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1.
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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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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
  • •OMICS distinguish cancer cells from resistant or cancer stem cells.
  • •Bactericidal antibiotics and mitochondria.
  • •Linezolid and anticancer therapy.
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4.
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Highlights
  • •Spatiotemporal microproteomics analysis of TBI.
  • •Injury site microproteomics reveal distinct phases in 10-day frame post TBI.
  • •Uninjured proteomic profile is restored in TBI at 10 days post injury.
  • Substantia nigra protein post 3 days suggest link to Parkinson's disease.
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5.
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Highlights
  • •Bayesian Beta-Binomial model integrates ion statistics with peptide ratio agreement.
  • •Model appropriately interprets information from low signal peptides.
  • •Confidence can be assigned even without replicates.
  • •Model adds sensitivity to detection of small changes.
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6.
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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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7.
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Highlights
  • •Cathepsin-L is introduced as a novel protease for HX-MS studies.
  • •Cathepsin-L improves resolution of traditionally challenging histone tails.
  • •Cathepsin-L can be readily combined with pepsin for improved protein coverage.
  • •In-solution dynamics of the H3.1 and H4 monomers reveal extensive EX1 kinetics.
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8.
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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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9.
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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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10.
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Highlights
  • •Definition of early systemin-responsive phosphorylation time course.
  • •Reconstruction of kinase-substrate relationships from phosphorylation time profiles.
  • •Phosphatase PLL5 rapidly dephosphorylated H+-ATPase LHA1 inducing alkalinization of the medium.
  • •MAP-Kinase MPK2 re-phosphorylated LHA1 after 15 minutes.
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11.
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Highlights
  • •Shotgun identification of neopeptides released from osteoarthritic cartilage.
  • •Specific endogenous peptides from the cartilage ECM are measured by MRM.
  • •Identification of neopeptides differentially generated from diseased tissue.
  • •The peptide DSNKIETIPN shows the best metrics as biomarker of OA cartilage.
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12.
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Highlights
  • •Atlantic salmon O-glycome expanded to 169 structures in three epithelia.
  • •Low interindividual variation amongst all populations and geographical regions.
  • •Small variations in glycosylation between geographical locations and fish size.
  • •Prominent fucosylation in gastrointestinal mucins from Tasmanian fish.
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13.
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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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14.
15.
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Highlights
  • •TMT labeling protocol with excellent intra- and interlaboratory reproducibility.
  • •Complete in-solution labeling of peptides using 1/8 of recommended TMT quantities.
  • •Demonstration of utility for deep-scale (phospho)proteome analysis.
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16.
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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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17.
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Highlights
  • •Development of a method for low-abundance small protein analysis in human plasma.
  • •Deep proteome profiling demonstrated unbiased identification of diverse factors.
  • •Method enabled identification of a novel human plasma protein C5ORF46.
  • •Analysis of intermittent fasting response showed changes in iron regulation.
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18.
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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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19.
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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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20.
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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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