Yee Bong Jing, Ali Nurul Ajeerah, Mohd-Naim Noor Faizah Binti, Ahmed Minhaz Uddin
Biosensors and Nanobiotechnology Laboratory, Integrated Science Building, Faculty of Science, Universiti Brunei Darussalam, Gadong 1410, Brunei Darussalam.
PAPRSB Institute of Health Science, Universiti Brunei Darussalam, Gadong 1410, Brunei Darussalam.
Chem Bio Eng. 2024 Jan 9;1(4):330-339. doi: 10.1021/cbe.3c00112. eCollection 2024 May 23.
Rapid and reliable molecular diagnostics employing target nucleic acids and small biomarkers are crucial strategies required for the precise detection of numerous diseases. Although diagnoses based on nucleic acid recognition are some of the most efficient and precise procedures, these tests often require expensive equipment and skilled professionals. Recent advancements in diagnostic innovations, particularly those based on clustered regularly interspaced short palindromic repeats (CRISPR), aim to provide thorough screening at homes, in clinics, and in the field. In comparison to traditional molecular techniques like PCR, CRISPR/Cas-based detection, using the single-stranded nucleic acid trans-cleavage abilities of Cas12 or Cas13, shows significant potential as a molecular diagnostic tool. It offers benefits such as attomolar-level sensitivity, single-base precision, and rapid turnover rates. Both Cas enzymes demonstrate exceptional specificity and sensitivity, holding substantial promise in disease diagnostics and beyond. Consequently, various amplification-free CRISPR/Cas-based detection methods have emerged, aiming to maintain sensitivity despite the absence of pre-amplification. This allows for the detection of non-nucleic acid targets and facilitates integration into point-of-care settings. This Review highlights current advances in amplification-free CRISPR/Cas detection systems in disease diagnostics and investigates their utility in point-of-care settings. Furthermore, the mechanisms of alternative CRISPR-based amplification-free detection of other small molecules, aside from nucleic acids, for disease diagnosis will also be briefly discussed.
采用靶核酸和小生物标志物的快速可靠分子诊断方法,是精确检测多种疾病所需的关键策略。尽管基于核酸识别的诊断方法是一些最有效、最精确的程序,但这些检测通常需要昂贵的设备和技术熟练的专业人员。诊断创新的最新进展,特别是基于成簇规律间隔短回文重复序列(CRISPR)的进展,旨在在家中、诊所和现场进行全面筛查。与聚合酶链反应(PCR)等传统分子技术相比,基于CRISPR/Cas的检测利用Cas12或Cas13的单链核酸反式切割能力,作为一种分子诊断工具显示出巨大潜力。它具有诸如阿托摩尔级灵敏度、单碱基精度和快速周转速度等优点。两种Cas酶都表现出卓越的特异性和灵敏度,在疾病诊断及其他领域具有巨大前景。因此,出现了各种基于CRISPR/Cas的无扩增检测方法,旨在即使在没有预扩增的情况下也能保持灵敏度。这使得能够检测非核酸靶标,并便于整合到即时检测环境中。本综述重点介绍了无扩增CRISPR/Cas检测系统在疾病诊断方面的当前进展,并研究了它们在即时检测环境中的实用性。此外,还将简要讨论基于CRISPR的其他小分子(除核酸外)用于疾病诊断的无扩增检测机制。