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1.
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Highlights
  • •PTMiner software for intelligent post-processing of open-search results.
  • •Unrestrictive modification site localization based on a Bayesian model.
  • •Extended transfer FDR estimation for accurate grouped FDR estimation.
  • •Comprehensive PTM characterization in a draft map of human proteome.
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2.
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Highlights
  • •Method for the analysis of response curves from thermal proteome profiling (TPP).
  • •NPARC uses nonparametric statistics and provides false discovery-rate (FDR) control.
  • •Increased proteome coverage and sensitivity to identify drug-binding proteins.
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3.
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Highlights
  • •New software to determine differentially expressed proteins in quantitative MS experiments.
  • •Applicable to any modern quantitative MS setup and study type, including clinical setups.
  • •Ultra-sensitive at strict FDR control, up to 1000 additional proteins in a single comparison.
  • •Easy to use, fast processing and readily available package, including user friendly manual.
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4.
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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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5.
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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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6.
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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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7.
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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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8.
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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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9.
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Highlights
  • •BioID with Golgi fractions identified C10orf76 as proximal to GBF1.
  • •Tagged C10orf76 overlaps with Golgi markers.
  • •C10orf76 binds GBF1 and exchanges rapidly between free and bound forms.
  • •C10orf76 is essential for maintenance of the Golgi and for secretion.
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10.
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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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11.
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Highlights
  • •microRNA-222 attenuates TGEV-induced mitochondrial dysfunction.
  • •microRNA-222 downregulates THBS1 and CD47.
  • •THBS1 is the target of microRNA-222 during TGEV infection.
  • •THBS1 and CD47 increase mitochondrial Ca2+ level and reduced mitochondrial membrane potential (MMP).
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12.
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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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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
  • •Kallikrein-related peptidase 7 is over expressed in ovarian cancer.
  • •Quantitative PROTOMAP and TAILS approaches identified putative substrates of KLK7.
  • •Pro-MMP10 is activated by KLK7.
  • •KLK7 cleaves thrombospondin 1 and IGFBP6 in vitro.
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15.
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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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16.
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Highlights
  • •Rapamycin and zinc induce moderate but significant mitochondrial proteome changes.
  • •The mitochondrial proteins processing system is robust under subtoxic conditions.
  • •Rapamycin and zinc perturb the mitochondrial proteins processing system.
  • •Rapamycin and zinc perturb the mitochondrial proteins homeostasis.
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17.
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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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18.
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Highlights
  • •HLA-B*40:02 and ERAP2 are risk factors for ankylosing spondylitis.
  • •The effects of ERAP2 on the B*40:02 peptidome are defined.
  • •ERAP2 has a major influence mainly due to alterations of N-terminal residues.
  • •These effects provide a basis for the association of ERAP2 with disease.
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19.
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Highlights
  • •Fast and simple capillary column packing protocol.
  • •Low-pressure packing at <100 bars from ultrahigh sorbent suspension concentration.
  • •Sorbent particle aggregation leading to blocking of the column entrance is avoided.
  • •Effective for long capillary UHPLC column packing with a wide range of sorbents.
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20.
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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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