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1.
Nucleic Acids Res ; 43(17): 8416-34, 2015 Sep 30.
Artículo en Inglés | MEDLINE | ID: mdl-26304538

RESUMEN

RNA viruses encode an RNA-dependent RNA polymerase (RdRp) that catalyzes the synthesis of their RNA(s). In the case of positive-stranded RNA viruses belonging to the order Nidovirales, the RdRp resides in a replicase subunit that is unusually large. Bioinformatics analysis of this non-structural protein has now revealed a nidoviral signature domain (genetic marker) that is N-terminally adjacent to the RdRp and has no apparent homologs elsewhere. Based on its conservation profile, this domain is proposed to have nucleotidylation activity. We used recombinant non-structural protein 9 of the arterivirus equine arteritis virus (EAV) and different biochemical assays, including irreversible labeling with a GTP analog followed by a proteomics analysis, to demonstrate the manganese-dependent covalent binding of guanosine and uridine phosphates to a lysine/histidine residue. Most likely this was the invariant lysine of the newly identified domain, named nidovirus RdRp-associated nucleotidyltransferase (NiRAN), whose substitution with alanine severely diminished the described binding. Furthermore, this mutation crippled EAV and prevented the replication of severe acute respiratory syndrome coronavirus (SARS-CoV) in cell culture, indicating that NiRAN is essential for nidoviruses. Potential functions supported by NiRAN may include nucleic acid ligation, mRNA capping and protein-primed RNA synthesis, possibilities that remain to be explored in future studies.


Asunto(s)
Nidovirales/enzimología , Nucleotidiltransferasas/química , ARN Polimerasa Dependiente del ARN/química , Proteínas Virales/química , Sitios de Unión , Secuencia Conservada , Equartevirus/enzimología , Equartevirus/fisiología , Guanosina/química , Guanosina Trifosfato/metabolismo , Manganeso/química , Nidovirales/genética , Nucleótidos/metabolismo , Nucleotidiltransferasas/metabolismo , Fosfatos/química , Poliproteínas/química , Poliproteínas/metabolismo , Estructura Terciaria de Proteína , ARN Polimerasa Dependiente del ARN/genética , ARN Polimerasa Dependiente del ARN/metabolismo , Coronavirus Relacionado al Síndrome Respiratorio Agudo Severo/enzimología , Coronavirus Relacionado al Síndrome Respiratorio Agudo Severo/fisiología , Uridina/química , Uridina Trifosfato/metabolismo , Proteínas Virales/genética , Proteínas Virales/metabolismo , Replicación Viral
2.
J Virol Methods ; 177(2): 174-83, 2011 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-21864579

RESUMEN

The ssRNA+ family Coronaviridae includes two subfamilies prototyped by coronaviruses and toroviruses that cause respiratory and enteric infections. To facilitate the identification of new distantly related members of the family Coronaviridae, we have developed a molecular assay with broad specificity. The consensus-degenerated hybrid oligonucleotide primer (CODEHOP) strategy was modified to design primers targeting the most conserved motifs in the RNA-dependent RNA polymerase locus. They were evaluated initially on RNA templates from virus-infected cells using a two-step RT-PCR protocol that was further advanced to a one-step assay. The sensitivity of the assay ranged from 10(2) to 10(6) and from 10(5) to 10(9) RNA copy numbers for individual corona-/torovirus templates when tested, respectively, with and without an excess of RNA from human cells. This primer set compared to that designed according to the original CODEHOP rules showed 10-10(3) folds greater sensitivity for 5 of the 6 evaluated corona-/torovirus templates. It detected 57% (32 of 56) of the respiratory specimens positive for 4 human coronaviruses, as well as stool specimens positive for a bovine torovirus. The high sensitivity and broad virus range of this assay makes it suitable for screening biological specimens in search for new viruses of the family Coronaviridae.


Asunto(s)
Coronavirus/aislamiento & purificación , Cartilla de ADN/genética , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa/métodos , Torovirus/aislamiento & purificación , Secuencia de Aminoácidos , Animales , Bovinos , Línea Celular , Secuencia Conservada , Coronavirus/clasificación , Coronavirus/genética , Infecciones por Coronavirus/diagnóstico , Infecciones por Coronavirus/virología , Cartilla de ADN/metabolismo , Humanos , Datos de Secuencia Molecular , Filogenia , ARN Viral/genética , Sensibilidad y Especificidad , Alineación de Secuencia , Torovirus/clasificación , Torovirus/genética , Infecciones por Torovirus/diagnóstico , Infecciones por Torovirus/virología , Cultivo de Virus
3.
Antiviral Res ; 87(2): 95-110, 2010 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-20153379

RESUMEN

This review focuses on bioinformatics technologies employed by the EU-sponsored multidisciplinary VIZIER consortium (Comparative Structural Genomics of Viral Enzymes Involved in Replication, FP6 PROJECT: 2004-511960, active from 1 November 2004 to 30 April 2009), to achieve its goals. From the management of the information flow of the project, to bioinformatics-mediated selection of RNA viruses and prediction of protein targets, to the analysis of 3D protein structures and antiviral compounds, these technologies provided a communication framework and integrated solutions for steady and timely advancement of the project. RNA viruses form a large class of major pathogens that affect humans and domestic animals. Such RNA viruses as HIV, Influenza virus and Hepatitis C virus are of prime medical concern today, but the identities of viruses that will threaten human population tomorrow are far from certain. To contain outbreaks of common or newly emerging infections, prototype drugs against viruses representing the Virus Universe must be developed. This concept was championed by the VIZIER project which brought together experts in diverse fields to produce a concerted and sustained effort for identifying and validating targets for antivirus therapy in dozens of RNA virus lineages.


Asunto(s)
Investigación Biomédica/organización & administración , Investigación Biomédica/tendencias , Biología Computacional/métodos , Enzimas/metabolismo , Virus ARN/enzimología , Proteínas Virales/metabolismo , Replicación Viral/efectos de los fármacos , Animales , Bases de Datos de Proteínas , Enzimas/química , Enzimas/genética , Unión Europea , Humanos , Estructura Terciaria de Proteína , Virus ARN/efectos de los fármacos , Virus ARN/genética , Proteínas Virales/química , Proteínas Virales/genética
4.
BMC Bioinformatics ; 9: 31, 2008 Jan 22.
Artículo en Inglés | MEDLINE | ID: mdl-18211675

RESUMEN

BACKGROUND: This paper discusses the problem of automated annotation. It is a continuation of the previous work on the A4-algorithm (Adaptive algorithm of automated annotation) developed by Leontovich and others. RESULTS: A number of new statistics for the automated annotation of biological sequences is introduced. All these statistics are based on the likelihood ratio criterion. CONCLUSION: Some of the statistics yield a prediction quality that is significantly higher (up to 1.5 times higher) in comparison with the results obtained with the A4-procedure.


Asunto(s)
Algoritmos , Interpretación Estadística de Datos , Bases de Datos Genéticas , Modelos Genéticos , Alineación de Secuencia/métodos , Análisis de Secuencia/métodos , Simulación por Computador , Funciones de Verosimilitud , Modelos Estadísticos , Reproducibilidad de los Resultados , Sensibilidad y Especificidad
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