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HIV-1核心的核输入及其与核孔相互作用的直接可视化

Direct visualization of HIV-1 core nuclear import and its interplay with the nuclear pore.

作者信息

Hou Zhen, Fronik Stanley, Shen Yao, Chen Long, Thompson Christopher, Neumann Sarah, Zhang Peijun

机构信息

Division of Structural Biology, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.

Section Electron Microscopy, Department of Cell and Chemical Biology, Leiden University Medical Center, Leiden, The Netherlands.

出版信息

EMBO Rep. 2025 Aug 29. doi: 10.1038/s44319-025-00567-6.

Abstract

Direct visualization of HIV-1 nuclear import through the nuclear pore complex (NPC) presents a technical challenge due to the rarity of this process. To enable systematic investigation, we developed a robust in situ system that mimics HIV-1 nuclear import in a near-native context using isolated HIV-1 virus like particles (VLP) cores and permeabilized CD4 + T lymphocyte (CEM) cells. This approach supports docking and translocation of abundant viral cores through nuclear pores into the nucleus. For high-resolution visualization, we implemented an integrated correlative approach to guide cryo-focused ion beam (cryo-FIB) milling and cryo-electron tomography (cryo-ET) imaging, enabling precise targeting and structural characterization of individual nuclear import events. Using this workflow, we visualized 510 HIV-1 VLP cores at distinct stages of nuclear import, capturing key snapshots of the full progression of nuclear import. Subsequent statistical and structural analyses allow classification of core morphologies and identification of translocation-associated remodeling in nuclear pores. This work provides a methodological foundation for dissecting HIV-1 and potentially other viruses nuclear import processes and post-entry events in a controlled and quantitative manner.

摘要

由于HIV-1通过核孔复合体(NPC)进行核输入的过程十分罕见,直接观察这一过程面临技术挑战。为了能够进行系统研究,我们开发了一种强大的原位系统,该系统使用分离的HIV-1病毒样颗粒(VLP)核心和通透化的CD4 + T淋巴细胞(CEM)细胞,在接近天然的环境中模拟HIV-1核输入。这种方法支持大量病毒核心通过核孔对接并转运到细胞核中。为了进行高分辨率观察,我们采用了一种综合相关方法来指导低温聚焦离子束(cryo-FIB)铣削和低温电子断层扫描(cryo-ET)成像,从而能够对单个核输入事件进行精确靶向和结构表征。使用这个工作流程,我们观察了处于核输入不同阶段的510个HIV-1 VLP核心,捕捉到了核输入全过程的关键瞬间。随后的统计和结构分析允许对核心形态进行分类,并识别核孔中与转运相关的重塑。这项工作为以可控和定量的方式剖析HIV-1以及潜在的其他病毒的核输入过程和进入后事件提供了方法学基础。

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