Evidence map›Paper›PMID 40650969›Full record

ArticleNucleic acids research2025

Structural and mechanistic insights into the sequential dsDNA cleavage by SpCas12f1.

Julene Madariaga-Marcos, Marius Baltramonaitis, Selgar Henkel-Heinecke, Dominik J Kauert, Patrick Irmisch, Greta Bigelyte-Stankeviciene, Arunas Silanskas, Tautvydas Karvelis, Virginijus Siksnys, Giedrius Sasnauskas and 1 more

Abstract read
In one paragraph

Article in Nucleic acids research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Stepwise DNA unwinding gates TnpB genome-editing activity.bioRxiv : the preprint server for biology · 2026
    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.

Julene Madariaga-MarcosPeter Debye Institute for Soft Matter Physics, Universität Leipzig, Leipzig 04103, Germany.
Marius BaltramonaitisInstitute of Biotechnology, Vilnius University Life Sciences Center, Vilnius 10257, Lithuania.
Selgar Henkel-HeineckePeter Debye Institute for Soft Matter Physics, Universität Leipzig, Leipzig 04103, Germany.
Dominik J KauertPeter Debye Institute for Soft Matter Physics, Universität Leipzig, Leipzig 04103, Germany.
Patrick IrmischPeter Debye Institute for Soft Matter Physics, Universität Leipzig, Leipzig 04103, Germany.
Greta Bigelyte-StankevicieneInstitute of Biotechnology, Vilnius University Life Sciences Center, Vilnius 10257, Lithuania.
Arunas SilanskasInstitute of Biotechnology, Vilnius University Life Sciences Center, Vilnius 10257, Lithuania.
Tautvydas KarvelisInstitute of Biotechnology, Vilnius University Life Sciences Center, Vilnius 10257, Lithuania.ORCID 0000-0002-0685-2947
Virginijus SiksnysInstitute of Biotechnology, Vilnius University Life Sciences Center, Vilnius 10257, Lithuania.ORCID 0000-0003-1983-2096
Giedrius SasnauskasInstitute of Biotechnology, Vilnius University Life Sciences Center, Vilnius 10257, Lithuania.
Ralf SeidelPeter Debye Institute for Soft Matter Physics, Universität Leipzig, Leipzig 04103, Germany.ORCID 0000-0002-6642-053X

Funding

Alexander von Humboldt FoundationDeutsche Forschungsgemeinschaft SE 1646/8-1Deutsche Forschungsgemeinschaft SPP2141European Research Council GA 724863German Research FoundationLeipzig UniversityMission-driven Implementation of Science and Innovation Programmes 02-002-P-0001New Generation LithuaniaResearch Council of Lithuania S-MIP-19-32
6 · The paper itself

Abstract

Miniature CRISPR-Cas12f1 effector complexes have recently attracted considerable interest for genome engineering applications due to their compact size. Unlike other Class 2 effectors, Cas12f1 functions as a homodimer bound to a single ∼200 nt RNA. While the basic biochemical properties of Cas12f1, such as its use of a single catalytic center for catalysis, have been characterized, the orchestration of the different events occurring during Cas12f1 reactions remained little explored. To gain insights into the dynamics and mechanisms involved in DNA recognition and cleavage by Cas12f1 from Syntrophomonas palmitatica (SpCas12f1), we solved the structure of SpCas12f1 bound to target DNA and employed single-molecule magnetic tweezers measurements in combination with ensemble kinetic measurements. Our data indicate that SpCas12f1 forms 18 bp R-loops, in which local contacts of the protein to the R-loop stabilize R-loop intermediates. DNA cleavage is catalyzed by a single SpCas12f1 catalytic center, which first rapidly degrades a ∼11 bp region on the nontarget strand by cutting at random sites. Subsequent target strand cleavage is slower and requires at least a nick in the nontarget strand.

Indexed as

Bacterial ProteinsCRISPR-Associated ProteinsDNADNA CleavageCatalytic DomainCRISPR-Cas SystemsKineticsModels, MolecularProtein BindingR-Loop StructuresBacterial ProteinsCRISPR-Associated ProteinsDNA

Identifiers

PMID40650969
PMCPMC12255294

What OpenQuestion holds

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Registered trials

None linked

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.