Ventura Gustavo Tavares, Costa Emmerson Corrêa Brasil da, Capaccia Anne Miranda, Mohana-Borges Ronaldo
Laboratório de Genômica Estrutural, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
PLoS One. 2014 Dec 31;9(12):e115941. doi: 10.1371/journal.pone.0115941. eCollection 2014.
The hepatitis C virus (HCV) infects 170 to 200 million people worldwide and is, therefore, a major health problem. The lack of efficient treatments that specifically target the viral proteins or RNA and its high chronicity rate make hepatitis C the cause of many deaths and hepatic transplants annually. The NS3 protein is considered an important target for the development of anti-HCV drugs because it is composed of two domains (a serine protease in the N-terminal portion and an RNA helicase/NTPase in the C-terminal portion), which are essential for viral replication and proliferation. We expressed and purified both the NS3 helicase domain (NS3hel) and the full-length NS3 protein (NS3FL) and characterized pH-dependent structural changes associated with the increase in their ATPase and helicase activities at acidic pH. Using intrinsic fluorescence experiments, we have observed that NS3hel was less stable at pH 6.4 than at pH 7.2. Moreover, binding curves using an extrinsic fluorescent probe (bis-ANS) and ATPase assays performed under different pH conditions demonstrated that the hydrophobic clefts of NS3 are significantly more exposed to the aqueous medium at acidic pH. Using fluorescence spectroscopy and anisotropy assays, we have also observed more protein interaction with DNA upon pH acidification, which suggests that the hydrophobic clefts exposure on NS3 might be related to a loss of stability that could lead it to adopt a more open conformation. This conformational change at acidic pH would stimulate both its ATPase and helicase activities, as well as its ability to bind DNA. Taken together, our results indicate that the NS3 protein adopts a more open conformation due to acidification from pH 7.2 to 6.4, resulting in a more active form at a pH that is found near Golgi-derived membranes. This increased activity could better allow NS3 to carry out its functions during HCV replication.
丙型肝炎病毒(HCV)在全球感染了1.7亿至2亿人,因此是一个重大的健康问题。由于缺乏专门针对病毒蛋白或RNA的有效治疗方法,且其慢性感染率很高,丙型肝炎每年导致许多人死亡并引发大量肝脏移植。NS3蛋白被认为是开发抗HCV药物的重要靶点,因为它由两个结构域组成(N端部分是丝氨酸蛋白酶,C端部分是RNA解旋酶/NTPase),这两个结构域对于病毒复制和增殖至关重要。我们表达并纯化了NS3解旋酶结构域(NS3hel)和全长NS3蛋白(NS3FL),并对酸性pH下与它们ATP酶和解旋酶活性增加相关的pH依赖性结构变化进行了表征。通过内在荧光实验,我们观察到NS3hel在pH 6.4时比在pH 7.2时更不稳定。此外,使用外在荧光探针(双-ANS)的结合曲线以及在不同pH条件下进行的ATP酶测定表明,NS3的疏水裂缝在酸性pH下明显更暴露于水性介质中。通过荧光光谱和各向异性测定,我们还观察到pH酸化后蛋白质与DNA的相互作用更多,这表明NS3上疏水裂缝的暴露可能与稳定性丧失有关,这可能导致其采用更开放的构象。酸性pH下的这种构象变化会刺激其ATP酶和解旋酶活性以及与DNA结合的能力。综上所述,我们的结果表明,由于从pH 7.2酸化到pH 6.4,NS3蛋白采用了更开放的构象,在高尔基体衍生膜附近的pH值下形成了更具活性的形式。这种增加的活性可以更好地使NS3在HCV复制过程中发挥其功能。