期刊
JOURNAL OF BIOLOGICAL CHEMISTRY
卷 278, 期 8, 页码 6596-6602出版社
AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M210164200
关键词
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资金
- NIAID NIH HHS [R21 AI047720, R01 AI047720, AI47720] Funding Source: Medline
Virion infectivity factor (Vif) is essential for the replication of human immunodeficiency virus type I (HIV-1) in vivo, but its function remains uncertain. Recently, we have shown that Vif proteins are able to form multimers, including dimers, trimers, or tetramers. Because the multimerization of Vif proteins is required for Vif function in the viral life cycle, we propose that it could be a novel target for anti-HIIV-1 therapeutics. Through a phage peptide display method, we have identified a set of 12-mer peptides containing a PXP motif that binds to HIV-1 Vif protein. These proline-enriched peptides potently inhibited the Vif-Vif interaction in vitro. We have also screened a set of synthesized Vif peptides (15-mer), which covers all the amino acids of the HIV-1 Vif protein sequence, for their ability to inhibit the Vif-Vif interaction in vitro. We demonstrated that Vif-derived proline-enriched peptides that contain the (PPLP164)-P-161 domain are able to inhibit the Vif-Vif interaction. Conversely, the deletion of the (PPLP164)-P-161 domain of Vif protein will significantly impair the capability of Vif proteins to interact with each other, indicating that the (PPLP164)-P-161 domain plays a key role in Vif multimerization. All these results demonstrate that the proline-enriched peptides block the multimerization of Vif through interfering with the polyproline interfaces of Vif formed by (PPLP164)-P-161 domain. Moreover, these peptides which inhibit the Vif-Vif interaction in vitro potently inhibit HIV-1 replication in the nonpermissive T-cells. We propose that this study starts a novel strategy to develop structural diverse inhibitors of Vif such as peptidomimetics or small organic molecules.
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