Cargando…
Highly active CRISPR-adaptation proteins revealed by a robust enrichment technology
Natural prokaryotic defense via the CRISPR–Cas system requires spacer integration into the CRISPR array in a process called adaptation. To search for adaptation proteins with enhanced capabilities, we established a robust perpetual DNA packaging and transfer (PeDPaT) system that uses a strain of T7...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415146/ https://www.ncbi.nlm.nih.gov/pubmed/37326009 http://dx.doi.org/10.1093/nar/gkad510 |
_version_ | 1785087457958559744 |
---|---|
author | Yosef, Ido Mahata, Tridib Goren, Moran G Degany, Or J Ben-Shem, Adam Qimron, Udi |
author_facet | Yosef, Ido Mahata, Tridib Goren, Moran G Degany, Or J Ben-Shem, Adam Qimron, Udi |
author_sort | Yosef, Ido |
collection | PubMed |
description | Natural prokaryotic defense via the CRISPR–Cas system requires spacer integration into the CRISPR array in a process called adaptation. To search for adaptation proteins with enhanced capabilities, we established a robust perpetual DNA packaging and transfer (PeDPaT) system that uses a strain of T7 phage to package plasmids and transfer them without killing the host, and then uses a different strain of T7 phage to repeat the cycle. We used PeDPaT to identify better adaptation proteins—Cas1 and Cas2—by enriching mutants that provide higher adaptation efficiency. We identified two mutant Cas1 proteins that show up to 10-fold enhanced adaptation in vivo. In vitro, one mutant has higher integration and DNA binding activities, and another has a higher disintegration activity compared to the wild-type Cas1. Lastly, we showed that their specificity for selecting a protospacer adjacent motif is decreased. The PeDPaT technology may be used for many robust screens requiring efficient and effortless DNA transduction. |
format | Online Article Text |
id | pubmed-10415146 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-104151462023-08-12 Highly active CRISPR-adaptation proteins revealed by a robust enrichment technology Yosef, Ido Mahata, Tridib Goren, Moran G Degany, Or J Ben-Shem, Adam Qimron, Udi Nucleic Acids Res Nucleic Acid Enzymes Natural prokaryotic defense via the CRISPR–Cas system requires spacer integration into the CRISPR array in a process called adaptation. To search for adaptation proteins with enhanced capabilities, we established a robust perpetual DNA packaging and transfer (PeDPaT) system that uses a strain of T7 phage to package plasmids and transfer them without killing the host, and then uses a different strain of T7 phage to repeat the cycle. We used PeDPaT to identify better adaptation proteins—Cas1 and Cas2—by enriching mutants that provide higher adaptation efficiency. We identified two mutant Cas1 proteins that show up to 10-fold enhanced adaptation in vivo. In vitro, one mutant has higher integration and DNA binding activities, and another has a higher disintegration activity compared to the wild-type Cas1. Lastly, we showed that their specificity for selecting a protospacer adjacent motif is decreased. The PeDPaT technology may be used for many robust screens requiring efficient and effortless DNA transduction. Oxford University Press 2023-06-16 /pmc/articles/PMC10415146/ /pubmed/37326009 http://dx.doi.org/10.1093/nar/gkad510 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Nucleic Acid Enzymes Yosef, Ido Mahata, Tridib Goren, Moran G Degany, Or J Ben-Shem, Adam Qimron, Udi Highly active CRISPR-adaptation proteins revealed by a robust enrichment technology |
title | Highly active CRISPR-adaptation proteins revealed by a robust enrichment technology |
title_full | Highly active CRISPR-adaptation proteins revealed by a robust enrichment technology |
title_fullStr | Highly active CRISPR-adaptation proteins revealed by a robust enrichment technology |
title_full_unstemmed | Highly active CRISPR-adaptation proteins revealed by a robust enrichment technology |
title_short | Highly active CRISPR-adaptation proteins revealed by a robust enrichment technology |
title_sort | highly active crispr-adaptation proteins revealed by a robust enrichment technology |
topic | Nucleic Acid Enzymes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415146/ https://www.ncbi.nlm.nih.gov/pubmed/37326009 http://dx.doi.org/10.1093/nar/gkad510 |
work_keys_str_mv | AT yosefido highlyactivecrispradaptationproteinsrevealedbyarobustenrichmenttechnology AT mahatatridib highlyactivecrispradaptationproteinsrevealedbyarobustenrichmenttechnology AT gorenmorang highlyactivecrispradaptationproteinsrevealedbyarobustenrichmenttechnology AT deganyorj highlyactivecrispradaptationproteinsrevealedbyarobustenrichmenttechnology AT benshemadam highlyactivecrispradaptationproteinsrevealedbyarobustenrichmenttechnology AT qimronudi highlyactivecrispradaptationproteinsrevealedbyarobustenrichmenttechnology |