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1.
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Highlights
  • •Monocytes are isolated from single donors after apheresis.
  • •Monocytes process CD16a and CD32a N-glycosylation differently by site and donor.
  • •CD16a with hybrid and oligomannose type N-glycans bind IgG1 Fc with stronger affinity than complex type.
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2.
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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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3.
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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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4.
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Highlights
  • •Affinity-based proteomics of infected macrophage cells.
  • Salmonella-modified membranes exhibit host-specific composition.
  • •Proteome differences explain some host-dependent pathophysiological differences.
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5.
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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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6.
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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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7.
8.
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Highlights
  • •Urinary proteomes of patients with recurrent UTI, renal scarring, and VUR.
  • •80 proteins differentially expressed, compared to healthy controls.
  • •62 proteins may be indicative of susceptibility for UTI.
  • •Altered acute phase response, extracellular matrix and carbohydrate metabolism.
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9.
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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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10.
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Highlights
  • •MS-based clinical assay that accurately determines phospho Rab10 occupancy.
  • •Stable isotope labeled phosphopeptide injected as a standard with endogenous tryptic phospho Rab peptide for accurate ratio determination.
  • •Determination of pRab levels in neutrophils of Parkinson disease patients.
  • •Relevance of pRab levels as marker of PD.
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11.
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Highlights
  • •Immunopeptidomics bears the potential to link diseases to antigen representation.
  • •We suggest to achieve this by analyzing the immunopeptidomes of cohorts of patients.
  • •Current mass spectrometry-based techniques to analyze immunopeptidomes are described.
  • •We term the proposed approach “Immunopeptidome-wide association studies” (IWAS).
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12.
13.
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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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14.
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Highlights
  • •Signaling networks can be highly heterogeneous across cells in a tissue.
  • •Various technologies allow analyzing signaling networks at single-cell resolution.
  • •The advantages and limitations of each single-cell approach are summarized.
  • •Confounding factors in single-cell signaling network analysis are discussed.
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15.
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Highlights
  • •Summarize the development of functional protein microarray.
  • •Application of functional proteome microarray in basic research.
  • •Application of functional proteome microarray in translational research.
  • •Fabrication of functional membrane protein array using virion display method.
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16.
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Highlights
  • •A detailed investigation of the protein extraction step from FFPE tissue is shown.
  • •Acidification during peptide wash increased peptide recovery of the SP3 method.
  • •LCM of substantia nigra enriched neuron-specific proteins including TH.
  • •>5,600 proteins were quantified using 3000 cells per sample from substantia nigra.
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17.
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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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18.
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Highlights
  • •Modern DIA methods contain high quality MS1 and MS2.
  • •We developed a statistical procedure incorporating MS1 and MS2.
  • •Benchmarking, the combined method outperformed the individual use of MS1 or MS2.
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19.
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Highlights
  • •Highly parallelizable 4D feature detection in ion mobility enhanced shotgun proteomics.
  • •Multidimensional non-linear mass, retention time and ion mobility recalibration.
  • •Collision cross section aware matching between runs.
  • •Label-free quantification of ion mobility MS data.
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20.
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Highlights
  • •Comprehensive molecular profiling of cutaneous and cerebellar metastasis variants.
  • •Identification of differentially regulated metastasis-associated molecules.
  • •Evidence for individually distinct patterns of metastasis-associated molecules.
  • •Highlighting the evident need for establishing meta-analyses strategies.
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