Evidence map›Paper›PMID 32290018›Full record

ArticlePhysical review. E2020

Directional allosteric regulation of protein filament length.

Adam S Jermyn, Wenxiang Cao, W Austin Elam, Enrique M De La Cruz, Milo M Lin

Open access · greenAbstract read
In one paragraph

Article in Physical review. E, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 36% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

Adam S JermynCenter for Computational Astrophysics,Flatiron Institute, New York, New York, 10010, USA.
Wenxiang CaoDepartment of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut 06511, USA.
W Austin ElamDepartment of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut 06511, USA.
Enrique M De La CruzDepartment of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut 06511, USA.
Milo M LinGreen Center for Molecular, Computational, and Systems Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
Yale University · USThe University of Texas Southwestern Medical Center · US

Funding

Actin filament mechanics and branched network turnoverR35GM136656 · NIGMS · YALE UNIVERSITY · PI ENRIQUE M DE LA CRUZ · 2020 to 2026
$4.0M
Actin filament elasticity and actin-binding protein functionR01GM097348 · NIGMS · YALE UNIVERSITY · PI DE LA CRUZ, ENRIQUE M · 2011 to 2018
$3.1M
NIGMS NIH HHS R01 GM097348NIGMS NIH HHS R35 GM136656
6 · The paper itself

Abstract

Cofilin and ADF are cytoskeleton remodeling proteins that cooperatively bind and fragment actin filaments. Bound cofilin molecules do not directly interact with each other, indicating that cooperative binding of cofilin is mediated by the actin filament lattice. Cofilactin is therefore a model system for studying allosteric regulation of self-assembly. How cofilin binding changes structural and mechanical properties of actin filaments is well established. Less is known about the interaction energies and the thermodynamics of filament fragmentation, which describes the collective manner in which the cofilin concentration controls mean actin filament length. Here, we provide a general thermodynamic framework for allosteric regulation of self-assembly, and we use the theory to predict the interaction energies of experimental actin filament length distributions over a broad range of cofilin binding densities and for multiple cofilactin variants. We find that bound cofilin induces changes in nearby actin-actin interactions, and that these allosteric effects are propagated along the filament to affect up to four neighboring cofilin-binding sites (i.e., beyond nearest-neighbor allostery). The model also predicts that cofilin differentially stabilizes and destabilizes longitudinal versus lateral actin-actin interactions, and that the magnitude, range, asymmetry, and even the sign of these interaction energies can be altered using different actin and cofilin mutational variants. These results demonstrate that the theoretical framework presented here can provide quantitative thermodynamic information governing cooperative protein binding and filament length regulation, thus revealing nanometer length-scale interactions from micron length-scale "wet-lab" measurements.

Indexed as

Allosteric RegulationCytoskeletal ProteinsModels, MolecularThermodynamicsCytoskeletal Proteins

Identifiers

PMID32290018
PMCPMC7758089
OpenAlexW3010929347

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.