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1.
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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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2.
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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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3.
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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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4.
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Highlights
  • •Kallikrein-related peptidase 7 is over expressed in ovarian cancer.
  • •Quantitative PROTOMAP and TAILS approaches identified putative substrates of KLK7.
  • •Pro-MMP10 is activated by KLK7.
  • •KLK7 cleaves thrombospondin 1 and IGFBP6 in vitro.
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5.
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Highlights
  • •In-depth proteome profiling of primary human myeloma cells
  • •Characteristics of myeloma cells are related to hypoxic bone marrow conditions
  • •Myeloma cells show specific immune evasion strategies
  • •Metabolic adaptations involve tumor and stroma cells
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6.
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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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7.
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Highlights
  • •Interplay of epithelial cells and internalized S. aureus was dissected over 96 h.
  • •Surviving host cells contain nonreplicating bacteria that persists in the cytoplasm.
  • •Competition over resources triggers temporal metabolic changes.
  • •Metabolic adaptation of host and bacteria determines the outcome of infection.
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8.
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Highlights
  • •A global lysine succinylome was investigated in A. hydrophila.
  • •The lysine succinylation modifications play crucial role on various metabolic pathways.
  • •Reversible succinylation on Lys23 and Lys30 regulates the activity of S-ribosylhomocysteine lyase LuxS.
  • •Lysine succinylation modifications of LuxS affect quorum sensing and metabolism.
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9.
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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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10.
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Highlights
  • •MEEC are a reliable endocardial in vitro model.
  • •Quantitative proteomics to characterize the NOTCH-driven endocardial secretome.
  • •NOTCH pathway status underlies different paracrine biological functions.
  • •New insights into secreted factors involved in cardiac valve development.
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11.
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Highlights
  • •Three novel Conodipines P1-3 in the injected venom of Conus purpurascens.
  • •Conodipines P1-3 have consensus catalytic characteristics of sPLA2.
  • •We determined multiple modification sites in Conodipines P1-3.
  • •Evaluated the activity of Conohyal-P1 by a MS-based method.
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12.
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Highlights
  • •nLC-MS/MS method to analyze immunoglobulin (Ig) N-glycopeptides from human serum.
  • •Multi-isotype, site-specific characterization of immunoglobulin N-glycosylation.
  • •IgA2 sequence and glycosylation-site variant analyses.
  • •Platform to define disease-specific N-glycan signatures for different Ig isotypes.
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13.
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Highlights
  • •Spatiotemporal microproteomics analysis of TBI.
  • •Injury site microproteomics reveal distinct phases in 10-day frame post TBI.
  • •Uninjured proteomic profile is restored in TBI at 10 days post injury.
  • Substantia nigra protein post 3 days suggest link to Parkinson's disease.
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14.
15.
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Highlights
  • •Proteogenomics and secretome comparison of human and zoonotic Staphylococcus aureus lineages.
  • •869 secreted proteins identified in eight S. aureus isolates of CC8, CC22 and CC398.
  • •CC398 lower secretion of surface proteins and higher secretion of hemolysins and exoenzymes.
  • •Regulatory differences in the secretomes could be linked to lower SigB activity in CC398.
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16.
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Highlights
  • •First report on the quantitative proteomic profiling of Drosophila lymph glands.
  • •Comparative proteomic analysis under conditions of perturbed blood cell homeostasis.
  • •Resource for identifying new regulators of insect and vertebrate hematopoiesis.
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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
  • •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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19.
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Highlights
  • •Quantitative proteomes and epigenetic regulation of T. gondii.
  • •Protein crotonylation and 2-hydroxyisobutylation in phenotypically different T. gondii parasites.
  • •Regulation of invasion regulation of T. gondii by protein modification.
  • •Lysine crotonylation and 2-hydroxyisobutylation regulated in multiple biological processes in phenotypically different T. gondii parasites.
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20.
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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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