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

Cell. 1987 Jun 5;49(5):679-85. doi: 10.1016/0092-8674(87)90544-7.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Cytoplasmic Granules / enzymology*
  • Endopeptidases / metabolism
  • Esterases / genetics
  • Esterases / metabolism*
  • Granzymes
  • Rats
  • Sequence Homology, Nucleic Acid
  • Serine Endopeptidases*
  • T-Lymphocytes, Cytotoxic / enzymology*

Substances

  • Esterases
  • serine esterase
  • Endopeptidases
  • Granzymes
  • Serine Endopeptidases