Protein Science, Vol 1, Issue 7 902-909, Copyright © 1992 by Cold Spring Harbor Laboratory Press

ARTICLE

Complete enzymatic deglycosylation of native sex steroid-binding protein (SBP or SHBG) of human and rabbit plasma: Effect on the steroid-binding activity

P. H. PETRA, P. R. GRIFFIN, J. R. YATES-III, K. MOORE and W. ZHANG
Department of Obstetrics & Gynecology and Department of Biochemistry, University of Washington, Seattle, Washington 98195

An enzymatic procedure for the complete removal of the N-linked and O-linked oligosaccharide side chains of the sex steroid-binding proteins (SBP or SHBG) of human and rabbit plasma under native conditions is described. Deglycosylation was catalyzed by N-glycanase, neuraminidase, and O-glycanase and was monitored by SDS-PAGE, lectin blotting, and molecular weight analyses by electrospray mass spectrometry. Digestion of rabbit SBP with N-glycanase generated a major 39,777-Da protein and two minor ones of 39,389 and 39,545 Da. The molecular weight of the major protein agrees with the molecular weight calculated from the sequence of the sugar-free polypeptide monomer (39,769 Da: Griffin, P.R., Kumar, S., Shabanowitz, J., Charbonneau, H., Namkung, P.C., Walsh, K.A., Hunt, D.F., & Petra, P.H., 1989, J. Biol. Chem. 264, 19066-19075), whereas the other two are deglycosylated proteolytic cleavage products lacking the TQR and TQ sequences at the amino-terminus. The N- and O-linked side chains of human SBP were removed by sequential digestion with N-glycanase and neuraminidase/O- glycanase. A 38,771-Da protein was generated, which agrees well with the molecular weight of the sugar-free polypeptide monomer (Walsh, K.A., Titani, K., Kumar, S., Hayes, R., & Petra, P.H., 1986, Biochemistry 25, 7584-7590). N-deglycosylation of human and rabbit SBP has no effect on the steroid-binding activity, but removal of the O-linked side chains of N-deglycosylated human SBP results in an apparent 50% loss of steroid-binding activity and an increase in the K(d) for the binding of 5{alpha}-dihydrotestosterone from 0.3 nM to 0.9 nM. There are no changes in steroid-binding specificity. The apparent loss of activity of O-deglycosylated human SBP is probably due to the small changes in the K(d), which could influence the equilibrium concentration of bound SBP when measured under standard assay conditions. We conclude that deglycosylation has very little effect on steroid-binding activity and that the oligosaccharide side chains must serve other functions in the physiology of SBP.
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