N-glycans of human protein C inhibitor: tissue-specific expression and function

• Published in: PloS one 2011-12, Vol.6 (12), p.e29011-e29011
• Main Authors: Sun, Wei, Grassi, Paola, Engström, Ake, Sooriyaarachchi, Sanjeewani, Ubhayasekera, Wimal, Hreinsson, Julius, Wånggren, Kjell, Clark, Gary F, Dell, Anne, Schedin-Weiss, Sophia
• Format: Article
• Language: English
• Subjects: Amino acids; Antigens; Biochemistry; Biokemi; Biology; Blood; Blood plasma; Catalysis; Chemistry; Children & youth; Childrens health; Chromatography; Constants; Crystallography; Gene Expression Regulation; Glycan; Humans; Inhibition; Kemi; Ligands; Male; Males; Mass spectrometry; Mass spectroscopy; MEDICIN; MEDICINE; Models, Molecular; N-glycans; N-glycosylation; Neurosciences; Organ Specificity; Polysaccharides; Prostate; Prostate cancer; Prostate specific antigen; Prostate-Specific Antigen - antagonists & inhibitors; Prostate-Specific Antigen - chemistry; Prostate-Specific Antigen - metabolism; Protease; Protease inhibitors; Protein C; Protein C inhibitor; Protein C Inhibitor - blood; Protein C Inhibitor - chemistry; Protein C Inhibitor - metabolism; Protein C Inhibitor - pharmacology; Protein Conformation; Proteins; Proteomics; Rate constants; Reproductive system; Semen; Semen - metabolism; Seminal plasma; Serine; Serine proteinase; Serine proteinase inhibitors; Serpin; Thrombin; Tissues; Urine; Womens health
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0029011

Protein C inhibitor (PCI) is a serpin type of serine protease inhibitor that is found in many tissues and fluids in human, including blood plasma, seminal plasma and urine. This inhibitor displays an unusually broad protease specificity compared with other serpins. Previous studies have shown that the N-glycan(s) and the NH₂-terminus affect some blood-related functions of PCI. In this study, we have for the first time determined the N-glycan profile of seminal plasma PCI, by mass spectrometry. The N-glycan structures differed markedly compared with those of both blood-derived and urinary PCI, providing evidence that the N-glycans of PCI are expressed in a tissue-specific manner. The most abundant structure (m/z 2592.9) had a composition of Fuc₃Hex₅HexNAc₄, consistent with a core fucosylated bi-antennary glycan with terminal Lewis(x). A major serine protease in semen, prostate specific antigen (PSA), was used to evaluate the effects of N-glycans and the NH₂-terminus on a PCI function related to the reproductive tract. Second-order rate constants for PSA inhibition by PCI were 4.3±0.2 and 4.1±0.5 M⁻¹ s⁻¹ for the natural full-length PCI and a form lacking six amino acids at the NH₂-terminus, respectively, whereas these constants were 4.8±0.1 and 29±7 M⁻¹ s⁻¹ for the corresponding PNGase F-treated forms. The 7-8-fold higher rate constants obtained when both the N-glycans and the NH₂-terminus had been removed suggest that these structures jointly affect the rate of PSA inhibition, presumably by together hindering conformational changes of PCI required to bind to the catalytic pocket of PSA.