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1.
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Highlights
  • •Novel two-dimensional separation system for identification of citrullinated peptides.
  • •Dedicated software developed for confident validation of citrullination.
  • P. gingivalis citrullinome: 78 proteins with a total of 161 citrullinated peptides.
  • •Confident discrimination of P. gingivalis OMVs from wild-type and PPAD mutants.
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2.
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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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3.
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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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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.
Factors promoting (orange) and suppressing (blue) the frequency of sexual commitment rate in Plasmodium falciparum.
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6.
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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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7.
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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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8.
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Microbes of interest can be engineered to improve the production of SCPs for human-food and animal-feed applications. These improvements include feedstock conversion, biomass accumulation, protein production, and the production of nutritional and functional compounds.
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9.
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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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10.
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Highlights
  • •Discovery of peptide biomarker candidates of respiratory tract pathogens S. pneumoniae, H. influenzae, M. catarrhalis and S. aureus as target pathogens.
  • •Peptide biomarker candidates were experimentally verified in clinical samples.
  • •Targeted MS using promising peptide biomarker candidates shown as proof-of-concept.
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11.
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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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12.
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Highlights
  • •An automated de novo sequencing program is evaluated with respect to different types of data.
  • •The number of unique high scoring de novo sequences that can be assigned to a data set provides a metric of overall data quality.
  • •A database suitability metric is presented for situations when the database choice is not obvious, or when the database quality is uncertain.
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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
  • •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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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
  • •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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18.
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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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19.
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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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20.
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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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