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1.
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Highlights
  • •Rapamycin and zinc induce moderate but significant mitochondrial proteome changes.
  • •The mitochondrial proteins processing system is robust under subtoxic conditions.
  • •Rapamycin and zinc perturb the mitochondrial proteins processing system.
  • •Rapamycin and zinc perturb the mitochondrial proteins homeostasis.
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4.
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Highlights
  • •iTRAQ-based analysis of saliva samples from oral cancer patients.
  • •Proteome profiling of saliva samples from patients with oral premalignant lesions.
  • •Verification of salivary biomarker candidates with MRM-MS and immunoassays.
  • •Identification of salivary proteins as potential biomarkers of oral cancer.
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5.
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Highlights
  • •Construction of threespine stickleback gill assay library using DDA proteomics
  • •Population-specific gill proteome signatures of four ecotypes identified by DIA
  • •HSP47 and extracellular matrix proteins highly elevated in warm-adapted sticklebacks
  • •Inflammasome and proteolytic proteins highly elevated in freshwater sticklebacks
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6.
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Highlights
  • •Auxin responsive proteins in Arabidopsis roots were identified from 3,514 detected proteins.
  • •All six auxin receptors are stable in response to hormone via novel MRM assays.
  • •The >100 differentially expressed proteins exhibit dynamic and transient responses to auxin.
  • •Phenotypic screening of the top responsive proteins uncovered several novel root mutants.
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7.
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Highlights
  • •Characterization of the phagosomal proteome comparing resting and LPS-treated BMDCs.
  • •Label-free quantification determined 2843 phagosomal proteins.
  • •Reduced recruitment of hydrolases and V-ATPase to phagosomes of LPS-treated cells.
  • •Increased recruitment of antigen cross-presentation molecules to these phagosomes.
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8.
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Highlights
  • •Identification of previously undetected chloroplast envelope proteins.
  • •Up to date manual annotation of genuine (or shared) envelope components.
  • •New hypotheses for localizations, functions, interactions among cell compartments.
  • •A new resource of significant value to the broader plant science community.
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9.
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Highlights
  • •Open source software for comprehensive HDX-MS data analysis.
  • •Automatic back-exchange correction options.
  • •Rigorous statistical analysis of the significance of uptake differences.
  • •High quality visualization tools.
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10.
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Highlights
  • •BioID and IP-MS were conducted to generate a global ZIKV-host protein interactome
  • •Interactome consists of >3000 high confidence ZIKV-host protein interactions
  • •Data mining indicates that ZIKV proteins interact with multiple host cell organelles
  • •An important role for peroxisomes in ZIKV infection is uncovered
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11.
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Highlights
  • •Comprehensive analysis of inter-individual variation of normal urinary proteome.
  • •Significant gender differences were observed.
  • •Proteins increased in female urine are enriched in immunological pathways.
  • •Estimated reference intervals of proteins as the baseline for biomarker discovery.
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12.
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Highlights
  • •Plant mitoribosomes contain several pentatricopeptide repeat proteins.
  • •The small mitoribosomal subunit is of an exceptionally large size.
  • •Protein units not directly related to translation may be attached to plant mitoribosomes to confer additional functions to these molecular machines.
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13.
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Highlights
  • •In-depth proteome profiling of primary human myeloma cells
  • •Characteristics of myeloma cells are related to hypoxic bone marrow conditions
  • •Myeloma cells show specific immune evasion strategies
  • •Metabolic adaptations involve tumor and stroma cells
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14.
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Highlights
  • •Quantitative phosphoproteome of BRAF drug-resistance in melanoma cells.
  • •Cytoskeletal proteins are downregulated in resistant vs. sensitive cells.
  • •Nestin is associated with an invasive phenotype and resistance to MEK and BRAF inhibitors.
  • •Nestin depletion affects PI3K/AKT and integrin signaling similar to resistant cells.
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15.
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Highlights
  • •Global proteomic remodeling alters antibiotic susceptibility in K. pneumoniae.
  • •Drug specific transport, sugar utilization, central metabolism, capsule synthesis.
  • •Common pathways of reactive oxygen scavenging, turnover of misfolded proteins.
  • •Integrated adjustments and unique drug-specific features for drug combinations.
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16.
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Highlights
  • •Establishment of a flow system allowing multi-omics analysis of S. aureus biofilms.
  • •Biofilm proteome profiling (intracellular and ECM) plus metabolic footprint analysis.
  • •Virulence factors and ribosomal proteins stabilize the ECM as moonlighting proteins.
  • •They act as electrostatic bridges between anionic cell surfaces, eDNA and metabolites.
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17.
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Highlights
  • •Proteogenomics and secretome comparison of human and zoonotic Staphylococcus aureus lineages.
  • •869 secreted proteins identified in eight S. aureus isolates of CC8, CC22 and CC398.
  • •CC398 lower secretion of surface proteins and higher secretion of hemolysins and exoenzymes.
  • •Regulatory differences in the secretomes could be linked to lower SigB activity in CC398.
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19.
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Highlights
  • •Quantitative microproteomics to study the CNS and PNS of the Twitcher mouse.
  • •10plex TMT experiments on corpus callosum, motor cortex and sciatic nerves extracts.
  • •More than 400 proteins groups deregulated between Twitcher and wildtype mice.
  • •New insights into the molecular mechanisms of Krabbe disease.
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20.
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Highlights
  • •Method to probe the isomeric variants of the glycans attached to purified proteins.
  • •Uses multiple rounds of glycosidase cleavage and lectin profiling.
  • •Computation integration of lectin-binding, glycan-array, and mass spectrometry data.
  • •Applied to microspots for compatibility with analyzing low-abundance proteins.
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