Three low molecular weight cysteine proteinase inhibitors of human seminal fluid: Purification and enzyme kinetic properties |
| |
Authors: | Vikash Kumar Yadav Nirmal Chhikara Kamaldeep Gill Sharmistha Dey Sarman Singh Savita Yadav |
| |
Institution: | 1. Department of Biophysics, All India Institute of Medical Sciences, Ansari Nagar, New Delhi 110029, India;2. Department of Lab Medicine, All India Institute of Medical Sciences, New Delhi 110029, India |
| |
Abstract: | The cystatins form a superfamily of structurally related proteins with highly conserved structural folds. They are all potent, reversible, competitive inhibitors of cysteine proteinases (CPs). Proteins from this group present differences in proteinase inhibition despite their high level of structural similarities. In this study, three cysteine proteinase inhibitors (CPIs) of low molecular weight were isolated from human seminal fluid (HSF) by affinity chromatography on carboxymethyl (CM)-papain–Sepharose column, purified using various chromatographic procedures and checked for purity on sodium-dodecyl PAGE (SDS-PAGE). Matrix-assisted laser desorption-ionization-time-of flight-mass spectrometry (MALDI-TOF-MS) identified these proteins as cystatin 9, cystatin SN, and SAP-1 (an N-terminal truncated form of cystatin S). All three CPIs suppressed the activity of papain potentially and showed remarkable heat stability. Interestingly SAP-1 also inhibits the activity of trypsin, chymotrypsin, pepsin, and PSA (prostate specific antigen) and acts as a cross-class protease inhibitor in in vitro studies. Using Surface Plasmon Resonance, we have also observed that SAP-1 shows a significant binding with all these proteases. These studies suggest that SAP-1 is a cross-class inhibitor that may regulate activity of various classes of proteases within the reproductive systems. To our knowledge, this is the first report about purification of CPIs from HSF; the identification of such proteins could provide better insights into the physiological processes and offer intimation for further research. |
| |
Keywords: | Chromatography Cross-class inhibition Cystatins Kinetics Papain Surface plasmon resonance |
本文献已被 ScienceDirect 等数据库收录! |
|