A family of serine esterases in lytic granules of cytolytic T lymphocytes
Details
Serval ID
serval:BIB_BD197D518435
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
A family of serine esterases in lytic granules of cytolytic T lymphocytes
Journal
Cell
ISSN
0092-8674 (Print)
Publication state
Published
Issued date
06/1987
Volume
49
Number
5
Pages
679-85
Notes
Journal Article
Research Support, Non-U.S. Gov't --- Old month value: Jun 5
Research Support, Non-U.S. Gov't --- Old month value: Jun 5
Abstract
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.
Keywords
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
Create date
24/01/2008 15:19
Last modification date
20/08/2019 15:31