Evidence map›Paper›PMID 38992021›Full record

ArticleNature communications2024

Turn-on protein switches for controlling actin binding in cells.

Unyime M Effiong, Hannah Khairandish, Isabela Ramirez-Velez, Yanran Wang, Brian Belardi

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 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Binding memory of liquid molecules.Nature communications · 2025
    Article
  4. Structure of the F-tractin-F-actin complex.The Journal of cell biology · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Unyime M EffiongMcKetta Department of Chemical Engineering, The University of Texas at Austin, Austin, TX, 78712, USA.ORCID 0009-0007-7637-4147
Hannah KhairandishMcKetta Department of Chemical Engineering, The University of Texas at Austin, Austin, TX, 78712, USA.
Isabela Ramirez-VelezMcKetta Department of Chemical Engineering, The University of Texas at Austin, Austin, TX, 78712, USA.
Yanran WangMcKetta Department of Chemical Engineering, The University of Texas at Austin, Austin, TX, 78712, USA.
Brian BelardiMcKetta Department of Chemical Engineering, The University of Texas at Austin, Austin, TX, 78712, USA. bdb@che.utexas.edu.ORCID 0000-0003-3608-0164

Funding

A Molecular Toolkit for Controlling and Probing Cell Junction-Actin InteractionsR35GM142941 · NIGMS · UNIVERSITY OF TEXAS AT AUSTIN · PI BELARDI, BRIAN · 2021 to 2025
$1.9M
National Science Foundation (NSF) 2218467NIGMS NIH HHS R35 GM142941U.S. Department of Health & Human Services | National Institutes of Health (NIH) R35GM142941Welch Foundation F-2055-20210327
6 · The paper itself

Abstract

Within a shared cytoplasm, filamentous actin (F-actin) plays numerous and critical roles across the cell body. Cells rely on actin-binding proteins (ABPs) to organize F-actin and to integrate its polymeric characteristics into diverse cellular processes. Yet, the multitude of ABPs that engage with and shape F-actin make studying a single ABP's influence on cellular activities a significant challenge. Moreover, without a means of manipulating actin-binding subcellularly, harnessing the F-actin cytoskeleton for synthetic biology purposes remains elusive. Here, we describe a suite of designed proteins, Controllable Actin-binding Switch Tools (CASTs), whose actin-binding behavior can be controlled with external stimuli. CASTs were developed that respond to different external inputs, providing options for turn-on kinetics and enabling orthogonality and multiplexing. Being genetically encoded, we show that CASTs can be inserted into native protein sequences to control F-actin association locally and engineered into structures to control cell and tissue shape and behavior.

Indexed as

Actin CytoskeletonActinsMicrofilament ProteinsProtein BindingAnimalsHumansKineticsProtein EngineeringActinsMicrofilament Proteins

Identifiers

PMID38992021
PMCPMC11239668

What OpenQuestion holds

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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.