Dárcio Ítalo Alves Teixeira, Luciana Magalhães Melo, Carlos Alberto de Almeida Gadelha, Rodrigo Maranguape Silva da Cunha, Carlos Bloch Jr., Gandhi Rádis-Baptista, Benildo Sousa Cavada, Vicente José de Figueirêdo Freitas
Published: March 17, 2006
Genet. Mol. Res. 5 (1) : 79-87
Cite this Article:
D.Ítalo Alv Teixeira, L.Magalhães Melo, C.Alberto de Gadelha, R.Maranguape da Cunha, C. Bloch, G. Rádis-Baptista, B.Sousa Cavada, V.José de F. Freitas (2006). Ion-exchange chromatography used to isolate a spermadhesin-related protein from domestic goat (Capra hircus) seminal plasma. Genet. Mol. Res. 5(1): 79-87.
About the Authors
Dárcio Ítalo Alves Teixeira, Luciana Magalhães Melo, Carlos Alberto de Almeida Gadelha, Rodrigo Maranguape Silva da Cunha, Carlos Bloch Jr., Gandhi Rádis-Baptista, Benildo Sousa Cavada, Vicente José de Figueirêdo Freitas
Corresponding author
V.J.F. Freitas
E-mail: vjff@uece.br
ABSTRACT
Mammalian seminal plasma contains among others, proteins called spermadhesins, which are the major proteins of boar and stallion seminal plasma. These proteins appear to be involved in capacitation and sperm-egg interaction. Previously, we reported the presence of a protein related to spermadhesins in goat seminal plasma. In the present study, we have further characterized this protein, and we propose ion-exchange chromatography to isolate this seminal protein. Semen was obtained from four adult Saanen bucks. Seminal plasma was pooled, dialyzed against distilled water and freeze-dried. Lyophilized proteins were loaded onto an ion-exchange chromatography column. Dialyzed-lyophilized proteins from the main peak of DEAE-Sephacel were applied to a C2/C18 column coupled to an RP-HPLC system, and the eluted proteins were lyophilized for electrophoresis. The N-terminal was sequenced and amino acid sequence similarity was determined using CLUSTAL W. Additionally, proteins from DEAE-Sephacel chromatography step were dialyzed and submitted to a heparin-Sepharose high-performance liquid chromatography. Goat seminal plasma after ion-exchange chromatography yielded 6.47 ± 0.63 mg (mean ± SEM) of the major retained fraction. The protein was designated BSFP (buck seminal fluid protein). BSFP exhibited N-terminal sequence homology to boar, stallion and bull spermadhesins. BSFP showed no heparin-binding capabilities. These results together with our previous data indicate that goat seminal plasma contains a protein that is structurally related to proteins of the spermadhesin family. Finally, this protein can be efficiently isolated by ion-exchange and reverse-phase chromatography.
Key words: Goat, Seminal plasma, Lectin, Spermadhesin.