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1.
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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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2.
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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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3.
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Highlights
  • •Zero-length chemical cross-linking of APOA1 peptides in HDL.
  • •Cross-links match antiparallel isomers of APOA dimers in molecular modeling.
  • •Identical MS/MS spectra of native and synthetic cross-linked peptides.
  • •First biochemical evidence of LL5/5 and LL5/4 isomers in human HDL.
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4.
5.
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Highlights
  • •Hsp70 homologs differ in their oligomeric properties in the presence of ATP.
  • •Human inducible Hsp70 forms ATP-dependent anti-parallel dimers with high propensity.
  • •Dimerization of ATP-bound Hsp70 is required for effective Hsp70-Hsp40 interaction.
  • •ATP-dependent interaction with Tomm34 TPR cochaperone disrupts Hsp70 dimer.
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6.
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Highlights
  • •Frequent genetic polymorphism affects the glycosylation pattern of fetuin.
  • •Personalized in-depth proteoform profiling of fetuin purified from 20 donors.
  • •Classification of serum donors into three different genotypes.
  • •Septic patients show increased level of fucosylation at N-glycolation site N176.
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7.
8.
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Highlights
  • •Quantitative microproteomics to study the CNS and PNS of the Twitcher mouse.
  • •10plex TMT experiments on corpus callosum, motor cortex and sciatic nerves extracts.
  • •More than 400 proteins groups deregulated between Twitcher and wildtype mice.
  • •New insights into the molecular mechanisms of Krabbe disease.
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9.
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Highlights
  • •Chemical proteomics strategy for quantitative profiling of phosphoprotein phosphatases.
  • •Compatible with quantitative multiplexing approaches.
  • •Applicable to many samples types including tissues from human to yeast.
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10.
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Highlights
  • •Automated analysis of protein complexes in proteomic experiments.
  • •Quantitative measurement of the coordinated changes in protein complex components.
  • •Interactive visualizations for exploratory analysis of proteomic results.
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11.
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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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12.
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Highlights
  • •Quantitative cross-linking mass spectrometry (QCLMS) was automated by Spectronaut.
  • •Data-independent acquisition (DIA) was adapted to QCLMS.
  • •Accuracy and precision of quantitation improves with DIA over DDA.
  • •QCLMS is now ready for use in complex samples.
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13.
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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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14.
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Highlights
  • •Functional role of a yet uncharacterized receptor kinase QSK1.
  • •Activation model for SIRK1 receptor kinase in a heteromer with QSK1.
  • •Role of QSK1 in substrate recruitment and stabilization of the complex.
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15.
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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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16.
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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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17.
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Highlights
  • •BioID with Golgi fractions identified C10orf76 as proximal to GBF1.
  • •Tagged C10orf76 overlaps with Golgi markers.
  • •C10orf76 binds GBF1 and exchanges rapidly between free and bound forms.
  • •C10orf76 is essential for maintenance of the Golgi and for secretion.
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18.
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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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19.
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Highlights
  • •Method to probe the isomeric variants of the glycans attached to purified proteins.
  • •Uses multiple rounds of glycosidase cleavage and lectin profiling.
  • •Computation integration of lectin-binding, glycan-array, and mass spectrometry data.
  • •Applied to microspots for compatibility with analyzing low-abundance proteins.
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20.
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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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