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1.
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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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2.
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Highlights
  • •Characterization of 12 proteins from across the P. falciparum sexual-stages as possible TBV targets.
  • •Heterologously expressed recombinant proteins recapitulate native parasite epitopes.
  • •Some recombinant proteins exhibit immunoreactivity when tested against sera from individuals from malaria-endemic Burkina Faso and Mali.
  • •Purified IgG against the antigen enolase moderately inhibits parasite development in the mosquito midgut.
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3.
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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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4.
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Highlights
  • •Quantitative proteomics of isolated lysosomes, autophagosomes and proteasomes.
  • •Pharmacological inhibition of proteasomes leads to their accumulation within lysosomes.
  • •Inhibition of classical autophagy pathways cannot completely block this process.
  • •Known autophagy adaptor proteins are not involved.
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5.
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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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6.
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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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7.
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Highlights
  • •Quantitative proteome interactions with 5 different C9ORF72 dipolypeptides (DPRs).
  • •The arg-rich DPRs promiscuously bound to the proteome compared with the other DPRs.
  • •Long repeat lengths of arg-rich DPRs, but not short lengths, stalled ribosomes.
  • •The arg-rich DPRs also reduced arginine methylation and actin cytoskeleton assembly.
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8.
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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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9.
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Highlights
  • •Universal and detergent-free proteomic sample preparation.
  • •Based on three simple mandatory steps (acidification, neutralization, digestion).
  • •Enhances proteome coverage especially for challenging samples.
  • •Improves quantitative reproducibility compared with ISD-Urea, FASP and SP3.
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10.
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Highlights
  • •A predictive modelling framework has been established to analyze IgG antibody responses against a large panel of P. falciparum-specific antigens to identify a specific antigen signature of NAI.
  • •An individual's immune status can be accurately predicted by measuring IgG responses against a small set of 15 defined parasite antigens.
  • •Proteins identified in the 15-antigen signature represent potential candidates for next-generation malaria vaccines or biomarkers for monitoring the impact of malaria interventions.
  • •The developed predictive framework can be adapted for developing novel surveillance and intervention tools for other infectious diseases.
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11.
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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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12.
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Highlights
  • db/db β-cells restores appropriate insulin stores and normalize secretory function.
  • •Numerous changes in the phosphorylation and sialylation states by euglycemic rest.
  • •Restoration of numerous dysfunctional biological processes following euglycemic rest.
  • •β-cell adaptive flexibility may lead to improvement in endogenous β-cell function.
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13.
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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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14.
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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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15.
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Highlights
  • •Quantifying ionizing radiation-induced oxidation in E. coli and D. radiodurans.
  • •Amelioration of protein damage dependent upon cellular components.
  • •GAPDH active site is highly modified and also IR-modified in H. sapiens.
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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
  • Pseudomonas aeruginosa growth increases in Aspergillus fumigatus culture filtrates.
  • A. fumigatus culture filtrates are characterized by a range of peptidases and proteases.
  • •LFQ proteomics characterizes the response of P. aeruginosa to A. fumigatus culture filtrates.
  • A. fumigatus creates an environment for P. aeruginosa to proliferate.
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18.
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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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19.
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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