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1.
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Highlights
  • •quantitative phosphoproteome analysis of TDM-activated macrophages.
  • •distinct Mincle-dependent and independent phosphorylation and gene regulations.
  • •Mincle-dependent activation of PI3K/AKT signaling by TDM.
  • •Mincle-independent macrophage response is linked to cell cycle regulation.
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2.
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Highlights
  • •A panel of HEK293 isogenic cell lines with knockout of GALNT genes.
  • •Identification of nonredundant O-glycosylation sites regulated by specific GalNAc-T isoforms.
  • •GalNAc-T7 and T10 contribute to follow-up activity in regions of high density O-glycosylation.
  • •GalNAc-T11 specifically controls O-glycosylation of specific linker regions in the low-density lipoprotein receptor related proteins.
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3.
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Highlights
  • •Phosphorylation on Y139 of the sheath protein IglB of Francisella.
  • •IglB substitutions Y139A, Y139D or Y139E prevent T6SS formation.
  • •Y139F substitution delays but does not abolish phagosomal escape in macrophages.
  • •Insight into the role of sheath phosphorylation in T6SS biogenesis.
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4.
5.
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Highlights
  • •MS-based method to detect native arginine-GlcNAcylation during Salmonella infection.
  • •Demonstration that SseK1 targets TRADD, whereas SseK3 targets the death receptors, TNFR1 and TRAILR.
  • •Evidence that effector overexpression results in misleading identification of host targets.
  • •Crystal structure of SseK3.
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6.
7.
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Highlights
  • •Proteomic landscapes of Drosophila somatic and reproductive tissues during aging.
  • •Pulsed metabolic labeling determines a decline in protein synthesis with age.
  • Drosophila model of human Parkinson's disease signifies an early-onset decline in protein synthesis.
  • •Collapse of proteostasis and mitochondria are early signals for normal aging.
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8.
9.
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Highlights
  • •Open source software for comprehensive HDX-MS data analysis.
  • •Automatic back-exchange correction options.
  • •Rigorous statistical analysis of the significance of uptake differences.
  • •High quality visualization tools.
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10.
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Highlights
  • •Quantitative proteomes of the 2016 WHO Neisseria gonorrhoeae reference strains.
  • •Novel gonorrhea vaccine candidates and potential global proteomic AMR markers.
  • •First large-scale proteomic profiling of gonorrhea vaccine candidates and AMR.
  • •A reference proteomics databank for gonococcal vaccine and AMR research endeavors.
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11.
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Highlights
  • •Atlantic salmon O-glycome expanded to 169 structures in three epithelia.
  • •Low interindividual variation amongst all populations and geographical regions.
  • •Small variations in glycosylation between geographical locations and fish size.
  • •Prominent fucosylation in gastrointestinal mucins from Tasmanian fish.
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12.
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Highlights
  • •Global proteomic remodeling alters antibiotic susceptibility in K. pneumoniae.
  • •Drug specific transport, sugar utilization, central metabolism, capsule synthesis.
  • •Common pathways of reactive oxygen scavenging, turnover of misfolded proteins.
  • •Integrated adjustments and unique drug-specific features for drug combinations.
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13.
14.
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Highlights
  • •MHC-II-bound peptide repertoires from DO-sufficient and DO-deficient cells.
  • •Fewer unique peptides and core epitopes were presented in the absence of DO.
  • •Immunopeptidome differences appeared to result from reduced DM editing.
  • •DO-dependent self-epitopes elicited CD4 T cell responses in mice.
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15.
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Highlights
  • •mRNA-seq, miRNA-seq, proteomes of P. fulvidraco, P. vachelli, hybrid Huangyou-1.
  • •Predicted miRNA-mRNA-protein pairs were found and validated by qRT-PCR and PRM.
  • •Immune, metabolism, digestion, absorption, proliferation, development generate heterosis.
  • •High parental gene/protein with low parental miRNAs inherit from the mother or father.
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16.
17.
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Highlights
  • •Establishment of a flow system allowing multi-omics analysis of S. aureus biofilms.
  • •Biofilm proteome profiling (intracellular and ECM) plus metabolic footprint analysis.
  • •Virulence factors and ribosomal proteins stabilize the ECM as moonlighting proteins.
  • •They act as electrostatic bridges between anionic cell surfaces, eDNA and metabolites.
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18.
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Highlights
  • •Quantitative (phospho)proteome analysis of antibiotic treatment in E. coli.
  • •Largest bacterial phosphorylation catalogue.
  • •Specific phosphorylation motifs changes during resistance development.
  • •Phosphorylation mediated signaling could be a potential target for drug design.
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19.
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Highlights
  • •Knockout of arginine methyltransferase Hmt1p in S. cerevisiae was investigated.
  • •RNA-seq and SILAC MS/MS found downregulation of phosphate-associated processes.
  • •Phosphate homeostasis and extracellular levels of acid phosphatases were perturbed.
  • •Pho4p was an in vitro Hmt1p substrate, but this was not confirmed in vivo.
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20.
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Highlights
  • •Proteome of mature boar spermatozoa from cauda epididymal and ejaculated sources were analyzed by iTRAQ-based LC-MS/MS.
  • •1,723 sperm proteins identified (974 of Sus scrofa taxonomy).
  • •1,602 sperm proteins quantified (960 of Sus scrofa taxonomy).
  • •32 Sus scrofa sperm proteins were differentially expressed among sperm sources.
  • •The proteome of boar spermatozoa is remodelled during ejaculation.
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