Evidence map›Paper›PMID 39396048›Full record

ArticleNature communications2024

Engineering tunable catch bonds with DNA.

Micah Yang, David T R Bakker, Isaac T S Li

Abstract read
In one paragraph

Article in Nature communications, 2024. 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. 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

3 authors.

Micah YangDepartment of Chemistry, The University of British Columbia, Kelowna, BC, Canada.ORCID 0009-0006-9822-2892
David T R BakkerDepartment of Chemistry, The University of British Columbia, Kelowna, BC, Canada.ORCID 0009-0005-5284-6205
Isaac T S LiDepartment of Chemistry, The University of British Columbia, Kelowna, BC, Canada. isaac.li@ubc.ca.ORCID 0000-0002-8450-5326

Funding

Canada Foundation for Innovation (Fondation canadienne pour l'innovation) 35492Canada Research Chairs (Chaires de recherche du Canada) CRC-2020-00143Gouvernement du Canada | Natural Sciences and Engineering Research Council of Canada (Conseil de Recherches en Sciences Naturelles et en Génie du Canada) RGPIN-2017-04407, RGPIN-2024-04352Michael Smith Foundation for Health Research (MSFHR) SCH-2020-0559
6 · The paper itself

Abstract

Unlike most adhesive bonds, biological catch bonds strengthen with increased tension. This characteristic is essential to specific receptor-ligand interactions, underpinning biological adhesion dynamics, cell communication, and mechanosensing. While artificial catch bonds have been conceived, the tunability of their catch behaviour is limited. Here, we present the fish-hook, a rationally designed DNA catch bond that can be finely adjusted to a wide range of catch behaviours. We develop models to design these DNA structures and experimentally validate different catch behaviours by single-molecule force spectroscopy. The fish-hook architecture supports a vast sequence-dependent behaviour space, making it a valuable tool for reprogramming biological interactions and engineering force-strengthening materials.

Indexed as

DNAMicroscopy, Atomic ForceNucleic Acid ConformationDNA

Identifiers

PMID39396048
PMCPMC11470926

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.