Hydrophilic/hydrophobic modified microchip for detecting multiple gene doping candidates using CRISPR-Cas12a and RPA

被引:3
|
作者
Zheng, Bingxin [1 ,2 ]
Yan, Jiayu [1 ,3 ]
Li, Tao [1 ,4 ,5 ]
Zhao, Yin [1 ]
Xu, Zhichen [1 ,2 ]
Rao, Ruotong [1 ,2 ]
Zhu, Jiang [1 ,2 ]
Hu, Rui [1 ,2 ]
Li, Ying [1 ,4 ,5 ]
Yang, Yunhuang [1 ,2 ]
机构
[1] Chinese Acad Sci, Wuhan Inst Phys & Math, Innovat Acad Precis Measurement Sci & Technol, Natl Ctr Magnet Resonance Wuhan,State Key Lab Magn, Wuhan 430071, Peoples R China
[2] Univ Chinese Acad Sci, Beijing, Peoples R China
[3] Shanghai Univ Sport, Shanghai Inst Doping Anal, Shanghai 200438, Peoples R China
[4] Hubei Univ Chinese Med, Sch Lab Med, 16 Huangjia Lake West Rd, Wuhan 430065, Peoples R China
[5] Hubei Shizhen Lab, 16 Huangjia Lake West Rd, Wuhan 430065, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Hydrophilic/hydrophobic modifications; CRISPR-Cas12a; Gene doping; Microfluidics; Multiplexed detection; ERYTHROPOIETIN; PLASMID; THERAPY;
D O I
10.1016/j.bios.2024.116631
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
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.
引用
收藏
页数:10
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