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1.
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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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2.
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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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3.
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Highlights
  • •HPV is being introduced as the primary test in cervical cancer screening programs.
  • •New biomarkers are needed for co-testing of women HPV positive in screening.
  • •Analysis of plasma from women with invasive cervical cancer identified a 11-marker panel.
  • •This signature shows high sensitivity and specificity to identify women with cancer.
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4.
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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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5.
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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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6.
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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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7.
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Highlights
  • •Frequent genetic polymorphism affects the glycosylation pattern of fetuin.
  • •Personalized in-depth proteoform profiling of fetuin purified from 20 donors.
  • •Classification of serum donors into three different genotypes.
  • •Septic patients show increased level of fucosylation at N-glycolation site N176.
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8.
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Highlights
  • •Profiling antibody responses of patients with naturally acquired malaria immunity.
  • •High-density peptide arrays featuring linear epitopes.
  • •Epitope mapping of known and potential novel vaccine candidates.
  • •Novel immunogenic epitopes discovered, and known antibody target motifs confirmed.
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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.
11.
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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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12.
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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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13.
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Highlights
  • •Method for the analysis of response curves from thermal proteome profiling (TPP).
  • •NPARC uses nonparametric statistics and provides false discovery-rate (FDR) control.
  • •Increased proteome coverage and sensitivity to identify drug-binding proteins.
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14.
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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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15.
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Highlights
  • •AP-DIA/SWATH analysis to identify TCTP-interacting proteins in NF1 tumor cells.
  • •A highly specific TCTPEF1A2 interaction but rather than TCTPEF1A1 interaction.
  • •TCTPEF1A2 interaction mediating formation of EF1A2-elogation factor complex.
  • •TCTPEF1A2 dependent translation machinery regulating NF1 tumor cell growth.
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18.
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Highlights
  • •First report on the quantitative proteomic profiling of Drosophila lymph glands.
  • •Comparative proteomic analysis under conditions of perturbed blood cell homeostasis.
  • •Resource for identifying new regulators of insect and vertebrate hematopoiesis.
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19.
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Highlights
  • •Fast and culture-free method for the identification of the 15 bacterial species causing UTIs.
  • •Combination of DIA analysis and machine learning algorithms to define a peptide signature.
  • •High accuracy, good linearity and reproducibility, sensitivity below standard threshold.
  • •Transferability to other laboratories and other mass spectrometers.
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20.
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Highlights
  • •Targeted mass spectrometry assay to quantify prion protein (PrP) in spinal fluid.
  • •Precise measurement of PrP peptide concentration across protein domains.
  • •Peptides are uniformly decreased in symptomatic prion disease patients.
  • •Assay applicable to humans and preclinical species for drug development.
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