Results 11 to 20 of about 7,205 (191)

Characterization of a thermostable Cas12a ortholog

open access: yesCell Insight, 2023
CRISPR-Cas12a has been used for genome editing and molecular diagnosis. The well-studied Cas12a orthologs have a T-rich PAM and are usually categorized as non-thermally stable enzymes.
Jing Wu   +8 more
doaj   +3 more sources

Programmable RNA detection with CRISPR-Cas12a

open access: yesNature Communications, 2023
Cas12a, a CRISPR-associated protein complex, has an inherent ability to cleave DNA substrates and is utilized in diagnostic tools to identify DNA molecules. We demonstrate that multiple orthologs of Cas12a activate trans-cleavage in the presence of split
Santosh R. Rananaware   +8 more
doaj   +5 more sources

Recent advances of Cas12a applications in bacteria [PDF]

open access: yesApplied Microbiology and Biotechnology, 2021
Abstract Clustered regularly interspaced short palindromic repeats (CRISPR)-mediated genome engineering and related technologies have revolutionized biotechnology over the last decade by enhancing the efficiency of sophisticated biological systems.
Meliawati Meliawati   +2 more
openaire   +2 more sources

Broad-spectrum enzymatic inhibition of CRISPR-Cas12a [PDF]

open access: yesNature Structural & Molecular Biology, 2019
Cas12a is a bacterial RNA-guided nuclease used widely for genome editing and, more recently, as a molecular diagnostic. In bacteria, Cas12a enzymes can be inhibited by bacteriophage-derived proteins, anti-CRISPRs (Acrs), to thwart clustered regularly interspaced short palindromic repeat (CRISPR) adaptive immune systems.
Gavin J. Knott   +6 more
openaire   +4 more sources

Aptamer-Linked CRISPR/Cas12a-Based Immunoassay

open access: yesAnalytical Chemistry, 2021
The clustered regularly interspaced short palindromic repeat (CRISPR)/Cas system has shown great promising applications in the area of nucleic acid biosensing. However, because of the dearth of versatile signal transduction strategies, this system is usually compromised to low versatility, moderate sensitivity, and complex operation for non-nucleic ...
Hui Li   +5 more
openaire   +3 more sources

Application of CRISPR-Cas12a temperature sensitivity for improved genome editing in rice, maize, and Arabidopsis

open access: yesBMC Biology, 2019
Background CRISPR-Cas12a (formerly Cpf1) is an RNA-guided endonuclease with distinct features that have expanded genome editing capabilities. Cas12a-mediated genome editing is temperature sensitive in plants, but a lack of a comprehensive understanding ...
Aimee A. Malzahn   +15 more
doaj   +1 more source

Sensitive Detection of KRAS Mutations by Clustered Regularly Interspaced Short Palindromic Repeats

open access: yesDiagnostics, 2021
Kirsten rat sarcoma viral oncogene (KRAS) is the isoform most frequently mutated in human tumors. Testing for activating KRAS mutations has important implications for diagnosis and the personalized medicine of cancers.
Huifen Zhou   +3 more
doaj   +1 more source

Establishment and application of a CRISPR-Cas12a-based RPA-LFS and fluorescence for the detection of Trichomonas vaginalis

open access: yesParasites & Vectors, 2022
Background Infection with Trichomonas vaginalis can lead to cervicitis, urethritis, pelvic inflammatory disease, prostatitis and perinatal complications and increased risk of HIV transmission.
Shan Li   +12 more
doaj   +1 more source

Efficient Targeted Mutagenesis Mediated by CRISPR-Cas12a Ribonucleoprotein Complexes in Maize

open access: yesFrontiers in Genome Editing, 2021
Recent advances in the development of CRISPR-Cas genome editing technologies have made it possible to perform targeted mutagenesis and precise gene replacement in crop plants. CRISPR-Cas9 and CRISPR-Cas12a are two main types of widely used genome editing
Shujie Dong   +16 more
doaj   +1 more source

Improved genome editing by an engineered CRISPR-Cas12a

open access: yesNucleic Acids Research, 2022
Abstract CRISPR-Cas12a is an RNA-guided, programmable genome editing enzyme found within bacterial adaptive immune pathways. Unlike CRISPR-Cas9, Cas12a uses only a single catalytic site to both cleave target double-stranded DNA (dsDNA) (cis-activity) and indiscriminately degrade single-stranded DNA (ssDNA) (trans-activity).
Enbo Ma   +9 more
openaire   +4 more sources

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