Functional nucleic acid biosensors utilizing rolling circle amplification

被引:81
作者
Bialy, Roger M. [1 ]
Mainguy, Alexa [1 ]
Li, Yingfu [1 ,2 ]
Brennan, John D. [1 ]
机构
[1] McMaster Univ, Biointerfaces Inst, 1280 Main St West, Hamilton, ON L8S 4O3, Canada
[2] McMaster Univ, Dept Biochem & Biomed Sci, 1280 Main St West, Hamilton, ON L8S 4K1, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院; 加拿大创新基金会;
关键词
MEDIATED ISOTHERMAL AMPLIFICATION; CASCADE SIGNAL AMPLIFICATION; QUARTZ-CRYSTAL MICROBALANCE; SURFACE-PLASMON RESONANCE; OF-CARE DIAGNOSTICS; IN-VITRO SELECTION; ULTRASENSITIVE ELECTROCHEMICAL DETECTION; STRAND-DISPLACEMENT AMPLIFICATION; DNAZYME FEEDBACK AMPLIFICATION; APTAMERIC RECOGNITION SYSTEM;
D O I
10.1039/d2cs00613h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Functional nucleic acids (FNAs), including DNA aptamers and DNAzymes, are finding increasing use as molecular recognition elements for point-of-care (POC) assays and sensors. An ongoing challenge in the development of FNA-based POC sensors is the ability to achieve detection of low levels of analyte without compromising assay time and ease of use. Rolling circle amplification (RCA) is a leading nucleic acid (NA) isothermal amplification method which can be coupled with FNAs for the ultrasensitive detection of non-NA targets. Herein we examine the key considerations required when designing FNA-coupled biosensors utilizing RCA. Specifically, we describe methods for using FNAs as inputs to regulate RCA, various modes of RCA amplification, and methods to detect the output of the RCA reaction, along with how these can be combined to allow detection of non-NA targets. Recent progress on development of portable optical and electrochemical POC devices that incorporate RCA is then described, followed by a summary of key challenges and opportunities in the field.
引用
收藏
页码:9009 / 9067
页数:59
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