Introducción. La producción de una proteína viral recombinante facilita la aplicación de diversas metodologías bioquímicas en investigación básica de los virus con relevancia clínica. Además, la obtención de un anticuerpo policlonal dirigido contra la proteína P permite el estudio de su función y está soportado en la inexistencia de un anticuerpo comercial dirigido contra esa proteína. Objetivo. Producir y caracterizar un anticuerpo policlonal dirigido contra la proteína P recombinante del virus de la rabia expresada en Escherichia coli. Materiales y métodos. El gen P que codifica para la proteína P del virus de la rabia, fue amplificado por reacción en cadena de la polimerasa de transcriptasa reversa y clonado en el vector de expresión PinPoint TM Xa-1 T (PROMEGA). La proteína recombinante P fue expresada en E. coli purificada por cromatografía de afinidad y usada para la producción del anticuerpo policlonal anti-P. El anticuerpo obtenido fue purificado y caracterizado por inmunocitoquímica con un sistema enzimático, inmunofluorescencia, Cell-ELISA fluorométrica y Western blotting. Resultados. La proteína recombinante se expresó eficientemente como una proteína de fusión biotinilada de aproximadamente 50 kd, que corresponde a la forma completa de la proteína P del virus de la rabia. El anticuerpo policlonal anti-P detectó con alta especificidad la proteína P en cultivos de neuronas sensoriales infectados con el virus de la rabia. Conclusión. La proteína P recombinante expresada en E. coli se constituyó en un antígeno específico para producir un anticuerpo policlonal que reconoce la proteína P nativa en células infectadas con el virus de la rabia. Palabras clave: virus de la rabia, inmunoquímica, fosfoproteínas, proteínas recombinantes, Escherichia coli. Production and characterization of a polyclonal antibody against rabies virus phosphoprotein Introduction. The expression of recombinant viral proteins has been a useful tool to study molecular biology and pathogenesis of virus infections. Because commercial specific antibodies to rabies virus phosphoprotein (P) are currently unavailable, these antibodies must be generated de novo in order to study the role of P protein during the infectious process. Objective. A polyclonal antibody was produced and characterized for use against the phosphoprotein (P) of rabies virus. The antibody was raised in rabbits with a recombinant viral phosphoprotein (P) produced in Escherichia coli. Materials and methods. Gene P coding for the viral phosphoprotein (P) was amplified by RT-PCR and cloned into the expression vector PinPointTM Xa-1 T. The recombinant protein P was expressed in Escherichia coli, purified by affinity chromatography and used to produce a polyclonal antibody anti-P. The antibody anti-P was purified and characterized by immunocytochemistry, immunofluorescence, fluorometric CELL-ELISA and Western blotting.
Rabies virus P protein participates as a regulating factor in viral transcription and replication; recent studies found an antitranscriptional and antireplicative effect of nerve growth factor (NGF) and Neurotrophin-3 (NT-3) in infected neuron cultures. We investigated here the specific effect of the neurotrophins on P protein, evaluating its synthesis and subcellular distribution in adult mouse dorsal root ganglia neuron cultures infected and treated with NGF or NT-3. The results showed that NGF, but not NT-3, caused an increase in the quantity of P protein and an accumulation of protein in neuronal bodies, revealing changes in transport to the neuritic processes.
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