Abstract

Abstract Here, we report a novel DNAzyme-based paper sensor to detect RNase H activity. The paper sensor was constructed by dropping a DNA/RNA duplex containing a guanine-rich DNA strand whose bases are complementary to the RNA strand, onto a Hybond™-N+ membrane. In the presence of RNase H, the RNA strand of the G-DNA/Cp-RNA duplex was hydrolyzed, which released G-DNA sequences to form a G-quadruplex/hemin HRP-mimetic DNAzyme after hemin was added to the membrane surface. Then, the formed DNAzymes catalyzed the oxidation of the TMB substrate, which changed the color of the paper sensor, thus realizing RNase H detection. Under the optimized conditions, a linear concentration range of 5∼ 60 U/mL with a limit of detection of 1.2 U/mL for RNase H was obtained. The paper sensor was also used to detect RNase H in complex biosamples containing cell lysates.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.