Literature DB >> 7751401

Effect of unphosphorylated smooth muscle myosin on caldesmon-mediated regulation of actin filament velocity.

K Y Horiuchi1, S Chacko.   

Abstract

The effect of smooth muscle myosin at different levels of light chain phosphorylation on caldesmon-mediated movement of actin filaments was investigated using an in vitro motility assay. Myosin at different levels of phosphorylation was obtained by mixing different proportions of fully phosphorylated and unphosphorylated myosin in monomeric form, while keeping the total myosin concentration constant. The average velocity of actin filaments containing tropomyosin was 1.20 +/- 0.046 microns s-1 at 30 degrees C with fully phosphorylated myosin. This velocity was not altered when the percentage of unphosphorylated myosin coated on the nitrocellulose surface was increased to 80%; further increases lowered the velocity. When the actin filaments with caldesmon bound at stoichiometric levels were used, filament velocity was unaffected until 50% of the myosin was unphosphorylated, but further increases in the percentage of unphosphorylated myosin induced a decrease in the velocity, and at 95% unphosphorylated myosin, filament movement had ceased. The decreased filament velocity in the presence of caldesmon was also observed when phosphorylated myosin was mixed with myosin rod instead of unphosphorylated myosin, but was not observed when the 38 kDa caldesmon C-terminal fragment, which lacks the myosin-binding domain, was used instead of intact caldesmon. These data indicate that the decreased filament velocity in the presence of caldesmon reflects the mechanical load produced by the tethering of actin to myosin through the interaction of the caldesmon N-terminal domain and the myosin S-2 region. The tethering effect mediated by caldesmon may play a role in smooth muscle contraction when a large number of myosin heads are dephosphorylated, as in force maintenance.

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Year:  1995        PMID: 7751401     DOI: 10.1007/BF00125306

Source DB:  PubMed          Journal:  J Muscle Res Cell Motil        ISSN: 0142-4319            Impact factor:   2.698


  42 in total

1.  Stoichiometry and stability of caldesmon in native thin filaments from sheep aorta smooth muscle.

Authors:  S Marston
Journal:  Biochem J       Date:  1990-12-01       Impact factor: 3.857

2.  Phosphorylation of caldesmon prevents its interaction with smooth muscle myosin.

Authors:  C Sutherland; M P Walsh
Journal:  J Biol Chem       Date:  1989-01-05       Impact factor: 5.157

Review 3.  The function of myosin and myosin light chain kinase phosphorylation in smooth muscle.

Authors:  K E Kamm; J T Stull
Journal:  Annu Rev Pharmacol Toxicol       Date:  1985       Impact factor: 13.820

4.  Functional domain of caldesmon.

Authors:  A Szpacenko; R Dabrowska
Journal:  FEBS Lett       Date:  1986-07-07       Impact factor: 4.124

5.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

6.  Preparation of myosin and its subfragments from rabbit skeletal muscle.

Authors:  S S Margossian; S Lowey
Journal:  Methods Enzymol       Date:  1982       Impact factor: 1.600

7.  Chemical energy usage during shortening and work production in mammalian smooth muscle.

Authors:  T M Butler; M J Siegman; S U Mooers
Journal:  Am J Physiol       Date:  1983-03

8.  Caldesmon binds to smooth muscle myosin and myosin rod and crosslinks thick filaments to actin filaments.

Authors:  S Marston; K Pinter; P Bennett
Journal:  J Muscle Res Cell Motil       Date:  1992-04       Impact factor: 2.698

9.  Binding of caldesmon to smooth muscle myosin.

Authors:  M Ikebe; S Reardon
Journal:  J Biol Chem       Date:  1988-03-05       Impact factor: 5.157

10.  The binding of caldesmon to actin and its effect on the ATPase activity of soluble myosin subfragments in the presence and absence of tropomyosin.

Authors:  L Velaz; M E Hemric; C E Benson; J M Chalovich
Journal:  J Biol Chem       Date:  1989-06-05       Impact factor: 5.157

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  12 in total

Review 1.  Random walks with thin filaments: application of in vitro motility assay to the study of actomyosin regulation.

Authors:  Steven Marston
Journal:  J Muscle Res Cell Motil       Date:  2003       Impact factor: 2.698

2.  Both N-terminal myosin-binding and C-terminal actin-binding sites on smooth muscle caldesmon are required for caldesmon-mediated inhibition of actin filament velocity.

Authors:  Z Wang; H Jiang; Z Q Yang; S Chacko
Journal:  Proc Natl Acad Sci U S A       Date:  1997-10-28       Impact factor: 11.205

3.  A simple method for automatic tracking of actin filaments in the motility assay.

Authors:  S B Marston; I D Fraser; W Bing; G Roper
Journal:  J Muscle Res Cell Motil       Date:  1996-08       Impact factor: 2.698

4.  Location of smooth-muscle myosin and tropomyosin binding sites in the C-terminal 288 residues of human caldesmon.

Authors:  P A Huber; I D Fraser; S B Marston
Journal:  Biochem J       Date:  1995-12-01       Impact factor: 3.857

5.  Contractile response of human anterior vaginal muscularis in women with and without pelvic organ prolapse.

Authors:  Gina M Northington; Maureen Basha; Lily A Arya; Alan J Wein; Samuel Chacko
Journal:  Reprod Sci       Date:  2010-12-30       Impact factor: 3.060

6.  Caldesmon exhibits a clustered distribution along individual chicken gizzard native thin filaments.

Authors:  K Mabuchi; Y Li; A Carlos; C L Wang; P Graceffa
Journal:  J Muscle Res Cell Motil       Date:  2001       Impact factor: 2.698

7.  Location and functional characterization of myosin contact sites in smooth muscle caldesmon.

Authors:  A V Vorotnikov; S B Marston; P A Huber
Journal:  Biochem J       Date:  1997-11-15       Impact factor: 3.857

Review 8.  Caldesmon and the regulation of cytoskeletal functions.

Authors:  C L Albert Wang
Journal:  Adv Exp Med Biol       Date:  2008       Impact factor: 2.622

9.  The role of caldesmon and its phosphorylation by ERK on the binding force of unphosphorylated myosin to actin.

Authors:  Horia Nicolae Roman; Nedjma B Zitouni; Linda Kachmar; Andrea Benedetti; Apolinary Sobieszek; Anne-Marie Lauzon
Journal:  Biochim Biophys Acta       Date:  2014-08-07

10.  Amino acid mutations in the caldesmon COOH-terminal functional domain increase force generation in bladder smooth muscle.

Authors:  Maoxian Deng; Ettickan Boopathi; Joseph A Hypolite; Tobias Raabe; Shaohua Chang; Stephen Zderic; Alan J Wein; Samuel Chacko
Journal:  Am J Physiol Renal Physiol       Date:  2013-08-28
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