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gp120 限制的释放导致 HIV-1 包膜糖蛋白的一种具有进入能力的中间状态。

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

作者信息

Herschhorn Alon, Ma Xiaochu, Gu Christopher, Ventura John D, Castillo-Menendez Luis, Melillo Bruno, Terry Daniel S, Smith Amos B, Blanchard Scott C, Munro James B, Mothes Walther, Finzi Andrés, Sodroski Joseph

机构信息

Department of Immunology Cancer and Virology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA

Department of Microbiology and Immunobiology, Harvard Medical School, Boston, Massachusetts, USA.

出版信息

mBio. 2016 Oct 25;7(5):e01598-16. doi: 10.1128/mBio.01598-16.

Abstract

UNLABELLED

Primary human immunodeficiency virus (HIV-1) envelope glycoprotein (Env) trimers [(gp120/gp41)] 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.

摘要

未标记

原代人免疫缺陷病毒(HIV-1)包膜糖蛋白(Env)三聚体[(gp120/gp41)]通常以亚稳态闭合构象(状态1)存在。与CD4受体结合会触发Env发生广泛的构象变化,以介导病毒进入。我们确定了在状态1中限制Env的特定gp120残基。这些限制残基的改变使状态1不稳定,使Env呈现出介于状态1和完全CD4结合状态(状态3)之间的功能性构象(状态2)。状态2占有率的增加与各状态之间较低的能量屏障相关。状态2是状态1和状态3之间所有转变的必经中间体。富含状态2的Env需要较低的CD4浓度来触发病毒进入,并能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一种Env构象;采样状态2可增加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。

重要性

HIV-1的包膜糖蛋白(Env)介导病毒进入,并且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。通过使Env不稳定,我们发现它呈现出一种中间状态,这种状态对于向具有进入能力的构象转变是功能性的且必不可少的。增加对这种状态的采样可增强HIV-1感染表达低水平CD4受体的细胞的能力,并使病毒能够逃避中和抗体和小分子抑制剂。这些发现为HIV-1 Env的功能和抑制提供了新的机制见解,并将有助于正在进行的对抗HIV-1的治疗和预防工作。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1496/5080382/5a459897c0a1/mbo0051630340001.jpg

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