DNA-Assisted CRISPR-Cas12a Enhanced Fluorescent Assay for Protein Detection in Complicated Matrices

被引:0
|
作者
Munusamy, Sathishkumar [1 ]
Zheng, Haiyan [1 ]
Jahani, Rana [1 ]
Zhou, Shuo [1 ]
Chen, Jun [1 ]
Kong, Juanhua [1 ]
Guan, Xiyun [1 ]
机构
[1] Univ Missouri, Dept Chem, Columbia, MO 65211 USA
来源
ACS APPLIED BIO MATERIALS | 2024年 / 8卷 / 01期
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
biomarkers; proteins; DNA barcodeamplification; complicated matrices; CRISPR; fluorescence; diseasediagnosis; IMMUNOSENSOR; AMPLIFICATION;
D O I
10.1021/acsabm.4c01600
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Proteins are important biological macromolecules that perform a wide variety of functions in the cell and human body, and can serve as important biomarkers for early diagnosis and prognosis of human diseases as well as monitoring the effectiveness of disease treatment. Hence, sensitive and accurate detection of proteins in human biospecimens is imperative. However, at present, there is no ideal method available for the detection of proteins in clinical samples, many of which are present at ultralow (less than 1 pM) concentrations and in complicated matrices. Herein, we report an ultrasensitive and selective DNA-assisted CRISPR-Cas12a enhanced fluorescent assay (DACEA) for protein detection with detection limits reaching as low as attomolar concentrations. The high assay sensitivity was accomplished through the combined DNA barcode amplification (by using dual-functionalized AuNPs) and CRISPR analysis, while the high selectivity and high resistance to the matrix effects of our method were accomplished via the formation of protein-antibody sandwich structure and the specific recognition of Cas12a (under the guidance of crRNA) toward the designed target ssDNA. Given its ability to accurately and sensitively detect trace amounts of proteins in complicated matrices, the DACEA protein assay platform pioneered in this work has a potential application in routine protein biomarker testing.
引用
收藏
页码:754 / 762
页数:9
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