Mechanism of action of mammalian cystatins

Pavlova, A., 2003. Mechanism of action of mammalian cystatins. Studies of inhibition of cysteine endoand exopeptidases by cystatins A and C. Doctor's dissertation. ISSN 1401-6257, ISBN 91-576-6379-3. Mammalian cystatins are tight-binding, reversible inhibitors of potentially destructive cysteine proteases, both endogenous and exogenous. The N-terminal region residues, Ile2 and especially Pro3, and the second binding loop residues, Leu73 and to some extent Pro74, of the family 1 cystatin, cystatin A, were shown to be essential for effective inhibition of papain and cathepsins L and B. Both regions were found to act in endopeptidase inhibition primarily by anchoring the enzymes in long-lived complexes with the inhibitor. However, in inhibition of the exopeptidase, cathepsin B, the N-terminal region also contributes to the high association rate. As previously shown for cystatin C, stopped-flow kinetics demonstrated a two-step mechanism of cystatin A binding to cathepsin B, with a conformational change in the second, rate-limiting step. In contrast, binding of cystatins A and C to a cathepsin B variant with an increased mobility of the occluding loop that blocks the active-site cleft occurred in an apparent one-step reaction. The second step of cathepsin B binding by cystatins was therefore concluded to involve displacement of the occluding loop. Cystatin C was shown to be a much better displacer of this loop than cystatin A. New effective and specific inhibitors of cysteine proteases were engineered by grafting individual binding regions of more potent cystatins into cystatin A. Introduction of motifs from the second binding loops of cystatins B or C into the corresponding loop of cystatin A increased the affinity for papain by ~10-fold. Moreover, replacement of the N-terminal region of cystatin A by that of cystatin C resulted in the affinity for cathepsin B being increased ~15-fold, to a level higher than that of any natural cystatin known. The latter chimeric inhibitor was as effective as cystatin C in displacing the occluding loop of cathepsin B, the rate of this step being increased by ~100-fold. The N-terminal region of a cystatin was thus concluded to promote occluding loop displacement by appropriately positioning the binding loops of the inhibitor entering the active-site cleft of cathepsin B.