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Comparative evaluation of stable TAFIa variants: importance of α‐helix 9 and β‐sheet 11 for TAFIa (in)stability
Author(s) -
CERESA E.,
DE MAEYER M.,
JONCKHEER A.,
PEETERS M.,
ENGELBORGHS Y.,
DECLERCK P. J.,
GILS A.
Publication year - 2007
Publication title -
journal of thrombosis and haemostasis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.947
H-Index - 178
eISSN - 1538-7836
pISSN - 1538-7933
DOI - 10.1111/j.1538-7836.2007.02720.x
Subject(s) - thrombomodulin , mutant , chemistry , carboxypeptidase , biochemistry , wild type , thrombin , helix (gastropod) , biology , enzyme , platelet , gene , ecology , snail , immunology
Summary. Background: Activated thrombin activatable fibrinolysis inhibitor (TAFIa) plays a pivotal role in fibrinolysis. TAFIa activity is regulated by a temperature‐dependent instability. This instability has not only complicated the study of structure–function relationships of TAFIa but has also prevented the crystallization of TAFIa. Furthermore, the TAFIa instability has severely compromised the development of activity inhibiting monoclonal antibodies. Recently, we combined all known stabilizing mutations (i.e. S305C, T325I, T329I, H333Y and H335Q) resulting in a synergistic (one hundred and eightyfold) stabilization of TAFIa at 37 °C. All these residues are located in an amino acid region (AA297‐335) consisting of α‐helix 9 and β‐sheet 11. Objectives: To provide a comparative evaluation of the characteristics of a panel of stable TAFIa mutants and an energy‐minimized model of the most stable TAFI variant. Results: The catalytic efficiency for activation of TAFI by thrombin/thrombomodulin was higher for all TAFI mutants compared with TAFI‐wild type (wt). Except for TAFI variants carrying T325I‐T329I, S305C‐T325I or S305C‐T325I‐T329I mutations, the catalytic efficiency for Hip‐Arg hydrolysis by TAFIa was similar for the TAFI mutants compared with the wild type. All TAFIa variants were equally well inhibited by potato tuber carboxypeptidase inhibitor (PTCI) and showed a significantly increased antifibrinolytic potential in accordance with their increased stability. Based on the intrinsic fluorescence decay of TAFIa, two independent structural transitions were found to be associated with the loss of functional activity. Conclusions: Using molecular dynamic calculations on both TAFI‐wt and TAFI‐S305C‐T325I‐T329I‐H333Y‐H335Q models, we were able to identify the molecular interactions that contribute to the increased stability of the mutants.