Literature DB >> 2553122

Chicken skeletal muscle has three Ca2+-dependent proteinases.

F H Wolfe1, S K Sathe, D E Goll, W C Kleese, T Edmunds, S M Duperret.   

Abstract

Chicken breast muscle has three Ca2+-dependent proteinases, two requiring millimolar Ca2+ (m-calpain and high m-calpain) and one requiring micromolar Ca2+ (mu-calpain). High m-calpain co-purifies with mu-calpain through successive DEAE-cellulose (steep gradient), phenyl-Sepharose, octylamine agarose, and Sephacryl S-300 columns, but elutes after mu-calpain when using a shallow KCl gradient to elute a DEAE-cellulose column. The mu- and m-calpains have 80 and 28 kDa polypeptides and are analogous to the mu- and m-calpains that have been purified from bovine, porcine and rabbit skeletal muscle. High m-calpain, which seems to be a new Ca2+-dependent proteinase, is still heterogeneous after the DEAE-cellulose column eluted with a shallow KCl gradient. Additional purification through two successive HPLC-DEAE columns and one HPLC-SW-4000 gel permeation column produces a fraction having six major polypeptides and 6-8 minor polypeptides on SDS-PAGE. A 74-76 kDa polypeptide in this fraction reacts in Western blots with monospecific, polyclonal anti-calpain antibodies that react with both the 80 kDa and the 28 kDa polypeptides of mu- or m-calpain. High m-calpain also is related to mu- and m-calpain in that it causes the same limited digestion of skeletal muscle myofibrils, has a similar pH optimum near pH 7.9-8.4, requires Ca2+ for activity, and reacts with the calpain inhibitor, calpastatin, and a variety of serine and cysteine proteinase inhibitors in a manner identical to mu- and m-calpain. High m-calpain differs from mu- and m-calpain in its elution off DEAE-cellulose columns and its requirement of 3800 microM Ca2+ for one-half maximal activity compared with 5.35 microM Ca2+ for mu-calpain and 420 microM Ca2+ for m-calpain. The physiological significance of high m-calpain in unclear. The presence of mu-calpain in chicken breast muscle suggests that all skeletal muscles contain both mu- and m-calpain, although the relative proportions of these two proteinases may vary in different species.

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Year:  1989        PMID: 2553122     DOI: 10.1016/0167-4838(89)90280-x

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  3 in total

1.  Calpain-PKC inter-relations in mouse hippocampus: a biochemical approach.

Authors:  K Touyarot; S Poussard; C Verret; B Aragon; P Cottin; X Nogues; J Micheau
Journal:  Neurochem Res       Date:  2000-06       Impact factor: 3.996

2.  Properties of easily releasable myofilaments: are they the first step in myofibrillar protein turnover?

Authors:  Girija Neti; Stefanie M Novak; Valery F Thompson; Darrel E Goll
Journal:  Am J Physiol Cell Physiol       Date:  2009-03-25       Impact factor: 4.249

3.  Protein kinase Calpha is a calpain target in cultured embryonic muscle cells.

Authors:  B Aragon; S Poussard; S Dulong; K Touyarot; E Dargelos; J J Brustis; D Levieux; A Ducastaing; P Cottin
Journal:  Mol Cell Biochem       Date:  2002-02       Impact factor: 3.396

  3 in total

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