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1.
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  • •Monocytes are isolated from single donors after apheresis.
  • •Monocytes process CD16a and CD32a N-glycosylation differently by site and donor.
  • •CD16a with hybrid and oligomannose type N-glycans bind IgG1 Fc with stronger affinity than complex type.
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2.
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  • •Label-free and dimethyl labeling MS analysis of 6 RBPs from Drosophila ovaries.
  • •Functionally related RBPs show overlapping proteomes.
  • •Selective co-purification of splicing factors and translational regulators.
  • •Validation of 26 novel interactions by co-immunoprecipitation.
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3.
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Highlights
  • •Two molecular groups in anal squamous carcinoma according proteomic profile.
  • •Differences in possible targeted processes such as metabolism or immune response.
  • •Different percentage of tumor lymphocyte infiltration.
  • •Difference in the frequency of ATM variants, related to PPAR inhibitors.
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4.
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Highlights
  • •A predominance of HLA-I bound deamidated peptides are generated through ERAD pathway.
  • •Deamidation of peptides with N-glycosylation motifs not in peptidome of HLA-II or proteolysis.
  • •Many precursors of ERAD generated deamidated peptides are glycoproteins.
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5.
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Highlights
  • •Urinary peptide profiling of youths with type 1 diabetes before clinical injury.
  • •Internal validation of uromodulin peptides by parallel reaction monitoring.
  • •Discovery of novel bioactivity of uromodulin peptides in vitro.
  • In silico prediction of proteases involved in uromodulin processing.
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6.
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Highlights
  • •Affinity-based proteomics of infected macrophage cells.
  • Salmonella-modified membranes exhibit host-specific composition.
  • •Proteome differences explain some host-dependent pathophysiological differences.
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7.
8.
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Highlights
  • •This study proposed a spectral library search method to accurately identify N-linked glycopeptides in human serum through LC-MS/MS with pMatchGlyco software.
  • •The identification depth of serum N-linked intact glycopeptides and glycoproteins was increased by combination of acetonitrile precipitation, HILIC enrichment and high-pH RPLC fractionation.
  • •22,677 unique serum N-linked intact glycopeptides corresponding to 526 N-linked glycoproteins were identified with N-glycosylation motif-specific FDR control.
  • •This study revealed the great microheterogeneity of N-linked glycoproteins in serum.
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9.
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Highlights
  • db/db β-cells restores appropriate insulin stores and normalize secretory function.
  • •Numerous changes in the phosphorylation and sialylation states by euglycemic rest.
  • •Restoration of numerous dysfunctional biological processes following euglycemic rest.
  • •β-cell adaptive flexibility may lead to improvement in endogenous β-cell function.
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10.
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Highlights
  • P. aeruginosa grown with exosiderophores and analyzed by proteomic and RT-qPCR.
  • •Catechol-type exosiderophores strongly induce the expression of their transporters.
  • •Repression of the endogenous iron uptake pathways.
  • •Complex phenotypic plasticity in the expression of the various iron-uptake pathways.
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11.
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Highlights
  • •Brain membrane protein extraction.
  • •Protein prenylation.
  • •Prenyl peptide capture and characterization by LC-MS/MS.
  • •HCD and EThcD peptide fragmentation.
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12.
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Highlights
  • •Proteomics analysis was performed in two murine models of Duchenne muscular dystrophy (mdx and mdx52) at three ages (8, 16 and 80 weeks) and compared with wild-type controls.
  • •High-resolution isoelectric focusing liquid chromatography-tandem mass spectrometry enabled the quantification of 4974 proteins in all samples.
  • •This study has revealed protein signatures of dystrophin deficiency and the progression of dystrophic pathology.
  • •In contrast, the proteomes of the mdx and mdx52 mice were highly similar.
  • •Pathway analysis revealed crosstalk between inflammatory, metabolic and muscle growth processes in dystrophic muscle.
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13.
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Highlights
  • Pseudomonas aeruginosa growth increases in Aspergillus fumigatus culture filtrates.
  • A. fumigatus culture filtrates are characterized by a range of peptidases and proteases.
  • •LFQ proteomics characterizes the response of P. aeruginosa to A. fumigatus culture filtrates.
  • A. fumigatus creates an environment for P. aeruginosa to proliferate.
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14.
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Highlights
  • •Changes in N-linked glycosylation in influenza A virus affect antigenicity of the virus.
  • •Glycosylation similarity can be quantified, even in heterogeneously glycosylated proteins.
  • •Glycosylation is measurably and site-specifically distinct in influenza from related strains.
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15.
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Highlights
  • •Sufficient tumor tissues are often unavailable large HLA peptidome discovery.
  • •Using patient derived xenograft (PDX) tumors can overcome this limitation.
  • •The large PDX HLA peptidomes expand significantly those of the original biopsies.
  • •The HLA peptidomes of the PDX tumors included many tumor antigens.
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16.
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Highlights
  • •Quantitative analysis of Plasmodium sexual stage egress secretome.
  • •Activated gametocytes release gender-related proteins.
  • •Gametocyte egress process involves different types of vesicles.
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17.
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Highlights
  • •Quantitative proteome interactions with 5 different C9ORF72 dipolypeptides (DPRs).
  • •The arg-rich DPRs promiscuously bound to the proteome compared with the other DPRs.
  • •Long repeat lengths of arg-rich DPRs, but not short lengths, stalled ribosomes.
  • •The arg-rich DPRs also reduced arginine methylation and actin cytoskeleton assembly.
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18.
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Highlights
  • •EGFR-TKI molecular response profiling covering 10138 proteins and 13486 mRNAs.
  • •EGFR-TKI combination therapy screen using a library of 528 compounds.
  • •Several new candidate EGFR-TKI escape mechanisms and combination therapy targets.
  • •Combined targeting of the oncogene BCL6 and EGFR results in synergy in NSCLC cells.
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19.
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Highlights
  • •In-depth proteomes of 4 SARS-CoV-2 cell line models (Vero E6, Calu-3, Caco-2, A549).
  • •Proteomic evidence for thousands of Chlorocebus sabaeus proteins.
  • •Proteomic response of Vero E6 cells to SARS-CoV-2 infection.
  • •Synthetic peptides, spectral libraries, and targeted assays for SARS-CoV-2 proteins.
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20.
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Highlights
  • •Urinary proteomes of patients with recurrent UTI, renal scarring, and VUR.
  • •80 proteins differentially expressed, compared to healthy controls.
  • •62 proteins may be indicative of susceptibility for UTI.
  • •Altered acute phase response, extracellular matrix and carbohydrate metabolism.
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