In granules of hematopoetic cells, dipeptidyl peptidase I (DPPI) processes
inactive proenzymes into active enzymes, e.g., lymphocyte progranzyme A. Ou
r goal was to develop in eversible inhibitors of intracellular DPPI. First,
we identified inhibitors with aqueous stability. Then we determined which
inhibitors were nontoxic, could enter cells and inactivate intracellular DP
PI. We screened nine dipeptide vinyl sulfone (VS) inhibitors (k(obs)/[I] >
72 M-1 s(-1)) and found six that were nontoxic. Foul affected intracellular
DPPI at < 25 muM These compounds contained only uncharged amino acid resid
ues; the two less reactive compounds contained charged Glu residues. The be
st one, Leu-Phe-VS-CH3, inactivated DPPI in cells with an ID50 of similar t
o 5 muM. This inhibitor was not the best inhibitor of purified DPPI. Longer
aqueous stabilities were important predictors of cellular efficacy. Leu-Ph
e-VS-CH3 had a half life of 97 min at the pH of the extracellular medium (7
.5) and 1302 min at pH 5.5 (the intracellular environment of DPPI). This VS
had no direct effect on granzyme activities. In contrast, the diazomethyl
ketone inhibitor Gly-Phe-CHN2 inhibited chymase activity. several good intr
a cellular DPPI VS inhibitors lacked reactivity with cathepsins B, H and L.
In conclusion, we have identified DPPI inhibitors suitable for cellular ap
plications. (C) 2001 Elsevier Science B.V. All rights reserved.