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Microinjection of mRNA coding for an anti-golgi antibody inhibits intracellular transport of a viral membrane protein

Messenger RNA was prepared from a hybridoma cell line secreting a monoclonal antibody (53FC3) directed against a luminal epitope of a Golgi membrane protein (M(r) = 135 kd) found in rodent cells. When this mRNA was microinjected into the cytoplasm of BHK cells, mouse IgG was seen to accumulate in th...

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Detalles Bibliográficos
Autores principales: Burke, Brian, Warren, Graham
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 1984
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7133283/
https://www.ncbi.nlm.nih.gov/pubmed/6323023
http://dx.doi.org/10.1016/0092-8674(84)90034-5
Descripción
Sumario:Messenger RNA was prepared from a hybridoma cell line secreting a monoclonal antibody (53FC3) directed against a luminal epitope of a Golgi membrane protein (M(r) = 135 kd) found in rodent cells. When this mRNA was microinjected into the cytoplasm of BHK cells, mouse IgG was seen to accumulate in the Golgi complex after 5–6 hr of incubation. No accumulation was seen in 3T3 cells which lack the epitope recognized by 53FC3. When microinjected BHK cells were infected with vesicular stomatitis virus, surface expression of the viral G protein was considerably reduced when compared with neighboring noninjected cells.