Evidence map›Paper›PMID 39083045›Full record

ArticleThe Journal of general physiology2024

Mechanisms of a novel regulatory light chain-dependent cardiac myosin inhibitor.

Kristina Kooiker, Qing-Fen Gan, Ming Yu, Na Sa, Saffie Mohran, Yuanhua Cheng, Galina Flint, Stephanie Neys, Chengqian Gao, Devin Nissen and 6 more

Abstract read
In one paragraph

Article in The Journal of general physiology, 2024. 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
–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

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Kristina KooikerDivision of Cardiology, Medicine, University of Washington, Seattle, WA, USA.ORCID 0000-0003-1817-9080
Qing-Fen GanBristol Myers Squibb Research , Brisbane, CA, USA.ORCID 0009-0002-7256-6778
Ming YuBristol Myers Squibb Research , Brisbane, CA, USA.ORCID 0009-0004-1074-8132
Na SaBristol Myers Squibb Research , Brisbane, CA, USA.ORCID 0000-0001-8599-4371
Saffie MohranDivision of Cardiology, Medicine, University of Washington, Seattle, WA, USA.ORCID 0000-0003-0728-9882
Yuanhua ChengDepartment of Bioengineering, University of Washington, Seattle, WA, USA.ORCID 0000-0003-4093-5006
Galina FlintCenter of Translational Muscle Research, University of Washington , Seattle, WA, USA.ORCID 0000-0003-3993-5156
Stephanie NeysDivision of Cardiology, Medicine, University of Washington, Seattle, WA, USA.ORCID 0009-0007-3455-9370
Chengqian GaoCollege of Basic Medical Sciences, Dalian Medical University , Dalian, China.ORCID 0009-0000-5107-5326
Devin NissenDepartment of Biology, Illinois Institute of Technology, Chicago, IL, USA.ORCID 0000-0001-9751-0901
Tim McMillenCenter of Translational Muscle Research, University of Washington , Seattle, WA, USA.ORCID 0000-0001-5261-3229
Anthony AsencioCenter of Translational Muscle Research, University of Washington , Seattle, WA, USA.ORCID 0000-0002-8147-0180
Weikang MaDepartment of Biology, Illinois Institute of Technology, Chicago, IL, USA.ORCID 0000-0001-9535-7114
Thomas C IrvingDepartment of Biology, Illinois Institute of Technology, Chicago, IL, USA.ORCID 0000-0003-4848-3323
Farid Moussavi-HaramiDivision of Cardiology, Medicine, University of Washington, Seattle, WA, USA.ORCID 0000-0002-0189-7214
Michael RegnierCenter of Translational Muscle Research, University of Washington , Seattle, WA, USA.ORCID 0000-0001-5437-9851

Funding

The Biophysics Collaborative Access Team (User Training and Outreach)P30GM138395 · NIGMS · ILLINOIS INSTITUTE OF TECHNOLOGY · PI THOMAS C IRVING · 2021 to 2026
$16.5M
From proteins to cells to tissues: A multi-scale assessment of biomechanical regulation by the myosin molecular motorRM1GM131981 · NIGMS · STANFORD UNIVERSITY · PI BERNSTEIN, DANIEL, MACK, DAVID LEE · 2019 to 2023
$10.3M
UW Center for Translational Muscle Research (Overall Application)P30AR074990 · NIAMS · UNIVERSITY OF WASHINGTON · PI Jennifer Michelle Davis · 2019 to 2026
$7.5M
Engineered Stem Cells for Cardiac RepairR01HL128368 · NHLBI · UNIVERSITY OF WASHINGTON · PI REGNIER, MICHAEL · 2018 to 2025
$6.1M
Experimental and Computational Studies in Genetic CardiomyopathiesR01HL157169 · NHLBI · UNIVERSITY OF WASHINGTON · PI Farid Moussavi-Harami · 2022 to 2026
$3.3M
Bioengineering Cardiovascular Training Grant (BCTG)T32EB032787 · NIBIB · UNIVERSITY OF WASHINGTON · PI MICHAEL REGNIER, Ying Zheng · 2022 to 2026
$969k
Effect of elevated dATP on contractile function and the Frank-Starling relationship in models of dilated cardiomyopathyK08HL128826 · NHLBI · UNIVERSITY OF WASHINGTON · PI MOUSSAVI-HARAMI, FARID · 2016 to 2021
$851k
Bristol Myers Squibb MyoKon 11456NHLBI NIH HHS K08 HL128826NHLBI NIH HHS R01 HL128368NHLBI NIH HHS R01 HL157169NIAMS NIH HHS P30 AR074990NIBIB NIH HHS T32 EB032787NIGMS NIH HHS P30 GM138395NIH HHS R01 HL128368University of Washington P30AR074990U.S. Department of Energy DE-AC02-06CH11357
6 · The paper itself

Abstract

Hypertrophic cardiomyopathy (HCM) is a genetic disease of the heart characterized by thickening of the left ventricle (LV), hypercontractility, and impaired relaxation. HCM is caused primarily by heritable mutations in sarcomeric proteins, such as β myosin heavy chain. Until recently, medications in clinical use for HCM did not directly target the underlying contractile changes in the sarcomere. Here, we investigate a novel small molecule, RLC-1, identified in a bovine cardiac myofibril high-throughput screen. RLC-1 is highly dependent on the presence of a regulatory light chain to bind to cardiac myosin and modulate its ATPase activity. In demembranated rat LV trabeculae, RLC-1 decreased maximal Ca2+-activated force and Ca2+ sensitivity of force, while it increased the submaximal rate constant for tension redevelopment. In myofibrils isolated from rat LV, both maximal and submaximal Ca2+-activated force are reduced by nearly 50%. Additionally, the fast and slow phases of relaxation were approximately twice as fast as DMSO controls, and the duration of the slow phase was shorter. Structurally, x-ray diffraction studies showed that RLC-1 moved myosin heads away from the thick filament backbone and decreased the order of myosin heads, which is different from other myosin inhibitors. In intact trabeculae and isolated cardiomyocytes, RLC-1 treatment resulted in decreased peak twitch magnitude and faster activation and relaxation kinetics. In conclusion, RLC-1 accelerated kinetics and decreased force production in the demembranated tissue, intact tissue, and intact whole cells, resulting in a smaller cardiac twitch, which could improve the underlying contractile changes associated with HCM.

Indexed as

Myocardial ContractionAnimalsCalciumCardiac MyosinsCattleMaleMyofibrilsMyosin Light ChainsRatsRats, Sprague-DawleyCalciumCardiac MyosinsMyosin Light Chains

Identifiers

PMID39083045
PMCPMC11291911

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Registered trials

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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.