Topological barrier to Cas12a activation by circular DNA nanostructures facilitates autocatalysis and transforms DNA/RNA sensing

Control of CRISPR/Cas12a trans -cleavage is crucial for biosensor development. Here, we show that small circular DNA nanostructures which partially match guide RNA sequences only minimally activate Cas12a ribonucleoproteins. However, linearizing these structures restores activation. Building on this...

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Vydáno v:	Nature communications Ročník 15; číslo 1; s. 1818 - 16
Hlavní autoři:	Deng, Fei, Li, Yi, Yang, Biyao, Sang, Rui, Deng, Wei, Kansara, Maya, Lin, Frank, Thavaneswaran, Subotheni, Thomas, David M., Goldys, Ewa M.
Médium:	Journal Article
Jazyk:	angličtina
Vydáno:	London Nature Publishing Group UK 05.03.2024 Nature Publishing Group Nature Portfolio
Témata:	631/208/4041/3196 631/45/147 631/45/603 96/10 Amplification Autocatalysis Biosensors Blood circulation Blood plasma Circular DNA Cleavage Colorimetry CRISPR CRISPR-Cas Systems Deoxyribonucleic acid DNA DNA - genetics DNA, Circular - genetics Gene sequencing gRNA Helicobacter pylori Humanities and Social Sciences multidisciplinary Mutation Nanostructure Nanostructures Nucleic acids Nucleotide sequence Reverse transcription Ribonucleic acid Ribonucleoproteins RNA RNA - genetics RNA, Guide, CRISPR-Cas Systems Room temperature Science Science (multidisciplinary) Severe acute respiratory syndrome coronavirus 2 Single-nucleotide polymorphism
ISSN:	2041-1723, 2041-1723
On-line přístup:	Získat plný text
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Shrnutí:	Control of CRISPR/Cas12a trans -cleavage is crucial for biosensor development. Here, we show that small circular DNA nanostructures which partially match guide RNA sequences only minimally activate Cas12a ribonucleoproteins. However, linearizing these structures restores activation. Building on this finding, an Autocatalytic Cas12a Circular DNA Amplification Reaction (AutoCAR) system is established which allows a single nucleic acid target to activate multiple ribonucleoproteins, and greatly increases the achievable reporter cleavage rates per target. A rate-equation-based model explains the observed near-exponential rate trends. Autocatalysis is also sustained with DNA nanostructures modified with fluorophore-quencher pairs achieving 1 aM level (<1 copy/μL) DNA detection (10 6 times improvement), without additional amplification, within 15 min, at room temperature. The detection range is tuneable, spanning 3 to 11 orders of magnitude. We demonstrate 1 aM level detection of SNP mutations in circulating tumor DNA from blood plasma, genomic DNA ( H. Pylori ) and RNA (SARS-CoV-2) without reverse transcription as well as colorimetric lateral flow tests of cancer mutations with ~100 aM sensitivity. The authors find that small circular DNA nanostructures which partially match gRNA sequences only minimally activate Cas12a. They report AutoCAR (Autocatalytic Cas12a Circular DNA Amplification Reaction) which allows a single nucleic acid target to activate multiple ribonucleoproteins, and increases reporter cleavage rates.
Bibliografie:	ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23
ISSN:	2041-1723 2041-1723
DOI:	10.1038/s41467-024-46001-8