A family of serine esterases in lytic granules of cytolytic T lymphocytes

Détails

ID Serval
serval:BIB_BD197D518435
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
A family of serine esterases in lytic granules of cytolytic T lymphocytes
Périodique
Cell
Auteur⸱e⸱s
Masson  D., Tschopp  J.
ISSN
0092-8674 (Print)
Statut éditorial
Publié
Date de publication
06/1987
Volume
49
Numéro
5
Pages
679-85
Notes
Journal Article
Research Support, Non-U.S. Gov't --- Old month value: Jun 5
Résumé
Cytoplasmic granules of cytolytic T lymphocytes (CTLs) contain, in addition to the pore-forming protein perforin, a family of highly homologous serine esterases, granzymes A-H. The serine esterase affinity label diisopropyl fluorophosphate reacts strongly with granzymes A and D, to a lesser extent with B, E, F, G, and H, and not at all with C and F. For granzymes A and D, synthetic substrates have been found. Antibodies raised against granzyme B strongly cross-react with A, G, and H, and antibodies to granzyme D recognize C, E, and F. These antigenic relationships correlate with similarities in the N-terminal amino acid sequences. At least 60% homology is observed between the eight proteins, and all are similar to rat mast cell protease 2. Sequence analysis suggests the identity of granzyme A with a protease predicted from a CTL-specific cDNA clone (H factor) and of granzyme B, G, or H with a protein encoded by the CTL-specific cDNA clone CTLA 1/CCP 1.
Mots-clé
Amino Acid Sequence Animals Cytoplasmic Granules/*enzymology Endopeptidases/metabolism Esterases/genetics/*metabolism Granzymes Rats Sequence Homology, Nucleic Acid *Serine Endopeptidases T-Lymphocytes, Cytotoxic/*enzymology
Pubmed
Web of science
Création de la notice
24/01/2008 15:19
Dernière modification de la notice
20/08/2019 15:31
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