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1.
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Highlights
  • •An innovative co-IP crosslinking proteomics study was designed for the TLR2 interactome.
  • •Proteomic profiling revealed combinatorial effects of simvastatin and Pam3CSK4 on the TLR2 interactome.
  • •ACTR1A and MARCKSL1 proteins were identified as potential interactors of TLR2 during the immune response.
  • •ACTR1A has important modulatory actions on the TLR2 pro-inflammatory signaling cascade.
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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
  • •1. Celastrol alleviated cholestatic liver injury.
  • •2. Celastrol inhibited the decrease of SIRT1 induced by deoxycholic acid.
  • •3. SIRT1-FXR signaling pathway mediated the effect of celastrol.
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4.
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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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5.
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Highlights
  • •Automated analysis of protein complexes in proteomic experiments.
  • •Quantitative measurement of the coordinated changes in protein complex components.
  • •Interactive visualizations for exploratory analysis of proteomic results.
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6.
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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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7.
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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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8.
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Highlights
  • •Multiplex epitope mapping/antigenic determinant identification in the gas phase.
  • •Intact transition and controlled dissociation of immune complexes by MS.
  • •Simultaneous identification and amino acid sequence determination of epitopes.
  • •Simplified in-solution sample handling because of ion manipulation and filtering by MS.
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9.
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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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10.
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Highlights
  • •Stability of oxidative phosphorylation subunits are reduced in a diet-induced mouse model of NAFLD.
  • •These changes are associated with impaired activities of electron transport chain complexes and ATP synthesis.
  • •Increased mitophagy contributed to enhanced degradation of mitochondrial proteins.
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11.
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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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12.
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Highlights
  • •Efficient sample preparation workflow for deep N-glycomics analysis from serum.
  • •Temperature gradient denaturing protocol to prevent protein precipitation.
  • •Decrease of free sugar content in serum enhanced PNGase F digestion efficiency.
  • •Modified evaporative labeling method increased fluorophore labeling yield.
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13.
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Highlights
  • •Enrichment of methyl peptides using two orthogonal techniques.
  • •Knockdown of PRMT1 leads to substantial changes in protein arginine “methylome”.
  • •Discrimination of ADMA and SDMA using characteristic neutral losses.
  • •Identification of PRMT1 targets and substrate scavenged by other PRMTs in the absence of PRMT1 activity.
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14.
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Highlights
  • •Database of PTM site-specific phosphorylation signatures of kinases, perturbations and signaling pathways (PTMsigDB).
  • •PTM signature enrichment analysis (PTM-SEA) outperformed gene-centric analysis in detection of EGF induced phospho signaling events.
  • •PI3K perturbation signatures were readily detected in PI3Ka inhibited human breast cancer cells.
  • •PTMsigDB and PTM-SEA can be freely accessed at https://github.com/broadinstitute/ssGSEA2.0.
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15.
16.
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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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17.
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Highlights
  • •OMICS distinguish cancer cells from resistant or cancer stem cells.
  • •Bactericidal antibiotics and mitochondria.
  • •Linezolid and anticancer therapy.
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18.
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Highlights
  • •Two-step cross-linking coupled with affinity purification to facilitate structural analysis of protein complexes.
  • •Integrated QXL-MS workflow for studying condition-dependent structural changes of protein complexes.
  • •Mechanistic insights on in vivo H2O2-induced conformational dynamics of proteasome complexes.
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19.
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Highlights
  • •Quantitative cross-linking mass spectrometry (QCLMS) was automated by Spectronaut.
  • •Data-independent acquisition (DIA) was adapted to QCLMS.
  • •Accuracy and precision of quantitation improves with DIA over DDA.
  • •QCLMS is now ready for use in complex samples.
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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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