Identification, characterization and purification of porcine Quiescin Q6-Sulfydryl Oxidase 2 protein
Journal
BMC Veterinary Research
Journal Volume
13
Journal Issue
1
Date Issued
2017
Author(s)
Abstract
Background: Post-spermiogenesis membrane surface modifications rely on molecules present in the reproductive tracts. Two isoforms (isoform 1 and 2) from Quiescin Q6-Sulfydryl Oxidase protein family have been identified in the male reproductive tract of rodent species. However, unlike isoform 1, scarce information is available for isoform 2, likely due to its lower expression level and lack of proper purification methods to obtain sufficient protein quantity for further assays. Results: This study demonstrated the presence of short and long forms of Quiescin Q6-Sulfydryl Oxidase 2 in boar, likely representing the secretory (short form) and transmembrane (long form) forms of Quiescin Q6-Sulfydryl Oxidase 2. Immunohistochemistry studies revealed the presence of Quiescin Q6-Sulfydryl Oxidase 2 in a broad range of porcine tissues; the pronounced vesicle-contained Quiescin Q6-Sulfydryl Oxidase 2 at the apical region of epididymis and seminal vesicles epithelium suggested its involvement in sperm physiology and its participation in semen formation. The majority of porcine Quiescin Q6-Sulfydryl Oxidase 2 could be purified via either antibody affinity column or be salted out using 10%-40% ammonium sulfate. Higher amount of low molecular weight Quiescin Q6-Sulfydryl Oxidase 2 observed in the seminal vesicle likely represents the secretory form of Quiescin Q6-Sulfydryl Oxidase 2 and reflects an exuberant secretory activity in this organ. Conclusions: We demonstrated for the first time, the presence of Quiescin Q6-Sulfydryl Oxidase 2 in porcine species; moreover, two forms of Quiescin Q6-Sulfydryl Oxidase 2 were identified and exhibited distinct molecular weights and properties during protein purification processes. This study also provided feasible Quiescin Q6-Sulfydryl Oxidase 2 purification methods from slaughterhouse materials that could potentially allow obtaining sufficient amount of Quiescin Q6-Sulfydryl Oxidase 2 for future functional investigations. ? 2017 The Author(s).
Other Subjects
ammonium sulfate; protein; quiescin q6 sulfydryl oxidase protein; unclassified drug; oxidoreductase; thiol oxidase; animal tissue; Article; controlled study; immunohistochemistry; immunoprecipitation; male; mouse; nonhuman; pig; protein analysis; protein expression; protein purification; protein structure; Western blotting; animal; chemistry; enzymology; epididymis; Institute for Cancer Research mouse; isolation and purification; metabolism; secretion (process); seminal vesicle; Animals; Epididymis; Immunohistochemistry; Male; Mice, Inbred ICR; Oxidoreductases; Seminal Vesicles; Swine
Type
journal article