Evidence map›Paper›PMID 37550424›Full record

ArticleNature biomedical engineering2024

Sensing the DNA-mismatch tolerance of catalytically inactive Cas9 via barcoded DNA nanostructures in solid-state nanopores.

Sarah E Sandler, Nicole E Weckman, Sarah Yorke, Akashaditya Das, Kaikai Chen, Richard Gutierrez, Ulrich F Keyser

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Nature biomedical engineering, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.3field-weighted citation impact, top 7% of its field
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

16 citing papers in PubMed, 30 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

Sarah E SandlerCavendish Laboratory, University of Cambridge, Cambridge, UK.ORCID 0000-0001-9689-8684
Nicole E WeckmanCavendish Laboratory, University of Cambridge, Cambridge, UK.ORCID 0000-0001-5894-4926
Sarah YorkeCavendish Laboratory, University of Cambridge, Cambridge, UK.ORCID 0000-0002-3511-4222
Akashaditya DasDepartment of Pathology, University of Cambridge, Cambridge, UK.
Kaikai ChenCavendish Laboratory, University of Cambridge, Cambridge, UK.ORCID 0000-0003-3170-0336
Richard GutierrezOxford Nanopore Technologies, Oxford Science Park, Oxford, UK.
Ulrich F KeyserCavendish Laboratory, University of Cambridge, Cambridge, UK. ufk20@cam.ac.uk.
University of Cambridge · GBOxford Nanopore Technologies (United Kingdom) · GBUniversity of Toronto · CA

Funding

EC | EC Seventh Framework Programm | FP7 Ideas: European Research Council (FP7-IDEAS-ERC - Specific Programme: 'Ideas ' Implementing the Seventh Framework Programme of the European Community for Research, Technological Development and Demonstration Activities (2007 to 2013)) ERC-2019-POC PoreDetect 899538RCUK | Engineering and Physical Sciences Research Council (EPSRC) EP/L015889/1RCUK | Engineering and Physical Sciences Research Council (EPSRC) EP/S022953/1
6 · The paper itself

Abstract

Single-molecule quantification of the strength and sequence specificity of interactions between proteins and nucleic acids would facilitate the probing of protein-DNA binding. Here we show that binding events between the catalytically inactive Cas9 ribonucleoprotein and any pre-defined short sequence of double-stranded DNA can be identified by sensing changes in ionic current as suitably designed barcoded linear DNA nanostructures with Cas9-binding double-stranded DNA overhangs translocate through solid-state nanopores. We designed barcoded DNA nanostructures to study the relationships between DNA sequence and the DNA-binding specificity, DNA-binding efficiency and DNA-mismatch tolerance of Cas9 at the single-nucleotide level. Nanopore-based sensing of DNA-barcoded nanostructures may help to improve the design of efficient and specific ribonucleoproteins for biomedical applications, and could be developed into sensitive protein-sensing assays.

Indexed as

NanoporesCRISPR-Cas SystemsDNANanotechnologyProteinsDNAProteins

Identifiers

PMID37550424
PMCPMC10963265
OpenAlexW4385638678

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.