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1.
Proc Natl Acad Sci U S A ; 109(35): 13996-4000, 2012 Aug 28.
Artigo em Inglês | MEDLINE | ID: mdl-22891297

RESUMO

Many pleomorphic, lipid-enveloped viruses encode matrix proteins that direct their assembly and budding, but the mechanism of this process is unclear. We have combined X-ray crystallography and cryoelectron tomography to show that the matrix protein of Newcastle disease virus, a paramyxovirus and relative of measles virus, forms dimers that assemble into pseudotetrameric arrays that generate the membrane curvature necessary for virus budding. We show that the glycoproteins are anchored in the gaps between the matrix proteins and that the helical nucleocapsids are associated in register with the matrix arrays. About 90% of virions lack matrix arrays, suggesting that, in agreement with previous biological observations, the matrix protein needs to dissociate from the viral membrane during maturation, as is required for fusion and release of the nucleocapsid into the host's cytoplasm. Structure and sequence conservation imply that other paramyxovirus matrix proteins function similarly.


Assuntos
Doença de Newcastle/virologia , Vírus da Doença de Newcastle/crescimento & desenvolvimento , Vírus da Doença de Newcastle/ultraestrutura , Nucleoproteínas/química , Proteínas Virais/química , Animais , Cristalografia por Raios X , Dimerização , Glicoproteínas/química , Glicoproteínas/metabolismo , Microscopia Eletrônica , Mononegavirais/ultraestrutura , Vírus da Doença de Newcastle/metabolismo , Nucleocapsídeo/química , Nucleocapsídeo/metabolismo , Nucleocapsídeo/ultraestrutura , Proteínas do Nucleocapsídeo , Nucleoproteínas/metabolismo , Estrutura Terciária de Proteína , Relação Estrutura-Atividade , Proteínas Virais/metabolismo , Vírion/química , Vírion/crescimento & desenvolvimento , Replicação Viral/fisiologia
2.
J Virol ; 83(10): 5109-16, 2009 May.
Artigo em Inglês | MEDLINE | ID: mdl-19279111

RESUMO

Here, we report the sequencing and classification of Nyamanini virus (NYMV) and Midway virus (MIDWV), two antigenically related viruses that were first isolated in 1957 and 1966, respectively. Although these viruses have been cultured multiple times from cattle egrets, seabirds, and their ticks, efforts to classify them taxonomically using conventional serological and electron microscopic approaches have failed completely. We used a random shotgun sequencing strategy to define the genomes of NYMV and MIDWV. Contigs of 11,631 and 11,752 nucleotides, representing the complete genome of NYMV and the near-complete genome of MIDWV, respectively, were assembled. Each virus genome was predicted to carry six open reading frames (ORFs). BLAST analysis indicated that only two of the ORF proteins of each virus, the putative nucleocapsid and polymerase, had detectable sequence similarity to known viral proteins. Phylogenetic analysis of these ORF proteins demonstrated that the closest relatives of NYNV and MIDWV are negative-stranded-RNA viruses in the order Mononegavirales. On the basis of their very limited sequence similarity to known viruses, we propose that NYMV and MIDWV define a novel genus, Nyavirus, in this order.


Assuntos
Genoma Viral , Mononegavirais/classificação , Filogenia , Vírus não Classificados/classificação , Animais , Chlorocebus aethiops , Mapeamento de Sequências Contíguas , Camundongos , Dados de Sequência Molecular , Mononegavirais/genética , Mononegavirais/ultraestrutura , Fases de Leitura Aberta , RNA Viral/genética , Carrapatos/virologia , Células Vero , Vírus não Classificados/genética , Vírus não Classificados/ultraestrutura
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