Global host proteomic responses to virus infection - read free eBook in online reader or directly download on the web page. Select files or add your book in reader. Download and read online ebook Global host proteomic responses to virus infection write by Kevin Coombs. This book was released on . Global host proteomic responses to virus infection available in PDF, EPUB and Kindle. The field of virology has seen explosive growth in the past few decades. A large amount of effort has gone into successfully delineating virus evolution, genetic diversity, immunology, pathogenesis, structure, vaccine development, viral gene expression and genomic replication strategies. In addition, considerable recent work has been focusing on cellular responses to infection as well as how viruses may induce transformation and oncogenesis. Viruses are obligate intracellular parasites and thus absolutely dependent upon host cells. Not surprisingly, they often cause profound changes in cells, including apoptosis, death and signalling, to name a few perturbations. Thus, the molecular signals for how viruses induce pathophysiological alterations in their hosts have been of growing recent interest. Cellular and organismal responses, such as those induced by virus infection, are invariably mediated by changes in gene and protein expression and modification. Thus, there has been keen interest in understanding how gene and protein expressions and modifications are quantitatively and qualitatively affected by such challenges. From a historical perspective, most early work that examined host protein responses to virus infection employed “biased” approaches, in which investigators targeted a limited number, or only one cellular molecule of interest. Completion of many organisms’ genome sequences has allowed the global “non-biased” simultaneous analysis of the entire repertoire of cellular mRNA species, the transcriptome, by gene micro-arrays. This has provided significant information about how cellular gene expressions are altered by virus-induced perturbations, but has not provided as much information about the encoded proteins. This results for several reasons, including, but not limited to the fact that gene expression levels cannot accurately predict protein expression levels, nor the types and extent of post-translational modifications, many genes encode multiple proteins through splice variants, and protein activity may be affected by a large number of conditions, including phosphorylation. Recent technological and bioinformatic approaches make it now possible to begin to extend similar global analyses to probe the cellular proteome, the repertoire of the actual effector molecules. One general strategy has been to take advantage of improved separations technologies, as well as greatly improved mass spectrometry resolution, to quantitatively or comparatively measure hundreds or thousands of proteins. Proteins from multiple conditions (i.e., mock-infected and infected) may be differentially labelled by various techniques, such as 2D-DIGE, ICAT, iTRAQ, SILAC, with 18O during peptide preparation, and/or by various other methods, and then compared to measure comparative alterations in the levels of proteins induced by the virus infection. Such analyses have also been extended by using “label-free” methods for more efficient multiplexing applications, and/or by examining specific protein modifications. In addition, concerted efforts to raise antibodies against all cellular proteins have resulted in the development of “antibody arrays,” which are also generally used for quantitative or comparative assays. Finally, while assays, such as the above, are generally limited to delineating the absolute amount of specific proteins, newer technologies have been developed that allow the simultaneous probing of hundreds of proteins’ functions. Assays, such as “Activity Based Protein Profiling”, are designed to probe enzymatic activity, with current focus on broad-spectrum proteases and other enzymatic classes. This Research Topic will provide an overview of many of these methods, as well as numerous specific examples of each approach, and how they are used to better delineate the ways viruses affect cellular responses during infection.
Proteomics Approaches to Unravel Virus - Vertebrate Host Interactions
Proteomics Approaches to Unravel Virus - Vertebrate Host Interactions - read free eBook in online reader or directly download on the web page. Select files or add your book in reader. Download and read online ebook Proteomics Approaches to Unravel Virus - Vertebrate Host Interactions write by . This book was released on 2021-04-30. Proteomics Approaches to Unravel Virus - Vertebrate Host Interactions available in PDF, EPUB and Kindle. Proteomics Approaches to Unravel Virus - Vertebrate Host Interactions, Volume 109 in the Advances in Virus Research series, highlights state-of-the art mass spectrometry techniques to elucidate the tight interplay of vertebrate viruses and their host cells. The volume includes chapters on Spatio-temporal resolution of host protein complexes during virus entry, Proteomic approaches to investigate gammaherpesvirus biology and associated tumorigenesis, Applications of Mass Spectrometry Imaging in Virus Research, Mapping surfaceome dynamics during viral infection, Characterization of proteolytic events in virus-host interactions, Dynamic protein network modulation upon viral infection, and much more. Discusses the latest methodological breakthroughs in mass spectrometry-based proteomics Reviews how technology has advanced our knowledge on virus-host interactions Provides future perspectives on proteomics research in virology
Global Quantitative Host Proteomic Assay of Infected Cells Highlight Virus Specific Protein Changes and Identify a Novel Role for Secretogranin Ii Protein in Virus Infections
Global Quantitative Host Proteomic Assay of Infected Cells Highlight Virus Specific Protein Changes and Identify a Novel Role for Secretogranin Ii Protein in Virus Infections - read free eBook in online reader or directly download on the web page. Select files or add your book in reader. Download and read online ebook Global Quantitative Host Proteomic Assay of Infected Cells Highlight Virus Specific Protein Changes and Identify a Novel Role for Secretogranin Ii Protein in Virus Infections write by Alicia Berard. This book was released on 2012. Global Quantitative Host Proteomic Assay of Infected Cells Highlight Virus Specific Protein Changes and Identify a Novel Role for Secretogranin Ii Protein in Virus Infections available in PDF, EPUB and Kindle. Viruses are obligate parasites that use the host cellular machinery to produce progeny virions. The host responds to this invading pathogen by induction of the immune system; however, the virus employs a variety of strategies to overcome these attacks. The complexity of the virus-host interaction is of great interest to researchers with aims to both characterize the relationship and target steps of the viral life cycle to hinder infection. Many targeted tactics employ single protein analysis; however, approaches that examine the whole set of virus/host interactions are available. Transcriptional alterations within host cells have been determined for many virus- host interactions by micro-array techniques; however little is known about the effects on cellular proteins. This study uses a quantitative mass spectrometric-based method, SILAC, to study differences in a host cell's proteome with infection by a virus. Mammalian reoviruses and herpes simplex viruses are prototypical viruses commonly studied to determine virus life cycle and interactions with hosts. Using three strains of reoviruses and one HSV1 strain, cells were infected to identify differentially regulated proteins at different times. Thousands of proteins were identified for each virus type, some up or down regulated after infection. Biological functions and network analyses were performed using online networking tools. These pathway analyses indicated numerous processes including cell death and inflammatory response are affected by T1L reovirus infection. Comparing reovirus strains revealed a greater overall proteomic change in host function when infected with the more pathogenic T3DC strain. For the HSV infection, host proteins altered during the different immediate early, earlyand late phases of infection helped characterize the host-virus interaction parallel to the virus life cycle. Overall, my study has characterized proteomic changes in different virus infection systems, identifying numerous novel cellular functional pathways and specific proteins altered during virus infections, specifically the secretogranin II protein that had opposite types of regulation in reoviruses and HSV and was examined for its effects on virus replication. Further studies on the novel proteomic characteristics may provide greater understanding to the complex virus-host interactome, leading to possible antiviral targets.
Proteomic Studies of the Influenza Virus-human Cell Interations
Proteomic Studies of the Influenza Virus-human Cell Interations - read free eBook in online reader or directly download on the web page. Select files or add your book in reader. Download and read online ebook Proteomic Studies of the Influenza Virus-human Cell Interations write by Yimeng Wang. This book was released on 2013. Proteomic Studies of the Influenza Virus-human Cell Interations available in PDF, EPUB and Kindle. Influenza A viruses (IAVs) continue to be a threat to human health. Despite extensive studies, the mechanisms underlying the IAVs-host interactions during IAV infection remain elusive. We employed quantitative proteomic methods to systematically explore the host cell protein expression responses to IAV infection and examine the function of a critical IAV protein called NS1 by identifying its host binding partners. Specifically, we used a 2-dimentional gel electrophoresis (2-DE) based proteomic method to screen host proteins whose expression was substantially altered by IAV. One critical protein named IkappaB kinase-gamma (IKKgamma) was found to be significantly down-regulated during IAV infection. Functional studies indicated that IKKgamma and IAVs were mutually inhibitory and IKKgamma might be the target for virus to inhibit IFN production. IAV protein NS1 is known to play critical roles in viral pathogenesis and host immune responses. Through 2-DE proteomic approach and mass spectrometry, we identified several novel host cellular proteins that were associated with NS1. First, we found that heterogeneous nuclear ribonucleoprotein A2/B1 (hnRNP A2/B1) interacted with NS1, affected replication, transcription, expression and nucleo-cytoplasmic translocation of NS1 mRNA, and the eventual whole virus replication. Second, two ATPase proteins, RUVBL1 and RUVBL2, were identified to associate with NS1 for regulation of cell apoptosis in the absence of IFNs. Third, based on previous finding of the interaction between a DEAD family protein designated as DDX100 and NS1 through a more sensitive proteomic approach called SILAC (stable isotope labeling with amino acids in cell culture), we found this interaction promoted virus replication through enhancing viral NS1 gene replication, transcription, and dsRNA unwinding. In summary, through quantitative proteomic, molecular and cell biology studies, we generated the global picture of host cell protein expression responses to IAV infection. For IAV NS1, several host cellular proteins were found to interact with NS1 to regulate the host cell action and virus proliferation.
RNA Viruses
RNA Viruses - read free eBook in online reader or directly download on the web page. Select files or add your book in reader. Download and read online ebook RNA Viruses write by Decheng Yang. This book was released on 2009. RNA Viruses available in PDF, EPUB and Kindle. This is the first comprehensive book on human/animal gene responses to RNA viral infections, including prevalent, emerging and re-emerging RNA viruses such as HIV, SARS-CoV, West Nile virus, influenza virus and many others. Human gene responses are reviewed by leading virologists worldwide in the following aspects: (i) the altered gene expression profiles at the transcriptional and translational levels detected with cutting-edge technologies such as cDNA microarray and proteomics; (ii) host innate and adapted immune responses to viral replication in target organs; (iii) virus-activated signal transduction pathways in cell survival, apoptosis and autophagosomal pathways; and (iv) the small interfering RNA/microRNA-mediated gene silencing pathway, a recently characterized new host defense mechanism against viral infection.
