Literature DB >> 10567705

Variability in the ratio of mutant to wildtype myosin heavy chain present in the soleus muscle of patients with familial hypertrophic cardiomyopathy. A new approach for the quantification of mutant to wildtype protein.

V Nier1, I Schultz, B Brenner, W Forssmann, M Raida.   

Abstract

The ratio of mutant to wildtype myosin heavy chain (beta-isoform, beta-MHC) in the soleus muscle of patients with familial hypertrophic cardiomyopathy was determined by a combination of HPLC, mass spectrometry and capillary zone electrophoresis. In two patients, one with a Val 606 Met mutation and another with a Gly 584 Arg mutation, the fraction of mutant beta-MHC was only 12+/-6% and 23+/-0.7% of total beta-MHC, respectively. These results demonstrate the necessity to determine the ratio of mutant to wildtype protein for the interpretation of functional studies on biopsy material from heterozygous patients with an inherited disease.

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Year:  1999        PMID: 10567705     DOI: 10.1016/s0014-5793(99)01433-7

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  17 in total

1.  Mutation of the myosin converter domain alters cross-bridge elasticity.

Authors:  Jan Köhler; Gerhard Winkler; Imke Schulte; Tim Scholz; William McKenna; Bernhard Brenner; Theresia Kraft
Journal:  Proc Natl Acad Sci U S A       Date:  2002-03-19       Impact factor: 11.205

2.  On mice, rabbits, and human heart failure.

Authors:  A J Marian
Journal:  Circulation       Date:  2005-05-10       Impact factor: 29.690

3.  Cardiomyopathy mutations reveal variable region of myosin converter as major element of cross-bridge compliance.

Authors:  B Seebohm; F Matinmehr; J Köhler; A Francino; F Navarro-Lopéz; A Perrot; C Ozcelik; W J McKenna; B Brenner; T Kraft
Journal:  Biophys J       Date:  2009-08-05       Impact factor: 4.033

4.  Mechanical and kinetic properties of β-cardiac/slow skeletal muscle myosin.

Authors:  Bernhard Brenner; Nils Hahn; Eva Hanke; Faramarz Matinmehr; Tim Scholz; Walter Steffen; Theresia Kraft
Journal:  J Muscle Res Cell Motil       Date:  2012-07-31       Impact factor: 2.698

5.  Transgenic rabbit model for human troponin I-based hypertrophic cardiomyopathy.

Authors:  Atsushi Sanbe; Jeanne James; Volkan Tuzcu; Selman Nas; Lisa Martin; James Gulick; Hanna Osinska; Sadayappan Sakthivel; Raisa Klevitsky; Kenneth S Ginsburg; Donald M Bers; Bruce Zinman; Edward G Lakatta; Jeffrey Robbins
Journal:  Circulation       Date:  2005-05-02       Impact factor: 29.690

6.  Molecular mechanism of the E99K mutation in cardiac actin (ACTC Gene) that causes apical hypertrophy in man and mouse.

Authors:  Weihua Song; Emma Dyer; Daniel J Stuckey; O'Neal Copeland; Man-Ching Leung; Christopher Bayliss; Andrew Messer; Ross Wilkinson; Jordi Lopez Tremoleda; Michael D Schneider; Sian E Harding; Charles S Redwood; Kieran Clarke; Kristen Nowak; Lorenzo Monserrat; Dominic Wells; Steven B Marston
Journal:  J Biol Chem       Date:  2011-05-26       Impact factor: 5.157

Review 7.  How do mutations in contractile proteins cause the primary familial cardiomyopathies?

Authors:  Steven B Marston
Journal:  J Cardiovasc Transl Res       Date:  2011-03-22       Impact factor: 4.132

8.  A novel mutation expands the genetic and clinical spectrum of MYH7-related myopathies.

Authors:  Nigel F Clarke; Kimberly Amburgey; James Teener; Sandra Camelo-Piragua; Akanchha Kesari; Jaya Punetha; Leigh B Waddell; Mark Davis; Nigel G Laing; Nicole Monnier; Kathryn N North; Eric P Hoffman; James J Dowling
Journal:  Neuromuscul Disord       Date:  2013-03-09       Impact factor: 4.296

9.  Faster cross-bridge detachment and increased tension cost in human hypertrophic cardiomyopathy with the R403Q MYH7 mutation.

Authors:  E Rosalie Witjas-Paalberends; Claudia Ferrara; Beatrice Scellini; Nicoletta Piroddi; Judith Montag; Chiara Tesi; Ger J M Stienen; Michelle Michels; Carolyn Y Ho; Theresia Kraft; Corrado Poggesi; Jolanda van der Velden
Journal:  J Physiol       Date:  2014-06-13       Impact factor: 5.182

10.  A novel technique based on a PNA hybridization probe and FRET principle for quantification of mutant genotype in fibrous dysplasia/McCune-Albright syndrome.

Authors:  Abdullah Karadag; Mara Riminucci; Paolo Bianco; Natasha Cherman; Sergei A Kuznetsov; Nga Nguyen; Michael T Collins; Pamela G Robey; Larry W Fisher
Journal:  Nucleic Acids Res       Date:  2004-04-19       Impact factor: 16.971

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