Molecular and Functional Properties of a Calpain Activator Protein Specific for μ-Isoforms*

  1. Sandro Pontremoli
  1. From the Institute of Biological Chemistry, University of Genoa, Viale Benedetto XV, 1-16132 Genoa, Italy

Abstract

A natural calpain activator protein has been isolated from bovine brain and characterized in its properties and molecular structure. The protein is a homodimer with a molecular mass of about 30 kDa and results in being almost identical to UK114 goat liver protein. Significant similarities with mouse HR12 protein were also observed, whereas a lower degree of similarity was found with a family of heat-responsive proteins named YJGF and YABJ fromHaemophilus influenzae and Bacillus subtilis, respectively.

The brain activator expresses a strict specificity for the μ-calpain isoform, being completely ineffective on the m-calpain form. As expected, also UK114 was found to possess calpain-activating properties, indistinguishable from those of bovine brain activator. A protein showing the same calpain-activating activity has been also isolated from human red cells, indicating that this factor is widely expressed. All these activators are efficient on μ-calpain independently from the source of the proteinase.

The high degree of specificity of the calpain activator for a single calpain isoform may be relevant for the understanding of sophisticated intracellular mechanisms underlying intracellular proteolysis. These data are indicating the existence of a new component of the Ca2+-dependent proteolytic system, constituted of members of a chaperonin-like protein family and capable of promoting intracellular calpain activation.

Footnotes

  • * The work was supported by grants from Ministero dell’ Universitá e della Ricerca Scientifica e Tecnologica and from the Associazione Italiana per la Ricerca sul Cancro.The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

  • To whom correspondence should be addressed. Tel.: 39-10-3538128; Fax: 39-10-518343 or 39-10-354415; E-mail:melloni{at}csita.unige.it.

  • Received December 17, 1997.
  • Revision received February 25, 1998.
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