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1.
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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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2.
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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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3.
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Highlights
  • •BioID and IP-MS were conducted to generate a global ZIKV-host protein interactome
  • •Interactome consists of >3000 high confidence ZIKV-host protein interactions
  • •Data mining indicates that ZIKV proteins interact with multiple host cell organelles
  • •An important role for peroxisomes in ZIKV infection is uncovered
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4.
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Highlights
  • •Single-pot workflow for manual or automated enrichment of N-terminal peptides.
  • •Sensitive enrichment of protein N termini from 10,000 cells or 2 μg crude proteome.
  • •Data independent acquisition improves precision of peptide level quantification.
  • •First degradomic analyses of sorted immune cells, single seedlings, and mitochondria from patient cells.
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5.
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Highlights
  • •Retention time shift can lead to inversion of elution order of peptides.
  • •Global alignment methods are suboptimal for alignment of distant runs.
  • •DIAlignR employs hybrid (global + local) RT alignment approach.
  • •DIAlignR can align swapped peaks accurately across distant runs.
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6.
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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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7.
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Highlights
  • •A global lysine succinylome was investigated in A. hydrophila.
  • •The lysine succinylation modifications play crucial role on various metabolic pathways.
  • •Reversible succinylation on Lys23 and Lys30 regulates the activity of S-ribosylhomocysteine lyase LuxS.
  • •Lysine succinylation modifications of LuxS affect quorum sensing and metabolism.
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8.
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Highlights
  • •Quantitative proteomes of the 2016 WHO Neisseria gonorrhoeae reference strains.
  • •Novel gonorrhea vaccine candidates and potential global proteomic AMR markers.
  • •First large-scale proteomic profiling of gonorrhea vaccine candidates and AMR.
  • •A reference proteomics databank for gonococcal vaccine and AMR research endeavors.
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9.
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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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10.
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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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11.
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Highlights
  • •Spatiotemporal microproteomics analysis of TBI.
  • •Injury site microproteomics reveal distinct phases in 10-day frame post TBI.
  • •Uninjured proteomic profile is restored in TBI at 10 days post injury.
  • Substantia nigra protein post 3 days suggest link to Parkinson's disease.
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12.
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Highlights
  • •Application of Sortase A to label protein N-termini across the whole proteome.
  • •Novel gel, proteomic and ELISA-based methods to determine N-myristoylation of proteins in cells, without metabolic labelling.
  • •Side by side mass spectrometric quantification of changes in protein N-myristoylation by two complementary methods.
  • •Improved Biotin-Neutravidin affinity enrichment protocol.
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13.
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Highlights
  • •Identification of previously undetected chloroplast envelope proteins.
  • •Up to date manual annotation of genuine (or shared) envelope components.
  • •New hypotheses for localizations, functions, interactions among cell compartments.
  • •A new resource of significant value to the broader plant science community.
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16.
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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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17.
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Highlights
  • •Selective release of IgG Fc glycans in crude serum by endoglycosidase S.
  • •CE-LIF-based measurements of IgG undergalactosylation levels (UGS).
  • •UGS as a biomarker: Stratification of non-alcoholic steatohepatitis patients and controls.
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18.
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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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19.
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Highlights
  • •First global study on laryngeal cells cultured with cigarette smoke enriched medium.
  • •Vocal fold fibroblasts increased production of ECM component hyaluronan.
  • •Expression of several fibrillar collagens was reduced.
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20.
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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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