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1.
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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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2.
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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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3.
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Highlights
  • •Mechanistic insights into ionic liquids and proteins at molecular level.
  • •Extractants prescreen for proteome analysis with MD simulation system.
  • •A loss-less sample preparation method developed for in-depth proteome profiling.
  • •Over 3,300 proteins were confidently identified from 1,000 HeLa cells in a 1 h run.
  • •Label-free quantitative proteome analysis of human liver cancer tissues.
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4.
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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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5.
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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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6.
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Highlights
  • •Cross-linked peptides are physically separated from mono-linked peptides in the gas-phase by TIMS ion mobility.
  • •Development of a novel data acquisition routine that a-priori distinguishes cross-linked from mono-linked peptides called caps-PASEF.
  • •First application of PhoX-driven cross-linking mass spectrometry on the timsTOF Pro.
  • •Application of cross-linking mass spectrometry to medium to high complexity samples.
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7.
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Highlights
  • •Rapid DIA-only library building with gas-phase fractionation.
  • •Recommended DIA acquisition strategies with staggered windows and forbidden zones.
  • •Optimized DIA instrument settings for several Thermo Orbitrap instruments.
  • •Data analysis tutorial using open source DIA software.
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8.
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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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9.
10.
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Highlights
  • •Higher AGC significantly improves quantitation quality in single-cell analysis.
  • •The boosting-to-sample ratio should be carefully evaluated and optimized.
  • •iBASIL allows for precise quantitation of 1,500 proteins from 104 AML single cells.
  • •iBASIL recapitulates major biological differences in different AML single cells.
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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
  • •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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13.
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Highlights
  • •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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14.
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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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15.
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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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16.
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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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17.
18.
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Highlights
  • •Comprehensive sialiomics of isolated rat synaptosomes.
  • •Site-specific modulation of sialic acids on surface glycoproteins after brief depolarization.
  • •Sialylation as dynamic modification important for synaptic depolarization-dependent processes.
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19.
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Highlights
  • •Quantitative proteomes of the cellular surface changes induced by mTORC1 signaling.
  • •Hit validation in human cancer cell lines and biopsies.
  • •Functional studies showing new drug targets to which cancer cells with hyperactive mTORC1 may be addicted.
  • •A new paradigm for drug development, namely targeting cell surface proteins regulated by mTORC1.
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20.
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Highlights
  • •TOF-SIMS allows to visualize normal brain and tumor border.
  • •Glioma samples can be subdivided into clinically relevant groups by TOF-SIMS data.
  • •TOF-SIMS allows to simultaneously detect proteins and metabolites in clinical samples.
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