van Gent D C, Oude Groeneger A A, Plasterk R H
Division of Molecular Biology, The Netherlands Cancer Institute, Amsterdam.
Nucleic Acids Res. 1993 Jul 25;21(15):3373-7. doi: 10.1093/nar/21.15.3373.
The human immunodeficiency virus integrase (HIV IN) protein cleaves two nucleotides off the 3' end of viral DNA and subsequently integrates the viral DNA into target DNA. IN exposes a specific phosphodiester bond near the viral DNA end to nucleophilic attack by water or other nucleophiles, such as glycerol or the 3' hydroxyl group of the viral DNA molecule itself. Wild-type IN has a preference for water as the nucleophile; we here describe a class of IN mutants that preferentially use the 3' hydroxyl group of viral DNA as nucleophile. The amino acids that are altered in this class of mutants map near the putative active-site residues Asp-116 and Glu-152. These results support a model in which multiple amino acid side-chains are involved in presentation of the (soluble) nucleophile. IN is probably active as an oligomeric complex, in which the subunits have non-equivalent roles; we here report that nucleophile selection is determined by the subunit that supplies the active site.
人类免疫缺陷病毒整合酶(HIV IN)蛋白从病毒DNA的3'末端切割下两个核苷酸,随后将病毒DNA整合到目标DNA中。IN使病毒DNA末端附近的特定磷酸二酯键暴露,以遭受水或其他亲核试剂(如甘油或病毒DNA分子自身的3'羟基)的亲核攻击。野生型IN优先选择水作为亲核试剂;我们在此描述一类优先使用病毒DNA的3'羟基作为亲核试剂的IN突变体。在这类突变体中发生改变的氨基酸位于推定的活性位点残基Asp-116和Glu-152附近。这些结果支持了一个模型,其中多个氨基酸侧链参与了(可溶性)亲核试剂的呈现。IN可能作为一种寡聚复合物发挥作用,其中亚基具有不等同的作用;我们在此报告,亲核试剂的选择由提供活性位点的亚基决定。