巨噬细胞上仿生DNA受体的修饰对病原体捕食的精确和逻辑操纵

IF 16 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Qingfei Sun, Yueyue Gui, Chong Fan, Jiaxiong Li, Xiaomeng Tan, Chao Li*, Jin Qiu* and Jiehua Ma*, 
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引用次数: 0

摘要

巨噬细胞使用模式识别受体(PRRs)来识别、捕获和吞噬病原体。重建人工系统来模拟这些受体来操纵巨噬细胞的捕食,在科学上令人兴奋,在技术上与抗感染相关。然而,制造具有可预测和稳定结构的合成prr模仿受体仍然是一个挑战。在此,我们使用环状适配体作为构建块来创建模拟PRRs功能的人工DNA受体(adr)。在巨噬细胞上修饰adr后,它们可以稳定地识别特定病原体,促进巨噬细胞的吞噬,类似于天然PRRs。作为动态结构,这些adr可以被外部DNA分子灵活激活或灭活,类似于蛋白质受体对小分子配体的反应。由于DNA反应的可编程性,可以引入布尔逻辑运算来逻辑地操纵巨噬细胞的捕食行为,表现出人工受体的特征。此外,adr可以与其他功能DNA基序(如CpG DNA)结合,以更高的效率增强巨噬细胞的活化和抗菌能力。总的来说,我们相信这种人工受体不仅拓宽了DNA纳米技术在细胞生物学中的应用,而且考虑到越来越多的耐多药细菌的出现,也有助于正在进行的重塑先天免疫系统以对抗感染的努力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Decoration of Biomimetic DNA Receptors on Macrophages for Precise and Logical Manipulation of Pathogen Predation

Decoration of Biomimetic DNA Receptors on Macrophages for Precise and Logical Manipulation of Pathogen Predation

Macrophages use pattern recognition receptors (PRRs) to recognize, capture, and phagocytize pathogens. Recreating artificial systems to mimic such receptors for manipulating macrophage predation is both scientifically exciting and technologically relevant to anti-infection. Nevertheless, fabricating synthetic PRR-mimicking receptors with a predictable and stable structure remains a challenge. Herein, we use circular aptamers as building blocks to create artificial DNA receptors (ADRs) that mimic the function of PRRs. After modification of ADRs on macrophages, they can stably recognize specific pathogens and promote the phagocytosis of macrophages, akin to natural PRRs. As dynamic structures, these ADRs can be flexibly activated or inactivated by external DNA molecules, akin to protein receptors responding to small-molecule ligands. Owing to the programmability of the DNA reaction, Boolean logic operations can be introduced to logically manipulate the predation behavior of macrophages, exhibiting the characteristics of artificial receptors. Furthermore, ADRs can be integrated with other functional DNA motifs, e.g., CpG DNA, to enhance the activation and antibacterial capacity of macrophages with higher efficiency. Overall, we believe that this artificial receptor not only broadens the application of DNA nanotechnology in cell biology but also contributes to ongoing efforts to remodel the innate immune system for fighting infection in consideration of the growing emergence of multidrug-resistant bacteria.

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来源期刊
ACS Nano
ACS Nano 工程技术-材料科学:综合
CiteScore
26.00
自引率
4.10%
发文量
1627
审稿时长
1.7 months
期刊介绍: ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.
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