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靶向细胞表面HIV-1包膜蛋白以抑制传染性病毒的形成。

Targeting cell surface HIV-1 Env protein to suppress infectious virus formation.

作者信息

Bastian Arangassery Rosemary, Ang Charles G, Kamanna Kantharaju, Shaheen Farida, Huang Yu-Hung, McFadden Karyn, Duffy Caitlin, Bailey Lauren D, Sundaram Ramalingam Venkat Kalyana, Chaiken Irwin

机构信息

Biochemistry and Molecular Biology, Drexel University College of Medicine, Philadelphia, PA 19102, United States; School of Biomedical Engineering, Science and Health Systems, Drexel University, Philadelphia, PA 19104, United States.

Biochemistry and Molecular Biology, Drexel University College of Medicine, Philadelphia, PA 19102, United States; School of Biomedical Engineering, Science and Health Systems, Drexel University, Philadelphia, PA 19104, United States.

出版信息

Virus Res. 2017 May 2;235:33-36. doi: 10.1016/j.virusres.2017.04.003. Epub 2017 Apr 6.

Abstract

HIV-1 Env protein is essential for host cell entry, and targeting Env remains an important antiretroviral strategy. We previously found that a peptide triazole thiol KR13 and its gold nanoparticle conjugate AuNP-KR13 directly and irreversibly inactivate the virus by targeting the Env protein, leading to virus gp120 shedding, membrane disruption and p24 capsid protein release. Here, we examined the consequences of targeting cell-surface Env with the virus inactivators. We found that both agents led to formation of non-infectious virus from transiently transfected HEK293T cells. The budded non-infectious viruses lacked Env gp120 but contained gp41. Importantly, budded virions also retained the capsid protein p24, in stark contrast to p24 leakage from viruses directly treated by these agents and arguing that the agents led to deformed viruses by transforming the cells at a stage before virus budding. We found that the Env inactivators caused gp120 shedding from the transiently transfected HEK293T cells as well as non-producer CHO-K1-gp160 cells. Additionally, AuNP-KR13 was cytotoxic against the virus-producing HEK293T and CHO-K1-gp160 cells, but not untransfected HEK293T or unmodified CHO-K1 cells. The results obtained reinforce the argument that cell-surface HIV-1 Env is metastable, as on virus particles, and provides a conformationally vulnerable target for virus suppression and infectious cell inactivation.

摘要

HIV-1包膜蛋白对于宿主细胞进入至关重要,靶向包膜蛋白仍然是一种重要的抗逆转录病毒策略。我们之前发现一种肽三唑硫醇KR13及其金纳米颗粒偶联物AuNP-KR13通过靶向包膜蛋白直接且不可逆地使病毒失活,导致病毒gp120脱落、膜破坏和p24衣壳蛋白释放。在此,我们研究了用病毒灭活剂靶向细胞表面包膜蛋白的后果。我们发现这两种试剂都导致从瞬时转染的HEK293T细胞形成无感染性的病毒。出芽的无感染性病毒缺乏Env gp120但含有gp41。重要的是,出芽的病毒粒子也保留了衣壳蛋白p24,这与这些试剂直接处理的病毒中p24泄漏形成鲜明对比,表明这些试剂在病毒出芽前的阶段通过转化细胞导致病毒变形。我们发现包膜蛋白灭活剂导致瞬时转染的HEK293T细胞以及非生产性CHO-K1-gp160细胞中的gp120脱落。此外,AuNP-KR13对产生病毒的HEK293T和CHO-K1-gp160细胞具有细胞毒性,但对未转染的HEK293T或未修饰的CHO-K1细胞没有细胞毒性。获得的结果强化了这样的观点,即细胞表面的HIV-1包膜蛋白与病毒颗粒上的一样是亚稳态的,并为病毒抑制和感染性细胞失活提供了一个构象易损靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4267/5555212/56b6793d075b/nihms888277f1.jpg

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