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1.
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Highlights
  • •Proteome analyses reveal RNF146 and TNKS1/2 substrates targeted for degradation.
  • •RNF146 KO and TNKS1/2 DKO cells display significantly different proteomes.
  • •RNF146 has both TNKS-dependent and -independent substrates.
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2.
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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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3.
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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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4.
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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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5.
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Highlights
  • •Epitope-tagging of a proteasome subunit allows for facile immuno-isolation.
  • •An engineered yeast strain permits capture of proteasome-associated substrates.
  • •MS/MS identified all 33 resident proteasome subunits in the 20S and 19S particles.
  • •Analysis of associated proteins and characterization of newly identified ERAD substrate.
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6.
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Highlights
  • •Quantitative analysis of Plasmodium sexual stage egress secretome.
  • •Activated gametocytes release gender-related proteins.
  • •Gametocyte egress process involves different types of vesicles.
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7.
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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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8.
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Highlights
  • •Guidelines for studying protein complexes via co-fractionation mass spectrometry.
  • •A novel procedure for profiling gold standard protein complexes in CF-MS data.
  • •Recommendations for efficient CF-MS fractionation collection.
  • •Scoring metric recommendations for precise and sensitive CF-MS data analysis.
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9.
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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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10.
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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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11.
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Highlights
  • •Integrated phosphoproteomics and analyses of newly synthesized proteins in neurons.
  • •Resource of temporal mGluR-induced signaling pathways upon DHPG stimulation.
  • •Validation of PKC, MAPK1, CAMKIIa, and CDK2 in mGluR-activation and signaling.
  • •Validation of Intersectin-1 in DHPG-induced AMPAR internalization.
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12.
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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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13.
14.
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Highlights
  • •Automated statistical approach for detecting uninformative features and outliers.
  • •Improved performance on relative protein quantification.
  • •An option in the open-source R-based software MSstats.
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15.
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Highlights
  • •XL-MS reveals new PPIs in yeast mitochondria under glycerol and glucose condition.
  • •Significant but limited results from quantitative XL-MS experiments.
  • •Ndi1 participates in a CIII2CIV2 respiratory supercomplex.
  • •Min8 promotes assembly of Cox12 into an intermediate complex IV.
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16.
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Highlights
  • •Novel statistical test combining missingness and quantitative profiles.
  • •Unification of different statistical tests into a PolySTest FDR provides higher robustness and confidence.
  • •PolySTest provides higher coverage of relevant biological pathways.
  • •User-friendly interactive web service for statistical analysis and visualization.
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17.
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Highlights
  • •FYN and ABL differentially regulate DCBLD Ser/Thr/Tyr phosphorylation.
  • •DCBLD1 and DCBLD2 interactomes are modulated by FYN and ABL.
  • •ABL drives a direct DCBLD2/14-3-3 interaction.
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18.
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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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19.
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Highlights
  • •Longitudinal monitoring of B cell subsets shows baseline antibody gene expression.
  • •A single, given CDR3 sequence can arise from more than one VJ gene combination.
  • •A healthy individual's V gene usage is stable irrespective of infection and subset.
  • •Surprisingly, class-switched antibodies can occur early in human B cell development.
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20.
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Highlights
  • •Quantitative proteomes of the cellular surface changes induced by mTORC1 signaling.
  • •Hit validation in human cancer cell lines and biopsies.
  • •Functional studies showing new drug targets to which cancer cells with hyperactive mTORC1 may be addicted.
  • •A new paradigm for drug development, namely targeting cell surface proteins regulated by mTORC1.
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