597876 CRISPR-Cas12a Mediated Universal Electrochemical Biosensing Platform (Faculty/Industry Candidate)

Thursday, November 19, 2020
Food, Pharmaceutical & Bioengineering Division (15) (PreRecorded+)
Yifan Dai1, Rodrigo A Somoza2, Wei Xu3, Jean F. Welter4, Arnold I. Caplan4 and Chung-Chiun Liu1, (1)Department of Chemical and Biomolecular Engineering, Case Western Reserve University, Cleveland, OH, (2)Biology, Case Western Reserve University, Cleveland, OH, (3)Department of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, (4)Biology, Case Western Reserve University

An accurate, rapid, and cost‐effective biosensor for the quantification of disease biomarkers is vital for the development of early‐diagnostic point‐of‐care systems. The recent discovery of the trans‐cleavage property of CRISPR type V effectors makes CRISPR a potential high‐accuracy bio‐recognition tool. Herein, a CRISPR‐Cas12a (cpf1) based electrochemical biosensor (E‐CRISPR) is demonstrated, which is more cost‐effective and portable than optical‐transduction‐based biosensors. Through optimizing the in vitro trans‐cleavage activity of Cas12a, E‐CRIPSR was used to detect viral nucleic acids, including human papillomavirus 16 (HPV‐16) and parvovirus B19 (PB‐19), with a picomolar sensitivity. An aptamer‐based E‐CRISPR cascade was further designed for the detection of transforming growth factor β1 (TGF‐β1) protein in clinical samples. As demonstrated, E‐CRISPR could enable the development of portable, accurate, and cost‐effective point‐of‐care diagnostic systems.

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See more of this Session: Sensors Enabled by Synthetic Biology
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