Determinants of chymotrypsin C cleavage specificity in the calcium‐binding loop of human cationic trypsinogen

A Szabó, M Sahin‐Tóth - The FEBS journal, 2012 - Wiley Online Library
The FEBS journal, 2012Wiley Online Library
The pancreatic serine protease chymotrypsin C (CTRC) cleaves the L eu81–G lu82 peptide
bond in the calcium‐binding loop of human cationic trypsinogen and thereby promotes its
degradation. This serves as a protective mechanism against ectopic trypsinogen activation
in the pancreas. In the present study, we demonstrate that cleavage of the Leu81–Glu82
peptide bond by CTRC is highly specific, and other human pancreatic chymotrypsins (CTRB
1, CTRB 2 and CTRL 1) and elastases (ELA 2A, ELA 3A and ELA 3 B) do not catalyze this …
The pancreatic serine protease chymotrypsin C (CTRC) cleaves the Leu81–Glu82 peptide bond in the calcium‐binding loop of human cationic trypsinogen and thereby promotes its degradation. This serves as a protective mechanism against ectopic trypsinogen activation in the pancreas. In the present study, we demonstrate that cleavage of the Leu81–Glu82 peptide bond by CTRC is highly specific, and other human pancreatic chymotrypsins (CTRB1, CTRB2 and CTRL1) and elastases (ELA2A, ELA3A and ELA3B) do not catalyze this reaction. To elucidate the mechanistic basis for CTRC specificity, we surveyed the primary (P1) cleavage preference of these pancreatic proteases on peptide substrates. We found that CTRC cleaved after a P1 Leu with at least tenfold higher catalytic efficiency than other enzymes tested. To assess extended sub‐site interactions, we introduced Ala mutations into human cationic trypsinogen at the P3, P1′ P3′ and P4′ amino acid positions, where P1–P1′ corresponds to Leu81–Glu82. Interestingly, CTRC‐mediated cleavage was stimulated threefold by mutation E82A and unaffected by mutations E79A and N84A, but all three mutations compromised specificity and resulted in increased cleavage by ELA2A. Mutation E85A decreased CTRC cleavage by twofold. Remarkably, other chymotrypsins and elastases did not cleave human cationic trypsinogen even with the L81F or L81A mutations, which introduced favorable P1 residues for these enzymes. We conclude that specific cleavage of the Leu81–Glu82 peptide bond in human cationic trypsinogen by CTRC is primarily determined by its distinctively high activity on leucyl peptide bonds, with the P1′ Glu82, P3′ Asn84 and P4′ Glu85 residues serving as additional specificity determinants.
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