Mommaerts W F, Vegh K, Seraydarian K, Meier K, Rittschof D
J Muscle Res Cell Motil. 1982 Jun;3(2):129-44. doi: 10.1007/BF00711938.
Procedures have been developed for the preparation of pure myosin heavy chain (h-myosin) by preparative gel electrophoresis, and for the characterization of h-myosin by cyanogen bromide peptide mapping. Major sources of error are the oxidation of methionine and the proteolytic splitting of the chain during purification. These errors have been eliminated. A peculiar feature is the doubling or quadrupling of a peptide of molecular weight 17 000. The results show structural differences between isomyosins derived from myonal types within the same animal, as well as interspecies differences.