Giri Kalyan, Scott Robert A, Maynard Ernest L
Department of Biochemistry and Molecular Biology, Uniformed Services University of the Health Sciences, Bethesda, Maryland 20814, USA.
Biochemistry. 2009 Aug 25;48(33):7969-78. doi: 10.1021/bi900677w.
Virion infectivity factor (Vif) is an HIV accessory protein that is essential for the infection of CD4(+) T cells. Vif recruits a Cullin 5 (Cul5)-based ubiquitin ligase that targets a host cytidine deaminase, apolipoprotein B mRNA editing enzyme catalytic polypeptide-like 3G (APOBEC3G), for proteasomal degradation. The Vif N-terminus binds APOBEC3G, and the C-terminus interacts with the Cul5-based ubiquitin ligase machinery. Within the C-terminus, a highly conserved H(108)-X(5)-C(114)-X(17-18)-C(133)-X(3-5)-H(139) (HCCH) motif binds zinc and is implicated in the Vif-Cul5 interaction. We have employed the biomimetic peptide HCCHp (HIV-1 Vif amino acids 101-142) in order to determine the zinc ligands and investigate the role of zinc binding in Cul5 recognition. Using CD spectroscopy, a competitive zinc binding assay, and a light scattering assay, we found that mutation of the conserved His and Cys residues in HCCHp had little effect on secondary structure but reduced zinc binding affinity and altered the aggregation properties of the peptides. X-ray absorption spectroscopy was used to study zinc coordination in wild-type HCCHp. The data are consistent with S(2)N(imid)(2) coordination and strongly suggest that His-108, Cys-114, Cys-133, and His-139 are zinc ligands. Mutation of one or both conserved Cys residues in HCCHp led to a decrease in Cys ligation, and an increase in the number of (N, O) ligands, with noninteger coordination numbers suggesting zinc site heterogeneity. A purified fragment of human Cul5 was found to inhibit zinc-induced aggregation of HCCHp, and pull-down experiments revealed that zinc binding to HCCHp increases the strength of the HCCHp-Cul5 interaction by 8-fold.
病毒体感染性因子(Vif)是一种HIV辅助蛋白,对CD4(+) T细胞的感染至关重要。Vif募集一种基于Cullin 5(Cul5)的泛素连接酶,该酶靶向宿主胞苷脱氨酶——载脂蛋白B mRNA编辑酶催化多肽样3G(APOBEC3G),使其通过蛋白酶体降解。Vif的N端与APOBEC3G结合,C端与基于Cul5的泛素连接酶机制相互作用。在C端,一个高度保守的H(108)-X(5)-C(114)-X(17 - 18)-C(133)-X(3 - 5)-H(139)(HCCH)基序结合锌,并参与Vif与Cul5的相互作用。我们使用了仿生肽HCCHp(HIV-1 Vif氨基酸101 - 142)来确定锌配体,并研究锌结合在Cul5识别中的作用。通过圆二色光谱、竞争性锌结合测定和光散射测定,我们发现HCCHp中保守的His和Cys残基的突变对二级结构影响不大,但降低了锌结合亲和力并改变了肽的聚集特性。利用X射线吸收光谱研究野生型HCCHp中的锌配位情况。数据与S(2)N(咪唑)(2)配位一致,并强烈表明His-108、Cys-114、Cys-133和His-139是锌配体。HCCHp中一个或两个保守Cys残基的突变导致Cys配位减少,(N, O)配体数量增加,非整数配位数表明锌位点存在异质性。发现人Cul5的一个纯化片段可抑制锌诱导的HCCHp聚集,下拉实验表明锌与HCCHp的结合使HCCHp与Cul5的相互作用强度增加了8倍。