Myosin cross-bridges do not form precise rigor bonds in hypertrophic heart muscle carrying troponin t mutations

K. Midde, V. Dumka, J. R. Pinto, P. Muthu, P. Marandos, I. Gryczynski, Z. Gryczynski, J. D. Potter, J. Borejdo

Research output: Contribution to journalArticle

4 Scopus citations


Distribution of orientations of myosin was examined in ex-vivo myofibrils from hearts of transgenic (Tg) mice expressing Familial Hypertrophic Cardiomyopathy (FHC) troponin T (TnT) mutations I79N, F110I and R278C. Humans are heterozygous for sarcomeric FHC mutations and so hypertrophic myocardium contains a mixture of the wild-type (WT) and mutated (MUT) TnT. If mutations are expressed at a low level there may not be a significant change in the global properties of heart muscle. In contrast, measurements from a few molecules avoid averaging inherent in the global measurements. It is thus important to examine the properties of only a few molecules of muscle. To this end, the lever arm of one out of every 60,000 myosin molecules was labeled with a fluorescent dye and a small volume within the A-band (~. 1 fL) was observed by confocal microscopy. This volume contained on average 5 fluorescent myosin molecules. The lever arm assumes different orientations reflecting different stages of acto-myosin enzymatic cycle. We measured the distribution of these orientations by recording polarization of fluorescent light emitted by myosin-bound fluorophore during rigor and contraction. The distribution of orientations of rigor WT and MUT myofibrils was significantly different. There was a large difference in the width and of skewness and kurtosis of rigor distributions. These findings suggest that the hypertrophic phenotype associated with the TnT mutations can be characterized by a significant increase in disorder of rigor cross-bridges.

Original languageEnglish (US)
Pages (from-to)409-418
Number of pages10
JournalJournal of Molecular and Cellular Cardiology
Issue number3
StatePublished - Sep 1 2011



  • Cardiac hypertrophy
  • Confocal microscopy
  • Mesoscopic measurements
  • Polarization of fluorescence
  • Troponin T

ASJC Scopus subject areas

  • Molecular Biology
  • Cardiology and Cardiovascular Medicine

Cite this

Midde, K., Dumka, V., Pinto, J. R., Muthu, P., Marandos, P., Gryczynski, I., Gryczynski, Z., Potter, J. D., & Borejdo, J. (2011). Myosin cross-bridges do not form precise rigor bonds in hypertrophic heart muscle carrying troponin t mutations. Journal of Molecular and Cellular Cardiology, 51(3), 409-418.