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基于双噬菌体展示肽共靶向的生物传感器,具有信号增强活性,用于金黄色葡萄球菌的比色检测。

Double phage displayed peptides co-targeting-based biosensor with signal enhancement activity for colorimetric detection of Staphylococcus aureus.

机构信息

School of Food Science and Technology, International Joint Laboratory on Food Safety, Synergetic Innovation Center of Food Safety and Quality Control, Jiangnan University, Wuxi, Jiangsu, 214122, China; Yixing Institute of Food and Biotechnology Co., Ltd, Yixing, 214200, China.

Comprehensive Technology Center of Zhangjiagang Customs, Zhangjiagang, Jiangsu, 215600, China.

出版信息

Biosens Bioelectron. 2024 Apr 1;249:116005. doi: 10.1016/j.bios.2024.116005. Epub 2024 Jan 4.

Abstract

The development of simple, fast, sensitive, and specific strategies for the detection of foodborne pathogenic bacteria is crucial for ensuring food safety and promoting human health. Currently, detection methods for Staphylococcus aureus still suffer from issues such as low specificity and low sensitivity. To address this problem, we proposed a sensitivity enhancement strategy based on double phage-displayed peptides (PDPs) co-targeting. Firstly, we screened two PDPs and analyzed their binding mechanisms through fluorescent localization, pull-down assay, and molecular docking. The two PDPs target S. aureus by binding to specific proteins on its outer membrane. Based on this phenomenon, a convenient and sensitive double PDPs colorimetric biosensor was developed. Double thiol-modified phage-displayed peptides (PDP-SH) enhance the aggregation of gold nanoparticles (AuNPs), whereas the specific interaction between the double PDPs and bacteria inhibits the aggregation of AuNPs, resulting in an increased visible color change before and after the addition of bacteria. This one-step colorimetric approach displayed a high sensitivity of 2.35 CFU/mL and a wide detection range from 10-2 × 10 CFU/mL. The combination with smartphone-based image analysis improved the portability of this method. This strategy achieves the straightforward, highly sensitive and portable detection of pathogenic bacteria.

摘要

开发简单、快速、灵敏和特异的食源性病原体检测策略对于保障食品安全和促进人类健康至关重要。目前,金黄色葡萄球菌的检测方法仍然存在特异性低、灵敏度低等问题。针对这一问题,我们提出了一种基于双噬菌体展示肽(PDP)共同靶向的灵敏度增强策略。首先,我们筛选了两个 PDP,并通过荧光定位、下拉实验和分子对接分析了它们的结合机制。这两个 PDP 通过与金黄色葡萄球菌外膜上的特定蛋白结合来靶向金黄色葡萄球菌。基于这一现象,我们开发了一种方便灵敏的双 PDP 比色生物传感器。双巯基修饰的噬菌体展示肽(PDP-SH)增强了金纳米粒子(AuNPs)的聚集,而双 PDP 与细菌之间的特异性相互作用抑制了 AuNPs 的聚集,导致在加入细菌前后可见颜色变化增加。这种一步比色法的灵敏度为 2.35 CFU/mL,检测范围从 10-2 × 10 CFU/mL。与基于智能手机的图像分析相结合,提高了该方法的便携性。该策略实现了对病原菌的直接、高灵敏和便携检测。

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