Journal article
Cathepsin H is an additional convertase of pro-granzyme B
ME D'Angelo, PI Bird, C Peters, T Reinheckel, JA Trapaniand, VR Sutton
Journal of Biological Chemistry | AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC | Published : 2010
Abstract
The serine protease granzyme B (GrB) is the most potent proapoptotic cytotoxin of the granule exocytosis pathway of cytotoxic lymphocytes. GrB is synthesized as a zymogen (proGrB) and activated in cytotoxic granules by the lysosomal cysteine protease cathepsin C (CatC) which removes the N-terminal dipeptide Gly-Glu. It has been shown recently that mice lacking CatC nonetheless express significant residual GrB activity, indicating the presence of additional proGrB convertases. Here, we describe an assay to assess activation of proGrB and show that the amino-peptidase cathepsin H (CatH) has proGrB convertase activity in vitro, whereas dipeptidylpeptidase II does not. We generated mice lacking ..
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Grants
Awarded by National Health and Medical Research Council of Australia (NHMRC)
Funding Acknowledgements
Supported by an Australian postgraduate award.Supported by Program Grant 490900 from the National Health and Medical Research Council of Australia (NHMRC). To whom correspondence may be addressed: Dept. of Biochemistry and Molecular Biology, Monash University, Clayton, 3800 Victoria, Australia. Tel.: 61-3-9902-9365; Fax: 61-3-99029500; E-mail: phillip.bird@med.monash.edu.au.Recipient of a senior fellowship from the NHMRC (288999).Supported by Program Grant 454569 from the NHMRC.