Generic placeholder image

Current Molecular Medicine

Editor-in-Chief

ISSN (Print): 1566-5240
ISSN (Online): 1875-5666

In Vitro Regulatory Effect of Epididymal Serpin CRES on Protease Activity of Proprotein Convertase PC4/PCSK4

Author(s): P. Mishra, Q. Qiu, A. Gruslin, Y. Hidaka, M. Mbikay and A. Basak

Volume 12, Issue 8, 2012

Page: [1050 - 1067] Pages: 18

DOI: 10.2174/156652412802480961

Price: $65

Abstract

PC4 or PCSK4 belongs to the 9-member superfamily of mammalian subtilases collectively called Proprotein Convertases or Proprotein Convertase Subtilisin/Kexins that convert inactive precursor proteins into their active mature forms by endoproteolytic cleavage. PC4-activity plays a crucial role in mammalian fertilization via activation of sperm surface proteins. PC4 knockout mice exhibit severely impaired male fertility due to premature sperm acrosome reaction. Regulation of sperm-PC4 activity during its storage and transport through epididymis is an important determinant for ultimate egg-binding and fertilizing capacities of sperms. Herein we show that epididymal serpin CRES (cystatin related epididymal spermatogenic) recombinant protein inhibits PC4 activity in vitro in a differential manner when measured against the fluorogenic substrate Boc- RVRR-MCA depending on its oligomeric state. Thus while CRES-dimer exhibits Ki ~8 μM, the corresponding monomer showed Ki > 100 μM. Both forms also blocked PC4-mediated processing of human proIGF-2 in human placenta tropoblast cell line with dimer being more efficient. Using specific inhibitors and substrates, we also demonstrated the presence of PC4-like activity and CRES protein in varying levels in the fluids of various epididymal compartments. Our observations suggest a potential function of CRES as a regulator of PC4 in sperm-egg interaction and fertilization.

Keywords: Proprotein convertase 4, proprotein convertase subtilisin kexin 4, serpin, epididymal fluid, cystatin related epididymal spermatogenic, inhibitor, protein aggregation, proprotein processing, yeast kexin, bacterial subtilisin, proneuropeptides, prohormones, maturation, autocatalysis, fertilization.


Rights & Permissions Print Cite
© 2024 Bentham Science Publishers | Privacy Policy