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1.
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Highlights
  • •Quantitative (phoshpo)proteome of primary cell cultures of patient-matched prostate CAF and NPF.
  • •Key CAF-associated proteins validated using orthogonal methodologies.
  • •LOXL2 inhibitors D-penicillamine and PXS-S2A impaired CAF migration and ECM alignment.
  • •Pre-treatment with LOXL2 inhibitors impaired migratory capacity of RWPE-2 cells in co-culture.
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2.
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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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3.
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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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4.
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Highlights
  • •Reported proteasomal spliced HLA peptides do not fit the consensus binding motifs.
  • •Their MS/MS spectrum matches suggest that many of them are ambiguous.
  • •Our workflow is based on de novo sequencing, alignment, and multiple search tools.
  • •The upper bound proportion of cis-spliced peptides is 2–6% and likely much smaller.
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5.
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Highlights
  • •Glycosylation is not currently considered in flu vaccine design.
  • •Glycosylation influences on immunodominance are not well understood.
  • •Identification of site-specific glycosylation using mass spectrometry has matured.
  • •New methods are needed to quantify site-specific glycosylation for vaccine design.
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6.
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Highlights
  • •Bayesian Beta-Binomial model integrates ion statistics with peptide ratio agreement.
  • •Model appropriately interprets information from low signal peptides.
  • •Confidence can be assigned even without replicates.
  • •Model adds sensitivity to detection of small changes.
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7.
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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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8.
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Highlights
  • •Cathepsin-L is introduced as a novel protease for HX-MS studies.
  • •Cathepsin-L improves resolution of traditionally challenging histone tails.
  • •Cathepsin-L can be readily combined with pepsin for improved protein coverage.
  • •In-solution dynamics of the H3.1 and H4 monomers reveal extensive EX1 kinetics.
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9.
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Highlights
  • •OMICS distinguish cancer cells from resistant or cancer stem cells.
  • •Bactericidal antibiotics and mitochondria.
  • •Linezolid and anticancer therapy.
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10.
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Highlights
  • •MaxQuant.Live controls Orbitrap mass analyzers in real-time.
  • •Freely available apps enable advanced data acquisition strategies.
  • •On-the-fly mass, retention time and intensity recalibration.
  • •Global targeting unifies shotgun and targeted proteomics.
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11.
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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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12.
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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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13.
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Highlights
  • •Quantitative changes in global proteome and ubiquitinome in Huntington's disease.
  • •Differential ubiquitination of wild-type and mutant Htt in mice brain.
  • •Enriched pathways include vesicle transport and mRNA processing.
  • •Correlation between protein and diGly site fold changes.
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14.
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Highlights
  • •Quantitative cross-linking mass spectrometry (QCLMS) was automated by Spectronaut.
  • •Data-independent acquisition (DIA) was adapted to QCLMS.
  • •Accuracy and precision of quantitation improves with DIA over DDA.
  • •QCLMS is now ready for use in complex samples.
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15.
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Highlights
  • •First global study on metabolic regulation of Nt-acetylation.
  • •Yeast cells maintain global Nt-acetylation levels during prolonged starvation.
  • •Nt-acetylation can in some cases be either up- or downregulated by starvation.
  • •Naa10/NatA affects the steady-state protein levels of Rsa3 and Rpl7a.
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16.
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Highlights
  • •Chromobodies are stabilized by antigen binding in live cells.
  • •Monitoring changes of endogenous protein levels in living cells with chromobodies.
  • •Broadly applicable system to generate turnover-accelerated chromobodies.
  • •Quantification of time- and dose-dependent compound effects.
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17.
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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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18.
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Highlights
  • •Enrichment of methyl peptides using two orthogonal techniques.
  • •Knockdown of PRMT1 leads to substantial changes in protein arginine “methylome”.
  • •Discrimination of ADMA and SDMA using characteristic neutral losses.
  • •Identification of PRMT1 targets and substrate scavenged by other PRMTs in the absence of PRMT1 activity.
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19.
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Highlights
  • •Proteome profiling of tissue interstitial fluids (TIFs) of oral cancer.
  • •Pathway of aminoacyl tRNA biosynthesis enriched in proteome of TIFs.
  • •Verification of nidogen-1 as a salivary biomarker of oral cancer.
  • •High correlation between elevated tissue level of nidogen-1 and poor survival.
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20.
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Highlights
  • •Temporal proteome profiling of lipotoxicity and glucolipotoxicity in β-cells
  • •Palmitate induced cholesterol metabolism earlier than fatty acid metabolism
  • •Setd8 promotes palmitate + glucose-stimulated INS-1 cell proliferation
  • •PA induced apoptosis partially via upregulation of Rhob in INS-1 cells
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