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通过响应性叠氮糖介导的代谢细胞标记,然后进行点击反应,在体内靶向感染宿主细胞。

Targeting infected host cells in vivo via responsive azido-sugar mediated metabolic cell labeling followed by click reaction.

机构信息

Department of Materials Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, United States.

Medical Research Center, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, Guangzhou, Guangdong, 510120, PR China.

出版信息

Biomaterials. 2020 Apr;238:119843. doi: 10.1016/j.biomaterials.2020.119843. Epub 2020 Feb 5.

Abstract

The early in vivo diagnosis of infectious disease foci is largely hindered by invasion and concealment of pathogens in host cells, making it difficult for conventional probes to detect and analyze intracellular pathogens. Taking advantage of the excessively produced reactive oxygen species (ROS) within host cells, herein we report the design of thiol-hemiketal blocked N-azidoacetyl galactosamine (AcGalNAzSP), an azido unnatural sugar bearing an unprecedent designed ROS-responsive moiety for targeted labelling of infected host cells. AcGalNAzSP showed great stability under physiological conditions, specifically released active unnatural sugar in host cells overproducing ROS, metabolically labeled infected host cells with azido groups, and enabled targeting in vivo infection sites by subsequent Click Chemistry reactions, substantiating an unprecedented approach for targeting infected host cells. This technique could be a powerful tool for early in vivo diagnosis and targeted treatment of infectious disease.

摘要

病原体在宿主细胞内的入侵和隐匿在很大程度上阻碍了传染病灶的早期体内诊断,使得传统探针难以检测和分析细胞内病原体。利用宿主细胞内过度产生的活性氧(ROS),我们在此报告了硫代-半缩醛封锁的 N-叠氮乙酰半乳糖胺(AcGalNAzSP)的设计,这是一种带有前所未有的 ROS 响应性部分的叠氮非天然糖,用于感染宿主细胞的靶向标记。AcGalNAzSP 在生理条件下具有很好的稳定性,在过度产生 ROS 的宿主细胞中特异性释放活性非天然糖,代谢性标记感染的宿主细胞上的叠氮基团,并通过后续的点击化学反应实现体内感染部位的靶向,为靶向感染宿主细胞提供了一种前所未有的方法。该技术可能成为传染病早期体内诊断和靶向治疗的有力工具。

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