Keck Graduate Institute, The Claremont Colleges, Claremont, CA, USA.
Cardea, San Diego, CA, USA.
Nat Biomed Eng. 2021 Jul;5(7):713-725. doi: 10.1038/s41551-021-00706-z. Epub 2021 Apr 5.
Simple and fast methods for the detection of target genes with single-nucleotide specificity could open up genetic research and diagnostics beyond laboratory settings. We recently reported a biosensor for the electronic detection of unamplified target genes using liquid-gated graphene field-effect transistors employing an RNA-guided catalytically deactivated CRISPR-associated protein 9 (Cas9) anchored to a graphene monolayer. Here, using unamplified genomic samples from patients and by measuring multiple types of electrical response, we show that the biosensors can discriminate within one hour between wild-type and homozygous mutant alleles differing by a single nucleotide. We also show that biosensors using a guide RNA-Cas9 orthologue complex targeting genes within the protospacer-adjacent motif discriminated between homozygous and heterozygous DNA samples from patients with sickle cell disease, and that the biosensors can also be used to rapidly screen for guide RNA-Cas9 complexes that maximize gene-targeting efficiency.
简单快速的单核苷酸特异性靶基因检测方法可能会开拓超越实验室环境的遗传研究和诊断领域。我们最近报道了一种生物传感器,用于使用液体门控石墨烯场效应晶体管对未扩增的靶基因进行电子检测,该传感器使用 RNA 引导的催化失活的 CRISPR 相关蛋白 9(Cas9)锚定在石墨烯单层上。在这里,我们使用来自患者的未扩增基因组样本,并通过测量多种类型的电响应,表明生物传感器可以在一个小时内区分野生型和纯合突变等位基因,它们之间仅相差一个核苷酸。我们还表明,针对间隔基序内基因的向导 RNA-Cas9 同系物复合物的生物传感器可以区分来自镰状细胞病患者的纯合和杂合 DNA 样本,并且生物传感器也可用于快速筛选最大限度地提高基因靶向效率的向导 RNA-Cas9 复合物。