| Literature DB >> 33820980 |
Sarah Balderston1,2, Jeffrey J Taulbee3, Elizabeth Celaya2, Kandace Fung1, Amanda Jiao2, Kasey Smith1, Reza Hajian1,2, Giedrius Gasiunas4,5, Simonas Kutanovas4, Daehwan Kim6, Jonathan Parkinson2, Kenneth Dickerson2, Juan-José Ripoll2, Regis Peytavi2, Hsiang-Wei Lu1,2, Francie Barron2, Brett R Goldsmith2, Philip G Collins3, Irina M Conboy6, Virginijus Siksnys4,5, Kiana Aran7,8,9.
Abstract
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.Entities:
Year: 2021 PMID: 33820980 DOI: 10.1038/s41551-021-00706-z
Source DB: PubMed Journal: Nat Biomed Eng ISSN: 2157-846X Impact factor: 25.671