High-fidelity detection of DNA combining the CRISPR/Cas9 system and hairpin probe
Methods that enable specific and sensitive detection of DNA are greatly required for high-fidelity sequence measurement and single-nucleotide variations (SNVs) genotyping. The CRISPR (clustered regularly interspaced short palindromic repeats)/Cas systems have provided revolutionary tools for detecti...
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Published in | Biosensors & bioelectronics Vol. 184; p. 113212 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
England
Elsevier B.V
15.07.2021
Elsevier BV |
Subjects | |
Online Access | Get full text |
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Summary: | Methods that enable specific and sensitive detection of DNA are greatly required for high-fidelity sequence measurement and single-nucleotide variations (SNVs) genotyping. The CRISPR (clustered regularly interspaced short palindromic repeats)/Cas systems have provided revolutionary tools for detecting nucleic acids. However, most of the current CRISPR/Cas-based DNA biosensing platforms suffer from inherent off-target effects of Cas proteins and require pre-amplification processes, which compromise the analytical fidelity. In this work, a CRISPR/Cas9-triggered hairpin probe-mediated biosensing method (namely CHP) was used to directly read the original DNA sequences, while effectively neutralizing the off-target effect and achieving high sensitivity. This technique can quantify DNA targets with a limit of detection (LOD) at the attomole level and identify SNVs with allelic fractions as low as 0.01%~0.1%. Moreover, we show that the CHP system is applicable in detecting mutations in serum samples without DNA isolation steps. Collectively, the CHP system is a sensitive and high-fidelity platform, which promises a great potential for providing robust tool for DNA sequence analysis and SNVs genotyping.
•The CHP system is a high-fidelity DNA biosensor combining CRISPR/Cas9 and hairpin probe.•The CHP system can neutralize the off-target effect of CRISPR/Cas9.•The CHP system can quantify DNA at attomole level and identify SNVs at low allelic fraction.•The CHP system can detect mutations in serum samples without DNA isolation steps. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0956-5663 1873-4235 1873-4235 |
DOI: | 10.1016/j.bios.2021.113212 |