Evidence map›Paper›PMID 22869697›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2012

Identification of an N-terminal inhibitory extension as the primary mechanosensory regulator of twitchin kinase.

Eleonore von Castelmur, Johan Strümpfer, Barbara Franke, Julijus Bogomolovas, Sonia Barbieri, Hiroshi Qadota, Petr V Konarev, Dmitri I Svergun, Siegfried Labeit, Guy M Benian and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

15 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. PK1 fromOpen biology · 2023
    Article
  6. Article
  7. Article
  8. Structural and mechanistic insights into mechanoactivation of focal adhesion kinase.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  9. Molecular stretching modulates mechanosensing pathways.Protein science : a publication of the Protein Society · 2017
    Review
  10. Twitchin kinase inhibits muscle activity.Molecular biology of the cell · 2017
    Article
  11. Mechanism of Focal Adhesion Kinase Mechanosensing.PLoS computational biology · 2015
    Article
  12. Article
  13. Article
  14. Article
  15. 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

12 authors at 4 institutions in 3 countries.

Eleonore von CastelmurInstitute of Integrative Biology, University of Liverpool, Liverpool, United Kingdom.
Johan Strümpfer
Barbara Franke
Julijus Bogomolovas
Sonia Barbieri
Hiroshi Qadota
Petr V Konarev
Dmitri I Svergun
Siegfried Labeit
Guy M Benian
Klaus Schulten
Olga Mayans
University of Liverpool · GBEmory University · USEuropean Molecular Biology Laboratory · DEUniversity of Illinois Urbana-Champaign · US

Funding

WHOLE CELL SIMULATIONP41RR005969 · NCRR · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI LUTHEY-SCHULTEN, ZAIDA · 1990 to 2011
$19.8M
Using C. elegans to study titin and obscurin (UNC-89)R01AR051466 · NIAMS · EMORY UNIVERSITY · PI BENIAN, GUY MARTIN · 2004 to 2009
$1.2M
Molecular Mechanisms of Cellular MechanicsR01GM073655 · NIGMS · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI SCHULTEN, KLAUS · 2006 to 2009
$1.0M
NCRR NIH HHS P41 RR005969NCRR NIH HHS P41-RR005969NIAMS NIH HHS R01 AR051466NIAMS NIH HHS R01-AR051466NIGMS NIH HHS R01 GM073655NIGMS NIH HHS R01-GM073655
6 · The paper itself

Abstract

Titin-like kinases are an important class of cytoskeletal kinases that intervene in the response of muscle to mechanical stimulation, being central to myofibril homeostasis and development. These kinases exist in autoinhibited states and, allegedly, become activated during muscle activity by the elastic unfolding of a C-terminal regulatory segment (CRD). However, this mechano-activation model remains controversial. Here we explore the structural, catalytic, and tensile properties of the multidomain kinase region of Caenorhabditis elegans twitchin (Fn(31)-Nlinker-kinase-CRD-Ig(26)) using X-ray crystallography, small angle X-ray scattering, molecular dynamics simulations, and catalytic assays. This work uncovers the existence of an inhibitory segment that flanks the kinase N-terminally (N-linker) and that acts synergistically with the canonical CRD tail to silence catalysis. The N-linker region has high mechanical lability and acts as the primary stretch-sensor in twitchin kinase, while the CRD is poorly responsive to pulling forces. This poor response suggests that the CRD is not a generic mechanosensor in this kinase family. Instead, the CRD is shown here to be permissive to catalysis and might protect the kinase active site against mechanical damage. Thus, we put forward a regulatory model where kinase inhibition results from the combined action of both N- and C-terminal tails, but only the N-terminal extension undergoes mechanical removal, thereby affording partial activation. Further, we compare invertebrate and vertebrate titin-like kinases and identify variations in the regulatory segments that suggest a mechanical speciation of these kinase classes.

Indexed as

Amino Acid SequenceAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCalmodulin-Binding ProteinsCatalysisCatalytic DomainCrystallography, X-RayModels, MolecularMolecular Sequence DataMuscle ProteinsProtein ConformationProtein Structure, TertiaryScattering, RadiationSequence Homology, Amino AcidX-RaysCaenorhabditis elegans ProteinsCalmodulin-Binding ProteinsMuscle Proteinsunc-22 protein, C elegans

Identifiers

PMID22869697
PMCPMC3427058
OpenAlexW2127104479

What OpenQuestion holds

Textmetadata
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.