Proteome Fishing for CRISPR/Cas12a-Based Orthogonal Multiplex Aptamer Sensing.
Shuangqin LiBaichuan JinYintao MaXu YangJinlong FanYueli XieChenlu XuXin DaiMengjie WangQiqi LiuTing FuYuan LiuWeihong TanPublished in: Journal of the American Chemical Society (2024)
Detection of serum protein biomarkers is extremely challenging owing to the superior complexity of serum. Here, we report a method of proteome fishing from the serum. It uses a magnetic nanoparticle-protein corona and a multiplexed aptamer panel, which we incubated with the nanoparticle-protein corona for biomarker recognition. To transfer protein biomarker detection to aptamer detection, we established a CRISPR/Cas12a-based orthogonal multiplex aptamer sensing (COMPASS) platform by profiling the aptamers of protein corona with clinical nonsmall cell lung cancer (NSCLC) serum samples. Furthermore, we determined the four out of nine (FOON) panel (including HE4, NSE, AFP, and VEGF165) to be the most cost-effective and accurate panel for COMPASS in NSCLC diagnosis. The diagnostic accuracy of NSCLC by the FOON panel with internal and external cohorts was 95.56% (ROC-AUC = 99.40%) and 89.58% (ROC-AUC = 95.41%), respectively. Our developed COMPASS technology circumvents the otherwise challenging multiplexed serum protein amplification problem and avoids aptamer degradation in serum. Therefore, this novel COMPASS could lead to the development of a facile, cost-effective, intelligent, and high-throughput diagnostic platform for large-cohort cancer screening.
Keyphrases
- high throughput
- crispr cas
- label free
- small cell lung cancer
- single cell
- gold nanoparticles
- protein protein
- sensitive detection
- real time pcr
- amino acid
- genome editing
- binding protein
- stem cells
- magnetic nanoparticles
- high resolution
- advanced non small cell lung cancer
- loop mediated isothermal amplification
- small molecule
- cell therapy
- bone marrow
- squamous cell carcinoma
- vascular endothelial growth factor
- mesenchymal stem cells
- reduced graphene oxide