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<titleInfo><title>RNA targeting unleashes indiscriminate nuclease activity of CRISPR–Cas12a2</title></titleInfo>


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<name type="personal">
  <namePart type="given">Jack Peter Kelly</namePart>
  <namePart type="family">Bravo</namePart>
  <role><roleTerm type="text">author</roleTerm> </role><identifier type="local">96aecfa5-8931-11ee-af30-aa6a5d6eee0e</identifier><description xsi:type="identifierDefinition" type="orcid">0000-0003-0456-0753</description></name>
<name type="personal">
  <namePart type="given">Thomson</namePart>
  <namePart type="family">Hallmark</namePart>
  <role><roleTerm type="text">author</roleTerm> </role></name>
<name type="personal">
  <namePart type="given">Bronson</namePart>
  <namePart type="family">Naegle</namePart>
  <role><roleTerm type="text">author</roleTerm> </role></name>
<name type="personal">
  <namePart type="given">Chase L.</namePart>
  <namePart type="family">Beisel</namePart>
  <role><roleTerm type="text">author</roleTerm> </role></name>
<name type="personal">
  <namePart type="given">Ryan N.</namePart>
  <namePart type="family">Jackson</namePart>
  <role><roleTerm type="text">author</roleTerm> </role></name>
<name type="personal">
  <namePart type="given">David W.</namePart>
  <namePart type="family">Taylor</namePart>
  <role><roleTerm type="text">author</roleTerm> </role></name>














<abstract lang="eng">Cas12a2 is a CRISPR-associated nuclease that performs RNA-guided, sequence-nonspecific degradation of single-stranded RNA, single-stranded DNA and double-stranded DNA following recognition of a complementary RNA target, culminating in abortive infection&lt;jats:sup&gt;1&lt;/jats:sup&gt;. Here we report structures of Cas12a2 in binary, ternary and quaternary complexes to reveal a complete activation pathway. Our structures reveal that Cas12a2 is autoinhibited until binding a cognate RNA target, which exposes the RuvC active site within a large, positively charged cleft. Double-stranded DNA substrates are captured through duplex distortion and local melting, stabilized by pairs of ‘aromatic clamp’ residues that are crucial for double-stranded DNA degradation and in vivo immune system function. Our work provides a structural basis for this mechanism of abortive infection to achieve population-level immunity, which can be leveraged to create rational mutants that degrade a spectrum of collateral substrates.</abstract>

<originInfo><publisher>Springer Nature</publisher><dateIssued encoding="w3cdtf">2023</dateIssued>
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<language><languageTerm authority="iso639-2b" type="code">eng</languageTerm>
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<relatedItem type="host"><titleInfo><title>Nature</title></titleInfo>
  <identifier type="issn">0028-0836</identifier>
  <identifier type="eIssn">1476-4687</identifier>
  <identifier type="MEDLINE">36599980</identifier><identifier type="doi">10.1038/s41586-022-05560-w</identifier>
<part><detail type="volume"><number>613</number></detail><detail type="issue"><number>7944</number></detail><extent unit="pages">582-587</extent>
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<short>J.P.K. Bravo, T. Hallmark, B. Naegle, C.L. Beisel, R.N. Jackson, D.W. Taylor, Nature 613 (2023) 582–587.</short>
<chicago>Bravo, Jack Peter Kelly, Thomson Hallmark, Bronson Naegle, Chase L. Beisel, Ryan N. Jackson, and David W. Taylor. “RNA Targeting Unleashes Indiscriminate Nuclease Activity of CRISPR–Cas12a2.” &lt;i&gt;Nature&lt;/i&gt;. Springer Nature, 2023. &lt;a href=&quot;https://doi.org/10.1038/s41586-022-05560-w&quot;&gt;https://doi.org/10.1038/s41586-022-05560-w&lt;/a&gt;.</chicago>
<ama>Bravo JPK, Hallmark T, Naegle B, Beisel CL, Jackson RN, Taylor DW. RNA targeting unleashes indiscriminate nuclease activity of CRISPR–Cas12a2. &lt;i&gt;Nature&lt;/i&gt;. 2023;613(7944):582-587. doi:&lt;a href=&quot;https://doi.org/10.1038/s41586-022-05560-w&quot;&gt;10.1038/s41586-022-05560-w&lt;/a&gt;</ama>
<ieee>J. P. K. Bravo, T. Hallmark, B. Naegle, C. L. Beisel, R. N. Jackson, and D. W. Taylor, “RNA targeting unleashes indiscriminate nuclease activity of CRISPR–Cas12a2,” &lt;i&gt;Nature&lt;/i&gt;, vol. 613, no. 7944. Springer Nature, pp. 582–587, 2023.</ieee>
<ista>Bravo JPK, Hallmark T, Naegle B, Beisel CL, Jackson RN, Taylor DW. 2023. RNA targeting unleashes indiscriminate nuclease activity of CRISPR–Cas12a2. Nature. 613(7944), 582–587.</ista>
<mla>Bravo, Jack Peter Kelly, et al. “RNA Targeting Unleashes Indiscriminate Nuclease Activity of CRISPR–Cas12a2.” &lt;i&gt;Nature&lt;/i&gt;, vol. 613, no. 7944, Springer Nature, 2023, pp. 582–87, doi:&lt;a href=&quot;https://doi.org/10.1038/s41586-022-05560-w&quot;&gt;10.1038/s41586-022-05560-w&lt;/a&gt;.</mla>
<apa>Bravo, J. P. K., Hallmark, T., Naegle, B., Beisel, C. L., Jackson, R. N., &amp;#38; Taylor, D. W. (2023). RNA targeting unleashes indiscriminate nuclease activity of CRISPR–Cas12a2. &lt;i&gt;Nature&lt;/i&gt;. Springer Nature. &lt;a href=&quot;https://doi.org/10.1038/s41586-022-05560-w&quot;&gt;https://doi.org/10.1038/s41586-022-05560-w&lt;/a&gt;</apa>
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