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Keywords: calpain
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Biochem J (2015) 465 (3): 405–412.
Published: 22 January 2015
...-unrelated inhibitors of calpain suppress formation of endocytic vacuoles, suggesting that this Ca 2+ -dependent protease is a mediator between Ca 2+ elevation and endocytic vacuole formation. Endocytic vacuoles are ‘initiating’ organelles in the development of acute pancreatitis. In the present study, we...
Includes: Multimedia, Supplementary data
Articles
Biochem J (2014) 459 (2): 355–368.
Published: 28 March 2014
...Teresa Arnandis; Ivan Ferrer-Vicens; Luis Torres; Concha García; Elena R. Garcia-Trevijano; Rosa Zaragoza; Juan R. Viña Calpains become activated in the mammary gland early during weaning, cleaving several proteins located mainly in the cell membrane, but also in other organelles such as lysosomes...
Includes: Supplementary data
Articles
Biochem J (2013) 453 (2): 303–310.
Published: 28 June 2013
... unknown. In the present paper, we demonstrate that skNAC regulates calpain activity. Specifically, we show that inhibition of skNAC gene expression leads to enhanced, and overexpression of the skNAC gene to repressed, activity of calpain 1 and, to a lesser extent, calpain 3 in myoblasts. In skNAC siRNA...
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Biochem J (2011) 436 (1): 113–121.
Published: 27 April 2011
..., analysed the consequences of defective myotilin degradation and tested whether disease-causing myotilin mutations result in altered protein turnover. The results indicate that myotilin is a substrate for the Ca 2+ -dependent protease calpain and identify two calpain cleavage sites in myotilin by MS. We...
Includes: Supplementary data
Articles
Biochem J (2010) 430 (3): 531–538.
Published: 27 August 2010
...André Struglics; Maria Hansson Mature aggrecan is generally C-terminally truncated at several sites in the CS (chondroitin sulfate) region. Aggrecanases and MMPs (matrix metalloproteinases) have been suggested to be responsible for this digestion. To identify whether calpain, a common intracellular...
Includes: Supplementary data
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Biochem J (2006) 394 (3): 715–725.
Published: 24 February 2006
...Ming Cheng Liu; Veronica Akle; Wenrong Zheng; Jitendra R. Dave; Frank C. Tortella; Ronald L. Hayes; Kevin K. W. Wang A major theme of TBI (traumatic brain injury) pathology is the over-activation of multiple proteases. We have previously shown that calpain-1 and -2, and caspase-3 simultaneously...
Includes: Supplementary data
Articles
Biochem J (2005) 389 (1): 223–231.
Published: 21 June 2005
... in RCP. PEST motifs play a role in targeting a protein for proteolytic degradation. We have demonstrated that RCP undergoes calcium-dependent degradation which can be prevented by specific calpain inhibitors. Using a mutant, lacking the three PEST sequences, RCP ΔPEST , we demonstrated...
Includes: Supplementary data
Articles
Biochem J (2005) 388 (3): 741–744.
Published: 07 June 2005
...Zoltán BOZÓKY; Anita ALEXA; Peter TOMPA; Peter FRIEDRICH Typical calpains in mammals become activated on binding of 8–12 Ca 2+ ions per enzyme molecule, giving an example of integrated, manifold regulation by calcium. Besides two identified Ca 2+ sites in catalytic domain II and several EF-hand...
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Biochem J (2004) 378 (2): 299–305.
Published: 01 March 2004
...Attila FARKAS; Peter TOMPA; Éva SCHÁD; Rita SINKA; Gáspár JÉKELY; Peter FRIEDRICH Calpain B is one of the two calpain homologues in Drosophila melanogaster that are proteolytically active. We studied its activation by Ca 2+ both in vitro and in vivo , in Schneider (S2) cells. Activation involves...
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Biochem J (2003) 376 (3): 625–632.
Published: 15 December 2003
...David S. PAUL; Anne W. HARMON; Courtney P. WINSTON; Yashomati M. PATEL Calpains are a family of non-lysosomal cysteine proteases. Recent studies have identified a member of the calpain family of proteases, calpain 10, as a putative diabetes-susceptibility gene that may be involved...
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Biochem J (2003) 375 (3): 643–651.
Published: 01 November 2003
... membrane. Here, we show that specific regions of the N-terminus of IP 3 -3KB are necessary and sufficient for efficient membrane localization of the protein. We also report that, in the presence of Ca 2+ , the kinase domain of IP 3 -3KB is cleaved from the membrane-anchoring region by calpain...
Articles
Biochem J (2003) 374 (2): 403–411.
Published: 01 September 2003
... that oxLDL-induced death of HMEC-1 cells is accompanied by activation of calpain. The μ-calpain inhibitor PD 151746 decreased oxLDL-induced cytotoxicity, whereas the general caspase inhibitor BAF (t-butoxycarbonyl-Asp-methoxyfluoromethylketone) had no effect. Also, oxLDL provoked calpain-dependent...
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Biochem J (2002) 368 (3): 905–913.
Published: 15 December 2002
..., PKC∊ or PKCΔ isoforms (CDα, CD∊ and CDΔ respectively) accumulated, and this accumulation was dependent on the activity of both calpain and caspase; and (2) transient expression of CDα, CD∊ or CDΔ sufficed to induce apoptosis. However, following this initial step of proteolytic activation, the pathways...
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Biochem J (2002) 365 (3): 791–799.
Published: 01 August 2002
... by the PtdIns-specific-PLC inhibitor ET-18-OCH 3 and the calpain inhibitor calpeptin, suggesting that 3-kinase activation in BBM lies downstream of PLC activation in BLM and is a calpain-mediated event. Moreover, the increase in immunoprecipitable PI3K-C2β activity, which is sensitive to wortmannin (10nM...
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Biochem J (2000) 351 (2): 403–411.
Published: 10 October 2000
... and breast cancer cell lines by Western-blot analysis shows a lack of tensin expression in most cancer cell lines, whereas these lines express considerable amounts of focal-adhesion molecules such as talin and focal-adhesion kinase. Finally, tensin is rapidly cleaved by a focal-adhesion protease, calpain II...