Evidence map›Paper›PMID 41305943›Full record

ArticleSmall (Weinheim an der Bergstrasse, Germany)2026

Effect of Load on Non-Muscle Myosin 2 Paralog Filaments in a Biomimetic Contractile Actin Array.

Philip Bleicher, David Han, Neil Billington, Ryan Hart, Christian A Combs, Shureed Qazi, Indra Chandrasekar, Jay R Knutson, James R Sellers

Abstract read
In one paragraph

Article in Small (Weinheim an der Bergstrasse, Germany), 2026. 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. Review
  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

9 authors.

Philip BleicherLaboratory of Molecular Physiology, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD, 20814, USA.ORCID 0000-0003-1788-0043
David HanLaboratory of Molecular Physiology, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD, 20814, USA.
Neil BillingtonLaboratory of Molecular Physiology, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD, 20814, USA.
Ryan HartEnabling Technologies Group, Sanford Research, Sioux Falls, SD, 57104, USA.
Christian A CombsNHLBI Light Microscopy Facility, National Institutes of Health, Bethesda, MD, 20814, USA.
Shureed QaziLaboratory of Advanced Microscopy and Biophotonics, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD, 20814, USA.
Indra ChandrasekarEnabling Technologies Group, Sanford Research, Sioux Falls, SD, 57104, USA.
Jay R KnutsonLaboratory of Advanced Microscopy and Biophotonics, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD, 20814, USA.
James R SellersLaboratory of Molecular Physiology, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD, 20814, USA.

Funding

ROLE OF PHOSPHORYLATION AS A REGULATORY MECHANISM IN MUSCLE CONTRACTIONZ01HL001786 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI SELLERS, JAMES R. · 1985 to 2008
$601k
Intramural NIH HHS Z01 HL001786NHLBI NIH HHS HL001786
6 · The paper itself

Abstract

Cells express three non-muscle myosin 2 (NM2) paralogs that form bipolar filaments of ≈30 motors each. Of these, NM2A and NM2B are best studied and show distinct enzymatic and mechanical properties. Although they can colocalize in cells, they also have unique localization patterns, suggesting functional differences. Most studies have examined these proteins interacting with actin under very low loads, but in cells they likely contribute to generating and maintaining cytoskeletal tension. Inspired by sarcomere-like tension generation in non-muscle cells, a minimal platform is reconstituted to study NM2 activity under load. Using micropatterned formin to align actin filaments in anti-parallel bundles, phosphorylated NM2 filaments are introduced to observe their interactions via TIRF (Total Internal Reflection Fluorescence) microscopy. NM2B contracts and bundles the actin filaments to form a tensed system. The rate of myosin filament movement slows, and many filaments completely stall. In contrast, NM2A moved faster but disrupted bundles via severing and retraction. FRET-based tension sensors revealed that both paralogs generate comparable tension despite these differing behaviors. This suggests that NM2A and NM2B play distinct mechanical roles in cells, with NM2B better suited for sustained tension and NM2A contributing to dynamic remodeling.

Indexed as

Actin CytoskeletonActinsBiomimeticsMyosin Type IIAnimalsFluorescence Resonance Energy TransferActinsMyosin Type IIFRETmicropatterningmyosinsarcomeretension sensor

Identifiers

PMID41305943
PMCPMC12802541

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.