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filingDate 2020-03-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7846ab3c09de94dcc2ae5dc4e24ed5b1
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publicationDate 2020-05-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-111172164-A
titleOfInvention A composition and method for arbitrary nucleic acid editing
abstract The present invention discloses a composition and method for any nucleic acid editing. A composition for carrying out targeted cleavage of any nucleic acid, comprising two main components: component A: oligonucleotide probe: the oligonucleotide probe is composed of two parts, one part is complementary to the target substrate, and the other part is complementary to the target substrate. A part has nucleic acid secondary structure; Component B: Endonuclease molecule: The endonuclease molecule can recognize the nucleic acid secondary structure of the oligonucleotide probe to bind to the probe, and can also cut DNA or RNA substrates. In the present invention, the secondary hairpin structure (stem-loop structure) on the oligonucleotide probe can be directly recognized by the endonuclease molecule to form a complex molecule. The probability that the complex molecule collides with the target substrate will be greater than the probability that two independently diffused molecules of the probe and the enzyme collide with the target substrate at the same time, thereby improving the efficiency of gene editing.
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Total number of triples: 601.