TY - JOUR
T1 - Pyroglutamyl diazomethyl ketone
T2 - Potent inhibitor of mammalian pyroglutamyl peptide hydrolase
AU - Wilk, Sherwin
AU - Friedman, Theodore C.
AU - Kline, Toni B.
N1 - Funding Information:
by an NIH grant
PY - 1985/7/31
Y1 - 1985/7/31
N2 - Pyroglutamyl peptide hydrolase (EC 3.4.11.8), a cysteine protease, cleaves the N-terminal pyroglutamyl residue from pyroglutamyl peptides such as thyrotropin releasing hormone. Pyroglutamyl diazomethyl ketone was synthesized as an active site directed inhibitor. Preincubation of the partially purified bovine brain enzyme with nanomolar concentrations of inhibitor produced rapid inactivation. Inhibitor concentrations five orders of magnitude higher did not inactivate other exo- and endopeptidases. A dose of 0.1 mg/kg administered intraperitoneally to mice totally inactivated the enzyme in all tissues studied including brain. Pyroglutamyl diazomethyl ketone should be of value in studies on the physiological role of this enzyme in the metabolism of pyroglutamyl-containing peptides.
AB - Pyroglutamyl peptide hydrolase (EC 3.4.11.8), a cysteine protease, cleaves the N-terminal pyroglutamyl residue from pyroglutamyl peptides such as thyrotropin releasing hormone. Pyroglutamyl diazomethyl ketone was synthesized as an active site directed inhibitor. Preincubation of the partially purified bovine brain enzyme with nanomolar concentrations of inhibitor produced rapid inactivation. Inhibitor concentrations five orders of magnitude higher did not inactivate other exo- and endopeptidases. A dose of 0.1 mg/kg administered intraperitoneally to mice totally inactivated the enzyme in all tissues studied including brain. Pyroglutamyl diazomethyl ketone should be of value in studies on the physiological role of this enzyme in the metabolism of pyroglutamyl-containing peptides.
UR - http://www.scopus.com/inward/record.url?scp=0022396951&partnerID=8YFLogxK
U2 - 10.1016/0006-291X(85)90468-1
DO - 10.1016/0006-291X(85)90468-1
M3 - Article
C2 - 2862865
AN - SCOPUS:0022396951
SN - 0006-291X
VL - 130
SP - 662
EP - 668
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 2
ER -