Suppr超能文献

HTLV-1 p8 和 Gag 向靶 T 细胞的转移依赖于 VASP,这是 p8 的一个新的相互作用伙伴。

Transfer of HTLV-1 p8 and Gag to target T-cells depends on VASP, a novel interaction partner of p8.

机构信息

Institute of Clinical and Molecular Virology, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany.

Division of Bioinformatics, Institute of Biochemistry, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany.

出版信息

PLoS Pathog. 2020 Sep 30;16(9):e1008879. doi: 10.1371/journal.ppat.1008879. eCollection 2020 Sep.

Abstract

The Human T-cell leukemia virus type 1 (HTLV-1) orf I-encoded accessory protein p8 is cleaved from its precursor p12, and both proteins contribute to viral persistence. p8 induces cellular protrusions, which are thought to facilitate transfer of p8 to target cells and virus transmission. Host factors interacting with p8 and mediating p8 transfer are unknown. Here, we report that vasodilator-stimulated phosphoprotein (VASP), which promotes actin filament elongation, is a novel interaction partner of p8 and important for p8 and HTLV-1 Gag cell-to-cell transfer. VASP contains an Ena/VASP homology 1 (EVH1) domain that targets the protein to focal adhesions. Bioinformatics identified a short stretch in p8 (amino acids (aa) 24-45) which may mediate interactions with the EVH1 domain of VASP. Co-immunoprecipitations confirmed interactions of VASP:p8 in 293T, Jurkat and HTLV-1-infected MT-2 cells. Co-precipitation of VASP:p8 could be significantly blocked by peptides mimicking aa 26-37 of p8. Mutational studies revealed that the EVH1-domain of VASP is necessary, but not sufficient for the interaction with p8. Further, deletion of the VASP G- and F-actin binding domains significantly diminished co-precipitation of p8. Imaging identified areas of partial co-localization of VASP with p8 at the plasma membrane and in protrusive structures, which was confirmed by proximity ligation assays. Co-culture experiments revealed that p8 is transferred between Jurkat T-cells via VASP-containing conduits. Imaging and flow cytometry revealed that repression of both endogenous and overexpressed VASP by RNA interference or by CRISPR/Cas9 reduced p8 transfer to the cell surface and to target Jurkat T-cells. Stable repression of VASP by RNA interference in chronically infected MT-2 cells impaired both p8 and HTLV-1 Gag transfer to target Jurkat T-cells, while virus release was unaffected. Thus, we identified VASP as a novel interaction partner of p8, which is important for transfer of HTLV-1 p8 and Gag to target T-cells.

摘要

人类 T 细胞白血病病毒 1(HTLV-1)orf I 编码的辅助蛋白 p8 从其前体 p12 中切割,这两种蛋白均有助于病毒的持续存在。p8 诱导细胞突起,这被认为有助于 p8 向靶细胞转移和病毒传播。与 p8 相互作用并介导 p8 转移的宿主因子尚不清楚。在这里,我们报告称,血管扩张刺激磷蛋白(VASP)可促进肌动蛋白丝伸长,是 p8 的一种新型相互作用伙伴,对于 p8 和 HTLV-1 Gag 细胞间转移至关重要。VASP 包含一个 Ena/VASP 同源 1(EVH1)结构域,该结构域将该蛋白靶向到粘着斑。生物信息学鉴定出 p8 中的一个短片段(氨基酸(aa)24-45),该片段可能介导与 VASP 的 EVH1 结构域的相互作用。共免疫沉淀实验证实了 293T、Jurkat 和 HTLV-1 感染的 MT-2 细胞中 VASP:p8 的相互作用。通过模拟 p8 的 aa26-37 的肽可显著阻断 VASP:p8 的共沉淀。突变研究表明,VASP 的 EVH1 结构域是与 p8 相互作用所必需的,但不是充分的。此外,VASP 的 G- 和 F-肌动蛋白结合结构域的缺失显著减少了 p8 的共沉淀。成像鉴定出 VASP 与质膜和突起结构中的 p8 部分共定位的区域,这通过邻近连接测定得到了证实。共培养实验表明,Jurkat T 细胞之间通过包含 VASP 的管进行 p8 的转移。成像和流式细胞术显示,通过 RNA 干扰或 CRISPR/Cas9 抑制内源性和过表达的 VASP,可减少 p8 转移到细胞表面和靶 Jurkat T 细胞,同时病毒释放不受影响。因此,我们确定 VASP 是 p8 的一种新型相互作用伙伴,对于 p8 和 HTLV-1 Gag 转移到靶 T 细胞至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac2d/7526893/cc39e5da9a46/ppat.1008879.g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验