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1.
2.
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Highlights
  • •Automated statistical approach for detecting uninformative features and outliers.
  • •Improved performance on relative protein quantification.
  • •An option in the open-source R-based software MSstats.
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3.
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Highlights
  • •Global and targeted phosphoproteomics in RICTOR-deficient brown adipocytes.
  • •RICTOR loss leads to higher levels of many interferon response-associated proteins.
  • •RICTOR loss dampens the dynamic insulin-dependent phosphoproteome response.
  • •ACLY S455, VIM S39, and EIF4B S422 are among the most dampened phosphosites.
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4.
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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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5.
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Highlights
  • •N-glycan patterns are distinct in pediatric and adult urine.
  • •Sex differences of N-glycans are much larger in adults.
  • •Pediatric urine has almost no sex differences in N-glycan levels.
  • •In adults, the majority of N-glycans were more abundant in males.
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6.
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Highlights
  • •Ectopic ATP synthase as a therapeutic target for gefitinib-resistant NSCLC.
  • •Multiomics uncovers the dynamic network in response to ecto-ATP synthase blockade.
  • •Ecto-ATP synthase blockade induces cytotoxicity by CK2/phospho-topo IIα/GAS5 axis.
  • •A positive feedforward circuit between phospho-topo IIα and lncRNA-GAS5.
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7.
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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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8.
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Highlights
  • •Integrated phosphoproteomics and analyses of newly synthesized proteins in neurons.
  • •Resource of temporal mGluR-induced signaling pathways upon DHPG stimulation.
  • •Validation of PKC, MAPK1, CAMKIIa, and CDK2 in mGluR-activation and signaling.
  • •Validation of Intersectin-1 in DHPG-induced AMPAR internalization.
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9.
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Highlights
  • •PRMT5 glutathionylation is increased in aged mice or under oxidative stress.
  • •Deglutathionylation of PRMT5 is catalyzed by glutaredoxin-1.
  • •PRMT5 glutathionylation decreases its methyltransferase activity.
  • •PRMT5 glutathionylation results in G2/M arrest and inhibits cell proliferation.
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10.
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Highlights
  • •Laser microdissection of highly vulnerable hippocampal region.
  • •Proteomic analysis of postmortem human brain tissue of AD and control cases.
  • •Decreased levels of presynaptic proteins, but not postsynaptic proteins, in AD.
  • •Immunohistochemistry verifies decreased levels of selected presynaptic proteins.
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11.
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Highlights
  • •Quantitative proteomics and machine learning to study plasma biomarkers in HCM.
  • •Six peptides are increased in plasma of LVH+ HCM compared to controls.
  • •Peptide biomarkers correlate with imaging markers of phenotype severity.
  • •Peptide biomarkers correlate with the estimated sudden cardiac death risk.
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12.
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Highlights
  • •cGAS acetylations and phosphorylations under basal and immune-stimulated states.
  • •K384 and K414 acetylations and S305 phosphorylation inhibit cGAS-mediated apoptosis.
  • •Acetylation at K198 stimulates cGAS-dependent interferon signaling.
  • •K198 acetylation is decreased upon herpesvirus infection.
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13.
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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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14.
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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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15.
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Highlights
  • •Immunopeptidomics bears the potential to link diseases to antigen representation.
  • •We suggest to achieve this by analyzing the immunopeptidomes of cohorts of patients.
  • •Current mass spectrometry-based techniques to analyze immunopeptidomes are described.
  • •We term the proposed approach “Immunopeptidome-wide association studies” (IWAS).
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16.
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Highlights
  • •Repeatable quantification of 200 proteins in dried blood spots.
  • •Determined lower limit of quantification, repeatability, parallelism and stability.
  • •Protein stability in DBS stored at ambient temperatures for up to 2 months.
  • •Concentration ranges for 200 proteins in 20 healthy individuals.
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17.
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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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18.
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Highlights
  • •DEqMS is a method for statistical analysis of quantitative MS-data.
  • •Variance estimates based on the actual MS-data structure.
  • •Improved statistical power and accuracy in protein differential analysis.
  • •DEqMS is available as a user-friendly R package in Bioconductor.
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19.
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Highlights
  • •Comprehensive molecular profiling of cutaneous and cerebellar metastasis variants.
  • •Identification of differentially regulated metastasis-associated molecules.
  • •Evidence for individually distinct patterns of metastasis-associated molecules.
  • •Highlighting the evident need for establishing meta-analyses strategies.
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20.
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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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