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. 1980 Sep 1;86(3):775–783. doi: 10.1083/jcb.86.3.775

Biochemical and ultrastructural aspects of Mr 165,000 M-protein in cross-striated chicken muscle

PMCID: PMC2110687  PMID: 6997322

Abstract

To better understand the relationship between the Mr 165,000 M-line protein (M-protein) and H-zone structure in skeletal and in cardiac muscle, as well as the possible interaction of M-protein with another skeletal muscle M-line component, the homodimeric creatine kinase isoenzyme composed of two M subunits (MM-CK), we performed biochemical, immunological, and ultrastructural studies on myofibrils extracted by different procedures. In contrast to MM-CK, M-protein could not be completely removed from myofibrils by low ionic strength extraction. Fab-fragments of antibodies against M-protein could not release M- protein quantitatively from either breast or heart myofibrils but remained bound to the myofibrillar structure, whereas monovalent antibodies against MM-CK cause the specific release of MM-CK and the concomitant disappearance of the M-line from chicken skeletal muscle myofibrils. When MM-CK was removed from skeletal myofibrils by low ionic strength extraction or, more specifically, by incubation with anti-MM-CK Fab, M-protein was still not released quantitatively upon treatment with anti-M-protein Fab as judged from immunofluorescence data. In the ultrastructural investigation of low ionic strength extracted muscle fibers, M protein could be localized in two stripes on both sides of the former M-line, suggesting a reduced attachment to the residual H-zone structure, whereas the specific removal of MM-CK resulted in the same dense staining pattern for M-protein within the M- line as observed in untreated fibers. However, the binding of M-protein to the residual M-line structure seemed to be reduced, as a considerable amount of this protein could be identified in the supernate of sequentially incubated myofibrils. The results indicate a strong binding of M-protein within the H-zone structure of skeletal as well as heart myofibrils.

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Selected References

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  1. Botts J., Stone D. B., Wang A. T., Mendelson R. A. Electron paramagnetic resonance and nanosecond fluorescence depolarization studies on creatine-phosphokinase interaction with myosin and its fragments. J Supramol Struct. 1975;3(2):141–145. doi: 10.1002/jss.400030206. [DOI] [PubMed] [Google Scholar]
  2. CORSI A., PERRY S. V. Some observations on the localization of myosin, actin and tropomyosin in the rabbit myofibril. Biochem J. 1958 Jan;68(1):12–17. doi: 10.1042/bj0680012. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Dawson D. M., Eppenberger H. M., Kaplan N. O. Creatine kinase: evidence for a dimeric structure. Biochem Biophys Res Commun. 1965 Nov 22;21(4):346–353. doi: 10.1016/0006-291x(65)90200-7. [DOI] [PubMed] [Google Scholar]
  4. Eaton B. L., Pepe F. A. M band protein. Two components isolated from chicken breast muscle. J Cell Biol. 1972 Dec;55(3):681–695. doi: 10.1083/jcb.55.3.681. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Eppenberger H. M., Dawson D. M., Kaplan N. O. The comparative enzymology of creatine kinases. I. Isolation and characterization from chicken and rabbit tissues. J Biol Chem. 1967 Jan 25;242(2):204–209. [PubMed] [Google Scholar]
  6. HUXLEY H. E. ELECTRON MICROSCOPE STUDIES ON THE STRUCTURE OF NATURAL AND SYNTHETIC PROTEIN FILAMENTS FROM STRIATED MUSCLE. J Mol Biol. 1963 Sep;7:281–308. doi: 10.1016/s0022-2836(63)80008-x. [DOI] [PubMed] [Google Scholar]
  7. HUXLEY H. E., HANSON J. Quantitative studies on the structure of cross-striated myofibrils. I. Investigations by interference microscopy. Biochim Biophys Acta. 1957 Feb;23(2):229–249. doi: 10.1016/0006-3002(57)90325-6. [DOI] [PubMed] [Google Scholar]
  8. Heizmann C. W., Eppenberger H. M. Glycogen debranching enzyme from chicken pectoralis muscle. Comparison with a 165 000 mol. wt myofibrillar protein. FEBS Lett. 1979 Sep 1;105(1):35–39. doi: 10.1016/0014-5793(79)80882-0. [DOI] [PubMed] [Google Scholar]
  9. Heizmann C. W., Eppenberger H. M. Isolation and characterization of glycogen phosphorylase b from chicken breast muscle: comparison with a protein extracted from the M. line. J Biol Chem. 1978 Jan 10;253(1):270–277. [PubMed] [Google Scholar]
  10. Herasymowych O. S., Mani R. S., Kay C. M. Isolation, purification and characterization of creatine kinase from bovine cardiac muscle. Biochim Biophys Acta. 1978 May 24;534(1):38–47. doi: 10.1016/0005-2795(78)90473-7. [DOI] [PubMed] [Google Scholar]
  11. Highsmith S., Kretzschmar K. M., O'Konski C. T., Morales M. F. Flexibility of myosin rod, light meromyosin, and myosin subfragment-2 in solution. Proc Natl Acad Sci U S A. 1977 Nov;74(11):4986–4990. doi: 10.1073/pnas.74.11.4986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Houk T. W., Jr, Putman S. V. Location of the creatine phosphokinase binding site of myosin. Biochem Biophys Res Commun. 1973 Dec 19;55(4):1271–1277. doi: 10.1016/s0006-291x(73)80031-2. [DOI] [PubMed] [Google Scholar]
  13. Knappeis G. G., Carlsen F. The ultrastructure of the M line in skeletal muscle. J Cell Biol. 1968 Jul;38(1):202–211. doi: 10.1083/jcb.38.1.202. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Kundrat E., Pepe F. A. The M band. Studies with fluorescent antibody staining. J Cell Biol. 1971 Feb;48(2):340–347. doi: 10.1083/jcb.48.2.340. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  16. Luther P., Squire J. Three-dimensional structure of the vertebrate muscle M-region. J Mol Biol. 1978 Nov 5;125(3):313–324. doi: 10.1016/0022-2836(78)90405-9. [DOI] [PubMed] [Google Scholar]
  17. Mani R. S., Kay C. M. Interaction studies of the 165 000 dalton protein component of the M-line with the S2 subfragment of myosin. Biochim Biophys Acta. 1978 Sep 26;536(1):134–141. doi: 10.1016/0005-2795(78)90059-4. [DOI] [PubMed] [Google Scholar]
  18. Masaki T., Takaiti O., Ebashi S. "M-substance", a new protein constituting the M-line of myofibrils. J Biochem. 1968 Dec;64(6):909–910. doi: 10.1093/oxfordjournals.jbchem.a128975. [DOI] [PubMed] [Google Scholar]
  19. Masaki T., Takaiti O. Purification of M-protein. J Biochem. 1972 Feb;71(2):355–357. doi: 10.1093/oxfordjournals.jbchem.a129774. [DOI] [PubMed] [Google Scholar]
  20. Morimoto K., Harrington W. F. Isolation and physical chemical properties of an M-line protein from skeletal muscle. J Biol Chem. 1972 May 25;247(10):3052–3061. [PubMed] [Google Scholar]
  21. PORTER R. R. The hydrolysis of rabbit y-globulin and antibodies with crystalline papain. Biochem J. 1959 Sep;73:119–126. doi: 10.1042/bj0730119. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Perriard J. C., Caravatti M., Perriard E. R., Eppenberger H. M. Quantitation of creatine kinase isoenzyme transition in differentiating chicken embryonic breast muscle and myogenic cell cultures by immunoadsorption. Arch Biochem Biophys. 1978 Nov;191(1):90–100. doi: 10.1016/0003-9861(78)90070-x. [DOI] [PubMed] [Google Scholar]
  23. SOBER H. A., PETERSON E. A. Protein chromatography on ion exchange cellulose. Fed Proc. 1958 Dec;17(4):1116–1126. [PubMed] [Google Scholar]
  24. Showe M. K., Isobe E., Onorato L. Bacteriophage T4 prehead proteinase. II. Its cleavage from the product of gene 21 and regulation in phage-infected cells. J Mol Biol. 1976 Oct 15;107(1):55–69. doi: 10.1016/s0022-2836(76)80017-4. [DOI] [PubMed] [Google Scholar]
  25. Sjöström M., Squire J. M. Cryo-ultramicrotomy and myofibrillar fine structure: a review. J Microsc. 1977 Dec;111(3):239–278. doi: 10.1111/j.1365-2818.1977.tb00067.x. [DOI] [PubMed] [Google Scholar]
  26. Sjöström M., Squire J. M. Fine structure of the A-band in cryo-sections. The structure of the A-band of human skeletal muscle fibres from ultra-thin cryo-sections negatively stained. J Mol Biol. 1977 Jan 5;109(1):49–68. doi: 10.1016/s0022-2836(77)80045-4. [DOI] [PubMed] [Google Scholar]
  27. Sommer J. R., Johnson E. A. Cardiac muscle. A comparative ultrastructural study with special reference to frog and chicken hearts. Z Zellforsch Mikrosk Anat. 1969;98(3):437–468. [PubMed] [Google Scholar]
  28. Strehler E. E., Pelloni G., Heizmann C. W., Eppenberger H. M. M-protein in chicken cardiac muscle. Exp Cell Res. 1979 Nov;124(1):39–45. doi: 10.1016/0014-4827(79)90255-6. [DOI] [PubMed] [Google Scholar]
  29. Stromer M. H., Hartshorne D. J., Mueller H., Rice R. V. The effect of various protein fractions on Z- and M-line reconstitution. J Cell Biol. 1969 Jan;40(1):167–178. doi: 10.1083/jcb.40.1.167. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Trinick J., Lowey S. M-protein from chicken pectoralis muscle: isolation and characterization. J Mol Biol. 1977 Jun 25;113(2):343–368. doi: 10.1016/0022-2836(77)90146-2. [DOI] [PubMed] [Google Scholar]
  31. Turner D. C., Wallimann T., Eppenberger H. M. A protein that binds specifically to the M-line of skeletal muscle is identified as the muscle form of creatine kinase. Proc Natl Acad Sci U S A. 1973 Mar;70(3):702–705. doi: 10.1073/pnas.70.3.702. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Wallimann T., Kuhn H. J., Pelloni G., Turner D. C., Eppenberger H. M. Localization of creatine kinase isoenzymes in myofibrils. II. Chicken heart muscle. J Cell Biol. 1977 Nov;75(2 Pt 1):318–325. doi: 10.1083/jcb.75.2.318. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Wallimann T., Pelloni G., Turner D. C., Eppenberger H. M. Monovalent antibodies against MM-creatine kinase remove the M line from myofibrils. Proc Natl Acad Sci U S A. 1978 Sep;75(9):4296–4300. doi: 10.1073/pnas.75.9.4296. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Wallimann T., Turner D. C., Eppenberger H. M. Localization of creatine kinase isoenzymes in myofibrils. I. Chicken skeletal muscle. J Cell Biol. 1977 Nov;75(2 Pt 1):297–317. doi: 10.1083/jcb.75.2.297. [DOI] [PMC free article] [PubMed] [Google Scholar]

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