| Literature DB >> 27990727 |
Yan Du1, Arti Pothukuchy1, Jimmy D Gollihar1, Armin Nourani1, Bingling Li2, Andrew D Ellington1.
Abstract
The detection of nucleic acid biomarkers for point-of-care (POC) diagnostics is currently limited by technical complexity, cost, and time constraints. To overcome these shortcomings, we have combined loop-mediated isothermal amplification (LAMP), programmable toehold-mediated strand-exchange signal transduction, and standard pregnancy test strips. The incorporation of an engineered hCG-SNAP fusion reporter protein (human chorionic gonadotropin-O6 -alkylguanine-DNA alkyltransferase) led to LAMP-to-hCG signal transduction on low-cost, commercially available pregnancy test strips. Our assay reliably detected as few as 20 copies of Ebola virus templates in both human serum and saliva and could be adapted to distinguish a common melanoma-associated SNP allele (BRAF V600E) from the wild-type sequence. The methods described are completely generalizable to many nucleic acid biomarkers, and could be adapted to provide POC diagnostics for a range of pathogens.Entities:
Keywords: SNAP protein; human chorionic gonadotropin; loop-mediated isothermal amplification (LAMP); nucleic acid amplification; pregnancy test strips
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Year: 2016 PMID: 27990727 PMCID: PMC5240841 DOI: 10.1002/anie.201609108
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336