Post-translational modifications of human thrombin-activatable fibrinolysis inhibitor (TAFI): evidence for a large shift in the isoelectric point and reduced solubility upon activation
- PMID: 16445295
- DOI: 10.1021/bi051956v
Post-translational modifications of human thrombin-activatable fibrinolysis inhibitor (TAFI): evidence for a large shift in the isoelectric point and reduced solubility upon activation
Abstract
Thrombin-activable fibrinolysis inhibitor (TAFI) is distinct from pancreatic procarboxypeptidase B in several ways. The enzymatic activity of TAFIa is unstable and decays with a half-life of a few minutes. During this study, we observed that (i) the isoelectric point (pI) of TAFI shifts dramatically from pH 5 toward pH 8 upon activation and (ii) TAFIa is significantly less soluble than TAFI. The structural bases for these observations were investigated by characterizing all post-translational modifications, including attached glycans and disulfide connectivity. The analyses revealed that all five potential N-glycosylation sites were utilized including Asn22, Asn51, Asn63, Asn86 (located in the activation peptide), and Asn219 (located in the catalytic domain). Asn219 was also found in an unglycosylated variant. Four of the glycans, Asn51, Asn63, Asn86, and Asn219 displayed microheterogeneity, while the glycan attached to Asn22 appeared to be homogeneous. In addition, bisecting GlcNAc attached to the trimannose core was detected, suggesting an origin other than the liver. Monosaccharide composition and LC-MS/MS analyses did not produce evidence for O glycosylation. TAFI contains eight cysteine residues, of which two, Cys69 and Cys383, are not involved in disulfides and contain free sulfhydryl groups. The remaining six cystines form disulfides, including Cys156-Cys169, Cys228-Cys252, and Cys243-Cys257. This pattern is homologous to pancreatic procarboxypeptidase B, and it is therefore unlikely that permutations in the cysteine connectivity are responsible for the enzymatic instability. LC-MS/MS analyses covering more than 90% of the TAFI amino acid sequence revealed no additional modifications. When these results are taken together, they suggest that the inherent instability of TAFIa is not caused by post-translational modifications. However, after activation, TAFIa loses 80% of the attached glycans, generating a large shift in pI and a propensity to precipitate. These changes are likely to significantly affect the properties of TAFIa as compared to TAFI.
Similar articles
-
Biochemical importance of glycosylation in thrombin activatable fibrinolysis inhibitor.Circ Res. 2008 Feb 15;102(3):295-301. doi: 10.1161/CIRCRESAHA.107.157099. Epub 2007 Dec 6. Circ Res. 2008. PMID: 18063813
-
An assay for measuring functional activated thrombin-activatable fibrinolysis inhibitor in plasma.Anal Biochem. 2008 Jan 1;372(1):32-40. doi: 10.1016/j.ab.2007.09.034. Epub 2007 Sep 29. Anal Biochem. 2008. PMID: 17967438
-
Thrombin activatable fibrinolysis inhibitor: a putative target to enhance fibrinolysis.Semin Thromb Hemost. 2013 Jun;39(4):365-72. doi: 10.1055/s-0033-1334488. Epub 2013 Mar 2. Semin Thromb Hemost. 2013. PMID: 23457049 Review.
-
Thrombin activatable fibrinolysis inhibitor (TAFI): a role in pre-eclampsia?Clin Chim Acta. 2007 Mar;378(1-2):1-6. doi: 10.1016/j.cca.2006.10.014. Epub 2006 Oct 26. Clin Chim Acta. 2007. PMID: 17184758 Review.
-
Posttranslational modifications of human inter-alpha-inhibitor: identification of glycans and disulfide bridges in heavy chains 1 and 2.Biochemistry. 1998 Jan 6;37(1):408-16. doi: 10.1021/bi971137d. Biochemistry. 1998. PMID: 9425062
Cited by
-
Flexibility of the thrombin-activatable fibrinolysis inhibitor pro-domain enables productive binding of protein substrates.J Biol Chem. 2010 Dec 3;285(49):38243-50. doi: 10.1074/jbc.M110.150342. Epub 2010 Sep 29. J Biol Chem. 2010. PMID: 20880845 Free PMC article.
-
Striatin is a novel modulator of cell adhesion.FASEB J. 2019 Apr;33(4):4729-4740. doi: 10.1096/fj.201801882R. Epub 2018 Dec 28. FASEB J. 2019. PMID: 30592649 Free PMC article.
-
α(1,3)-Fucosyltransferases FUT4 and FUT7 control murine susceptibility to thrombosis.Am J Pathol. 2013 Jun;182(6):2082-93. doi: 10.1016/j.ajpath.2013.02.010. Epub 2013 Apr 2. Am J Pathol. 2013. PMID: 23562273 Free PMC article.
-
Virtual 2-D map of the fungal proteome.Sci Rep. 2021 Mar 23;11(1):6676. doi: 10.1038/s41598-021-86201-6. Sci Rep. 2021. PMID: 33758316 Free PMC article.
-
The crystal structure of thrombin-activable fibrinolysis inhibitor (TAFI) provides the structural basis for its intrinsic activity and the short half-life of TAFIa.J Biol Chem. 2008 Oct 24;283(43):29416-23. doi: 10.1074/jbc.M804003200. Epub 2008 Jul 31. J Biol Chem. 2008. PMID: 18669641 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Molecular Biology Databases
Research Materials
Miscellaneous