作者: Björg Rafnar , Gregory J Tobin , Kunio Nagashima , Matthew A Gonda , Eggert Gunnarsson
DOI: 10.1016/S0168-1702(97)00141-X
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摘要: Abstract Two different recombinant visna virus (VV) gag -baculoviruses were constructed for the expression of precursor VV Gag in insect cells. Both viruses expressed proteins migrating on SDS–PAGE at predicted rate precursor, Pr50 . However, differences seen morphology virus-like particles produced. Monoclonal antibody directed against capsid protein (p25) and sera from sheep infected with ovine lentiviruses reacted to both 50-kDa proteins. A env -baculovirus was constructed, substituting sequences encoding signal peptide Env murine IFN- γ analogue. Sera lentivirus immunoblots two approximately 100 200 kDa found plasma membrane cells -recombinant virus. Sheep immunized either or developed high titers ELISA. The serum ascitic fluid mice native processed immunoblots, whereas gp135 a putative oligomer gp135. responded specifically by lymphocyte proliferation vitro.