Evidence map›Paper›PMID 37774939›Full record

ArticleJournal of theoretical biology2023

Inferring local molecular dynamics from the global actin network structure: A case study of 2D synthetic branching actin networks.

Minghao W Rostami, Brittany E Bannish, Kelsey Gasior, Rebecca L Pinals, Calina Copos, Adriana T Dawes

Open access · greenAbstract read
In one paragraph

Article in Journal of theoretical biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 41% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
  2. 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

6 authors at 6 institutions in 1 country.

Minghao W RostamiDepartment of Mathematics and Statistics, Binghamton University, Binghamton, NY, USA. Electronic address: mrostami@binghamton.edu.
Brittany E BannishDepartment of Mathematics and Statistics, University of Central Oklahoma, Edmond, OK, USA. Electronic address: BBannish@uco.edu.
Kelsey GasiorDepartment of Applied and Computational Mathematics and Statistics, University of Notre Dame, Notre Dame, IN, USA. Electronic address: kgasior2@nd.edu.
Rebecca L PinalsPicower Institute for Learning and Memory, Massachusetts Institute of Technology, Boston, MA, USA. Electronic address: rpinals@mit.edu.
Calina CoposDepartment of Biology and Department of Mathematics, Northeastern University, Boston, MA, USA. Electronic address: c.copos@northeastern.edu.
Adriana T DawesDepartment of Mathematics and Department of Molecular Genetics, The Ohio State University, Columbus, OH, USA. Electronic address: dawes.33@math.ohio-state.edu.
Binghamton University · USMassachusetts Institute of Technology · USNortheastern University · USThe Ohio State University · USUniversity of Central Oklahoma · USUniversity of Notre Dame · US

Funding

Mathematical investigation of dynein-mediated centrosome positioning in polarized cellsR01GM132651 · NIGMS · OHIO STATE UNIVERSITY · PI DAWES, ADRIANA · 2019 to 2022
$1.4M
NIGMS NIH HHS R01 GM132651
6 · The paper itself

Abstract

Cells rely on their cytoskeleton for key processes including division and directed motility. Actin filaments are a primary constituent of the cytoskeleton. Although actin filaments can create a variety of network architectures linked to distinct cell functions, the microscale molecular interactions that give rise to these macroscale structures are not well understood. In this work, we investigate the microscale mechanisms that produce different branched actin network structures using an iterative classification approach. First, we employ a simple yet comprehensive agent-based model that produces synthetic actin networks with precise control over the microscale dynamics. Then we apply machine learning techniques to classify actin networks based on measurable network density and geometry, identifying key mechanistic processes that lead to particular branched actin network architectures. Extensive computational experiments reveal that the most accurate method uses a combination of supervised learning based on network density and unsupervised learning based on network symmetry. This framework can potentially serve as a powerful tool to discover the molecular interactions that produce the wide variety of actin network configurations associated with normal development as well as pathological conditions such as cancer.

Indexed as

ActinsMolecular Dynamics SimulationActin CytoskeletonActinsActinAgent-based modelBranched actin networkCell cytoskeletonLamellipodiumMachine learning

Identifiers

PMID37774939
PMCPMC10842209
OpenAlexW4387079127

What OpenQuestion holds

Textmetadata
LicenceTDM
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.