Role of the Viral Capsid in HIV-1 Integration

病毒衣壳在 HIV-1 整合中的作用

• 批准号: 10199944
• 负责人: Chandravanu Dash
• 金额: $ 37万
• 依托单位: MEHARRY MEDICAL COLLEGE
• 依托单位国家: 美国
• 财政年份: 2019
• 资助国家: 美国
• 起止时间: 2019-07-15 至 2024-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10199944
• 关键词: AIDS/HIV problem; Antiviral Agents; Antiviral Therapy; Area; Binding; Biochemical; Biochemistry; Biological Assay; Biology; Capsid; Capsid Proteins; Cell Nucleus; Cell fusion; Cells; Cellular Membrane; Clinic; Clinical; Complex; Coupling; Cultured Cells; Cytoplasm; DNA Integration; Data; Dependence; Development; Disease Management; Drug Targeting; Drug usage; Environment; Exhibits; Face; Fractionation; Goals; HIV; HIV Infections; HIV-1; In Vitro; Infection; Integrase; Integration Host Factors; Knowledge; Life Cycle Stages; Link; Measures; Mediating; Membrane; Modeling; Morphology; Nuclear; Nuclear Pore Complex; Pathway interactions; Play; Proteins; Proviruses; Reaction; Regimen; Reporting; Research; Resistance; Reverse Transcription; Role; Sucrose; Testing; United States National Institutes of Health; Variant; Viral; Virus; Virus Integration; antiretroviral therapy; base; design; drug development; inhibitor/antagonist; multidisciplinary; mutant; next generation; novel; pandemic disease; side effect; skills; small molecule; small molecule inhibitor; therapeutic target; viral DNA; viral resistance

ABSTRACT The ongoing HIV pandemic has resulted in ~1.2 million infections in the US and ~37 million infections worldwide. In spite of considerable progress in HIV/AIDS research, anti-retroviral therapy (ART) remains the only treatment option for HIV-1 infection. While ART has been highly effective in controlling the virus and making HIV infection a manageable disease, the drugs used in the ART regimen are expensive, cause side effects, and face viral resistance. Thus, there is an urgent need for continued development of drugs against novel cellular and viral targets. HIV-1 capsid protein (CA) is an important viral therapeutic target that is currently clinically unexploited. Recently, Gilead developing a highly potent CA-targeting inhibitor as next generation of antivirals. However, successful transition of these CA-specific inhibitors to the clinic require clear understanding of the anti-viral mechanisms and the delineating CA’s role in HIV-1 infection. Our studies are designed to understand the mechanism by which HIV-1 CA controls viral integration. HIV enters the target cell by fusion of the viral membrane with the cellular membrane, releasing the viral capsid core into the cytoplasm of the target cell. Functional studies of HIV-1 variants indicate that the proper assembly, morphology, and stability of the capsid core are all essential for HIV-1 infectivity. While it is well established that HIV-1 CA facilitates reverse transcription, recent data shows that CA is also a key determinant of the ability of HIV-1 to enter the nucleus of the target cell. In particular, CA is genetically and functionally implicated in nuclear entry of the reverse transcribed provirus, by mediating interactions with cellular factors. A key knowledge gap is the role of CA in viral integration-a critical post-nuclear entry step of HIV-1 infection. We hypothesize that HIV-1 CA protein directly influences viral DNA integration. To test this hypothesis we propose three specific aims: Aim 1. To define the effects of capsid stability on HIV-1 preintegration complex (PIC) activity and viral DNA integrity. Aim 2. To determine whether integration activity is dependent on CA levels in the PICs. Aim 3. To determine the role of known capsid-binding host proteins in defining PIC-associated CA levels and PIC activity. To test a direct link between HIV-1 CA and viral DNA integration, we have developed a novel model by coupling a biochemical approach that quantitatively measures PIC-associated integration activity to the use of the CA-specific inhibitor as probes. In addition, we have assembled a multidisciplinary team with expertise in PIC biochemistry (Dash), capsid biology (Aiken) and retroviral integration (Engelman). Therefore, the proposed studies will generate new knowledge on the mechanism by which CA regulates HIV-1 integration and define the antiviral effects of CA-inhibitors to facilitate the development of novel CA-based anti-viral therapies (a High-Priority HIV/AIDS research area of the NIH).

摘要 持续的艾滋病毒大流行导致美国约120万人感染， 国际吧尽管在艾滋病毒/艾滋病研究方面取得了相当大的进展，但抗逆转录病毒疗法（ART）仍然是艾滋病毒/艾滋病治疗的主要手段。 HIV-1感染的唯一治疗选择。虽然ART在控制病毒方面非常有效， 使艾滋病毒感染成为一种可控制的疾病，ART方案中使用的药物昂贵， 影响，并面临病毒抵抗。因此，迫切需要继续开发药物， 新的细胞和病毒靶点。HIV-1衣壳蛋白（CA）是一种重要的病毒治疗靶点， 目前临床上尚未开发。最近，吉利德开发了一种高效的CA靶向抑制剂， 抗病毒药物的产生。然而，这些CA特异性抑制剂向临床的成功过渡需要明确的 了解抗病毒机制和描绘CA在HIV-1感染中的作用。我们的研究是 旨在了解HIV-1 CA控制病毒整合的机制。 HIV通过病毒膜与细胞膜的融合进入靶细胞，释放出 病毒衣壳核心进入靶细胞的细胞质。HIV-1变异体的功能研究表明， 衣壳核心的适当组装、形态和稳定性对于HIV-1的感染性都是必需的。虽然 众所周知，HIV-1 CA促进逆转录，最近的数据表明，CA也是一个关键， HIV-1进入靶细胞核的能力的决定因素。特别是，CA是遗传性的， 在功能上与逆转录前病毒的核进入有关，通过介导与 细胞因子一个关键的知识差距是CA在病毒整合中的作用，这是病毒进入核后的关键步骤。 HIV-1感染。我们假设HIV-1 CA蛋白直接影响病毒DNA整合。测试 根据这一假设，我们提出了三个具体目标：目标1。确定衣壳稳定性对HIV-1的影响 整合前复合物（PIC）活性和病毒DNA完整性。目标2.要确定集成活动是否 取决于太平洋岛屿国家的CA水平。目标3。为了确定已知的帽蛋白结合宿主蛋白在 定义PIC相关的CA水平和PIC活动。检测HIV-1 CA和病毒DNA之间的直接联系 整合，我们已经开发了一种新的模型，通过耦合的生化方法，定量 测量PIC相关的整合活性以使用CA特异性抑制剂作为探针。另外我们 组建了一个多学科团队，拥有PIC生物化学（Dash），衣壳生物学（Aiken）和 逆转录病毒整合（Engelman）。因此，拟议的研究将产生关于 CA调节HIV-1整合的机制，并确定CA抑制剂的抗病毒作用，以促进 新的基于CA的抗病毒疗法的开发（NIH的高优先级HIV/AIDS研究领域）。