Search results for "protein engineering"

showing 10 items of 54 documents

Complexes of carbon nanotubes with ions and macromolecules : studies on electronic conduction properties

2014

electronic transportprotein engineeringhemicellulosecarbon nanotubealkali-dopingbiosensornanomaterials
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Homology modeling using simulated annealing of restrained molecular dynamics and conformational search calculations with CONGEN: application in predi…

1997

We have developed an automatic approach for homology modeling using restrained molecular dynamics and simulated annealing procedures, together with conformational search algorithms available in the molecular mechanics program CONGEN (Bruccoleri RE, Karplus M, 1987, Biopolymers 26:137-168). The accuracy of the method is validated by "predicting" structures of two homeodomain proteins with known three-dimensional structures, and then applied to predict the three-dimensional structure of the homeodomain of the murine Msx-1 transcription factor. Regions of the unknown protein structure that are highly homologous to the known template structure are constrained by "homology distance constraints,"…

Models MolecularSaccharomyces cerevisiae ProteinsProtein ConformationMSX1 Transcription FactorMolecular Sequence DataSaccharomyces cerevisiaeBiologyProtein EngineeringBiochemistryProtein Structure SecondaryMolecular dynamicsMiceProtein structureAnimalsComputer SimulationHomology modelingAmino Acid SequenceMolecular BiologyHomeodomain ProteinsMSX1 Transcription FactorSequence Homology Amino AcidNuclear ProteinsProtein engineeringProtein superfamilyengrailedRepressor ProteinsCrystallographyAntennapedia Homeodomain ProteinThreading (protein sequence)AlgorithmsInformation SystemsTranscription FactorsResearch ArticleProtein science : a publication of the Protein Society
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Introduction of histidine residues into avidin subunit interfaces allows pH-dependent regulation of quaternary structure and biotin binding

2003

AbstractIn order to turn the subunit association and biotin binding of avidin into pH-sensitive phenomena, we have replaced individually three amino acid residues in avidin (Met96, Val115 and Ile117) with histidines in the 1–3 interface, and in combination with a histidine conversion in the 1–2 interface (Trp110). The single replacements Met96His and Val115His in the 1–3 interface were found to have a clear effect on the quaternary structure of avidin, since subunit associations of these mutants became pH-dependent. The histidine replacement in the 1–2 interface affected the biotin-binding properties of the mutants, in particular reversibility of binding and protein–ligand complex formation…

Models MolecularBiotin bindingInsectaProtein subunitBiophysicsBiotinBiosensing TechniquesBiochemistryCell LineProtein structureStructural BiologyGeneticsAnimalsHistidinepH dependenceProtein Structure QuaternaryMolecular BiologyHistidinebiologyChemistryCell BiologyProtein engineeringHydrogen-Ion ConcentrationAvidinRecombinant ProteinsMolecular WeightProtein SubunitsSpectrometry FluorescenceAmino Acid SubstitutionBiochemistryBiotinylationBiophysicsbiology.proteinProtein quaternary structureProtein engineeringBaculoviridaeProtein BindingAvidinFEBS Letters
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Analysis of Structure-Activity Relationships of the Bowman-Birk Inhibitor of Serine Proteinases

1993

Proteinase inhibitors are a class of the various dietary inhibitors of mutagenesis and carcinogenesis (Hayatsu et al., 1988). Schelp and Pongpaew (1988) have recently hypothesized that protection against cancer may result from an increase of endogenous proteinase inhibitors such as α2-macroglobulin induced by diets that are low in calories and fat. The Bowman-Birk inhibitor (BBI) of serine proteinases, a double-headed polypeptide-inhibitor of trypsin and chymotrypsin, is one of the most potent cancer chemopreventive agents (Yavelow et al., 1983, 1985). Recently, this property has been substantiated in an in vivo investigation using mice (St. Clair et al., 1990) that were exposed to dimethyl…

chemistry.chemical_classificationChymotrypsinmedicine.diagnostic_testbiologyProteolysisElastaseRational designProteolytic enzymesProtein engineeringTrypsinAmino acidchemistryBiochemistrymedicinebiology.proteinmedicine.drug
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Engineering of a DNA Polymerase for Direct m6A Sequencing

2017

Methods for the detection of RNA modifications are of fundamental importance for advancing epitranscriptomics. N6-methyladenosine (m6A) is the most abundant RNA modification in mammalian mRNA and is involved in the regulation of gene expression. Current detection techniques are laborious and rely on antibody-based enrichment of m6A-containing RNA prior to sequencing, since m6A modifications are generally "erased" during reverse transcription (RT). To overcome the drawbacks associated with indirect detection, we aimed to generate novel DNA polymerase variants for direct m6A sequencing. Therefore, we developed a screen to evolve an RT-active KlenTaq DNA polymerase variant that sets a mark for…

0301 basic medicineAdenosineRNA-dependent RNA polymeraseDNA-Directed DNA Polymerase010402 general chemistryProtein Engineering01 natural sciencesCatalysis03 medical and health sciencesDNA polymerasesSequencing by hybridization[SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry Molecular Biology/Genomics [q-bio.GN]TheoryofComputation_ANALYSISOFALGORITHMSANDPROBLEMCOMPLEXITYRNA polymerase IRNA MessengerPolymerasebiologyOligonucleotideN6-methyladenosineReverse Transcriptase Polymerase Chain ReactionCommunicationMultiple displacement amplificationHigh-Throughput Nucleotide Sequencing[SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry Molecular Biology/Molecular biologyGeneral ChemistryDNA MethylationRNA modificationMolecular biologyReverse transcriptaseCommunications0104 chemical sciencesSequencing by ligationenzyme engineering030104 developmental biologyComputingMethodologies_PATTERNRECOGNITIONddc:540biology.proteinepitranscriptomicsRNA Methylation
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Reductive modification of genetically encoded 3-nitrotyrosine sites in alpha synuclein expressed in E.coli

2019

Tyrosine nitration is a post-translational protein modification relevant to various pathophysiological processes. Chemical nitration procedures have been used to generate and study nitrated proteins, but these methods regularly lead to modifications at other amino acid residues. A novel strategy employs a genetic code modification that allows incorporation of 3-nitrotyrosine (3-NT) during ribosomal protein synthesis to generate a recombinant protein with defined 3-NT-sites, in the absence of other post-translational modifications. This approach was applied to study the generation and stability of the 3-NT moiety in recombinant proteins produced in E.coli. Nitrated alpha-synuclein (ASYN) was…

lcsh:R5-920Escherichia coli ProteinsGenetic VectorsGreen Fluorescent ProteinsGene ExpressionProtein EngineeringRecombinant Proteinslcsh:Biology (General)ddc:570Escherichia colialpha-SynucleinHumansTyrosineCloning MolecularAlpha synuclein Nitration 3-Nitrotyrosine 3-Aminotyrosine E.colilcsh:Medicine (General)Oxidation-Reductionlcsh:QH301-705.5Metabolic Networks and PathwaysResearch Paper
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HIF-1α and Pro-Inflammatory Signaling Improves the Immunomodulatory Activity of MSC-Derived Extracellular Vesicles

2021

Despite the strong evidence for the immunomodulatory activity of mesenchymal stromal cells (MSCs), clinical trials have so far failed to clearly show benefit, likely reflecting methodological shortcomings and lack of standardization. MSC-mediated tissue repair is commonly believed to occur in a paracrine manner, and it has been stated that extracellular vesicles (EVs) secreted by MSCs (EVMSC) are able to recapitulate the immunosuppressive properties of parental cells. As a next step, clinical trials to corroborate preclinical studies should be performed. However, effective dose in large mammals, including humans, is quite high and EVs industrial production is hindered by the proliferative s…

MaleT-Lymphocytesmedicine.medical_treatmentCellimmunomodulationProtein Engineeringlcsh:ChemistryMiceHypersensitivity Delayedlcsh:QH301-705.5TelomeraseCells CulturedSpectroscopyMice Inbred BALB CGeneral MedicineRecombinant ProteinsComputer Science ApplicationsCell biologyCytokinemedicine.anatomical_structurehypoxia-inducible factor 1-alphaCytokinesmesenchymal stromal cellsGenetic VectorsGreen Fluorescent ProteinsBiologyMesenchymal Stem Cell TransplantationArticleCatalysisCell LineViral vectorInorganic ChemistryExtracellular VesiclesYoung AdultParacrine signallingIn vivomedicineAnimalsHumansPhysical and Theoretical ChemistryMolecular BiologyDental PulpCell ProliferationT-cellsLentivirusOrganic ChemistryMesenchymal stem cellMesenchymal Stem CellsHypoxia-Inducible Factor 1 alpha SubunitIn vitrolcsh:Biology (General)lcsh:QD1-999Cell cultureInternational Journal of Molecular Sciences
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Dual film-like organelles enable spatial separation of orthogonal eukaryotic translation

2021

Summary Engineering new functionality into living eukaryotic systems by enzyme evolution or de novo protein design is a formidable challenge. Cells do not rely exclusively on DNA-based evolution to generate new functionality but often utilize membrane encapsulation or formation of membraneless organelles to separate distinct molecular processes that execute complex operations. Applying this principle and the concept of two-dimensional phase separation, we develop film-like synthetic organelles that support protein translation on the surfaces of various cellular membranes. These sub-resolution synthetic films provide a path to make functionally distinct enzymes within the same cell. We use t…

Protein designComputational biologyBiology2D phase separationArticleGeneral Biochemistry Genetics and Molecular BiologySynthetic biologyEukaryotic translationOrganelleHumansRNA MessengerAmino AcidsOrganellesmembrane signalingsynthetic biomolecular condensatesProteinsTranslation (biology)Intracellular MembranesProtein engineeringGenetic codeenzyme engineeringHEK293 Cellsgenetic code expansionEukaryotic CellsGenetic CodeProtein Biosynthesisorthogonal translationsynthetic biologyRibosomesFunction (biology)Cell
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Controlling quaternary structure assembly: subunit interface engineering and crystal structure of dual chain avidin.

2006

Dual chain avidin (dcAvd) is an engineered avidin form, in which two circularly permuted chicken avidin monomers are fused into one polypeptide chain. DcAvd can theoretically form two different pseudotetrameric quaternary assemblies because of symmetry at the monomer-monomer interfaces. Here, our aim was to control the assembly of the quaternary structure of dcAvd. We introduced the mutation I117C into one of the circularly permuted domains of dcAvd and scanned residues along the 1-3 subunit interface of the other domain. Interestingly, V115H resulted in a single, disulfide locked quaternary assembly of dcAvd, whereas I117H could not guide the oligomerisation process even though it stabilis…

Models MolecularStereochemistryProtein subunitBiotinGene ExpressionCrystal structureCrystallography X-RayLigandsProtein EngineeringProtein–protein interactionchemistry.chemical_compoundBiotinStructural BiologyAnimalsDisulfidesProtein Structure QuaternaryMolecular BiologyChromatography High Pressure LiquidbiologyProtein engineeringHydrogen-Ion ConcentrationAvidinCrystallographyProtein SubunitsMonomerchemistryMutationbiology.proteinChromatography GelThermodynamicsProtein quaternary structureChickensAvidinJournal of molecular biology
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Chicken Avidin-related Protein 4/5 Shows Superior Thermal Stability when Compared with Avidin while Retaining High Affinity to Biotin

2003

The protein chicken avidin is a commonly used tool in various applications. The avidin gene belongs to a gene family that also includes seven other members known as the avidin-related genes (AVR). We report here on the extremely high thermal stability and functional characteristics of avidin-related protein AVR4/5, a member of the avidin protein family. The thermal stability characteristics of AVR4/5 were examined using a differential scanning calorimeter, microparticle analysis, and a microplate assay. Its biotin-binding properties were studied using an isothermal calorimeter and IAsys optical biosensor. According to these analyses, in the absence of biotin AVR4/5 is clearly more stable (T…

Models MolecularStreptavidinProtein DenaturationBiotin bindingMolecular modelProtein familyMolecular Sequence DataBiotinProtein EngineeringBiochemistryAvian Proteinschemistry.chemical_compoundBiotinAnimalsThermal stabilityAmino Acid SequenceProtein Structure QuaternaryMolecular BiologyThermostabilityChromatographybiologyTemperatureCell BiologyAvidinRecombinant ProteinschemistryMutagenesis Site-Directedbiology.proteinChickensAvidinJournal of Biological Chemistry
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