Literature DB >> 6123314

Degradation of smooth-muscle myosin by trypsin-like serine proteinases.

J Kay, R F Siemankowski, L M Siemankowski, D E Goll.   

Abstract

1. Hydrolysis of the myosins from smooth and from skeletal muscle by a rat trypsin-like serine proteinase and by bovine trypsin at pH 7 is compared. 2. Proteolysis of the heavy chains of both myosins by the rat enzyme proceeds at rates approx. 20 times faster than those obtained with bovine trypsin. Whereas cleavage of skeletal-muscle myosin heavy chain by both enzymes results in the generation of conventional products i.e. heavy meromyosin and light meromyosin, the heavy chain of smooth-muscle myosin is degraded into a fragment of mol. wt. 150000. This is dissimilar from heavy meromyosin and cannot be converted into heavy meromyosin. It is shown that proteolysis of the heavy chain takes place in the head region. 3. The 'regulatory' light chain (20kDa) of smooth-muscle myosin is degraded very rapidly by the rat proteinase. 4. The ability of smooth-muscle myosin to have its ATPase activity activated by actin in the presence of a crude tropomyosin fraction on introduction of Ca2+ is diminished progressively during exposure to the rat proteinase. The rate of loss of the Ca2+-activated actomyosin ATPase activity is very similar to the rate observed for proteolysis of the heavy chain and 3-4 times slower than the rate of removal of the so-called 'regulatory' light chain. 5. The significance of these findings in terms of the functional organization of the smooth muscle myosin molecule is discussed. 6. Since the degraded myosin obtained after exposure to very small amounts of the rat proteinase is no longer able to respond to Ca2+, i.e. the functional activity of the molecule has been removed, the implications of a similar type of proteolysis operating in vivo are considered for myofibrillar protein turnover in general, but particularly with regard to the initiation of myosin degradation, which is known to take place outside the lysosome (i.e. at neutral pH).

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Year:  1982        PMID: 6123314      PMCID: PMC1163640          DOI: 10.1042/bj2010267

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  44 in total

1.  Comparative studies on the structure and aggregative properties of the myosin molecule. I. The structure of the lobster myosin molecule.

Authors:  R F Siemankowski; C R Zobel
Journal:  J Mechanochem Cell Motil       Date:  1976-03

2.  A relationship between Ca2+ sensitivity and phosphorylation of gizzard actomyosin.

Authors:  M O Aksoy; D Williams; E M Sharkey; D J Hartshorne
Journal:  Biochem Biophys Res Commun       Date:  1976-03-08       Impact factor: 3.575

3.  The effect of phosphorylation of gizzard myosin on actin activation.

Authors:  A Górecka; M O Aksoy; D J Hartshorne
Journal:  Biochem Biophys Res Commun       Date:  1976-07-12       Impact factor: 3.575

4.  A simple method of preparing actin-free myosin from smooth muscle.

Authors:  S Ebashi
Journal:  J Biochem       Date:  1976-01       Impact factor: 3.387

5.  Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane.

Authors:  G Fairbanks; T L Steck; D F Wallach
Journal:  Biochemistry       Date:  1971-06-22       Impact factor: 3.162

6.  Comparative studies of human smooth and striated muscle myosins.

Authors:  U Gröschel-Stewart
Journal:  Biochim Biophys Acta       Date:  1971-02-16

7.  Molecular weight estimation of polypeptide chains by electrophoresis in SDS-polyacrylamide gels.

Authors:  A L Shapiro; E Viñuela; J V Maizel
Journal:  Biochem Biophys Res Commun       Date:  1967-09-07       Impact factor: 3.575

8.  A Ca2+-activated protease possibly involved in myofibrillar protein turnover. Partial characterization of the purified enzyme.

Authors:  W R Dayton; W J Reville; D E Goll; M H Stromer
Journal:  Biochemistry       Date:  1976-05-18       Impact factor: 3.162

9.  A Ca2+-activated protease possibly involved in myofibrillar protein turnover. Purification from porcine muscle.

Authors:  W R Dayton; D E Goll; M G Zeece; R M Robson; W J Reville
Journal:  Biochemistry       Date:  1976-05-18       Impact factor: 3.162

10.  Selective control of the degradation of normal and aberrant proteins in Reuber H35 hepatoma cells.

Authors:  S E Knowles; F J Ballard
Journal:  Biochem J       Date:  1976-06-15       Impact factor: 3.857

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  7 in total

1.  Degradation of myofibrillar proteins by trypsin-like serine proteinases.

Authors:  J Kay; L M Siemankowski; R F Siemankowski; J A Greweling; D E Goll
Journal:  Biochem J       Date:  1982-02-01       Impact factor: 3.857

2.  Isolation of silica-dependent protein from rat lung with special reference to development of fibrosis.

Authors:  M Aalto; E Kulonen; J Pikkarainen
Journal:  Br J Exp Pathol       Date:  1989-04

3.  Purification of a neutral proteinase, associated with the actomyosin complex, from uterine myometrium.

Authors:  R Barth; M Hoechst; E G Afting
Journal:  Biochem J       Date:  1984-09-15       Impact factor: 3.857

4.  Lipase-induced alterations of fatty acid synthesis by subcellular fractions from germinating pea (Pisum sativum L.).

Authors:  J Sanchez; B R Jordan; J Kay; J L Harwood
Journal:  Biochem J       Date:  1982-05-15       Impact factor: 3.857

5.  Immunolocalization of cathepsin D in normal and neoplastic human tissues.

Authors:  W A Reid; M J Valler; J Kay
Journal:  J Clin Pathol       Date:  1986-12       Impact factor: 3.411

6.  Myosin accumulation and striated muscle myopathy result from the loss of muscle RING finger 1 and 3.

Authors:  Jens Fielitz; Mi-Sung Kim; John M Shelton; Shuaib Latif; Jeffrey A Spencer; David J Glass; James A Richardson; Rhonda Bassel-Duby; Eric N Olson
Journal:  J Clin Invest       Date:  2007-09       Impact factor: 14.808

7.  Dense bodies and actin polarity in vertebrate smooth muscle.

Authors:  M Bond; A V Somlyo
Journal:  J Cell Biol       Date:  1982-11       Impact factor: 10.539

  7 in total

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