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1.
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Highlights
  • •Urinary peptide profiling of youths with type 1 diabetes before clinical injury.
  • •Internal validation of uromodulin peptides by parallel reaction monitoring.
  • •Discovery of novel bioactivity of uromodulin peptides in vitro.
  • In silico prediction of proteases involved in uromodulin processing.
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2.
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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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3.
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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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4.
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Highlights
  • P. aeruginosa grown with exosiderophores and analyzed by proteomic and RT-qPCR.
  • •Catechol-type exosiderophores strongly induce the expression of their transporters.
  • •Repression of the endogenous iron uptake pathways.
  • •Complex phenotypic plasticity in the expression of the various iron-uptake pathways.
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5.
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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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6.
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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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7.
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Highlights
  • •Quantitative analysis of Plasmodium sexual stage egress secretome.
  • •Activated gametocytes release gender-related proteins.
  • •Gametocyte egress process involves different types of vesicles.
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8.
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Highlights
  • •Used affinity-enrichable, isotopically coded, and MS-cleavable crosslinker.
  • •Targeted acquisition strategy based on isotopic-coding described and evaluated.
  • •Novel data analysis pipeline developed provides improved crosslink identification.
  • •Large dataset reveals hundreds of mitochondrial protein-protein interactions.
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9.
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Highlights
  • •pY phosphoproteomes and dedicated ranking analyses for 16 AML cell lines.
  • •RTK drivers, 6 mutant cell lines confirmed, identification for 4 more cell lines.
  • •MAPK1/3 phosphorylation for cell lines without TK driver, indicating RAS mutation.
  • •Drug target space phosphorylation correlates with drug IC50s in specific cell lines.
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10.
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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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11.
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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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12.
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Highlights
  • •ProAlanase is a powerful protease for efficient low pH disulfide bond mapping.
  • •High suitability for analysis of histone family members and their PTMs.
  • •Accurate phosphorylation profiling in proline-rich proteins.
  • •Sequence coverage increase and full de novo sequencing in combination with trypsin.
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13.
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Highlights
  • •Simultaneous quantification of Bait, Prey and Reporter at the single cell level.
  • •Two hours of reaction are enough instead of 24–48 h for conventional assays.
  • •Potential expression problems of the Bait and Prey can be easily detected.
  • •True positive PPIs feature a distinct pattern of Reporter level versus Bait/Prey level.
  • •PPIs with unknown affinities can be ranked using an affinity ladder.
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14.
15.
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Highlights
  • •In-depth proteomes of 4 SARS-CoV-2 cell line models (Vero E6, Calu-3, Caco-2, A549).
  • •Proteomic evidence for thousands of Chlorocebus sabaeus proteins.
  • •Proteomic response of Vero E6 cells to SARS-CoV-2 infection.
  • •Synthetic peptides, spectral libraries, and targeted assays for SARS-CoV-2 proteins.
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16.
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Highlights
  • •Changes in N-linked glycosylation in influenza A virus affect antigenicity of the virus.
  • •Glycosylation similarity can be quantified, even in heterogeneously glycosylated proteins.
  • •Glycosylation is measurably and site-specifically distinct in influenza from related strains.
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17.
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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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18.
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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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19.
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Highlights
  • •All six binding sites in PANWT are occupied by ADP- or ATP-type nucleotides.
  • •PANKA Walker A mutant substoichiometrically binds ATP- but not ADP-type nucleotides.
  • •PAN hexamer dissociation of the solution origin characteristics was observed in MS.
  • •We posit that the PAN hexamer dissociation proceeds within the ESI droplets.
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20.
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Highlights
  • •Acute inhibition of growth-regulatory AGC-kinases Sch9, PKA and Ypk1.
  • •Phospho-proteomic profiling of 6373 phsopho-sites.
  • •Ypk1 regulates phospho-sites in RRxS/T-context and functionally overlaps with PKA.
  • •Ypk1 and PKA activate trehalase activity of Nth1.
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