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1.
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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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2.
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Highlights
  • •Repeatable quantification of 200 proteins in dried blood spots.
  • •Determined lower limit of quantification, repeatability, parallelism and stability.
  • •Protein stability in DBS stored at ambient temperatures for up to 2 months.
  • •Concentration ranges for 200 proteins in 20 healthy individuals.
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3.
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Highlights
  • •N-glycosylation site analysis of the hemipteran pest insect Nilaparvata lugens.
  • •Differential N-glycosylation of proteins is observed between male and female adults.
  • •Sex-specific glycoproteins are involved in insect reproduction.
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4.
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Highlights
  • •A predominance of HLA-I bound deamidated peptides are generated through ERAD pathway.
  • •Deamidation of peptides with N-glycosylation motifs not in peptidome of HLA-II or proteolysis.
  • •Many precursors of ERAD generated deamidated peptides are glycoproteins.
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5.
6.
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Highlights
  • •N-glycan patterns are distinct in pediatric and adult urine.
  • •Sex differences of N-glycans are much larger in adults.
  • •Pediatric urine has almost no sex differences in N-glycan levels.
  • •In adults, the majority of N-glycans were more abundant in males.
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7.
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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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8.
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Highlights
  • •The gut mucosal-luminal interface is a spatiotemporal heterogeneous ecosystem.
  • •Proteomics and metaproteomics are tools to study the host and microbiome functionality.
  • •Insights into functional diversity, biomass, and matter flow can be obtained.
  • •Such data can be complementary inputs for building ecology models of the microbiome.
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9.
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Highlights
  • •Activity based serine hydrolase profiles in 11 fractions along the murine small intestine.
  • •AADAC and Ces2e activity profiles correlate with chylomicron secretion.
  • •Ces2e shows the highest activity based enrichment in the entire small intestine.
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10.
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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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11.
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Highlights
  • •Guidelines for studying protein complexes via co-fractionation mass spectrometry.
  • •A novel procedure for profiling gold standard protein complexes in CF-MS data.
  • •Recommendations for efficient CF-MS fractionation collection.
  • •Scoring metric recommendations for precise and sensitive CF-MS data analysis.
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12.
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Highlights
  • •Quantitative proteomics and machine learning to study plasma biomarkers in HCM.
  • •Six peptides are increased in plasma of LVH+ HCM compared to controls.
  • •Peptide biomarkers correlate with imaging markers of phenotype severity.
  • •Peptide biomarkers correlate with the estimated sudden cardiac death risk.
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13.
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Highlights
  • •Future proteomic analyses for longitudinal studies and P4 medicine arguably require ≥1M samples/day.
  • •Proteome depth/coverage is commonly the focus whereas analytical speed is typically neglected.
  • •A compromise between analytical depth and speed is needed for future large-scale studies.
  • •Ultrahigh-speed ‘omic’ analyses require tools that are intrinsically fast such as laser-based MS.
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14.
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Highlights
  • •Co-elution stands out as a global interactome mapping method.
  • •Benefits include all-to-all protein analysis and measurement of interactome perturbations.
  • •Different separation, quantification and bioinformatic strategies are available.
  • •Design considerations depend largely on system under study.
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15.
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Highlights
  • •OpenPepXL is a new XL-MS identification tool with a high sensitivity.
  • •It is available for all common operating systems and remote computing environments.
  • •OpenPepXL is open source and supports open OpenPepXL is available as part of OpenMS data formats like mzML and mzIdentML.
  • •at https://www.openms.de/openpepxl.
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16.
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Highlights
  • •Peptide-based screens provide a scalable approach to study protein-protein interactions.
  • •These screens help to characterize the function of structurally disordered regions.
  • •The impact of posttranslational modifications can be directly investigated.
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17.
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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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18.
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Highlights
  • •In-depth profiling of the serum proteome in early-stage COVID-19 patients.
  • •A landscape of inflammation and immune signaling related to the SARS-CoV-2 infection.
  • •CCL2 and CXCL10 medicated cytokine signaling pathways may correlate with neutrophil and lymphocyte respectively.
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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
  • •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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