Purification of vitellogenin from the plasma of Indian freshwater murrel, Channa punctatus (Bloch) by different methods: a comparative study.

Plasma from estrogenized, [32P] NaH2PO4-injected murrel, Channa punctatus was collected in the presence of proteolytic inhibitors and subjected to different separation procedures singly or in combination, viz., gel filtration chromatography on Ultrogel AcA 34, ion-exchange chromatography on DEAE sephacel, or selective precipitation with dimethylformamide or with Mg2+: EDTA in order to isolate vitellogenin from other plasma proteins. The results show that chromatography on Ultrogel or DEAE sephacel yields intact vitellogenin whereas prior precipitation with DMF or with Mg2+: EDTA results in either co-precipitation of other plasma proteins or in the cleavage of phosvitin-like material from the native vitellogenin molecule.

Structures and properties of vitellin isolated from Triatominae species

Se realizaron estudios comparativos de los pesos moleculares composicion quimica e identidad inmunológica de la vitelina (VN) de distintas especies de triatominos. Se determinó que la VN es una lipoglicofosfoproteina con 12.76% de hidratos de carbono 12.53% de lipidos y 0.6% de fósforo unido a mas aproteica. La VN nativa muestra por filtración en gel una única banda de 310 KDa. La VN delipidizada muestra por PAGE SDS una banda principal de 175 KDa coincidente con la banda hallada en la vitellogenina (VG). La composición de aminoácidos fue similar en las cuatro especies ensayadas