively be used in AIDS therapy by the combined treatment methods to be used in combination with other AIDS therapies. In the present invention, the peptide can be effectively selected using a characteristic panning method using agarose beads.
机译:本发明提供了抑制CD4(细胞受体)和gp120(人免疫缺陷病毒1型的外膜蛋白)(以下缩写为“ HIV-1”)的相互作用的肽,其用途和该肽。特别地,筛选方法由12个氨基酸,脯氨酸(脯氨酸)的氨基酸4,氨基酸6是苯丙氨酸(苯丙氨酸)和其余氨基酸肽作为细胞受体CD4组成。抑制与HIV-1外膜蛋白gp120相互作用的本发明小到可以化学合成,但具有现有的获得性免疫缺陷综合症(简称为“ AIDS”)。它在HIV-1病毒感染的早期阶段起作用,这与“ HIV-1病毒”的作用阶段完全不同。由于膜特异地抑制了gp120蛋白的相互作用,并且可以发展成为一种新的AIDS治疗药物,这种肽可以通过与其他艾滋病疗法相结合的联合治疗方法,可以有效地用于艾滋病疗法。在本发明中,可以使用使用琼脂糖珠的特征性淘选方法来有效地选择肽。

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