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1.
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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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2.
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Highlights
  • •Mapping kinase-substrate relationships is vital in discovering new tuberculosis drug targets.
  • •LC-MS/MS-based phosphoproteomics expand mycobacterial STPK substrate catalogues.
  • •We review and integrate MS-generated datasets on novel candidate substrates.
  • •Validation studies are necessary to confirm true physiological substrates of STPKs.
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3.
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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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4.
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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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5.
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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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6.
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Highlights
  • •A novel HLA-ABC-triple knockout cell model to study the HLA-B*51 peptidome.
  • •Enrichment of the unconventional non-Pro/Ala2 HLA-B*51 peptides following ERAP1 silencing.
  • •Knockdown of ERAP1 increases the length of non-Pro/Ala2 and Ala2 peptides, not that of Pro2.
  • •ERAP1 regulation of HLA-B*51 cell surface expression is cell type dependent.
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7.
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Highlights
  • •Growth in the bile salt deoxycholate (DOC) induces virulence proteins in C. jejuni.
  • •A putative symporter Cj0025c is associated with DOC growth and cystine transport.
  • •Deletion of cj0025c results in loss of cystine transport and a sulfur starved proteotype.
  • •Cj0025c is required for wild-type virulence phenotypes including human cell invasion.
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8.
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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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9.
10.
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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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11.
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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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12.
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Highlights
  • •Provision of data generated on the basis of a gold standard spike-in sample set.
  • •Choice of spectral library has great impact on identification and quantification.
  • •DIA is superior to DDA in quantification reproducibility, specificity and accuracy.
  • •DIA outperforms DDA in the quantification of low protein amounts.
  • •Quantification on peptide level is generally preferable.
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13.
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Highlights
  • •Cross-linked peptides are physically separated from mono-linked peptides in the gas-phase by TIMS ion mobility.
  • •Development of a novel data acquisition routine that a-priori distinguishes cross-linked from mono-linked peptides called caps-PASEF.
  • •First application of PhoX-driven cross-linking mass spectrometry on the timsTOF Pro.
  • •Application of cross-linking mass spectrometry to medium to high complexity samples.
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14.
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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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15.
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Highlights
  • •Sufficient tumor tissues are often unavailable large HLA peptidome discovery.
  • •Using patient derived xenograft (PDX) tumors can overcome this limitation.
  • •The large PDX HLA peptidomes expand significantly those of the original biopsies.
  • •The HLA peptidomes of the PDX tumors included many tumor antigens.
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16.
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Highlights
  • •Curation of 2066 phosphorylated HLA class I peptides from immunopeptidomics data.
  • •Determination of 22 HLA class I binding motifs for phosphorylated peptides.
  • •Observation of a higher frequency of phosphorylated ligands binding HLA-C molecules.
  • •Development of a predictor of phosphorylated peptide interactions with HLA class I.
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17.
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Highlights
  • •Statistical approach for differential abundance analysis for proteomic experiments with TMT labeling.
  • •Applicable to large-scale experiments with complex or unbalanced design.
  • •An open-source R/Bioconductor package compatible with popular data processing tools.
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18.
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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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19.
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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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20.
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Highlights
  • •Proteome of airway secretions derived from mock- and hRSV-infected WD-PBEC cultures.
  • •A polarised secretome in uninfected WD-PBECs, skewed in hRSV-infected cultures.
  • •CXCL6, CXCL16, CECACAM1 and CSF3 induced only upon hRSV-infection.
  • •Detection of CXCL6, CXCL16 and CSF3 in NPAs from hRSV-positive children.
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