Evidence map›Paper›PMID 36778082›Full record

ArticleNature catalysis2022

Principles of target DNA cleavage and the role of Mg2+ in the catalysis of CRISPR-Cas9.

Łukasz Nierzwicki, Kyle W East, Jonas M Binz, Rohaine V Hsu, Mohd Ahsan, Pablo R Arantes, Erin Skeens, Martin Pacesa, Martin Jinek, George P Lisi and 1 more

Abstract read
In one paragraph

Article in Nature catalysis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

39 citing papers in PubMed.

  1. Review
  2. Biophysical characterization ofSensors & diagnostics · 2026
    Article
  3. Article
  4. Review
  5. Controlled dynamic remodeling of the spliceosome active site enables the first step of splicing.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. A Cryptic Binding Pocket Regulates the Metal-Dependent Activity of Cas9.bioRxiv : the preprint server for biology · 2025
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Łukasz NierzwickiDepartment of Bioengineering, University of California Riverside, 900 University Avenue, Riverside, CA 52512, United States.
Kyle W EastDepartment of Molecular Biology, Cell Biology & Biochemistry, Brown University, Providence, RI, United States.
Jonas M BinzDepartment of Biochemistry, University of Zürich, Winterthurerstrasse 190, CH-8057 Zurich, Switzerland.
Rohaine V HsuDepartment of Bioengineering, University of California Riverside, 900 University Avenue, Riverside, CA 52512, United States.
Mohd AhsanDepartment of Bioengineering, University of California Riverside, 900 University Avenue, Riverside, CA 52512, United States.
Pablo R ArantesDepartment of Bioengineering, University of California Riverside, 900 University Avenue, Riverside, CA 52512, United States.
Erin SkeensDepartment of Molecular Biology, Cell Biology & Biochemistry, Brown University, Providence, RI, United States.
Martin PacesaDepartment of Biochemistry, University of Zürich, Winterthurerstrasse 190, CH-8057 Zurich, Switzerland.
Martin JinekDepartment of Biochemistry, University of Zürich, Winterthurerstrasse 190, CH-8057 Zurich, Switzerland.
George P LisiDepartment of Molecular Biology, Cell Biology & Biochemistry, Brown University, Providence, RI, United States.
Giulia PalermoDepartment of Bioengineering, University of California Riverside, 900 University Avenue, Riverside, CA 52512, United States.

Funding

Investigating the metal-dependent function, allostery and inhibition of CRISPR-Cas9R01GM141329 · NIGMS · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI PALERMO, GIULIA · 2021 to 2025
$1.7M
Studies of Allostery between Multi-domain Proteins and Nucleic Acid ComplexesR01GM136815 · NIGMS · YALE UNIVERSITY · PI BATISTA, VICTOR S · 2021 to 2024
$1.4M
NIGMS NIH HHS R01 GM136815NIGMS NIH HHS R01 GM141329
6 · The paper itself

Abstract

At the core of the CRISPR-Cas9 genome-editing technology, the endonuclease Cas9 introduces site-specific breaks in DNA. However, precise mechanistic information to ameliorating Cas9 function is still missing. Here, multi-microsecond molecular dynamics, free-energy and multiscale simulations are combined with solution NMR and DNA cleavage experiments to resolve the catalytic mechanism of target DNA cleavage. We show that the conformation of an active HNH nuclease is tightly dependent on the catalytic Mg

Identifiers

PMID36778082
PMCPMC9909973

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.