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1.
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Highlights
  • •Rapamycin and zinc induce moderate but significant mitochondrial proteome changes.
  • •The mitochondrial proteins processing system is robust under subtoxic conditions.
  • •Rapamycin and zinc perturb the mitochondrial proteins processing system.
  • •Rapamycin and zinc perturb the mitochondrial proteins homeostasis.
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2.
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Highlights
  • •Temporal proteome profiling of lipotoxicity and glucolipotoxicity in β-cells
  • •Palmitate induced cholesterol metabolism earlier than fatty acid metabolism
  • •Setd8 promotes palmitate + glucose-stimulated INS-1 cell proliferation
  • •PA induced apoptosis partially via upregulation of Rhob in INS-1 cells
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3.
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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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4.
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Highlights
  • •Characterization of the phagosomal proteome comparing resting and LPS-treated BMDCs.
  • •Label-free quantification determined 2843 phagosomal proteins.
  • •Reduced recruitment of hydrolases and V-ATPase to phagosomes of LPS-treated cells.
  • •Increased recruitment of antigen cross-presentation molecules to these phagosomes.
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5.
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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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6.
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Highlights
  • •Quantitative changes in global proteome and ubiquitinome in Huntington's disease.
  • •Differential ubiquitination of wild-type and mutant Htt in mice brain.
  • •Enriched pathways include vesicle transport and mRNA processing.
  • •Correlation between protein and diGly site fold changes.
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7.
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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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8.
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Highlights
  • •Changes to the proteome of skin fibroblasts subjected to reductive stress have been quantitated.
  • •Only a small set of proteins is selectively diminished upon exposure to reductants.
  • •Collagens (COL1A2 and COL6A2) emerge as sentinels of reductive stress.
  • •Reductive stress triggers receptor-independent Akt phosphorylation at Ser473.
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9.
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Highlights
  • •First global study on laryngeal cells cultured with cigarette smoke enriched medium.
  • •Vocal fold fibroblasts increased production of ECM component hyaluronan.
  • •Expression of several fibrillar collagens was reduced.
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10.
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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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11.
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Highlights
  • •In-depth proteome underpins the gland ontogeny and age-specific activity of the HGs.
  • •The well-developed acini in the HGs of NBs promote the RJ secretary activities.
  • •The enhanced protein and energy metabolism in the HGs boost the stronger RJ secretion of RJBs.
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12.
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Highlights
  • •Feeding mice a western-style obesogenic diet resulted in dramatic changes in fecal microbial proteome.
  • •Basal fecal microbial proteome, but not microbiome, composition was associated with extent of diet-induced obesity.
  • •A major feature of fecal microbial proteome of high-responder mice was enriched motility-related proteins.
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13.
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Highlights
  • •Chromobodies are stabilized by antigen binding in live cells.
  • •Monitoring changes of endogenous protein levels in living cells with chromobodies.
  • •Broadly applicable system to generate turnover-accelerated chromobodies.
  • •Quantification of time- and dose-dependent compound effects.
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14.
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Highlights
  • •Method for the analysis of response curves from thermal proteome profiling (TPP).
  • •NPARC uses nonparametric statistics and provides false discovery-rate (FDR) control.
  • •Increased proteome coverage and sensitivity to identify drug-binding proteins.
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15.
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Highlights
  • •Highly glycosylated matrisome proteins and their binding partners comprise extracellular networks that mediate tissue-specific cellular microenvironments.
  • •Elucidation of roles of matrisome molecules in disease mechanisms requires detailed mapping of matrisome glycosylation and other post-translational modifications.
  • •We review tissue workup methods for matrisome proteomics, glycomics and glycoproteomics.
  • •The combination of proteomics, glycomics and glycoproteomics profiles matrisome protein modifications distinct from those studied by immunohistochemistry.
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16.
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Highlights
  • •Development of a method for low-abundance small protein analysis in human plasma.
  • •Deep proteome profiling demonstrated unbiased identification of diverse factors.
  • •Method enabled identification of a novel human plasma protein C5ORF46.
  • •Analysis of intermittent fasting response showed changes in iron regulation.
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17.
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Highlights
  • •Bayesian Beta-Binomial model integrates ion statistics with peptide ratio agreement.
  • •Model appropriately interprets information from low signal peptides.
  • •Confidence can be assigned even without replicates.
  • •Model adds sensitivity to detection of small changes.
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18.
19.
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Highlights
  • •Comprehensive analysis of inter-individual variation of normal urinary proteome.
  • •Significant gender differences were observed.
  • •Proteins increased in female urine are enriched in immunological pathways.
  • •Estimated reference intervals of proteins as the baseline for biomarker discovery.
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20.
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Highlights
  • •Construction of threespine stickleback gill assay library using DDA proteomics
  • •Population-specific gill proteome signatures of four ecotypes identified by DIA
  • •HSP47 and extracellular matrix proteins highly elevated in warm-adapted sticklebacks
  • •Inflammasome and proteolytic proteins highly elevated in freshwater sticklebacks
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