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可视化不可见之物:可视化细菌蛋白及宿主-病原体相互作用的新方法。

Visualizing the invisible: novel approaches to visualizing bacterial proteins and host-pathogen interactions.

作者信息

Singh Moirangthem Kiran, Kenney Linda J

机构信息

Department of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, TX, United States.

Sealy Center for Structural Biology, University of Texas Medical Branch, Galveston, TX, United States.

出版信息

Front Bioeng Biotechnol. 2024 Feb 13;12:1334503. doi: 10.3389/fbioe.2024.1334503. eCollection 2024.

DOI:10.3389/fbioe.2024.1334503
PMID:38415188
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10898356/
Abstract

Host-pathogen interactions play a critical role in infectious diseases, and understanding the underlying mechanisms is vital for developing effective therapeutic strategies. The visualization and characterization of bacterial proteins within host cells is key to unraveling the dynamics of these interactions. Various protein labeling strategies have emerged as powerful tools for studying host-pathogen interactions, enabling the tracking, localization, and functional analysis of bacterial proteins in real-time. However, the labeling and localization of secreted type III secretion system (T3SS) effectors in host cells poses technical challenges. Conventional methods disrupt effector stoichiometry and often result in non-specific staining. Bulky fluorescent protein fusions interfere with effector secretion, while other tagging systems such as 4Cys-FLaSH/Split-GFP suffer from low labeling specificity and a poor signal-to-noise ratio. Recent advances in state-of-the-art techniques have augmented the existing toolkit for monitoring the translocation and dynamics of bacterial effectors. This comprehensive review delves into the bacterial protein labeling strategies and their application in imaging host-pathogen interactions. Lastly, we explore the obstacles faced and potential pathways forward in the realm of protein labeling strategies for visualizing interactions between hosts and pathogens.

摘要

宿主-病原体相互作用在传染病中起着关键作用,了解其潜在机制对于制定有效的治疗策略至关重要。宿主细胞内细菌蛋白的可视化和表征是揭示这些相互作用动态的关键。各种蛋白质标记策略已成为研究宿主-病原体相互作用的有力工具,能够实时追踪、定位和功能分析细菌蛋白。然而,宿主细胞中分泌型III型分泌系统(T3SS)效应器的标记和定位带来了技术挑战。传统方法会破坏效应器的化学计量,并且常常导致非特异性染色。庞大的荧光蛋白融合体会干扰效应器的分泌,而其他标记系统,如4Cys-FLaSH/分裂绿色荧光蛋白,存在标记特异性低和信噪比差的问题。最先进技术的最新进展扩充了现有的监测细菌效应器转位和动态的工具集。这篇综述深入探讨了细菌蛋白标记策略及其在成像宿主-病原体相互作用中的应用。最后,我们探讨了在可视化宿主与病原体相互作用的蛋白质标记策略领域所面临的障碍和潜在的前进途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d517/10898356/83a7d338c5fc/fbioe-12-1334503-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d517/10898356/3e56e36e4996/fbioe-12-1334503-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d517/10898356/f239e6f3d698/fbioe-12-1334503-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d517/10898356/83a7d338c5fc/fbioe-12-1334503-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d517/10898356/3e56e36e4996/fbioe-12-1334503-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d517/10898356/f239e6f3d698/fbioe-12-1334503-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d517/10898356/83a7d338c5fc/fbioe-12-1334503-g003.jpg

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Nat Commun. 2022 Jan 14;13(1):314. doi: 10.1038/s41467-022-27956-y.
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Nat Commun. 2021 Nov 18;12(1):6715. doi: 10.1038/s41467-021-27025-w.
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