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动态可变形纳米界面促进高效病原体捕获与传感

Efficient Pathogen Capture and Sensing Promoted by Dynamic Deformable Nanointerfaces.

作者信息

Cao Ying, Wu Na, Li Hui-Da, Xue Jing-Wen, Wang Rui, Yang Ting, Wang Jian-Hua

机构信息

Department of Chemistry, Research Center for Analytical Sciences, College of Sciences, Northeastern University, Box 332, Shenyang, 110819, China.

出版信息

Small. 2022 Dec;18(51):e2203962. doi: 10.1002/smll.202203962. Epub 2022 Nov 3.

Abstract

The M13 bacteriophage (M13 phage) has emerged as an attractive bionanomaterial due to its chemistry/gene modifiable feature and unique structures. Herein, a dynamic deformable nanointerface is fabricated taking advantage of the unique feature of the M13 phage for ultrasensitive detection of pathogens. PIII proteins at the tip of the M13 phage are genetically modified to display 6His peptide for site-specific anchoring onto Ni-NTA microbeads, whereas pVIII proteins along the side of the M13 phage are orderly arranged with thousands of aptamers and their complementary strands (c-apt). The flexible M13 nanofibers with rich recognition sites act as octopus tentacles, resulting in a 19-fold improvement in the capture affinity toward the target. The competitive binding of the target pathogen releases c-apts and initiates rolling circle amplification (RCA). The sway motion of M13 nanofibers accelerates the diffusion of c-apts, thus promoting RCA efficiency. Benefiting from the strengthened capture ability toward the target and the accelerated RCA process, three-orders of magnitude improvement in the sensitivity is achieved, with a detection limit of 8 cfu mL for Staphylococcus aureus. The promoted capture ability and assay performance highlights the essential role of the deformable feature of the engineered interface. This may provide inspiration for the construction of more efficient reaction interfaces.

摘要

M13噬菌体因其可化学修饰/基因编辑的特性和独特的结构,已成为一种极具吸引力的生物纳米材料。在此,利用M13噬菌体的独特特性构建了一种动态可变形纳米界面,用于超灵敏检测病原体。对M13噬菌体尖端的PIII蛋白进行基因改造,使其展示6His肽,以便位点特异性锚定在Ni-NTA微珠上,而沿M13噬菌体侧面的pVIII蛋白则与数千个适体及其互补链(c-apt)有序排列。具有丰富识别位点的柔性M13纳米纤维充当章鱼触手,使对靶标的捕获亲和力提高了19倍。靶标病原体的竞争性结合释放c-apts并启动滚环扩增(RCA)。M13纳米纤维的摆动运动加速了c-apts的扩散,从而提高了RCA效率。得益于对靶标的增强捕获能力和加速的RCA过程,灵敏度提高了三个数量级,对金黄色葡萄球菌的检测限为8 cfu/mL。增强的捕获能力和检测性能突出了工程化界面可变形特性的重要作用。这可能为构建更高效的反应界面提供灵感。

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