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1.
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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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2.
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Highlights
  • •HLA-B*27:05 and ERAP2 are risk factors for ankylosing spondylitis.
  • •The effects of ERAP2 on the B*27:05 ligandome are defined.
  • •P1, P2, P3, P7, and PΩ peptide positions are influenced by ERAP2.
  • •These effects provide a basis for the association of ERAP2 with the autoimmune disease.
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3.
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Highlights
  • •DEqMS is a method for statistical analysis of quantitative MS-data.
  • •Variance estimates based on the actual MS-data structure.
  • •Improved statistical power and accuracy in protein differential analysis.
  • •DEqMS is available as a user-friendly R package in Bioconductor.
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4.
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Highlights
  • •Salivary secretion was increased by mouth rinsing with TRP channel agonists.
  • •The salivary proteome varied over time and was changed by TRP channel stimulation.
  • •Immunoreactive Cystatin S was increased in saliva after TRPV1 stimulation.
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5.
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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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6.
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Highlights
  • •Epitope-tagging of a proteasome subunit allows for facile immuno-isolation.
  • •An engineered yeast strain permits capture of proteasome-associated substrates.
  • •MS/MS identified all 33 resident proteasome subunits in the 20S and 19S particles.
  • •Analysis of associated proteins and characterization of newly identified ERAD substrate.
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7.
8.
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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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9.
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Highlights
  • •Label-free and dimethyl labeling MS analysis of 6 RBPs from Drosophila ovaries.
  • •Functionally related RBPs show overlapping proteomes.
  • •Selective co-purification of splicing factors and translational regulators.
  • •Validation of 26 novel interactions by co-immunoprecipitation.
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10.
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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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11.
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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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12.
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Highlights
  • •Increased proteome coverage with Orbitrap Exploris 480 MS and FAIMS using single compensation voltages and short LC gradients.
  • •Towards single-cell proteomics with high-sensitivity analysis of 5 ng HeLa with more than 1,000 proteins identified in 5 minutes using FAIMS and DIA.
  • •Deep proteome profiling across twelve rat organs tissues by label-free quantitation using DIA compared to TMT-multiplexing and turboTMT acquisition using phi-SDM.
  • •Rapid and sensitive phosphoproteomics with automated enrichment using Ti-IMAC magnetic beads and direct DIA analysis.
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13.
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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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14.
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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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15.
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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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16.
17.
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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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18.
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Highlights
  • •Validation of an omic method for antigen identification using LC-MS/MS.
  • •Validation of accuracy, precision, specificity, limit of detection and robustness.
  • •Validation according to the current FDA and EMA guidelines.
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19.
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Highlights
  • •New quality assessment metrics to evaluate proteome-wide cross-linking mass spectrometry (XL-MS) data sets.
  • •New “MS3-centric” cross-link search engine named MaXLinker with high sensitivity and specificity.
  • •More than 9300 cross-links from our human proteome-wide XL-MS study.
  • •Orthogonal experimental validation of novel interactions identified in our study.
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20.
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Highlights
  • •Human spermatozoa possess cells of poor morphology that lack nuclear integrity.
  • •These cells can be isolated by density separation.
  • •Mass spectrometry reveals their nuclei contain excess protein.
  • •TOP2A is a promising marker of this poor nuclear development.
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