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1.
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Highlights
  • •Proteomic landscapes of Drosophila somatic and reproductive tissues during aging.
  • •Pulsed metabolic labeling determines a decline in protein synthesis with age.
  • Drosophila model of human Parkinson's disease signifies an early-onset decline in protein synthesis.
  • •Collapse of proteostasis and mitochondria are early signals for normal aging.
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2.
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Highlights
  • •quantitative phosphoproteome analysis of TDM-activated macrophages.
  • •distinct Mincle-dependent and independent phosphorylation and gene regulations.
  • •Mincle-dependent activation of PI3K/AKT signaling by TDM.
  • •Mincle-independent macrophage response is linked to cell cycle regulation.
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3.
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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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4.
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Highlights
  • •C9, GSN, PON1, and PON3 validated as serum biomarker candidates of EAC.
  • •Multimarker panel with AUROC of 0.93 to aid current endoscopy surveillance of BE.
  • •Induction of tissue C9 in BE, dysplastic BE and EAC.
  • •Alteration of complement pathway glycoproteins during BE-EAC pathogenesis.
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5.
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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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6.
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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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7.
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Highlights
  • •BioID with Golgi fractions identified C10orf76 as proximal to GBF1.
  • •Tagged C10orf76 overlaps with Golgi markers.
  • •C10orf76 binds GBF1 and exchanges rapidly between free and bound forms.
  • •C10orf76 is essential for maintenance of the Golgi and for secretion.
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8.
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Highlights
  • •A global lysine succinylome was investigated in A. hydrophila.
  • •The lysine succinylation modifications play crucial role on various metabolic pathways.
  • •Reversible succinylation on Lys23 and Lys30 regulates the activity of S-ribosylhomocysteine lyase LuxS.
  • •Lysine succinylation modifications of LuxS affect quorum sensing and metabolism.
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9.
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Highlights
  • •PTMiner software for intelligent post-processing of open-search results.
  • •Unrestrictive modification site localization based on a Bayesian model.
  • •Extended transfer FDR estimation for accurate grouped FDR estimation.
  • •Comprehensive PTM characterization in a draft map of human proteome.
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10.
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Highlights
  • •We studied mid-pregnancy alcohol exposure and baboon fetal cerebral artery.
  • •238 proteins differed between control and alcohol-exposed fetuses near-term.
  • •Proteins of metabolic pathways represented one of the major targets of alcohol.
  • •Alcohol effect on the development of fetal brain vessels is persistent.
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11.
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Highlights
  • •Hsp70 homologs differ in their oligomeric properties in the presence of ATP.
  • •Human inducible Hsp70 forms ATP-dependent anti-parallel dimers with high propensity.
  • •Dimerization of ATP-bound Hsp70 is required for effective Hsp70-Hsp40 interaction.
  • •ATP-dependent interaction with Tomm34 TPR cochaperone disrupts Hsp70 dimer.
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12.
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Highlights
  • •Pre-formed and offset gradients for high throughput, robustness and peptide re-focusing.
  • •Minimal cross-contamination by disposable trap columns and partial elution.
  • •Single shot DIA measurements achieve >5000 proteins in 21 min.
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13.
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Highlights
  • •Microvesicle proteomics of 187 utero-tubal lavage samples for early diagnosis of HGOC.
  • •Machine learning-based classification of a 9-protein signature with high predictive power.
  • •Signature has 70‥ sensitivity and 76.2‥ specificity, predicting stage I lesions.
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14.
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Highlights
  • •Mice lacking Wip1 display spermatogenesis defects at the late-stage germ cell types.
  • •Proteome and phosphoproteome profiling reveals impaired dynamics of testis junction.
  • •Elevated levels of cytokines may lead to abnormal BTB structure and spermatogenesis.
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15.
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Highlights
  • •Changes to the proteome of skin fibroblasts subjected to reductive stress have been quantitated.
  • •Only a small set of proteins is selectively diminished upon exposure to reductants.
  • •Collagens (COL1A2 and COL6A2) emerge as sentinels of reductive stress.
  • •Reductive stress triggers receptor-independent Akt phosphorylation at Ser473.
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16.
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Highlights
  • •Chromobodies are stabilized by antigen binding in live cells.
  • •Monitoring changes of endogenous protein levels in living cells with chromobodies.
  • •Broadly applicable system to generate turnover-accelerated chromobodies.
  • •Quantification of time- and dose-dependent compound effects.
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17.
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Highlights
  • •Quantitative (phospho)proteome analysis of antibiotic treatment in E. coli.
  • •Largest bacterial phosphorylation catalogue.
  • •Specific phosphorylation motifs changes during resistance development.
  • •Phosphorylation mediated signaling could be a potential target for drug design.
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18.
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Highlights
  • •Glycosylation is not currently considered in flu vaccine design.
  • •Glycosylation influences on immunodominance are not well understood.
  • •Identification of site-specific glycosylation using mass spectrometry has matured.
  • •New methods are needed to quantify site-specific glycosylation for vaccine design.
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19.
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Highlights
  • •MaxQuant.Live controls Orbitrap mass analyzers in real-time.
  • •Freely available apps enable advanced data acquisition strategies.
  • •On-the-fly mass, retention time and intensity recalibration.
  • •Global targeting unifies shotgun and targeted proteomics.
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20.
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Highlights
  • •Quantitative changes in global proteome and ubiquitinome in Huntington's disease.
  • •Differential ubiquitination of wild-type and mutant Htt in mice brain.
  • •Enriched pathways include vesicle transport and mRNA processing.
  • •Correlation between protein and diGly site fold changes.
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