THE ACID STABILIZATION OF PLASMINOGEN-ACTIVATOR INHIBITOR-1 DEPENDS ON PROTONATION OF A SINGLE GROUP THAT AFFECTS LOOP INSERTION INTO BETA-SHEET-A

The serpin plasminogen activator inhibitor-1 (PAI-1) spontaneously ado pts an inactive or latent conformation by inserting the N-terminal par t of the reactive center loop as strand 4 into the major beta-sheet (s heet A), To examine factors that may regulate reactive loop insertion in PAI-1, we determined the inactivation rate of the inhibitor in the pH range 4.5-13, Below pH 9, inactivation led primarily to latent PAI- 1, and one predominant effect of pH on the corresponding rate constant could be observed, Protonation of a group exhibiting a pK(alpha) of 7 .6 (25 degrees C, ionic strength = 0.15 M) reduced the rate of formati on of latent PAI-1 by a factor of 35, from 0.17 h(-1) at pH 9 to about 0.005 h(-1) below pH 6. The ionization with a pK(alpha) 7.6 was found to have no effect on the rate by which PAI-1 inhibits trypsin and is therefore unlikely to change the flexibility of the loop or the orient ation of the reactive center, The peptides Ac-TEASSSTA and Ac-TVASSSTA (cf. P14-P7 in the reactive loop of PAI-1) formed stable complexes wi th PAI-1 and converted the inhibitor to a substrate for tissue type pl asminogen activator, We found that peptide binding and formation of la tent PAI-1 are mutually exclusive events, similarly affected by the pK (alpha) 7.6 ionization. This is direct evidence that external peptides can substitute for strand 4 in beta-sheet A of PAI-1 and that the pR( alpha) 7.6 ionization regulates insertion of complementary, internal o r external, strands into this position, A model that accounts for the observed pH effects is presented, and the identity of the ionizing gro up is discussed based on the structure of latent PAI-1, The group is t entatively identified as His-143 in helix F, located on top of sheet A .