Isolation and Characterization of Myosin from Subjects with Asymmetric Sepatal Hypertrophy

Human cardiac myosin isolated from operatively obtained samples of ventricular septum and left ventricular free wall of subjects with asymmetric septal hypertrophy (ASH) was compared, with respect to structural and enzymatic propesrties, to myosin isolated from hearts of subjects without heart disease. The following parameters were studied(1) activation of myosin ATP-ase activity by K+-EDTA and Ca2+, (2) molecular weight of the heavy and light chains of myosin as determined by electrophoretic migration in polyacrylamide-sodium dodecyl sulfate (SDS) gels, and (3) ability to form bipolar aggregates at low ionic strength, as examined by electron microscopy. No difference was present in any of these parameters between human cardiac myosin from subjects with ASH and from subjects without heart disease. Thus, the genetic defect present in subjects with ASH is not expressed in the particular structural and functional characteristics of myosin evaluated in this study.

[1]  I. J. Don Asymmetric septal hypertrophy. , 1976, Minnesota medicine.

[2]  D. Zipes,et al.  The site of functional right bundle branch block in the intact canine heart. , 1975, Advances in cardiology.

[3]  J. Léger,et al.  Human cardiac myosin ATPase and light subunits. A comparative study. , 1975, Biochimica et biophysica acta.

[4]  A. Salel,et al.  Chronological effects of mild pressure overload on myosin ATPase activity in the canine right ventricle. , 1975, Journal of molecular and cellular cardiology.

[5]  W. Henry,et al.  Asymmetric Septal Hypertrophy (ASH) in Infancy , 1974, Circulation.

[6]  W. Roberts,et al.  Differences in Distribution of Myocardial Abnormalities in Patients with Obstructive and Nonobstructive Asymmetric Septal Hypertrophy (ASH): Echocardiographic and Gross Anatomic Findings , 1974, Circulation.

[7]  T. Katagiri,et al.  Studies on the substructure of myosin in cardiac hypertrophy. Characterization of light chains. , 1974, Biochimica et biophysica acta.

[8]  W. Roberts,et al.  Differences in distribution of myocardial abnormalities in patients with obstructive and nonobstructive asymmetric septal hypertrophy (ASH). Light and electron microscopic findings. , 1974, Circulation.

[9]  W. Henry,et al.  Familial prevalence and genetic transmission of idiopathic hypertrophic subaortic stenosis. , 1973, The New England journal of medicine.

[10]  R. Macalpin,et al.  Left ventricular hypertrophy diagnosed by echocardiography. , 1973, The New England journal of medicine.

[11]  W. Henry,et al.  Asymmetric Septal Hypertrophy: Echocardiographic Identification of the Pathognomonic Anatomic Abnormality of IHSS , 1973, Circulation.

[12]  Roberts Wc Valvular, subvalvular and supravalvular aortic stenosis: morphologic features. , 1973 .

[13]  W. Roberts Valvular, subvalvular and supravalvular aortic stenosis: morphologic features. , 1973, Cardiovascular clinics.

[14]  V. Ferrans,et al.  Myocardial Ultrastructure in Idiopathic Hypertrophic Subaortic Stenosis: A Study of Operatively Excised Left Ventricular Outflow Tract Muscle in 14 Patients , 1972, Circulation.

[15]  R. Myerburg,et al.  Physiology of Canine Intraventricular Conduction and Endocardial Excitation , 1972, Circulation research.

[16]  T. Pollard,et al.  Isolation and characterization of myosin and two myosin fragments from human blood platelets. , 1971, Proceedings of the National Academy of Sciences of the United States of America.

[17]  D. Wallach,et al.  Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane. , 1971, Biochemistry.

[18]  W. J. Mueller,et al.  Propagation of Impulses across the Purkinje Fiber‐Muscle Junctions in the Dog Heart , 1970, Circulation research.

[19]  K. Weber,et al.  The reliability of molecular weight determinations by dodecyl sulfate-polyacrylamide gel electrophoresis. , 1969, The Journal of biological chemistry.

[20]  W. J. Mueller,et al.  Interaction of Transmembrane Potentials in Canine Purkinje Fibers and at Purkinje Fiber‐Muscle Junctions , 1969, Circulation research.

[21]  J. Carney,et al.  AN ELECTRON MICROSCOPE STUDY OF CANINE CARDIAC MYOSIN AND SOME OF ITS AGGREGATES , 1966, The Journal of cell biology.

[22]  H. Huxley,et al.  ELECTRON MICROSCOPE STUDIES ON THE STRUCTURE OF NATURAL AND SYNTHETIC PROTEIN FILAMENTS FROM STRIATED MUSCLE. , 1963, Journal of molecular biology.

[23]  A. L. Brown,et al.  The Clinical, Hemodynamic, and Pathologic Diagnosis of Muscular Subvalvular Aortic Stenosis , 1961, Circulation.

[24]  L. B. Bradley,et al.  The relationship between sulfhydryl groups and the activation of myosin adenosinetriphosphatase. , 1956, The Journal of biological chemistry.

[25]  O. H. Lowry,et al.  Protein measurement with the Folin phenol reagent. , 1951, The Journal of biological chemistry.