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

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

The Journal of physiology (2014-06-15)
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

The first mutation associated with hypertrophic cardiomyopathy (HCM) is the R403Q mutation in the gene encoding β-myosin heavy chain (β-MyHC). R403Q locates in the globular head of myosin (S1), responsible for interaction with actin, and thus motor function of myosin. Increased cross-bridge relaxation kinetics caused by the R403Q mutation might underlie increased energetic cost of tension generation; however, direct evidence is absent. Here we studied to what extent cross-bridge kinetics and energetics are related in single cardiac myofibrils and multicellular cardiac muscle strips of three HCM patients with the R403Q mutation and nine sarcomere mutation-negative HCM patients (HCMsmn). Expression of R403Q was on average 41 ± 4% of total MYH7 mRNA. Cross-bridge slow relaxation kinetics in single R403Q myofibrils was significantly higher (P < 0.0001) than in HCMsmn myofibrils (0.47 ± 0.02 and 0.30 ± 0.02 s(-1), respectively). Moreover, compared to HCMsmn, tension cost was significantly higher in the muscle strips of the three R403Q patients (2.93 ± 0.25 and 1.78 ± 0.10 μmol l(-1) s(-1) kN(-1) m(-2), respectively) which showed a positive linear correlation with relaxation kinetics in the corresponding myofibril preparations. This correlation suggests that faster cross-bridge relaxation kinetics results in an increase in energetic cost of tension generation in human HCM with the R403Q mutation compared to HCMsmn. Therefore, increased tension cost might contribute to HCM disease in patients carrying the R403Q mutation.

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Imidazole, ACS reagent, ≥99% (titration)
Imidazole, for molecular biology, ≥99% (titration)
Imidazole, ReagentPlus®, 99%
Imidazole, puriss. p.a., ≥99.5% (GC)
Imidazole buffer Solution, BioUltra, 1 M in H2O
Imidazole, BioUltra, ≥99.5% (GC)
Imidazole, anhydrous, free-flowing, Redi-Dri, ACS reagent, ≥99%
Imidazole, BioUltra, for molecular biology, ≥99.5% (GC)
Imidazole, Pharmaceutical Secondary Standard; Certified Reference Material
Imidazole, ≥99% (titration), crystalline
Imidazole, United States Pharmacopeia (USP) Reference Standard
Imidazole, ReagentPlus®, 99%, Redi-Dri, free-flowing
Ondansetron impurity E, European Pharmacopoeia (EP) Reference Standard
Imidazole, for molecular biology, ≥99% (titration), free-flowing, Redi-Dri
Imidazole, European Pharmacopoeia (EP) Reference Standard