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1.
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Highlights
  • •NCMR is crucial for substrate recognition and activity regulation.
  • •MASTL conserves a cryptic C-Lobe in the non-conserved middle region.
  • •MASTL450 containing the cryptic C-lobe is observed in cancer cell lines.
  • •Key phosphorylation sites for MASTL provide an activation model.
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3.
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Highlights
  • •We used phosphoproteomics to reveal the underlying mechanisms of drug synergy on EGFR and ROCK co-inhibition in TNBC cells.
  • •EGFR inhibition alone induces autophagy activation in TNBC cells as a cytoprotective mechanism.
  • •Combinatorial treatment leads to impaired autophagic flux resulting in a strong accumulation of autophagic vacuoles.
  • •We hypothesize that ROCKi-induced cytoskeletal changes impair autophagosome clearance ultimately leading to cell death.
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4.
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Highlights
  • •TOP: robust, bio-friendly FFPE proteome extraction method with less fixation bias.
  • •Proteome of MSI-H colorectal cancer identifies immunobiology key elements.
  • •MSI-H tumor displays an “INFg-STAT1 centric signature”.
  • •Long-term IFNg induction In-vitro mimicks MSI-H signature.
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5.
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Highlights
  • •pY phosphoproteomes and dedicated ranking analyses for 16 AML cell lines.
  • •RTK drivers, 6 mutant cell lines confirmed, identification for 4 more cell lines.
  • •MAPK1/3 phosphorylation for cell lines without TK driver, indicating RAS mutation.
  • •Drug target space phosphorylation correlates with drug IC50s in specific cell lines.
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7.
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Highlights
  • •CD73 is one of the most upregulated proteins in the radioresistant cells.
  • •CD73 upregulation confers radioresistance and irradiation-induced apoptosis.
  • •CD73 confers radioresistance potentially through inactivating protein BAD.
  • •Elevated CD73 is required for maintaining the resistant cells in a mesenchymal state.
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8.
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Highlights
  • •SRPK1 is overexpressed in endometrial cancer and associated with poor survival.
  • •SRPK1 promotes endometrial cancer cell growth under nutrient-deprived conditions.
  • •Activation of EGFR-IGF1R-AKT signaling promotes resistance to SRPK1 inhibitors.
  • •Co-targeting SRPK1 and EGFR-IGF1R synergize blocking endometrial cancer cell growth.
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9.
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Highlights
  • •Proteome analyses reveal RNF146 and TNKS1/2 substrates targeted for degradation.
  • •RNF146 KO and TNKS1/2 DKO cells display significantly different proteomes.
  • •RNF146 has both TNKS-dependent and -independent substrates.
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10.
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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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11.
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Highlights
  • •XL-MS reveals new PPIs in yeast mitochondria under glycerol and glucose condition.
  • •Significant but limited results from quantitative XL-MS experiments.
  • •Ndi1 participates in a CIII2CIV2 respiratory supercomplex.
  • •Min8 promotes assembly of Cox12 into an intermediate complex IV.
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12.
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Highlights
  • •HuProt array-based identification of autoantigens in serum of early lung cancer.
  • •Independent validation of early lung cancer biomarker candidates with ELISA.
  • •Bioinformatics-aided identification of a biomarker panel.
  • •Independent verification of the panel with ELISA and immunohistochemistry.
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13.
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Highlights
  • •Cecal Ligation Puncture (CLP) mouse model to study sepsis-induced kidney disease.
  • •Quantitative global proteome and phosphoproteome profiling of mouse kidneys.
  • •Highly significant candidate markers for onset and progression of AKI to CKD.
  • •Mechanistic insights into sepsis-associated kidney injuries.
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14.
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Highlights
  • •Longitudinal monitoring of B cell subsets shows baseline antibody gene expression.
  • •A single, given CDR3 sequence can arise from more than one VJ gene combination.
  • •A healthy individual's V gene usage is stable irrespective of infection and subset.
  • •Surprisingly, class-switched antibodies can occur early in human B cell development.
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16.
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Highlights
  • •Organelle profiling maps capture localizations of 1000s of proteins in one experiment.
  • •Comparing maps +/− perturbation reveals disease mechanisms & cellular responses.
  • •A conceptual guide to planning and interpreting organellar profiling experiments.
  • •A cross-study consensus set of human organellar marker proteins.
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17.
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Highlights
  • •Simultaneous quantification of Bait, Prey and Reporter at the single cell level.
  • •Two hours of reaction are enough instead of 24–48 h for conventional assays.
  • •Potential expression problems of the Bait and Prey can be easily detected.
  • •True positive PPIs feature a distinct pattern of Reporter level versus Bait/Prey level.
  • •PPIs with unknown affinities can be ranked using an affinity ladder.
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18.
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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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19.
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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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20.
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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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