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2.
J Virol ; 75(22): 10721-9, 2001 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-11602713

RESUMO

The VP22 protein of herpes simplex virus type 2 (HSV-2) is a major component of the virion tegument. Previous work with HSV-1 indicated that VP22 is phosphorylated during infection, and phosphorylation may play a role in modulating VP22 localization in infected cells. It is not clear, however, when phosphorylation occurs in infected cells or how it is regulated. Less is known about the synthesis and phosphorylation of HSV-2 VP22. To study the complete biosynthetic history of HSV-2 VP22, we generated a monoclonal antibody to the carboxy terminus of VP22. Using immunoprecipitation and Western blot analyses, we show that HSV-2 VP22 can be found in three distinct isoforms in infected cells, two of which are phosphorylated. Like HSV-1 VP22, HSV-2 VP22 is synthesized ca. 4 h after infection, and the isoform later incorporated into virions is hypophosphorylated. In addition, we demonstrate for the first time (i) that newly synthesized VP22 is phosphorylated rapidly after synthesis, (ii) that this phosphorylation occurs in a virus-dependent manner, (iii) that the HSV-2 kinase UL13 is capable of inducing phosphorylation of VP22 in the absence of other viral proteins, (iv) that phosphorylated VP22 is very stable in infected cells, (v) that phosphorylated isoforms of VP22 are gradually dephosphorylated late in infection to produce the virion tegument form, and (vi) that this dephosphorylation occurs independently of viral DNA replication or virion assembly. These results indicate that HSV-2 VP22 is a stable protein that undergoes highly regulated, virus-dependent phosphorylation events in infected cells.


Assuntos
Herpesvirus Humano 2/metabolismo , Proteínas Estruturais Virais/metabolismo , Animais , Anticorpos Monoclonais/imunologia , Chlorocebus aethiops , Herpesvirus Humano 2/patogenicidade , Fosforilação , Isoformas de Proteínas , Proteínas Quinases/fisiologia , Transfecção , Células Vero , Proteínas Estruturais Virais/análise , Proteínas Estruturais Virais/imunologia
3.
Hosp Cost Manag Account ; 4(9): 1-6, 1992 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-10122658

RESUMO

This article has provided a look into the use of the reciprocal method as an alternative to more conventional methods of hospital service department cost allocation methods. The reciprocal method can be used with readily available software and with data that are largely already known. This method will provide not only appropriate allocation values for financial reporting but data that can be used for hospital decision making. In the highly competitive and sometimes hostile environment in which hospitals now fight to survive, any additional relevant data--especially that generated at almost no additional cost--should be provided to managers to help in the decision-making process.


Assuntos
Contabilidade/métodos , Alocação de Custos/métodos , Administração Financeira de Hospitais/métodos , Departamentos Hospitalares/economia , Tomada de Decisões Gerenciais , Relações Interdepartamentais , Estados Unidos
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