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1.
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Highlights
  • H. pylori dysregulates the in vivo gastric proteome of gerbils in a strain-specific manner.
  • H. pylori increases RABEP2 and G3BP2 levels in cell culture.
  • H. pylori upregulates RABEP2 and G3BP2 in gerbil and human gastric epithelium.
  • •Levels of RABEP2 and G3BP2 increase with severity of malignant lesions in vivo.
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2.
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Highlights
  • •HLA-B*40:02 and ERAP2 are risk factors for ankylosing spondylitis.
  • •The effects of ERAP2 on the B*40:02 peptidome are defined.
  • •ERAP2 has a major influence mainly due to alterations of N-terminal residues.
  • •These effects provide a basis for the association of ERAP2 with disease.
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3.
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Highlights
  • •R-10G is a mono-sulfated glycan antigen of human iPS and ES cells on podocalyxin.
  • •R-10G and nonsulfated i are reciprocal antigens on type 2 glycan backbones.
  • •TRA-1–60 and -81 and FC10.2 are antigens expressed on unsulfated type 1 backbones.
  • •These assignments open the way to probing their roles in podocalyxin-signaling.
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4.
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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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5.
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Highlights
  • •HLA-B*51 and ERAP1, but not ERAP2, are risk factors for Behçet's disease.
  • •The HLA-B*51 peptidome and the effects of ERAP1 and ERAP2 on it are analyzed.
  • •ERAP1 and ERAP2 alter multiple features of the HLA-B*51 peptidome in distinct ways.
  • •Both enzymes act independently with complementary and partially redundant functions.
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6.
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Highlights
  • •AP-DIA/SWATH analysis to identify TCTP-interacting proteins in NF1 tumor cells.
  • •A highly specific TCTPEF1A2 interaction but rather than TCTPEF1A1 interaction.
  • •TCTPEF1A2 interaction mediating formation of EF1A2-elogation factor complex.
  • •TCTPEF1A2 dependent translation machinery regulating NF1 tumor cell growth.
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7.
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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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8.
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Highlights
  • •Quantitative (phoshpo)proteome of primary cell cultures of patient-matched prostate CAF and NPF.
  • •Key CAF-associated proteins validated using orthogonal methodologies.
  • •LOXL2 inhibitors D-penicillamine and PXS-S2A impaired CAF migration and ECM alignment.
  • •Pre-treatment with LOXL2 inhibitors impaired migratory capacity of RWPE-2 cells in co-culture.
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9.
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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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10.
11.
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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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12.
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Highlights
  • •microRNA-222 attenuates TGEV-induced mitochondrial dysfunction.
  • •microRNA-222 downregulates THBS1 and CD47.
  • •THBS1 is the target of microRNA-222 during TGEV infection.
  • •THBS1 and CD47 increase mitochondrial Ca2+ level and reduced mitochondrial membrane potential (MMP).
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13.
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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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14.
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Highlights
  • •Glycosylation is not currently considered in flu vaccine design.
  • •Glycosylation influences on immunodominance are not well understood.
  • •Identification of site-specific glycosylation using mass spectrometry has matured.
  • •New methods are needed to quantify site-specific glycosylation for vaccine design.
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15.
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Highlights
  • •1. Celastrol alleviated cholestatic liver injury.
  • •2. Celastrol inhibited the decrease of SIRT1 induced by deoxycholic acid.
  • •3. SIRT1-FXR signaling pathway mediated the effect of celastrol.
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16.
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Highlights
  • •Definition of early systemin-responsive phosphorylation time course.
  • •Reconstruction of kinase-substrate relationships from phosphorylation time profiles.
  • •Phosphatase PLL5 rapidly dephosphorylated H+-ATPase LHA1 inducing alkalinization of the medium.
  • •MAP-Kinase MPK2 re-phosphorylated LHA1 after 15 minutes.
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17.
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Highlights
  • •The proteomes of L. lactis MG1363 and phage p2 at different stages of infection were characterized.
  • •16% (226/1412) of the bacterial proteins detected were unique to infected cultures.
  • •A targeted approach using synthetic peptides improved the coverage of phage p2 proteome.
  • •By means of proteogenomics, we uncovered a conserved phage protein coded by a previously unannotated gene.
  • •Deletion of the bacterial gene llmg_0219 (unknown function) impedes phage p2 infection.
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18.
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Highlights
  • •Incrementally build mzML 1.1, and mzIdentML 1.2 files in Python over a file stream.
  • •Traverse controlled vocabularies using common mapping patterns.
  • •Generate byte offset index as the document streams.
  • •Manage referential integrity on-the-fly.
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19.
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Highlights
  • •MaxQuant.Live controls Orbitrap mass analyzers in real-time.
  • •Freely available apps enable advanced data acquisition strategies.
  • •On-the-fly mass, retention time and intensity recalibration.
  • •Global targeting unifies shotgun and targeted proteomics.
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20.
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Highlights
  • •OMICS distinguish cancer cells from resistant or cancer stem cells.
  • •Bactericidal antibiotics and mitochondria.
  • •Linezolid and anticancer therapy.
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