Home LiteratureArticle Details
PMID: 3417855 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Interaction of C-protein with pH 8.0 synthetic thick filaments prepared from the myosin of vertebrate skeletal muscle.

Journal of muscle research and cell motility ·Vol. 9 ·No. 2 ·1988-04-00 ·Pages 174-83

Davis JS

Abstract

The assembly mechanism of synthetic thick filaments of purified myosin formed at pH 8.0 has been extensively studied. These filaments were chosen for experimentation since they share a number of structural features, as well as aspects of the kinetics of their assembly, with native filaments. C-protein copolymerization consistently favours the formation of longer synthetic filaments with the diameter of the crossbridge region remaining comparable to that of the native filament. At moderate concentrations the close-to-symmetrical length distribution typical of pH 8.0 filaments is altered to a distribution with a steep rising, and extended tailing edge towards longer filament lengths. The asymmetric length distributions probably originate from an at least partial exclusion of C-protein from the equivalent of the accessory-protein binding stripes adjacent to the bare zone from which C-protein is apparently excluded in vivo. An outer limit to C-protein binding exists in native filaments. This does not appear to be the case in vitro since filaments significantly longer than the native appear stabilized by C-protein. A minimum of three types of C-protein binding can be resolved. Physiological stoichiometries of C-protein (0 to approximately 0.3 mole ratios) lower the critical concentration of myosin (not length equilibrated) and increase filament length. The lack of a significant change in filament turbidity as these high-affinity sites are occupied is indicative of a C-protein-induced change in the structure of the synthetic filaments. A second set of binding sites occupied at higher mole ratios of C-protein: myosin (approximately 0.3-1.0) are typified by a marked increase in the specific turbidity of the filaments; a result consistent with the addition of weight to such a structure. The precedent of C-protein binding to the subfragment-2 portion of the myosin molecule provides a plausible basis for these observations. A third phase characterized by a less marked increase in turbidity occurs between 1-2:1 (and possibly higher) C-protein: myosin mole ratios. The molecular basis of this process is not immediately apparent.

MeSH Terms
Actin Cytoskeleton/metabolism Animals Carrier Proteins Cytoskeleton/metabolism Hydrogen-Ion Concentration Muscle Proteins/metabolism Myosins/metabolism Rabbits
Chemicals
Carrier Proteins Muscle Proteins myosin-binding protein C Myosins
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Davis J S
Department of Biology, Johns Hopkins University, Baltimore, Maryland 21218.
References (29)
29 references, click to expand
  1. The interaction of C-protein with heavy meromyosin and subfragment-2.
    Biochem J. 1978 Jun 1;171(3):813-6 PMID: 352343
  2. C-protein from rabbit soleus (red) muscle.
    Biochem J. 1981 May 1;195(2):463-9 PMID: 6797400
  3. The myosin filament. III. C-protein.
    J Mol Biol. 1975 Dec 25;99(4):609-17 PMID: 814246
  4. Axial arrangement of crossbridges in thick filaments of vertebrate skeletal muscle.
    J Mol Biol. 1976 Apr 5;102(2):325-32 PMID: 1271466
  5. Preparation of C-protein, H-protein, X-protein, and phosphofructokinase.
    Methods Enzymol. 1982;85 Pt B:130-8 PMID: 6214690
  6. Disassembly kinetics of thick filaments in rabbit skeletal muscle fibers. Effects of ionic strength, Ca2+ concentration, pH, temperature, and cross-bridges on the stability of thick filament structure.
    Biophys J. 1985 Mar;47(3):267-75 PMID: 2983792
  7. Effects of C-protein on synthetic myosin filament structure.
    Biophys J. 1979 Sep;27(3):433-46 PMID: 263692
  8. Direct visualization of the myosin crossbridge helices on relaxed rabbit psoas thick filaments.
    J Mol Biol. 1983 Nov 25;171(1):105-9 PMID: 6685773
  9. Polypeptide chains of intermediate molecular weight in myosin preparations.
    FEBS Lett. 1971 Jun 2;15(1):40-44 PMID: 11945810
  10. Frog skeletal muscle thick filaments are three-stranded.
    J Cell Biol. 1983 Jun;96(6):1797-802 PMID: 6602135
  11. The structure of C-protein and X-protein molecules and a polymer of X-protein.
    J Mol Biol. 1985 Jul 20;184(2):297-309 PMID: 3839853
  12. The aggregation characteristics of column-purified rabbit skeletal myosin in the presence and absence of C-protein at pH 7.0.
    Biophys J. 1982 Feb;37(2):433-40 PMID: 6895856
  13. Myosin filamentogenesis: effects of pH and ionic concentration.
    J Mol Biol. 1966 Sep;20(2):391-401 PMID: 5970667
  14. 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 PMID: 839534
  15. Studies on the formation and physical chemical properties of synthetic myosin filaments.
    Biochemistry. 1966 Nov;5(11):3474-87 PMID: 5972328
  16. Interaction of C-protein with myosin, myosin rod and light meromyosin.
    J Mol Biol. 1975 Sep 5;97(1):1-9 PMID: 1100851
  17. The reconstruction of myosin filaments in rabbit psoas muscle from solubilized myosin.
    J Muscle Res Cell Motil. 1986 Apr;7(2):97-109 PMID: 3711312
  18. Periodic charge distributions in the myosin rod amino acid sequence match cross-bridge spacings in muscle.
    Nature. 1982 Sep 16;299(5880):226-31 PMID: 7202124
  19. Resting myosin cross-bridge configuration in frog muscle thick filaments.
    J Cell Biol. 1986 Feb;102(2):610-8 PMID: 3484742
  20. Interaction of C-protein with myosin.
    J Biochem. 1980 May;87(5):1413-20 PMID: 6893044
  21. H-protein and X-protein. Two new components of the thick filaments of vertebrate skeletal muscle.
    J Mol Biol. 1983 Nov 5;170(3):675-98 PMID: 6415290
  22. Kinetics and thermodynamics of the assembly of the parallel- and antiparallel-packed sections of synthetic thick filaments of skeletal myosin: a pressure-jump study.
    Biochemistry. 1985 Sep 10;24(19):5263-9 PMID: 4074693
  23. The ultrastructural location of C-protein, X-protein and H-protein in rabbit muscle.
    J Muscle Res Cell Motil. 1986 Dec;7(6):550-67 PMID: 3543050
  24. Pressure-jump studies on the length-regulation kinetics of the self-assembly of myosin from vertebrate skeletal muscle into thick filament.
    Biochem J. 1981 Aug 1;197(2):309-14 PMID: 7198910
  25. The influence of pressure on the self-assembly of the thick filament from the myosin of vertebrate skeletal muscle.
    Biochem J. 1981 Aug 1;197(2):301-8 PMID: 7198909
  26. A new protein of the thick filaments of vertebrate skeletal myofibrils. Extractions, purification and characterization.
    J Mol Biol. 1973 Mar 15;74(4):653-76 PMID: 4269687
  27. A model for length-regulation in thick filaments of vertebrate skeletal myosin.
    Biophys J. 1986 Sep;50(3):417-22 PMID: 3756294
  28. The myosin dimer: an intermediate in the self-assembly of the thick filament of vertebrate skeletal muscle.
    FEBS Lett. 1982 Apr 19;140(2):293-7 PMID: 7084470
  29. The location of C-protein in rabbit skeletal muscle.
    Proc R Soc Lond B Biol Sci. 1976 Mar 16;192(1109):451-61 PMID: 4802
Article Info
Journal
Journal of muscle research and cell motility
Abbr.
J Muscle Res Cell Motil
ISSN
0142-4319
Published
1988-04-00
Pages
174-83
Language
English
Region
Netherlands
NLM ID
8006298
Subset
IM
Grants
NIADDK NIH HHS · AM-04349 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com