Mujica Michael López, Tamborelli Alejandro, Castellaro Andrés, Barcudi Danilo, Rubianes María D, Rodríguez Marcela C, Saka Héctor A, Bocco José L, Dalmasso Pablo R, Rivas Gustavo A
INFIQC, CONICET-UNC, Departamento de Fisicoquímica, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Ciudad Universitaria, 5000, Córdoba, Argentina.
CIQA, CONICET, Departamento de Ingeniería Química, Facultad Regional Córdoba, Universidad Tecnológica Nacional, Maestro López esq. Cruz Roja Argentina, 5016, Córdoba, Argentina.
Biosens Bioelectron X. 2022 Dec;12:100222. doi: 10.1016/j.biosx.2022.100222. Epub 2022 Sep 13.
We report two novel genosensors for the quantification of SARS-CoV-2 nucleic acid using glassy carbon electrodes modified with a biocapture nanoplatform made of multi-walled carbon nanotubes (MWCNTs) non-covalently functionalized with avidin (Av) as a support of the biotinylated-DNA probes. One of the genosensors was based on impedimetric transduction offering a non-labelled and non-amplified detection of SARS-CoV-2 nucleic acid through the increment of [Fe(CN)] charge transfer resistance. This biosensor presented an excellent analytical performance, with a linear range of 1.0 × 10 M - 1.0 × 10 M, a sensitivity of (5.8 ± 0.6) x 10 Ω M (r = 0.994), detection and quantification limits of 0.33 aM and 1.0 aM, respectively; and reproducibilities of 5.4% for 1.0 × 10 M target using the same MWCNTs-Av-bDNAp nanoplatform, and 6.9% for 1.0 × 10 M target using 3 different nanoplatforms. The other genosensor was based on a sandwich hybridization scheme and amperometric transduction using the streptavidin(Strep)-biotinylated horseradish peroxidase (bHRP)/hydrogen peroxide/hydroquinone (HQ) system. This genosensor allowed an extremely sensitive quantification of the SARS-CoV-2 nucleic acid, with a linear range of 1.0 × 10 M - 1.0 × 10 M, detection limit at zM level, and a reproducibility of 11% for genosensors prepared with the same MWCNTs-Av-bDNAp nanoplatform. As a proof-of-concept, and considering the extremely high sensitivity, the genosensor was challenged with highly diluted samples obtained from SARS-CoV-2 RNA PCR amplification.
我们报道了两种新型基因传感器,用于定量检测严重急性呼吸综合征冠状病毒2(SARS-CoV-2)核酸。该传感器采用玻碳电极,电极上修饰有生物捕获纳米平台,该平台由多壁碳纳米管(MWCNT)制成,并用抗生物素蛋白(Av)进行非共价功能化,以支持生物素化DNA探针。其中一种基因传感器基于阻抗传感,通过[Fe(CN)]电荷转移电阻的增加,对SARS-CoV-2核酸进行无标记、无扩增检测。该生物传感器具有出色的分析性能,线性范围为1.0×10⁻¹² M - 1.0×10⁻⁶ M,灵敏度为(5.8±0.6)×10⁴ Ω M⁻¹(r = 0.994),检测限和定量限分别为0.33 aM和1.0 aM;使用相同的MWCNTs-Av-bDNAp纳米平台对1.0×10⁻⁸ M靶标的重现性为5.4%,使用3种不同纳米平台对1.0×10⁻¹⁰ M靶标的重现性为6.9%。另一种基因传感器基于夹心杂交方案和安培传感,使用链霉亲和素(Strep)-生物素化辣根过氧化物酶(bHRP)/过氧化氢/对苯二酚(HQ)系统。该基因传感器能够对SARS-CoV-2核酸进行极其灵敏的定量,线性范围为1.0×10⁻¹² M - 1.0×10⁻⁶ M,检测限达到zeptomolar水平,使用相同的MWCNTs-Av-bDNAp纳米平台制备的基因传感器的重现性为11%。作为概念验证,并考虑到其极高的灵敏度,该基因传感器用从SARS-CoV-2 RNA PCR扩增获得的高度稀释样品进行测试。