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1.
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Highlights
  • •Auxin responsive proteins in Arabidopsis roots were identified from 3,514 detected proteins.
  • •All six auxin receptors are stable in response to hormone via novel MRM assays.
  • •The >100 differentially expressed proteins exhibit dynamic and transient responses to auxin.
  • •Phenotypic screening of the top responsive proteins uncovered several novel root mutants.
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2.
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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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3.
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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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4.
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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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5.
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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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6.
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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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7.
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Highlights
  • •Cathepsin-L is introduced as a novel protease for HX-MS studies.
  • •Cathepsin-L improves resolution of traditionally challenging histone tails.
  • •Cathepsin-L can be readily combined with pepsin for improved protein coverage.
  • •In-solution dynamics of the H3.1 and H4 monomers reveal extensive EX1 kinetics.
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8.
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Highlights
  • •Application of Sortase A to label protein N-termini across the whole proteome.
  • •Novel gel, proteomic and ELISA-based methods to determine N-myristoylation of proteins in cells, without metabolic labelling.
  • •Side by side mass spectrometric quantification of changes in protein N-myristoylation by two complementary methods.
  • •Improved Biotin-Neutravidin affinity enrichment protocol.
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9.
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Highlights
  • •Production of sera with different levels of protection against rodent Plasmodium.
  • •Generation of immunomic and proteomic data sets enriched in protective antigens.
  • •Prediction of the most likely protective antigens using a weighted scoring system.
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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
  • •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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12.
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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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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.
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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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15.
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Highlights
  • •BioID and IP-MS were conducted to generate a global ZIKV-host protein interactome
  • •Interactome consists of >3000 high confidence ZIKV-host protein interactions
  • •Data mining indicates that ZIKV proteins interact with multiple host cell organelles
  • •An important role for peroxisomes in ZIKV infection is uncovered
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16.
17.
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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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18.
19.
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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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20.
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Highlights
  • •Reported proteasomal spliced HLA peptides do not fit the consensus binding motifs.
  • •Their MS/MS spectrum matches suggest that many of them are ambiguous.
  • •Our workflow is based on de novo sequencing, alignment, and multiple search tools.
  • •The upper bound proportion of cis-spliced peptides is 2–6% and likely much smaller.
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