Unknown

Dataset Information

0

Integrated Micropillar Polydimethylsiloxane Accurate CRISPR Detection System for Viral DNA Sensing.


ABSTRACT: A fully Integrated Micropillar Polydimethylsiloxane Accurate CRISPR deTection (IMPACT) system is developed for viral DNA detection. This powerful system is patterned with high-aspect-ratio micropillars to enhance reporter probe binding. After surface modification and probe immobilization, the CRISPR-Cas12a/crRNA complex is injected into the fully enclosed microchannel. With the presence of a double-stranded DNA target, the CRISPR enzyme is activated and denatures the single-stranded DNA reporters from the micropillars. This collateral cleavage releases fluorescence reporters into the assay, and the intensity is linearly proportional to the target DNA concentration ranging from 0.1 to 10 nM. Importantly, this system does not rely on the traditional dye-quencher-labeled probe, thus reducing the fluorescence background presented in the assay. Furthermore, our one-step detection protocol is performed on-chip at isothermal conditions (37 °C) without using complicated and time-consuming off-chip probe hybridization and denaturation. This miniaturized and fully packed IMPACT chip demonstrates sensitive and accurate DNA detection within 120 min and paves ways to the next-generation point-of-care diagnostics, responding to emerging and deadly pathogen outbreaks.

SUBMITTER: Hass KN 

PROVIDER: S-EPMC7594154 | biostudies-literature | 2020 Oct

REPOSITORIES: biostudies-literature

altmetric image

Publications

Integrated Micropillar Polydimethylsiloxane Accurate CRISPR Detection System for Viral DNA Sensing.

Hass Kenneth N KN   Bao Mengdi M   He Qian Q   Liu Li L   He Jiacheng J   Park Myeongkee M   Qin Peiwu P   Du Ke K  

ACS omega 20201013 42


A fully Integrated Micropillar Polydimethylsiloxane Accurate CRISPR deTection (IMPACT) system is developed for viral DNA detection. This powerful system is patterned with high-aspect-ratio micropillars to enhance reporter probe binding. After surface modification and probe immobilization, the CRISPR-Cas12a/crRNA complex is injected into the fully enclosed microchannel. With the presence of a double-stranded DNA target, the CRISPR enzyme is activated and denatures the single-stranded DNA reporter  ...[more]

Similar Datasets

| S-EPMC8301860 | biostudies-literature
| S-EPMC9070391 | biostudies-literature
| S-EPMC3829920 | biostudies-other
| S-EPMC7191753 | biostudies-literature
| S-EPMC9396441 | biostudies-literature
| S-EPMC4318258 | biostudies-literature
| S-EPMC5717174 | biostudies-literature
| S-EPMC7553042 | biostudies-literature
| S-EPMC10522547 | biostudies-literature
| S-EPMC10796118 | biostudies-literature