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活细胞中单病毒追踪的量子点技术

Single-virus tracking with quantum dots in live cells.

机构信息

State Key Laboratory of Medicinal Chemical Biology, Frontiers Science Center for New Organic Matter, Tianjin Key Laboratory of Biosensing and Molecular Recognition, Research Center for Analytical Sciences, College of Chemistry, School of Medicine and Frontiers Science Center for Cell Responses, Nankai University, Tianjin, P. R. China.

Haihe Laboratory of Sustainable Chemical Transformations, Tianjin, China.

出版信息

Nat Protoc. 2023 Feb;18(2):458-489. doi: 10.1038/s41596-022-00775-7. Epub 2022 Nov 30.

Abstract

Single-virus tracking (SVT) offers the opportunity to monitor the journey of individual viruses in real time and to explore the interactions between viral and cellular structures in live cells, which can assist in characterizing the complex infection process and revealing the associated dynamic mechanisms. However, the low brightness and poor photostability of conventional fluorescent tags (e.g., organic dyes and fluorescent proteins) greatly limit the development of the SVT technique, and challenges remain in performing multicolor SVT over long periods of time. Owing to the outstanding photostability, high brightness and narrow emission with tunable color range of quantum dots (QDs), QD-based SVT (QSVT) enables us to follow the fate of individual viruses interacting with different cellular structures at the single-virus level for milliseconds to hours, providing more accurate and detailed information regarding viral infection in live cells. So far, the QSVT technique has yielded spectacular achievements in uncovering the mechanisms associated with virus entry, trafficking and egress. Here, we provide a detailed protocol for QSVT implementation using the viruses that we have previously studied systematically as an example. The specific procedures for performing QSVT experiments in live cells are described, including virus preparation, the QD labeling strategies, imaging approaches, image processing and data analysis. The protocol takes 1-2 weeks from the preparation of viruses and cellular specimens to image acquisition, and 1 d for image processing and data analysis.

摘要

单病毒追踪 (SVT) 提供了实时监测单个病毒轨迹的机会,并可探索活细胞中病毒和细胞结构之间的相互作用,有助于对复杂的感染过程进行特征描述,并揭示相关的动态机制。然而,传统荧光标记物(如有机染料和荧光蛋白)的亮度低、光稳定性差,极大地限制了 SVT 技术的发展,并且在长时间内进行多色 SVT 仍然具有挑战性。由于量子点 (QDs) 具有出色的光稳定性、高亮度和窄的发射谱(可调谐的颜色范围),基于 QD 的 SVT (QSVT) 使我们能够在单病毒水平上实时追踪与不同细胞结构相互作用的单个病毒的命运,从而提供有关活细胞中病毒感染的更准确和详细的信息。迄今为止,QSVT 技术在揭示与病毒进入、运输和出芽相关的机制方面取得了引人瞩目的成就。在此,我们以我们之前系统研究的病毒为例,提供了详细的 QSVT 实施方案。本文描述了在活细胞中进行 QSVT 实验的具体步骤,包括病毒制备、QD 标记策略、成像方法、图像处理和数据分析。从病毒和细胞标本的准备到图像采集,该方案大约需要 1-2 周的时间,而图像处理和数据分析则需要 1 天。

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