Evidence map›Paper›PMID 23297410›Full record

ArticleThe Journal of biological chemistry2013

Single molecule force spectroscopy on titin implicates immunoglobulin domain stability as a cardiac disease mechanism.

Brian R Anderson, Julius Bogomolovas, Siegfried Labeit, Henk Granzier

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

25 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. A Case Study Identified a New Mutation in theInternational journal of general medicine · 2025
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Single-particle virology.Biophysical reviews · 2020
    Review
  11. Article
  12. Article
  13. Article
  14. Titin mutations and muscle disease.Pflugers Archiv : European journal of physiology · 2019
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. The genetic basis of hypertrophic cardiomyopathy in cats and humans.Journal of veterinary cardiology : the official journal of the European Society of Veterinary Cardiology · 2015
    Review
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

4 authors at 2 institutions in 2 countries.

Brian R AndersonDepartment of Physics, University of Arizona, Tucson, Arizona 85724, USA.
Julius Bogomolovas
Siegfried Labeit
Henk Granzier
Heidelberg University · DEUniversity of Arizona · US

Funding

Function of Giant Sarcomere Matrix Proteins in MuscleR01HL062881 · NHLBI · WASHINGTON STATE UNIVERSITY · PI GRANZIER, HENK L. · 1999 to 2018
$6.4M
Computational and Mathematical Modeling of Biomedical SystemsT32GM084905 · NIGMS · UNIVERSITY OF ARIZONA · PI SECOMB, TIMOTHY W. · 2009 to 2018
$2.2M
NHLBI NIH HHS HL062881NHLBI NIH HHS R01 HL062881NIGMS NIH HHS GM084905NIGMS NIH HHS T32 GM084905
6 · The paper itself

Abstract

Titin plays crucial roles in sarcomere organization and cardiac elasticity by acting as an intrasarcomeric molecular spring. A mutation in the tenth Ig-like domain of titin's spring region is associated with arrhythmogenic cardiomyopathy, a disease characterized by ventricular arrhythmias leading to cardiac arrest and sudden death. Titin is the first sarcomeric protein linked to arrhythmogenic cardiomyopathy. To characterize the disease mechanism, we have used atomic force microscopy to directly measure the effects that the disease-linked point mutation (T16I) has on the mechanical and kinetic stability of Ig10 at the single molecule level. The mutation decreases the force needed to unfold Ig10 and increases its rate of unfolding 4-fold. We also found that T16I Ig10 is more prone to degradation, presumably due to compromised local protein structure. Overall, the disease-linked mutation weakens the structural integrity of titin's Ig10 domain and suggests an Ig domain disease mechanism.

Indexed as

Amino Acid SequenceAnimalsCardiomyopathiesConnectinHeart DiseasesImmunoglobulinsKineticsLikelihood FunctionsMiceMicroscopy, Atomic ForceMolecular Sequence DataMonte Carlo MethodMuscle ProteinsMutationMyocardiumProtein DenaturationConnectinImmunoglobulinsMuscle ProteinsProtein Kinases

Identifiers

PMID23297410
PMCPMC3581406
OpenAlexW2049883744

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.