Search results for "viral"

showing 10 items of 2737 documents

Aortic Stiffness in HIV Infection with and without Antiretroviral Therapy. A Meta-analysis of Observational Studies

2020

Background: The risk of Cardiovascular (CV) events is higher in HIV-infected patients (HIV+) compared to HIV-uninfected persons (HIV−). Large artery stiffness, a well-documented predictor of adverse CV prognosis, may mediate this enhanced risk. It is usually assessed by measuring aortic Pulse Wave Velocity (aPWV). Studies examining arterial stiffness in HIV+ yielded inconsistent results. We performed a meta-analysis with the aim to evaluate the association of HIV infection and its therapy [Antiretroviral Therapy (ART)] with aPWV. Design and Method: The Standardized Mean Difference (SMD) and corresponding 95% confidence intervals were calculated for aPWV in different comparison groups. Stati…

cardiovascular riskmedicine.medical_specialtySettore MED/09 - Medicina Internaaortic stiffnessSettore MED/17 - Malattie Infettivebusiness.industrypulse wave velocityHIV infection cardiovascular risk pulse wave velocity aortic stiffnessHuman immunodeficiency virus (HIV)virus diseasesSpecialties of internal medicineGeneral Medicinemedicine.disease_causeHIV infectionAntiretroviral therapyRC581-951Meta-analysisInternal medicineRC666-701MedicineDiseases of the circulatory (Cardiovascular) systemObservational studyAortic stiffnessbusinessPulse wave velocityArtery Research
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Repression of Human Papillomavirus Oncogene Expression under Hypoxia Is Mediated by PI3K/mTORC2/AKT Signaling

2019

Oncogenic HPV types are major human carcinogens. Under hypoxia, HPV-positive cancer cells can repress the viral E6/E7 oncogenes and induce a reversible growth arrest. This response could contribute to therapy resistance, immune evasion, and tumor recurrence upon reoxygenation. Here, we uncover evidence that HPV oncogene repression is mediated by hypoxia-induced activation of canonical PI3K/mTORC2/AKT signaling. AKT-dependent downregulation of E6/E7 is only observed under hypoxia and occurs, at least in part, at the transcriptional level. Quantitative proteome analyses identify additional factors as candidates to be involved in AKT-dependent E6/E7 repression and/or hypoxic PI3K/mTORC2/AKT ac…

cervical cancerAKT1Down-RegulationAKT2Mechanistic Target of Rapamycin Complex 2mTORC2MicrobiologyHost-Microbe Biology03 medical and health sciences0302 clinical medicineVirologyCell Line TumorHumansHypoxiahuman papillomavirustumor virusPsychological repressionMechanistic target of rapamycinProtein kinase BPapillomaviridaePI3K/AKT/mTOR pathway030304 developmental biology0303 health sciencesOncogenebiologyAKTOncogene Proteins ViralQR1-502030220 oncology & carcinogenesisHost-Pathogen InteractionsCancer researchbiology.proteinddc:004Phosphatidylinositol 3-KinaseProto-Oncogene Proteins c-aktResearch ArticleSignal TransductionmBio
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Polymers with antiviral properties: A brief review.

2021

Viruses that are pathogenic to humans and livestock pose a serious epidemiological threat and challenge the world's population. The SARS-CoV-2/COVID-19 pandemic has made the world aware of the scale of the threat. The surfaces of various materials can be a source of viruses that remain temporarily contagious in the environment. Few polymers have antiviral effects that reduce infectivity or the presence of a virus in the human environment. Some of the effects are due to certain physical properties, e.g., high hydrophobicity. Other materials owe their antiviral activity to a modified physicochemical structure favoring the action on specific virus receptors or on their biochemistry. Current re…

chemistry.chemical_classification2019-20 coronavirus outbreakeducation.field_of_studyHuman environmentCoronavirus disease 2019 (COVID-19)010405 organic chemistryResearch areasPolymersSevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2)PopulationCOVID-19NanotechnologyGeneral MedicinePolymer010402 general chemistry01 natural sciencesAntiviral AgentsVirus0104 chemical scienceschemistryHumanseducationPolimery w medycynie
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Structural Properties of Carnation Mottle Virus p7 Movement Protein and Its RNA-binding Domain

2001

Plant viral movement proteins (MPs) participate actively in the intra- and intercellular movement of RNA plant viruses to such an extent that MP dysfunction impairs viral infection. However, the molecular mechanism(s) of their interaction with cognate nucleic acids are not well understood, partly due to the lack of structural information. In this work, a protein dissection approach was used to gain information on the structural and RNA-binding properties of this class of proteins, as exemplified by the 61-amino acid residue p7 MP from carnation mottle virus (CarMV). Circular dichroism spectroscopy showed that CarMV p7 is an alpha/beta RNA-binding soluble protein. Using synthetic peptides de…

chemistry.chemical_classificationBinding SitesCarlavirusC-terminusMolecular Sequence DataRNA-Binding ProteinsRNACell BiologyBiologyAlanine scanningBiochemistryProtein Structure SecondaryAmino acidViral ProteinsProtein structureBiochemistrychemistryRNAAmino Acid SequenceBinding siteMolecular BiologyPeptide sequenceBinding domainJournal of Biological Chemistry
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Characterization of the DNA-binding activity of the E1 and E2 proteins and the E1/E2 complex of human papillomavirus type 33.

1997

The E1 and E2 proteins of papillomaviruses are essential for the initiation of viral DNA replication. We have purified the E2 protein of human papillomavirus type 33 (HPV-33) by immunoaffinity chromatography. The purified E2 protein bound with high affinity to all four consensus binding sites of HPV-33 (Kd approximately equal to 2 x 10(-10)M). A putative E2 binding site differing at one position in the second stem of the palindrome was not bound by E2. The E1 protein of HPV-33 purified by affinity chromatography using glutathione S-transferase as tag displayed specific DNA-binding activity in footprint analyses protecting HPV-33 nucleotides 7896 to 7909/1 to 18 from DNasel digestion. Hypers…

chemistry.chemical_classificationBinding SitesPalindromeOncogene Proteins ViralGlutathioneBiologyVirologyMolecular biologyDNA-Binding ProteinsDNA binding sitechemistry.chemical_compoundViral Envelope ProteinschemistryAffinity chromatographyVirologySense (molecular biology)HumansNucleotideBinding siteDigestionPapillomaviridaeProtein BindingJournal of General Virology
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Deoxyribonucleases in Herpes simplex Virus Type 1 and 2 Infected Primary Rabbit Kidney Cells

1980

Abstract In primary rabbit kidney cells infected with herpes simplex virus four different neutral deoxyribonuclease activities can be detected by means of the deoxyribonuclease assay in DNA-containing polyacrylamide gels following their separation by discelectrophoresis. The method is suitable to follow independently the change in each activity of the different enzymes using only about 5 × 105 cells for each assay during the time-course of infection. Under these conditions one enzyme activity is constant, two disappear while the activity of a fourth one present only in infected cells, increases.

chemistry.chemical_classificationDeoxyribonucleasesbiologyChemistryDeoxyribonucleaseCell Transformation ViralKidneymedicine.disease_causeVirologyGeneral Biochemistry Genetics and Molecular BiologyEnzyme assayKineticsHerpes simplex virusEnzymemedicinebiology.proteinRabbit kidneyAnimalsSimplexvirusRabbitsDeoxyribonucleasesCells CulturedZeitschrift für Naturforschung C
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Biochemical and Kinetic Analyses of NS5B RNA-Dependent RNA Polymerase of the Hepatitis C Virus

1998

The biochemical properties of the RNA-dependent RNA polymerase (RdRp) of the hepatitis C virus were analyzed. A hexahistidine affinity-tagged NS5B fusion protein was expressed with recombinant baculoviruses in insect cells and purified to near homogeneity. Enzymatic activity of the purified protein was inhibited by KCl or high concentrations of NaCl and was absolutely dependent on Mg2+, which could be replaced by Mn2+. NS5B was found to be processive and able to copy long heteropolymeric templates with an elongation rate of 150-200 nucleotides/min at 22 degreesC. Kinetic constants were determined for all four nucleoside triphosphates and different templates. In case of a heteropolymeric RNA…

chemistry.chemical_classificationHepatitis C virusvirusesRNARNA-dependent RNA polymeraseHepacivirusBiologyViral Nonstructural ProteinsRibonucleosidemedicine.disease_causeRNA-Dependent RNA PolymeraseMolecular biologySubstrate Specificitychemistry.chemical_compoundKineticsBiochemistrychemistryRNA polymeraseVirologymedicineHumansNucleotideNS5BNucleosideVirology
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Potent SARS-CoV-2 mRNA Cap Methyltransferase Inhibitors by Bioisosteric Replacement of Methionine in SAM Cosubstrate

2021

Viral mRNA cap methyltransferases (MTases) are emerging targets for the development of broad-spectrum antiviral agents. In this work, we designed potential SARS-CoV-2 MTase Nsp14 and Nsp16 inhibitors by using bioisosteric substitution of the sulfonium and amino acid substructures of the cosubstrate S-adenosylmethionine (SAM), which serves as the methyl donor in the enzymatic reaction. The synthetically accessible target structures were prioritized using molecular docking. Testing of the inhibitory activity of the synthesized compounds showed nanomolar to submicromolar IC50 values for five compounds. To evaluate selectivity, enzymatic inhibition of the human glycine N-methyltransferase invol…

chemistry.chemical_classificationMessenger RNALetterMethyltransferaseMethioninebiologySARS-CoV-2SulfoniumOrganic ChemistryNsp16MTase inhibitorsNsp14BiochemistryCofactorAmino acidantiviral drugschemistry.chemical_compoundEnzymeBiochemistrychemistryDrug DiscoveryGlycinebiology.proteinSAM analoguesACS Medicinal Chemistry Letters
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A quantum mechanics/molecular mechanics study of the protein-ligand interaction for inhibitors of HIV-1 integrase.

2007

Human immunodeficiency virus type-1 integrase (HIV-1 IN) is an essential enzyme for effective viral replication. Diketo acids such as L-731,988 and S-1360 are potent and selective inhibitors of HIV-1 IN. In this study, we used molecular dynamics simulations, within the hybrid quantum mechanics/molecular mechanics (QM/MM) approach, to determine the protein-ligand interaction energy between HIV-1 IN and L-731,988 and 10 of its derivatives and analogues. This hybrid methodology has the advantage that it includes quantum effects such as ligand polarisation upon binding, which can be very important when highly polarisable groups are embedded in anisotropic environments, as for example in metal-c…

chemistry.chemical_classificationModels MolecularbiologyChemistryStereochemistryOrganic ChemistryProteinsGeneral ChemistryInteraction energyHIV IntegraseLigand (biochemistry)LigandsMolecular mechanicsCatalysisIntegraseMolecular dynamicsEnzymeViral replicationComputational chemistryQuantum mechanicsbiology.proteinQuantum TheoryHIV Integrase InhibitorsProtein ligandChemistry (Weinheim an der Bergstrasse, Germany)
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Inhibition of herpesvirus DNA synthesis by 9-beta-D-arabinofuranosyladenine in cellular and cell-free systems.

1977

9-beta-D-Arabinofuranosyladenine 5'-triphosphate (ara-ATP) is an inhibitor both of DNA polymerase-alpha and -beta from noninfected rabbit kidney cells and of the DNA-dependent DNA polymerase induced by herpes simplex virus Type 1 (strain IES). The studies were performed with partially purified enzymes, and each of the different polymerase preparations contained only one DNA-dependent DNA polymerase species. These enzymes were inhibited in a competitive manner. The HSV-induced DNA-dependent DNA polymerase was 39-fold more sensitive to ara-ATP than was cellular DNA polymerase-beta and 116-fold more sensitive than cellular DNA polymerase-alpha. The affinity of the HSV-induced enzyme for ara-AT…

chemistry.chemical_classificationVirus CultivationbiologyDNA synthesisCell-Free SystemChemistryDNA polymeraseGeneral Neurosciencemedicine.disease_causeMolecular biologyGeneral Biochemistry Genetics and Molecular BiologyEnzyme assayProliferating cell nuclear antigenchemistry.chemical_compoundHerpes simplex virusEnzymeHistory and Philosophy of ScienceDNA Viralbiology.proteinmedicineSimplexvirusPolymeraseDNAVidarabineNucleic Acid Synthesis InhibitorsAnnals of the New York Academy of Sciences
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