Abstract:
:Rubella virosomes were prepared from performed liposomes and detergent solubilized viral hemagglutinin. The liposomes were made from lecithin/dicetyl phosphate (3.5 : 1) films resuspended in NTE buffer and sonicated. Viral hemagglutinin was prepared from purified virus after solubilization with Triton X-100 and centrifugation through a sucrose gradient containing beta-D-octylglucoside. Electron microscopy of the rate zonal purified virosomes, showed virus-like structures of 40 - 80 nm. The virosomes retained the biological activity of the hemagglutinin and had a buoyant density of 1.2 g/cm3.
journal_name
J Virol Methodsjournal_title
Journal of virological methodsauthors
Trudel M,Marchessault F,Payment Pdoi
10.1016/0166-0934(81)90069-0subject
Has Abstractpub_date
1981-11-01 00:00:00pages
187-92issue
4eissn
0166-0934issn
1879-0984pii
0166-0934(81)90069-0journal_volume
3pub_type
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