Institute of Complex Systems, Structural Biochemistry (ICS-6), Forschungszentrum Jülich, 52425, Jülich, Germany.
Institut für Physikalische Biologie, Heinrich-Heine-Universität Düsseldorf, 40225, Düsseldorf, Germany.
Sci Rep. 2017 Jul 20;7(1):5979. doi: 10.1038/s41598-017-06319-4.
HIV-1 Nef is an important pathogenic factor for HIV/AIDS pathogenesis. Studies have shown that the association of Nef with the inner leaflet of the plasma membrane and with endocytic and perinuclear vesicles is essential for most activities of Nef. Using purified recombinant proteins in pull-down assays and by co-immunoprecipitation assays we demonstrate that Nef binds directly and specifically to all GABARAP family members, but not to LC3 family members. Based on nuclear magnetic resonance (NMR) experiments we showed that Nef binds to GABARAP via two surface exposed hydrophobic pockets. S53 and F62 of GABARAP were identified as key residues for the interaction with Nef. During live-cell fluorescence microscopy an accumulation of Nef and all GABARAP family members in vesicular structures throughout the cytoplasm and at the plasma membrane was observed. This plasma membrane accumulation was significantly reduced after knocking down GABARAP, GABARAPL1 and GABARAPL2 with respective siRNAs. We identified GABARAPs as the first known direct interaction partners of Nef that are essential for its plasma membrane localization.
HIV-1 Nef 是 HIV/AIDS 发病机制的一个重要致病因素。研究表明,Nef 与质膜的内小叶以及内吞和核周小泡的关联对于 Nef 的大多数活性都是必不可少的。通过纯化的重组蛋白下拉实验和共免疫沉淀实验,我们证明 Nef 可以直接和特异地与所有 GABARAP 家族成员结合,但不与 LC3 家族成员结合。基于核磁共振(NMR)实验,我们表明 Nef 通过两个暴露于表面的疏水性口袋与 GABARAP 结合。GABARAP 的 S53 和 F62 被确定为与 Nef 相互作用的关键残基。在活细胞荧光显微镜下,观察到 Nef 和所有 GABARAP 家族成员在整个细胞质和质膜中的囊泡结构中积累。用相应的 siRNA 敲低 GABARAP、GABARAPL1 和 GABARAPL2 后,这种质膜积累显著减少。我们确定 GABARAPs 是 Nef 的第一个已知的直接相互作用伙伴,对于其质膜定位是必不可少的。