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Inhibition of Human Immunodeficiency Virus Envelope Glycoprotein- Mediated Single Cell Lysis by Low-Molecular-Weight Antagonists of Viral Entry

机译:低分子重量病毒拮抗剂对人免疫缺陷病毒包膜糖蛋白介导的单细胞裂解的抑制作用。

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摘要

The coexpression of human immunodeficiency virus type 1 (HIV-1) envelope glycoproteins and receptors leads to the lysis of single cells by a process that is dependent upon membrane fusion. This cell lysis was inhibited by low-molecular-weight compounds that interfere with receptor binding or with receptor-induced conformational transitions in the envelope glycoproteins. A peptide, T20, potently inhibited cell-cell fusion but had no effect on single cell lysis mediated by the HIV-1 envelope glycoproteins. Thus, critical events in the lysis of single cells by the HIV-1 envelope glycoproteins occur in intracellular compartments accessible only to small inhibitory compounds.
机译:人类免疫缺陷病毒1型(HIV-1)包膜糖蛋白和受体的共表达通过依赖于膜融合的过程导致单细胞裂解。低分子量化合物会抑制这种细胞溶解,这些化合物会干扰受体结合或包膜糖蛋白中受体诱导的构象转变。 T20肽有效抑制细胞-细胞融合,但对HIV-1包膜糖蛋白介导的单细胞裂解没有影响。因此,HIV-1包膜糖蛋白在单细胞裂解中的关键事件发生在只有小抑制性化合物才能进入的细胞室内。

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