Evidence map›Paper›PMID 35549081›Full record

ArticleACS macro letters2021

Motor-Driven Restructuring of Cytoskeleton Composites Leads to Tunable Time-Varying Elasticity.

Janet Y Sheung, Daisy H Achiriloaie, Christopher Currie, Karthik Peddireddy, Aaron Xie, Jessalyn Simon-Parker, Gloria Lee, Michael J Rust, Moumita Das, Jennifer L Ross and 1 more

Abstract read
In one paragraph

Article in ACS macro letters, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

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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

11 authors.

Janet Y SheungW. M. Keck Science Department, Scripps College, Pitzer College, and Claremont McKenna College, 925 N. Mills Ave., Claremont, California 91711, United States.ORCID 0000-0003-4694-9740
Daisy H AchiriloaieW. M. Keck Science Department, Scripps College, Pitzer College, and Claremont McKenna College, 925 N. Mills Ave., Claremont, California 91711, United States.
Christopher CurrieDepartment of Physics and Biophysics, University of San Diego, 5998 Alcala Park, San Diego, California 92110, United States.
Karthik PeddireddyDepartment of Physics and Biophysics, University of San Diego, 5998 Alcala Park, San Diego, California 92110, United States.ORCID 0000-0003-4282-5484
Aaron XieW. M. Keck Science Department, Scripps College, Pitzer College, and Claremont McKenna College, 925 N. Mills Ave., Claremont, California 91711, United States.
Jessalyn Simon-ParkerW. M. Keck Science Department, Scripps College, Pitzer College, and Claremont McKenna College, 925 N. Mills Ave., Claremont, California 91711, United States.
Gloria LeeDepartment of Physics and Biophysics, University of San Diego, 5998 Alcala Park, San Diego, California 92110, United States.
Michael J RustDepartment of Molecular Genetics and Cell Biology, University of Chicago, Chicago, Illinois 60637, United States.
Moumita DasSchool of Physics and Astronomy, Rochester Institute of Technology, Rochester, New York 14623, United States.
Jennifer L RossDepartment of Physics, Syracuse University, Syracuse, New York 13244, United States.
Rae M Robertson-AndersonDepartment of Physics and Biophysics, University of San Diego, 5998 Alcala Park, San Diego, California 92110, United States.ORCID 0000-0003-4475-4667

Funding

Biomimetic cytoskeleton and advanced microscopy to reveal intracellular DNA dynamics and distributionsR15GM123420 · NIGMS · UNIVERSITY OF SAN DIEGO · PI MCGORTY, RYAN, ROBERTSON-ANDERSON, RAE MARIE · 2017 to 2022
$939k
NIGMS NIH HHS R15 GM123420
6 · The paper itself

Abstract

The composite cytoskeleton, comprising interacting networks of semiflexible actin and rigid microtubules, generates forces and restructures by using motor proteins such as myosins to enable key processes including cell motility and mitosis. Yet, how motor-driven activity alters the mechanics of cytoskeleton composites remains an open challenge. Here, we perform optical tweezers microrheology and confocal imaging of composites with varying actin-tubulin molar percentages (25-75, 50-50, and 75-25), driven by light-activated myosin II motors, to show that motor activity increases the elastic plateau modulus by over 2 orders of magnitude by active restructuring of both actin and microtubules that persists for hours after motor activation has ceased. Nonlinear microrheology measurements show that motor-driven restructuring increases the force response and stiffness and suppresses actin bending. The 50-50 composite exhibits the most dramatic mechanical response to motor activity due to the synergistic effects of added stiffness from the microtubules and sufficient motor substrate for pronounced activity.

Indexed as

ActinsCytoskeletonElasticityMicrotubulesMyosinsActinsMyosins

Identifiers

PMID35549081
PMCPMC9239751

What OpenQuestion holds

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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.