Ellencrona Karin, Syed Asim, Johansson Magnus
School of Life Sciences, Södertörn University, S-14189 Huddinge, Sweden and Department of Genetics, Microbiology and Toxicology, Stockholm University, S-106 91, Stockholm, Sweden.
Biol Chem. 2009 Apr;390(4):319-23. doi: 10.1515/BC.2009.041.
Dengue virus (DENV) and tick-borne encephalitis virus (TBEV) are flaviviruses, which can cause lethal hemorrhagic fever and encephalitis, respectively. Here, we demonstrate that the TBEV-NS5 and DENV-NS5 proteins use an internal binding mechanism to target human PDZ proteins. TBEV-NS5 has high affinity to regulating synaptic membrane exocytosis-2 (RIMS2) and Scribble, whereas DENV-NS5 binds primarily to the tight junction protein zonula occludens-1 (ZO-1). Targeting of TBEV-NS5 to the plasma membrane is stabilised by ZO-1; however, DENV-NS5 co-localises with ZO-1 in the nucleus. These interactions have potential important roles in the ability of flaviviruses to manipulate cell proliferation, junction permeability and the interferon pathways.
登革病毒(DENV)和蜱传脑炎病毒(TBEV)均为黄病毒,分别可导致致命的出血热和脑炎。在此,我们证明TBEV-NS5和DENV-NS5蛋白利用一种内部结合机制靶向人类PDZ蛋白。TBEV-NS5对调节突触膜胞吐作用-2(RIMS2)和scribble具有高亲和力,而DENV-NS5主要与紧密连接蛋白闭合蛋白-1(ZO-1)结合。ZO-1可稳定TBEV-NS5定位于质膜;然而,DENV-NS5与ZO-1在细胞核中共定位。这些相互作用在黄病毒操纵细胞增殖、连接通透性和干扰素途径的能力方面具有潜在的重要作用。