Search results for "Structural Biology."

showing 10 items of 822 documents

Impact of High pH Stress on Yeast Gene Expression: A Comprehensive Analysis of mRNA Turnover During Stress Responses.

2015

Environmental alkalinisation represents a stress condition for yeast Saccharomyces cerevisiae, to which this organism responds with extensive gene expression remodelling. We show here that alkaline pH causes an overall decrease in the transcription rate (TR) and a fast destabilisation of mRNAs, followed by a more prolonged stabilisation phase. In many cases, augmented mRNA levels occur without the TR increasing, which can be attributed to mRNA stabilisation. In contrast, the reduced amount of mRNAs is contributed by both a drop in the TR and mRNA stability. A comparative analysis with other forms of stress shows that, unlike high pH stress, heat-shock, osmotic and oxidative stresses present…

Saccharomyces cerevisiae ProteinsTranscription GeneticRNA StabilitySaccharomyces cerevisiaeBiophysicsSaccharomyces cerevisiaeOxidative phosphorylationBiochemistryStress (mechanics)Stress PhysiologicalStructural BiologyGene Expression Regulation FungalGene expressionGeneticsRNA MessengerDestabilisationRNA Processing Post-TranscriptionalMolecular BiologyGeneMessenger RNAbiologyHydrogen-Ion Concentrationbiology.organism_classificationYeastCell biologyBiochemistryGene-Environment Interaction
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Urmylation and tRNA thiolation functions of ubiquitin-like Uba4·Urm1 systems are conserved from yeast to man

2015

AbstractThe ubiquitin-like protein Urm1 from budding yeast and its E1-like activator Uba4 have dual roles in protein urmylation and tRNA thiolation pathways. To study whether these are conserved among eukaryotes, we used gene shuffles to replace the yeast proteins by their human counterparts, hURM1 and hUBA4/MOCS3. As judged from biochemical and genetical assays, hURM1 and hUBA4 are functional in yeast, albeit at reduced efficiencies. They mediate urmylation of the peroxiredoxin Ahp1, a known urmylation target in yeast, and support tRNA thiolation. Similar to hUBA4, yeast Uba4 itself is modified by Urm1 and hURM1 suggesting target overlap between eukaryal urmylation pathways. In sum, our st…

Saccharomyces cerevisiae ProteinsUba4 (hUBA4/MOCS3)Saccharomyces cerevisiaeBiophysicstRNA thiolationSaccharomyces cerevisiaeBiochemistryUbiquitin-like urmylationRNA TransferUbiquitinStructural BiologyAnticodonGeneticsHumansUbiquitinsMolecular BiologyProtein urmylationGeneUrm1 (hURM1)Conserved SequenceSequence Homology Amino AcidbiologyActivator (genetics)TRNA thiolationCell Biologybiology.organism_classificationNucleotidyltransferasesYeastBiochemistrySulfurtransferasesbiology.proteinPeroxiredoxinHeLa CellsFEBS Letters
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Elucidating the picocyanobacteria salinity divide through ecogenomics of new freshwater isolates

2022

Abstract Background Cyanobacteria are the major prokaryotic primary producers occupying a range of aquatic habitats worldwide that differ in levels of salinity, making them a group of interest to study one of the major unresolved conundrums in aquatic microbiology which is what distinguishes a marine microbe from a freshwater one? We address this question using ecogenomics of a group of picocyanobacteria (cluster 5) that have recently evolved to inhabit geographically disparate salinity niches. Our analysis is made possible by the sequencing of 58 new genomes from freshwater representatives of this group that are presented here, representing a 6-fold increase in the available genomic data. …

SalinityProteomePhysiologyFresh WaterCell BiologyPlant ScienceCyanobacteriaGeneral Biochemistry Genetics and Molecular BiologyQRStructural BiologyGeneral Agricultural and Biological SciencesEcology Evolution Behavior and SystematicsEcosystemDevelopmental BiologyBiotechnologyBMC Biology
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Poly-sarcosine and poly(ethylene-glycol) interactions with proteins investigated using molecular dynamics simulations

2018

Nanoparticles coated with hydrophilic polymers often show a reduction in unspecific interactions with the biological environment, which improves their biocompatibility. The molecular determinants of this reduction are not very well understood yet, and their knowledge may help improving nanoparticle design. Here we address, using molecular dynamics simulations, the interactions of human serum albumin, the most abundant serum protein, with two promising hydrophilic polymers used for the coating of therapeutic nanoparticles, poly(ethylene-glycol) and poly-sarcosine. By simulating the protein immersed in a polymer-water mixture, we show that the two polymers have a very similar affinity for the…

SarcosineBiocompatibilityPoly-peptoidlcsh:BiotechnologyBiophysicsFOS: Physical sciencesNanoparticle02 engineering and technologyCondensed Matter - Soft Condensed MatterProtein aggregation010402 general chemistry01 natural sciencesBiochemistryNanoparticle protein coronachemistry.chemical_compoundMolecular dynamicsAdsorptionStructural Biologylcsh:TP248.13-248.65GeneticsmedicinePhysics - Biological Physicschemistry.chemical_classificationBiomolecules (q-bio.BM)MD simulationPolymer021001 nanoscience & nanotechnologyHuman serum albuminPEG0104 chemical sciencesComputer Science ApplicationsQuantitative Biology - BiomoleculeschemistryChemical engineeringBiological Physics (physics.bio-ph)FOS: Biological sciencesSoft Condensed Matter (cond-mat.soft)Poly-sarcosine0210 nano-technologyResearch ArticleBiotechnologymedicine.drug
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A facile method to determine pore size distribution in porous scaffold by using image processing

2015

Abstract Image processing permits scientists to investigate morphological properties of three-dimensional structures starting from their bi-dimensional gray-scale representation. In many cases porous structure with complex architecture has to be designed in order to attempt specific properties such in the case of scaffold for tissue engineering. Traditional morphological characterization, like scanning electron microscopy, should be coupled with quantitative information such as pore size distribution (PSD) in order to get a deeper understanding of the influence of the porous structure on tissue regeneration processes and on other related applications, it is remarkable to study a quantitativ…

ScaffoldMaterials scienceScanning electron microscopeGeneral Physics and AstronomyNanotechnologyImage processingCell BiologyPorosimetryPore size distributionCharacterization (materials science)ScaffoldImage processingTissue engineeringStructural BiologyGeneral Materials ScienceRepresentation (mathematics)PorosityMicron
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Two changes of the same nucleotide confer resistance to diuron and antimycin in the mitochondrial cytochrome b gene of Schizosaccharomyces pombe

1988

AbstractDiuron (3-(3,4-dichlorophenyl)-1,1-dimethylurea) and antimycin, both inhibitors of mitochondrial respiration, block electron flow between cytochromes b and c1. Mutants resistant to either drug have been selected using Schizosaccharomyces pombe strains with an extrachromosomally inherited mutator. In analogy to Saccharomyces cerevisiae these mutational sites were assumed to map in the cytochrome b gene. DNA sequence analysis showed that two changes in the same nucleotide are responsible for resistance to antimycin and diuron. Analysis of resistant and sensitive progeny of crosses between the mutants and the wild type confirmed the correlation between mutational alteration and resista…

Sequence analysisSaccharomyces cerevisiaeMutantGenes FungalMolecular Sequence DataBiophysicsAntimycin AMutational alterationBiochemistryAntimycin resistanceSpecies SpecificityStructural BiologySchizosaccharomycesGenetics(Schizosaccharomyces pombe)AnimalsHumansNucleotideAmino Acid SequenceMolecular BiologyGeneDNA sequence analysischemistry.chemical_classificationbiologyBase SequenceCytochrome bWild typeDrug Resistance MicrobialCell Biologybiology.organism_classificationCytochrome b GroupMitochondrial cytochrome b geneMolecular biologyDiuron resistancechemistryBiochemistryGenesDiuronSchizosaccharomyces pombeSaccharomycetalesMutator strainFEBS Letters
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A new interpretation and practical aspects of the direct-methods modulus sum function. VIII

2001

Since the first publication of the direct-methods modulus sum function [Rius (1993). Acta Cryst. A49, 406-409], the application of this function to a variety of situations has been shown in a series of seven subsequent papers. In this way, much experience about this function and its practical use has been gained. It is thought by the authors that it is now the right moment to publish a more complete study of this function which also considers most of this practical knowledge. The first part of the study relates, thanks to a new interpretation, this function to other existing phase-refinement functions, while the second shows, with the help of test calculations on a selection of crystal stru…

Series (mathematics)Direct methodProteinsTangentField (mathematics)Function (mathematics)Biomechanical PhenomenaInterpretation (model theory)Moment (mathematics)Structural BiologyDirect methodsCalculusCrystallizationAlgorithmsMathematicsActa Crystallographica Section A Foundations of Crystallography
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Iteratively reweighted least squares in crystal structure refinements

2011

The use of robust techniques in crystal structure multipole refinements of small molecules as an alternative to the commonly adopted weighted least squares is presented and discussed. As is well known, the main disadvantage of least-squares fitting is its sensitivity to outliers. The elimination from the data set of the most aberrant reflections (due to both experimental errors and incompleteness of the model) is an effective practice that could yield satisfactory results, but it is often complicated in the presence of a great number of bad data points, whose one-by-one elimination could become unattainable. This problem can be circumvented by means of a robust least-squares regression that…

Settore GEO/06 - MineralogiaLeast trimmed squarescomputer.software_genreRegressionRobust regressionIteratively reweighted least squaresData setRobust regression outlier refinementData pointStructural BiologyOutlierSensitivity (control systems)Data miningcomputerAlgorithmMathematicsActa Crystallographica Section A Foundations of Crystallography
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Correction to: FASTA/Q data compressors for MapReduce-Hadoop genomics: space and time savings made easy

2022

Following publication of the original article [1], the authors identified that the affiliations of Giuseppe Cattaneo and Raffaele Giancarlo were interchanged. The correct affiliations are given below. The correct affiliation of Giuseppe Cattaneo is: 2Dipartimento di Informatica, Università di Salerno, Fisciano, Italy. The correct affiliation of Raffaele Giancarlo is: 3Dipartimento di Matematica ed Informatica, Università di Palermo, Palermo, Italy. The original article [1] has been corrected.

Settore INF/01 - InformaticaStructural BiologyApplied MathematicsData CompressionMolecular BiologyBiochemistryComputer Science ApplicationsBMC Bioinformatics
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Speeding up the Consensus Clustering methodology for microarray data analysis

2010

Abstract Background The inference of the number of clusters in a dataset, a fundamental problem in Statistics, Data Analysis and Classification, is usually addressed via internal validation measures. The stated problem is quite difficult, in particular for microarrays, since the inferred prediction must be sensible enough to capture the inherent biological structure in a dataset, e.g., functionally related genes. Despite the rich literature present in that area, the identification of an internal validation measure that is both fast and precise has proved to be elusive. In order to partially fill this gap, we propose a speed-up of Consensus (Consensus Clustering), a methodology whose purpose…

Settore INF/01 - Informaticalcsh:QH426-470Computer scienceResearchApplied MathematicsStability (learning theory)InferenceApproximation algorithmcomputer.software_genreNon-negative matrix factorizationIdentification (information)lcsh:GeneticsComputingMethodologies_PATTERNRECOGNITIONComputational Theory and Mathematicslcsh:Biology (General)Structural BiologyConsensus clusteringBenchmark (computing)Data mininginternal validation measures data mining microarray data NMFCluster analysiscomputerMolecular Biologylcsh:QH301-705.5Algorithms for Molecular Biology
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