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Release of gp120 Restraints Leads to an Entry-Competent Intermediate State of the HIV-1 Envelope Glycoproteins

机译:gp120约束物的释放导致进入竞争状态的HIV-1信封糖蛋白进入中间状态。

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ABSTRACT Primary human immunodeficiency virus (HIV-1) envelope glycoprotein (Env) trimers [(gp120/gp41)_(3)] typically exist in a metastable closed conformation (state 1). Binding the CD4 receptor triggers Env to undergo extensive conformational changes to mediate virus entry. We identified specific gp120 residues that restrain Env in state 1. Alteration of these restraining residues destabilized state 1, allowing Env to populate a functional conformation (state 2) intermediate between state 1 and the full CD4-bound state (state 3). Increased state 2 occupancy was associated with lower energy barriers between the states. State 2 was an obligate intermediate for all transitions between state 1 and state 3. State 2-enriched Envs required lower CD4 concentrations to trigger virus entry and more efficiently infected cells expressing low levels of CD4. These Envs were resistant to several broadly neutralizing antibodies and small-molecule inhibitors. Thus, state 2 is an Env conformation on the virus entry pathway; sampling state 2 increases the adaptability of HIV-1 to different host cell receptor levels and immune environments. Our results provide new insights into the conformational regulation of HIV-1 entry. IMPORTANCE The envelope glycoproteins (Env) of HIV-1 mediate virus entry and are the sole targets of neutralizing antibodies. Understanding the way that Env promotes HIV-1 entry can expedite drug and vaccine development. By destabilizing Env, we found that it assumes an intermediate state that is functional and obligate for transitions to entry-competent conformations. Increased sampling of this state enhances the ability of HIV-1 to infect cells that express low levels of the CD4 receptor and allows the virus to evade neutralizing antibodies and small-molecule inhibitors. These findings provide new mechanistic insights into the function and inhibition of HIV-1 Env and will contribute to ongoing therapeutic and prevention efforts to combat HIV-1.
机译:摘要人类原发性人类免疫缺陷病毒(HIV-1)包膜糖蛋白(Env)三聚体[(gp120 / gp41)_(3)]通常以亚稳态封闭构型存在(状态1)。结合CD4受体触发Env进行广泛的构象变化,以介导病毒进入。我们鉴定了在状态1中抑制Env的特定gp120残基。这些抑制性残基的改变使状态1不稳定,从而使Env可以填充介于状态1和完整CD4结合状态(状态3)之间的功能性构象(状态2)。状态2的占用增加与状态之间较低的能垒相关。状态2是状态1和状态3之间所有转换的专心中间产物。富含状态2的Envs需要较低的CD4浓度才能触发病毒进入,并且需要更有效地感染表达低水平CD4的细胞。这些Env对几种广泛中和的抗体和小分子抑制剂具有抗性。因此,状态2是病毒进入途径上的Env构象;采样状态2可提高HIV-1对不同宿主细胞受体水平和免疫环境的适应性。我们的结果为HIV-1进入的构象调控提供了新的见解。重要信息HIV-1的包膜糖蛋白(Env)介导病毒进入,是中和抗体的唯一靶标。了解Env促进HIV-1进入的方式可以加快药物和疫苗的开发。通过破坏Env的稳定性,我们发现它处于一个中间状态,该状态是功能性的,并且有义务过渡到具有入口功能的构象。增加这种状态的采样可以增强HIV-1感染表达CD4受体水平低的细胞的能力,并使病毒能够逃避中和抗体和小分子抑制剂。这些发现提供了对HIV-1 Env的功能和抑制作用的新的机械学见解,将有助于对抗HIV-1的正在进行的治疗和预防工作。

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