Search results for "proteomics."

showing 10 items of 523 documents

Herceptin-resistance in breast cancer cells: a proteomic study.

2009

HER-2 is a cell membrane protein that belongs to the ErbB family of receptor tyrosine kinases (HER-1, HER-2, HER-3, HER-4). The over-expression of HER-2, which results in the 25-30% of breast cancer patients, is considered a predictive and prognostic marker for breast cancer malignancy and invasiveness and makes HER-2 an excellent therapeutic target. In the last years new therapeutic strategies have been improved in order to better deal tumor diseases an to minimize collateral effects due to classic chemotherapy in patients. In this way, a new approach was the somministration of humanized antibodies directed against tumor-associated molecular targets. Among these ones Herceptin, an anti-neo…

Herceptin breast cancer proteomicsSettore BIO/06 - Anatomia Comparata E Citologia
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Exploration of extracellular vesicles from Ascaris suum provides evidence of parasite–host cross talk

2019

The prevalent porcine helminth, Ascaris suum, compromises pig health and reduces farm productivity worldwide. The closely related human parasite, A. lumbricoides, infects more than 800 million people representing a disease burden of 1.31 million disability-adjusted life years. The infections are often chronic in nature, and the parasites have a profound ability to modulate their hosts' immune responses. This study provides the first in-depth characterisation of extracellular vesicles (EVs) from different developmental stages and body parts of A. suum and proposes the role of these vesicles in the host-parasite interplay. The release of EVs from the third- (L3) and fourth-stage (L4) larvae a…

Histology030231 tropical medicineascaris suumProteomicsMicrobiology03 medical and health sciences0302 clinical medicineImmune systemproteomicsAntigenImmunityhost–parasite interactionsParasite hostinglcsh:QH573-671Ascaris suumAscaris suum030304 developmental biologymiRNA0303 health sciencesbiologylcsh:CytologyCell Biologybiology.organism_classificationimmunityMicrovesicleshost-parasite interactionsHuman parasiteextracellular vesiclesmirna
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�ber den Feinbau der Schwimmblase von Anguilla vulgaris L.

1961

HistologyChemistrySwim bladderBiophysicsCell BiologyProteomicsElectron microscopicPathology and Forensic MedicineZeitschrift f�r Zellforschung und Mikroskopische Anatomie
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The Complex Regulatory Role of Cytomegalovirus Nuclear Egress Protein pUL50 in the Production of Infectious Virus

2021

The regulation of the nucleocytoplasmic release of herpesviral capsids is defined by the process of nuclear egress. Due to their large size, nuclear capsids are unable to traverse via nuclear pores, so that herpesviruses evolved to develop a vesicular transport pathway mediating their transition through both leaflets of the nuclear membrane. This process involves regulatory proteins, which support the local distortion of the nuclear envelope. For human cytomegalovirus (HCMV), the nuclear egress complex (NEC) is determined by the pUL50-pUL53 core that initiates multicomponent assembly with NEC-associated proteins and capsids. Hereby, pUL50 serves as a multi-interacting determinant that recru…

Human cytomegalovirusGene Expression Regulation ViralProteomicsefficiency of infectious virus productionQH301-705.5Nuclear Envelope[SDV]Life Sciences [q-bio]virusesQuantitative proteomicsCytomegalovirusconditional expressionGenome Viralnuclear egress complex (NEC)Virus ReplicationArticleCell LineViral ProteinsCapsidNEC protein pUL50DNA PackagingmedicineHumansddc:610Biology (General)Nuclear poreNuclear membraneregulation of viral replicationGenes Immediate-EarlyCell Nucleusfunctional propertiesChemistryVirionGeneral MedicineFibroblastsmedicine.diseaseCell biologyVesicular transport protein[SDV] Life Sciences [q-bio]Kineticsmedicine.anatomical_structureLytic cycleCapsidhuman cytomegalovirusLamin
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Proteomic Analyses of Human Cytomegalovirus Strain AD169 Derivatives Reveal Highly Conserved Patterns of Viral and Cellular Proteins in Infected Fibr…

2014

Human cytomegalovirus (HCMV) particle morphogenesis in infected cells is an orchestrated process that eventually results in the release of enveloped virions. Proteomic analysis has been employed to reveal the complexity in the protein composition of these extracellular particles. Only limited information is however available regarding the proteome of infected cells preceding the release of HCMV virions. We used quantitative mass spectrometry to address the pattern of viral and cellular proteins in cells, infected with derivatives of the AD169 laboratory strain. Our analyses revealed a remarkable conservation in the patterns of viral and of abundant cellular proteins in cells, infected for 2…

Human cytomegalovirusTime FactorsProteomeviruseslcsh:QR1-502MorphogenesisCytomegalovirusBiologyVirus ReplicationProteomicslcsh:MicrobiologyMass SpectrometryArticleCell LineproteomicsVirologyExtracellularmedicineHumanshuman cytomegalovirus; proteomics; mass spectrometry; virions; expression patternProteinsViral tegumentFibroblastsmedicine.diseaseVirologyCell biologyInfectious DiseasesViral replicationhuman cytomegalovirusCell cultureexpression patternHost-Pathogen InteractionsProteomevirionsViruses
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Proteome adaptations under contrasting soil phosphate regimes of Rhizophagus irregularis engaged in a common mycorrhizal network.

2021

International audience; For many plants, their symbiosis with arbuscular mycorrhizal fungi plays a key role in the acquisition of mineral nutrients such as inorganic phosphate (Pi), in exchange for assimilated carbon. To study gene regulation and function in the symbiotic partners, we and others have used compartmented microcosms in which the extra-radical mycelium (ERM), responsible for mineral nutrient supply for the plants, was separated by fine nylon nets from the associated host roots and could be harvested and analysed in isolation. Here, we used such a model system to perform a quantitative comparative protein profiling of the ERM of Rhizophagus irregularis BEG75, forming a common my…

Hyphal growthRhizophagus irregularisProteomicsProteomeNitrogen[SDV]Life Sciences [q-bio]Glyoxylate cyclemycorrhizal symbiosisMicrobiologyPlant RootsPhosphatesFungal Proteins03 medical and health sciencesSoilNutrientcommon mycelial networkSymbiosisGeneticsMycorrhizal networkSymbiosisMycelium030304 developmental biology2. Zero hungerphosphate nutrition0303 health sciencesbiology030306 microbiologyfungiFungi15. Life on landextra-radical myceliumbiology.organism_classificationshotgun proteomicBiochemistryProteomeFungal genetics and biology : FGB
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Neuroproteomics in the auditory brainstem: candidate proteins for ultrafast and precise information processing.

2014

In the mammalian auditory brainstem, the cochlear nuclear complex (CN) and the superior olivary complex (SOC) feature structural and functional specializations for ultrafast (<1 ms) and precise information processing. Their proteome, the basis for structure and function, has been rarely analyzed so far. Here we identified and quantified the protein profiles of three major auditory brainstem regions of adult rats, the CN, the SOC, and the inferior colliculus (IC). The rest of the brain served as a reference. Via label-free quantitative mass spectrometry and 2-D DIGE/MALDI-MS, we identified 584 and 297 proteins in the plasma membrane/synaptic vesicle proteome and the cytosolic proteome, respe…

Inferior colliculusCochlear NucleusMaleNeurofilamentProteomeSuperior Olivary ComplexCell BiologyBiologyCochlear nucleusSynaptotagmin 1Inferior ColliculiCell biologyRatsRats Sprague-DawleyCellular and Molecular NeuroscienceNeuroproteomicsOrgan SpecificitySuperior olivary complexProteomeotorhinolaryngologic diseasesAnimalsBrainstemMolecular BiologyNeuroscienceMolecular and cellular neurosciences
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Mass spectrometry applications

2012

The history of proteomics dates back to the discovery of two-dimensional gels in the 1970s, which provided the first feasible way of displaying hundreds or thousands of proteins on a single gel. Despite mass spectrometry being restricted for a long time to small and thermostable compounds, the development in the late 1980s of two techniques for the routine and general formation of molecular ions of intact biomolecules changed this situation and mass spectrometry has become an indispensable tool for proteomics research. The aim of this chapter is to review the major types of MS instruments used in proteomics analysis and to discuss strategies for the analysis of whole proteins and peptides o…

Ion-mobility spectrometry–mass spectrometryLiquid chromatography–mass spectrometryChemistryLife ScienceComputational biologyDirect electron ionization liquid chromatography–mass spectrometry interfaceProteomicsMass spectrometryMozzarella cheeseMass spectrometry imaging
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Drift time-specific collision energies enable deep-coverage data-independent acquisition proteomics.

2013

A data-independent acquisition (DIA) mass spectrometry approach, ultradefinition (UD)MSE, offers high reproducibility and improved proteome coverage over alternative DIA and data-dependent acquisition workflows. We present a data-independent acquisition mass spectrometry method, ultradefinition (UD) MSE. This approach utilizes ion mobility drift time-specific collision-energy profiles to enhance precursor fragmentation efficiency over current MSE and high-definition (HD) MSE data-independent acquisition techniques. UDMSE provided high reproducibility and substantially improved proteome coverage of the HeLa cell proteome compared to previous implementations of MSE, and it also outperformed a…

IonsProteomicsReproducibilityProteomeSoftware toolCoverage dataCell BiologyBiologyProteomicsCollisionBioinformaticsMass spectrometryBiochemistryPeptide Fragmentsbody regionsTandem Mass SpectrometryProteomeHumansMolecular BiologyAlgorithmSoftwareBiotechnologyChromatography LiquidHeLa CellsNature methods
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Proteomic Analyses Reveal an Acidic Prime Side Specificity for the Astacin Metalloprotease Family Reflected by Physiological Substrates

2011

Astacins are secreted and membrane-bound metalloproteases with clear associations to many important pathological and physiological processes. Yet with only a few substrates described their biological roles are enigmatic. Moreover, the lack of knowledge of astacin cleavage site specificities hampers assay and drug development. Using PICS (proteomic identification of protease cleavage site specificity) and TAILS (terminal amine isotopic labeling of substrates) degradomics approaches >3000 cleavage sites were proteomically identified for five different astacins. Such broad coverage enables family-wide determination of specificities N- and C-terminal to the scissile peptide bond. Remarkably, me…

KeratinocytesModels MolecularProteomicsVascular Endothelial Growth Factor AProteasesmedicine.medical_treatmentProteolysisMolecular Sequence DataBiologyCleavage (embryo)BiochemistryCell LineSubstrate SpecificityAnalytical Chemistry03 medical and health sciencesTandem Mass SpectrometrymedicineHumansAmino Acid SequenceMolecular BiologyPeptide sequencePhylogeny030304 developmental biologyEnzyme Precursors0303 health sciencesProteaseStaining and LabelingEdman degradationmedicine.diagnostic_testResearch030302 biochemistry & molecular biologyTioproninMetalloendopeptidasesTerminal amine isotopic labeling of substratesRecombinant ProteinsKineticsBiochemistryProteolysisKallikreinsAstacinPeptidesSequence AlignmentChromatography LiquidMolecular &amp; Cellular Proteomics
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