CRISPR-Powered Aptasensor for Diagnostics of Alzheimer's Disease

被引:5
|
作者
Jia, Zhengyang [1 ]
Maghaydah, Yazeed [2 ]
Zdanys, Kristina [3 ]
Kuchel, George A. [2 ]
Diniz, Breno Satler [2 ,3 ]
Liu, Changchun [1 ]
机构
[1] Univ Connecticut, Hlth Ctr, Dept Biomed Engn, Farmington, CT 06030 USA
[2] Univ Connecticut, Ctr Hlth, Ctr Aging, Farmington, CT 06030 USA
[3] Univ Connecticut, Dept Psychiat, Div Geriatr Psychiat & Behav Hlth, Hlth Ctr, Farmington, CT 06030 USA
关键词
Alzheimer'sdisease diagnosis; amyloid beta biomarkerquantification; CRISPR-Cas12a detection; aptasensor; fluorescence detection; CEREBROSPINAL-FLUID; BIOMARKERS; OLIGOMERS; CSF; AGGREGATION; RATIO;
D O I
10.1021/acssensors.3c02167
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Alzheimer's disease (AD) is a neurodegenerative disorder and the most common cause of dementia, characterized by the accumulation of amyloid beta (A beta) peptides in the brain. Here, we present a simple, rapid, and affordable CRISPR-powered aptasensor for the quantitative detection of A beta 40 and A beta 42 biomarkers in cerebrospinal fluid (CSF) samples, enabling early and accurate diagnostics of AD patients. The aptasensor couples the high specificity of aptamers for A beta biomarkers with CRISPR-Cas12a-based fluorescence detection. The CRISPR-powered aptasensor enables us to detect A beta 40 and A beta 42 in CSF samples within 60 min, achieving a detection sensitivity of 1 pg/mL and 0.1 pg/mL, respectively. To validate its clinical utility, we quantitatively detected A beta 40 and A beta 42 biomarkers in clinical CSF samples. Furthermore, by combining CSF A beta 42 levels with the c-(A beta 42)/c-(A beta 40) ratio, we achieved an accurate diagnostic classification of AD patients and healthy individuals, showing superior performance over the conventional ELISA method. We believe that our innovative aptasensor approach holds promise for the early diagnostic classification of AD patients.
引用
收藏
页码:398 / 405
页数:8
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