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dc.contributor.author정철현-
dc.contributor.author김인산-
dc.contributor.author전용문-
dc.contributor.author이계준-
dc.contributor.author구지영-
dc.contributor.author최유희-
dc.contributor.author장윤수-
dc.contributor.author유지현-
dc.contributor.author정유경-
dc.contributor.author이승환-
dc.contributor.author김진수-
dc.contributor.author이상화-
dc.contributor.author배상수-
dc.date.accessioned2021-06-09T04:20:25Z-
dc.date.available2021-06-09T04:20:25Z-
dc.date.issued2018-07-
dc.identifier.citationVOL 9-2777-11-
dc.identifier.issn2041-1723-
dc.identifier.other51105-
dc.identifier.urihttp://pubs.kist.re.kr/handle/201004/67878-
dc.description.abstractCas12a (also called Cpf1) is a representative type V-A CRISPR effector RNA-guided DNA endonuclease, which provides an alternative to type II CRISPR&#8211-
dc.description.abstractCas9 for genome editing. Previous studies have revealed that Cas12a has unique features distinct from Cas9, but the detailed mechanisms of target searching and DNA cleavage by Cas12a are still unclear. Here, we directly observe this entire process by using single-molecule fluorescence assays to study Cas12a from Acidaminococcus sp. (AsCas12a). We determine that AsCas12a ribonucleoproteins search for their on-target site by a one-dimensional diffusion along elongated DNA molecules and induce cleavage in the two DNA strands in a well-defined order, beginning with the non-target strand. Furthermore, the protospacer-adjacent motif (PAM) for AsCas12a makes only a limited contribution of DNA unwinding during R-loop formation and shows a negligible role in the process of DNA cleavage, in contrast to the Cas9 PAM.-
dc.publisherNature Communications-
dc.subject유전자 가위-
dc.subjectCRISPR-
dc.subjectCas12a-
dc.subjectCpf1-
dc.subjectSingle Molecule FRET-
dc.subjectSingle Molecule Tracking-
dc.subjectMolecular Mechanism-
dc.titleDirect observation of DNA target searching and cleavage by CRISPR-Cas12a-
dc.typeArticle-
dc.relation.page2777-12777-11-
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