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1.
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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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2.
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Highlights
  • •Multi-omics analysis on mode of action of novel antimalarial, JPC-3210
  • •JPC-3210 has rapid parasite killing kinetics.
  • •Metabolomics and peptidomics demonstrated JPC-3210 inhibits hemoglobin digestion.
  • •Proteomics demonstrated JPC-3210 enriches for translation regulation proteins.
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3.
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Highlights
  • •Acute inhibition of growth-regulatory AGC-kinases Sch9, PKA and Ypk1.
  • •Phospho-proteomic profiling of 6373 phsopho-sites.
  • •Ypk1 regulates phospho-sites in RRxS/T-context and functionally overlaps with PKA.
  • •Ypk1 and PKA activate trehalase activity of Nth1.
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4.
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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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5.
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Highlights
  • •CD73 is one of the most upregulated proteins in the radioresistant cells.
  • •CD73 upregulation confers radioresistance and irradiation-induced apoptosis.
  • •CD73 confers radioresistance potentially through inactivating protein BAD.
  • •Elevated CD73 is required for maintaining the resistant cells in a mesenchymal state.
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6.
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Highlights
  • •Human spermatozoa possess cells of poor morphology that lack nuclear integrity.
  • •These cells can be isolated by density separation.
  • •Mass spectrometry reveals their nuclei contain excess protein.
  • •TOP2A is a promising marker of this poor nuclear development.
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7.
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Highlights
  • •Used affinity-enrichable, isotopically coded, and MS-cleavable crosslinker.
  • •Targeted acquisition strategy based on isotopic-coding described and evaluated.
  • •Novel data analysis pipeline developed provides improved crosslink identification.
  • •Large dataset reveals hundreds of mitochondrial protein-protein interactions.
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8.
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Highlights
  • •Brain membrane protein extraction.
  • •Protein prenylation.
  • •Prenyl peptide capture and characterization by LC-MS/MS.
  • •HCD and EThcD peptide fragmentation.
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9.
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Highlights
  • •OpenPepXL is a new XL-MS identification tool with a high sensitivity.
  • •It is available for all common operating systems and remote computing environments.
  • •OpenPepXL is open source and supports open OpenPepXL is available as part of OpenMS data formats like mzML and mzIdentML.
  • •at https://www.openms.de/openpepxl.
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10.
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Highlights
  • •N-glycan patterns are distinct in pediatric and adult urine.
  • •Sex differences of N-glycans are much larger in adults.
  • •Pediatric urine has almost no sex differences in N-glycan levels.
  • •In adults, the majority of N-glycans were more abundant in males.
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11.
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Highlights
  • •Mitochondrial heart N terminome shows aminopeptidase processing after MTS cleavage.
  • •CLPP-deficiency alters protein processing patterns in mouse heart mitochondria.
  • •Candidate substrates identified by N termini accumulation and interaction with inactive ClpXP.
  • •UQCRC1, HSPA9 and OAT validated biochemically as high confidence ClpXP substrates.
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12.
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Highlights
  • •Proteomes and phosphoproteomes of radiosensitive and radioresistant PDAC cell lines.
  • •Common activation of DDR is proven by ATM activity on known and novel substrates.
  • •Resistant cells bear raised NQO1 expression, actin dynamics including FAK activity.
  • •Inhibitors of CHEK Rabusertib and FAK Defactinib radiosensitize PDAC cells.
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13.
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Highlights
  • •Sufficient tumor tissues are often unavailable large HLA peptidome discovery.
  • •Using patient derived xenograft (PDX) tumors can overcome this limitation.
  • •The large PDX HLA peptidomes expand significantly those of the original biopsies.
  • •The HLA peptidomes of the PDX tumors included many tumor antigens.
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14.
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Highlights
  • •Urinary proteomes of patients with recurrent UTI, renal scarring, and VUR.
  • •80 proteins differentially expressed, compared to healthy controls.
  • •62 proteins may be indicative of susceptibility for UTI.
  • •Altered acute phase response, extracellular matrix and carbohydrate metabolism.
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15.
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Highlights
  • •Quantitative proteomics of isolated lysosomes, autophagosomes and proteasomes.
  • •Pharmacological inhibition of proteasomes leads to their accumulation within lysosomes.
  • •Inhibition of classical autophagy pathways cannot completely block this process.
  • •Known autophagy adaptor proteins are not involved.
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16.
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Highlights
  • •Repeatable quantification of 200 proteins in dried blood spots.
  • •Determined lower limit of quantification, repeatability, parallelism and stability.
  • •Protein stability in DBS stored at ambient temperatures for up to 2 months.
  • •Concentration ranges for 200 proteins in 20 healthy individuals.
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17.
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Highlights
  • •Co-elution stands out as a global interactome mapping method.
  • •Benefits include all-to-all protein analysis and measurement of interactome perturbations.
  • •Different separation, quantification and bioinformatic strategies are available.
  • •Design considerations depend largely on system under study.
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18.
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Highlights
  • •PRMT5 glutathionylation is increased in aged mice or under oxidative stress.
  • •Deglutathionylation of PRMT5 is catalyzed by glutaredoxin-1.
  • •PRMT5 glutathionylation decreases its methyltransferase activity.
  • •PRMT5 glutathionylation results in G2/M arrest and inhibits cell proliferation.
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19.
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Highlights
  • •Laser microdissection of highly vulnerable hippocampal region.
  • •Proteomic analysis of postmortem human brain tissue of AD and control cases.
  • •Decreased levels of presynaptic proteins, but not postsynaptic proteins, in AD.
  • •Immunohistochemistry verifies decreased levels of selected presynaptic proteins.
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20.
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Highlights
  • •Cecal Ligation Puncture (CLP) mouse model to study sepsis-induced kidney disease.
  • •Quantitative global proteome and phosphoproteome profiling of mouse kidneys.
  • •Highly significant candidate markers for onset and progression of AKI to CKD.
  • •Mechanistic insights into sepsis-associated kidney injuries.
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