High-Yield and Quantitative Purification Method for HIV Which Minimizes Forces Applied to Virions Utilized to Investigate Maturation of HIV-1 via Cryo-Electron Tomography.

IF 3.8 3区 医学 Q2 VIROLOGY
Viruses-Basel Pub Date : 2025-03-03 DOI:10.3390/v17030364
Benjamin Preece, Wiley Peppel, Rodrigo Gallegos, Gillian Ysassi, Gabriel Clinger, Nicole Bohn, Broti Adhikary, Luiza Mendonça, David Belnap, Michael Vershinin, Saveez Saffarian
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Abstract

HIV is a lentivirus characterized by its cone shaped mature core. Visualization and structural examination of HIV requires the purification of virions to high concentrations. The yield and integrity of these virions are crucial for ensuring a uniform representation of all viral particles in subsequent analyses. In this study, we present a method for the purification of HIV virions which minimizes the forces applied to virions while maximizing the efficiency of collection. This method, which relies on virion sedimentation simulations, allows us to capture between 1000 and 5000 HIV virions released from individual HEK293 cells after transfection with the NL4.3 HIV backbone. We utilized this approach to investigate HIV core formation from several constructs: pNL4-3(RT:D185A&D186A) with an inactive reverse transcriptase, NL4.3(IN: V165A&R166A) with a type-II integrase mutation, and NL4.3(Ψ: Δ(105-278)&Δ(301-332)) featuring an edited Ψ packaging signal. Notably, virions from NL4.3(Ψ: Δ(105-278)&Δ(301-332)) displayed a mixed population, comprising immature virions, empty cores, and cores with detectable internal density. Conversely, virions derived from NL4.3(IN: V165A&R166A) exhibited a type II integrase mutant phenotype characterized by empty cores and RNP density localized around the cores, consistent with previous studies. In contrast, virions released from pNL4-3(RT:D185A&D186A) displayed mature cores containing detectable RNP density. We suggest that the sedimentation simulations developed in this study can facilitate the characterization of enveloped viruses.

利用冷冻电子断层扫描研究HIV-1成熟过程的一种高效、定量的HIV纯化方法。
HIV是一种慢病毒,其特征是其成熟核呈锥形。艾滋病毒的可视化和结构检查需要将病毒粒子纯化到高浓度。这些病毒粒子的产量和完整性对于确保在随后的分析中所有病毒颗粒的均匀代表至关重要。在这项研究中,我们提出了一种纯化HIV病毒粒子的方法,该方法可以最大限度地减少施加在病毒粒子上的力,同时最大限度地提高收集效率。这种方法依赖于病毒粒子沉降模拟,使我们能够捕获在转染NL4.3 HIV主干后从单个HEK293细胞释放的1000到5000个HIV病毒粒子。我们利用这种方法研究了几种构建体的HIV核心形成:具有非活性逆转录酶的pNL4-3(RT:D185A&D186A),具有ii型整合酶突变的NL4.3(IN: V165A&R166A),以及具有编辑Ψ包装信号的NL4.3(Ψ: Δ(105-278)&Δ(301-332))。值得注意的是,NL4.3的病毒粒子(Ψ: Δ(105-278)&Δ(301-332))呈现混合种群,包括未成熟病毒粒子、空核和内部密度可检测的核。相反,NL4.3衍生的病毒粒子(IN: V165A&R166A)表现出II型整合酶突变表型,其特征是空核和核周围的RNP密度,与先前的研究一致。相比之下,pNL4-3(RT: d185a和d186a)释放的病毒粒子显示出含有可检测RNP密度的成熟核。我们认为,本研究中建立的沉降模拟可以促进包膜病毒的表征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Viruses-Basel
Viruses-Basel VIROLOGY-
CiteScore
7.30
自引率
12.80%
发文量
2445
审稿时长
1 months
期刊介绍: Viruses (ISSN 1999-4915) is an open access journal which provides an advanced forum for studies of viruses. It publishes reviews, regular research papers, communications, conference reports and short notes. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. We also encourage the publication of timely reviews and commentaries on topics of interest to the virology community and feature highlights from the virology literature in the ''News and Views'' section. Electronic files or software regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material.
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