Platinum nanoparticles (PtNPs)-based CRISPR/Cas12a platform for detection of nucleic acid and protein in clinical samples

被引:8
作者
Liang, Jiajie [1 ,2 ,4 ]
Teng, Peijun [1 ]
Hu, Liangshan [3 ]
He, Guanbo [4 ]
Song, Qifang [1 ]
Zhang, Ying [1 ]
Peng, Bin [1 ]
Li, Gan [1 ]
Xiao, Wei [3 ]
Cao, Donglin [3 ]
Tang, Yong [1 ]
机构
[1] Jinan Univ, Dept Bioengn, Coll Life Sci & Technol, Guangdong Prov Engn Res Ctr Antibody Drug & Immun, Guangzhou 510632, Peoples R China
[2] Jinan Univ, Affiliated Hosp 1, Dept Oncol, Guangzhou 510632, Peoples R China
[3] Guangdong Second Prov Gen Hosp, Dept Lab Med, Guangzhou 510317, Peoples R China
[4] Guangdong Biowings Tech Ltd, Foshan 528000, Peoples R China
关键词
Noble metal nanocatalysts; CRISPR/Cas12a; Nucleic acid detection; Protein detection; Biosensor SARS-CoV-2; DIAGNOSTICS;
D O I
10.1016/j.aca.2022.340203
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Early rapid screening diagnostic assay is essential for the identification, prevention, and evaluation of many contagious or refractory diseases. The optical density transducer created by platinum nanoparticles (PtNPs) (OD-CRISPR) is reported in the present research as a cheap and easy-to-execute CRISPR/Cas12a-based diagnostic platform. The OD-CRISPR uses PtNPs, with ultra-high peroxidase-mimicking activity, to increase the detection sensitivity, thereby enabling the reduction of detection time and cost. The OD-CRISPR can be utilized to identify nucleic acid or protein biomarkers within an incubation time of 30-40min in clinical specimens. In the case of taking severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) N gene as an instance, when compared to a quantitative reverse transcription-polymerase chain reaction (RT-qPCR), the OD-CRISPR test attains a sensitivity of 79.17% and a specificity of 100%. In terms of detecting prostate-specific antigen (PSA), aptamer-based OD-CRISPR assay achieves the least discoverable concentration of 0.01 ng mL(-1). In general, the OD-CRISPR can detect nucleic acid and protein biomarkers, and is a potential strategy for early rapid screening diagnostic tools.
引用
收藏
页数:7
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