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1.
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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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2.
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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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3.
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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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4.
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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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5.
6.
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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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7.
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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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8.
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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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9.
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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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10.
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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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11.
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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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12.
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Highlights
  • •Developed a data processing pipeline to format phosphopeptide identifications.
  • •Identified the preferred substrate motif for FLT3 and mutant kinases.
  • •Designed and validated a panel of pan-FTL3 artificial substrates.
  • •Monitored FLT3 and mutant kinase activity through FAStide phosphorylation.
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13.
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Highlights
  • •MHC-II-bound peptide repertoires from DO-sufficient and DO-deficient cells.
  • •Fewer unique peptides and core epitopes were presented in the absence of DO.
  • •Immunopeptidome differences appeared to result from reduced DM editing.
  • •DO-dependent self-epitopes elicited CD4 T cell responses in mice.
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14.
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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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15.
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Highlights
  • •HLA-B*40:02 and ERAP2 are risk factors for ankylosing spondylitis.
  • •The effects of ERAP2 on the B*40:02 peptidome are defined.
  • •ERAP2 has a major influence mainly due to alterations of N-terminal residues.
  • •These effects provide a basis for the association of ERAP2 with disease.
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16.
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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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17.
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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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18.
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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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19.
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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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20.
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Highlights
  • •Proteome profiling of tissue interstitial fluids (TIFs) of oral cancer.
  • •Pathway of aminoacyl tRNA biosynthesis enriched in proteome of TIFs.
  • •Verification of nidogen-1 as a salivary biomarker of oral cancer.
  • •High correlation between elevated tissue level of nidogen-1 and poor survival.
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