PARTIAL-PURIFICATION AND CHARACTERIZATION OF A PROTEIN IN PORCINE FOLLICULAR-FLUID WHICH RESTRICTS SPERM-EGG INTERACTION IN-VITRO

Citation
J. Ramsoondar et al., PARTIAL-PURIFICATION AND CHARACTERIZATION OF A PROTEIN IN PORCINE FOLLICULAR-FLUID WHICH RESTRICTS SPERM-EGG INTERACTION IN-VITRO, Canadian journal of veterinary research, 59(1), 1995, pp. 8-14
Citations number
33
Categorie Soggetti
Veterinary Sciences
ISSN journal
08309000
Volume
59
Issue
1
Year of publication
1995
Pages
8 - 14
Database
ISI
SICI code
0830-9000(1995)59:1<8:PACOAP>2.0.ZU;2-Z
Abstract
An attempt was made to isolate, and characterize a component in preovu latory porcine follicular fluid (pFF) which has a restricting effect o n sperm-egg interaction in vitro. Using the zona-free hamster ova (egg s) penetration assay as an in vitro test system, it was shown previous ly that the numbers of porcine spermatozoa attached to or penetrated i nto each egg and the number of eggs with sperm attached or penetrated decreased significantly as the concentration of pFF was increased in t he culture medium. In the present study, the component in pFF having t hese effects was shown to be a heat stable, nonsteroidal substance whi ch retained its activity after dialysis, lyophilization and gel filtra tion chromatography. The activity was also found to be present in preo vulatory homologous serum. Separation of the material on protein type gel filtration columns with detection at 280 nm, together with the ban ding seen with Coomassie staining on sodium dodecyl sulfate-polyacryla mide gel electrophoresis (SDS-PAGE), suggests that it is a protein. Ba sed on high pressure liquid chromatographic separation (HPLC) and SDS- PAGE analyses, the bioactivity could be due to a single protein of 87 kD or to one or more of three smaller proteins, possibly disaggregated products of the 87 kD protein, in the range of 26-28 kD.