Revista: | Revista Brasileira de Zootecnia |
Base de datos: | PERIÓDICA |
Número de sistema: | 000445516 |
ISSN: | 1516-3598 |
Autores: | Felix, Bruna Alves1 Otávio, Kamila de Sousa1 Martins, Jorge André Matias2 Santos, Fágner Cavalcante Patrocínio dos3 Velho, Ana Luiza Malhado Cazaux de Souza4 Vasconcelos, Fábio Roger1 Bezerra, Maria Júlia Barbosa1 Moura, Arlindo A1 |
Instituciones: | 1Universidade Federal do Ceara, Departamento de Zootecnia, Fortaleza, Ceara. Brasil 2Universidade Federal do Cariri, Centro de Ciências Agrarias e da Biodiversidade, Juazeiro do Norte, Ceara. Brasil 3Universidade Estadual do Ceara, Faculdade de Veterinaria, Fortaleza, Ceara. Brasil 4Centro Universitario Dinamica das Cataratas, Foz do Iguacu, Parana. Brasil |
Año: | 2020 |
Volumen: | 49 |
País: | Brasil |
Idioma: | Inglés |
Tipo de documento: | Artículo |
Enfoque: | Experimental, analítico |
Resumen en inglés | The objective of the present study was to develop a methodology to obtain the enriched fraction of ram seminal vesicle protein 14 (RSVP14). The study was developed using Morada Nova rams, from which semen samples were collected weekly. Seminal plasma proteins were precipitated with cold ethanol, and then 6.15 mg/mL of total proteins were subjected to liquid gelatin affinity chromatography using a Gelatin-Sepharose matrix coupled to an automated chromatographic system. Proteins were eluted into four fractions (A, B, C, and D), in which A and B contained non-gelatin-binding proteins, and C and D fractions contained gelatin-binding proteins. Gels were analyzed by Quantity One software, in which five protein bands were detected in fraction D, with molecular weights between 12 and 30 kDa. The gelatin-binding proteins (fraction D) were loaded into a HiTrap™ Heparin HP affinity column. Two chromatographic fractions were separated (D1 and D2), in which D1 contained non-heparin-binding proteins, and D2 contained heparin-binding proteins. Proteins from the last two peaks were subjected to 12.5% SDS-PAGE and Western Blot. Two bands with molecular weight of 14 and 24 kDa, contained in fraction D1, were excised from gel and subjected to tandem mass spectrometry, identifying the proteins RSVP14 and RSVP24. Thus, the chromatographic methods of the present study are efficient to capture the enriched fraction of RSVP14 |
Disciplinas: | Medicina veterinaria y zootecnia |
Palabras clave: | Ovinos y caprinos, Carneros, Ovis aries, Proteómica, Espermatozoides |
Keyword: | Sheep and goats, Rams, Ovis aries, Proteomics, Spermatozoa |
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