清脆的
背景(考古学)
软件可移植性
多路复用
纳米技术
多路复用
计算生物学
Cas9
微流控
实验室晶片
质粒
计算机科学
基因
材料科学
生物信息学
生物
遗传学
电信
古生物学
程序设计语言
作者
Bingxin Zheng,Jiayu Yan,Tao Li,Yin Zhao,Zhichen Xu,Ruotong Rao,Jiang Zhu,Rui Hu,Ying Li,Yunhuang Yang
标识
DOI:10.1016/j.bios.2024.116631
摘要
With significant advancements in understanding gene functions and therapy, the potential misuse of gene technologies, particularly in the context of sports through gene doping (GD), has come to the forefront. This raises concerns regarding the need for point-of-care testing of various GD candidates to counter illicit practices in sports. However, current GD detection techniques, such as PCR, lack the portability required for on-site multiplexed detection. In this study, we introduce an integrated microfluidics-based chip for multiplexed gene doping detection, termed MGD-Chip. Through the strategic design of hydrophilic and hydrophobic channels, MGD-Chip enables the RPA and CRISPR-Cas12a assays to be sequentially performed on the device, ensuring minimal interference and cross-contamination. Six potential GD candidates were selected and successfully tested simultaneously on the platform within 1 h. Demonstrating exceptional specificity, the platform achieved a detection sensitivity of 0.1 nM for unamplified target plasmids and 1 aM for amplified ones. Validation using mouse models established by injecting IGFI and EPO transgenes confirmed the platform's efficacy in detecting gene doping in real samples. This technology, capable of detecting multiple targets using portable elements, holds promise for real-time GD detection at sports events, offering a rapid, highly sensitive, and user-friendly solution to uphold the integrity of sports competitions.
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