Department of Biomedical Engineering, The Chinese University of Hong Kong, Hong Kong SAR, China.
Department of Biomedical Engineering, The Chinese University of Hong Kong, Hong Kong SAR, China; Department of Chemical and Biological Engineering, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong SAR, China.
Biosens Bioelectron. 2024 Dec 15;266:116695. doi: 10.1016/j.bios.2024.116695. Epub 2024 Aug 30.
Scalable electronic devices that can detect target biomarkers from clinical samples hold great promise for point-of-care nucleic acid testing, but still cannot achieve the detection of target molecules at an attomolar range within a short timeframe (<1 h). To tackle this daunting challenge, we integrate graphene field-effect transistors (GFETs) with exponential target recycling and hybridization chain reaction (TRHCR) to detect oligonucleotides (using miRNA as a model disease biomarker), achieving a detection limit of 100 aM and reducing the sensing time by 30-fold, from 15 h to 30 min. In contrast to traditional linear TRHCR, our exponential TRHCR enables the target miRNA to initiate an autocatalytic system with exponential kinetics, significantly accelerating the reaction speed. The resulting reaction products, long-necked double-stranded polymers with a negative charge, are effectively detected by the GFET through chemical gating, leading to a shift in the Dirac voltage. Therefore, by monitoring the magnitude of this voltage shift, the target miRNA is quantified with high sensitivity. Consequently, our approach successfully detects 22-mer miRNA at concentrations as low as 100 aM in human serum samples, achieving the desired short timeframe of 30 min, which is congruent with point-of-care testing, and demonstrates superior specificity against single-base mismatched interfering oligonucleotides.
可扩展的电子设备能够从临床样本中检测目标生物标志物,这对即时核酸检测具有重要意义,但它们仍然无法在短时间内(<1 小时)达到检测目标分子纳摩尔级别的精度。为了解决这一艰巨的挑战,我们将石墨烯场效应晶体管(GFET)与指数靶标循环和杂交链式反应(TRHCR)相结合,用于检测寡核苷酸(以 miRNA 作为疾病生物标志物模型),检测限达到 100 aM,并将检测时间缩短 30 倍,从 15 小时缩短至 30 分钟。与传统的线性 TRHCR 相比,我们的指数 TRHCR 使靶标 miRNA 能够启动具有指数动力学的自动催化系统,显著加快了反应速度。所得的反应产物是带有负电荷的长颈双链聚合物,通过化学门控可被 GFET 有效检测,导致 Dirac 电压发生偏移。因此,通过监测该电压偏移的幅度,可以实现对目标 miRNA 的高灵敏度定量。因此,我们的方法成功地在人类血清样本中检测到浓度低至 100 aM 的 22 -mer miRNA,实现了 30 分钟的理想短时间检测窗口,符合即时检测的要求,并对单碱基错配的干扰寡核苷酸具有优异的特异性。