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1.
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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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2.
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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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3.
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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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4.
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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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5.
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Highlights
  • •Higher AGC significantly improves quantitation quality in single-cell analysis.
  • •The boosting-to-sample ratio should be carefully evaluated and optimized.
  • •iBASIL allows for precise quantitation of 1,500 proteins from 104 AML single cells.
  • •iBASIL recapitulates major biological differences in different AML single cells.
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6.
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Highlights
  • •Curation of 2066 phosphorylated HLA class I peptides from immunopeptidomics data.
  • •Determination of 22 HLA class I binding motifs for phosphorylated peptides.
  • •Observation of a higher frequency of phosphorylated ligands binding HLA-C molecules.
  • •Development of a predictor of phosphorylated peptide interactions with HLA class I.
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7.
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Highlights
  • •Organelle profiling maps capture localizations of 1000s of proteins in one experiment.
  • •Comparing maps +/− perturbation reveals disease mechanisms & cellular responses.
  • •A conceptual guide to planning and interpreting organellar profiling experiments.
  • •A cross-study consensus set of human organellar marker proteins.
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8.
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Highlights
  • •Mechanistic insights into ionic liquids and proteins at molecular level.
  • •Extractants prescreen for proteome analysis with MD simulation system.
  • •A loss-less sample preparation method developed for in-depth proteome profiling.
  • •Over 3,300 proteins were confidently identified from 1,000 HeLa cells in a 1 h run.
  • •Label-free quantitative proteome analysis of human liver cancer tissues.
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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
  • •In depth performance assessment of leading tools for differential protein abundance.
  • •Novel fast modular framework MSqRobSum for robust protein summarization and inference.
  • •MsqRobSum outperforms leading protein summarization-based tools.
  • •MSqRobSum is on par with top-performing peptide based tool MSqRob.
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11.
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Highlights
  • •MS-based clinical assay that accurately determines phospho Rab10 occupancy.
  • •Stable isotope labeled phosphopeptide injected as a standard with endogenous tryptic phospho Rab peptide for accurate ratio determination.
  • •Determination of pRab levels in neutrophils of Parkinson disease patients.
  • •Relevance of pRab levels as marker of PD.
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12.
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Highlights
  • •Quantitative proteome of neonatal, young, and aged OPCs.
  • •50% of the proteome is differentially expressed between neonatal and adult OPCs.
  • •Myelin proteins are increased, and cholesterol synthesis proteins decreased with age.
  • •Proteins associated with other neurodegenerative diseases are increased in aged OPCs.
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13.
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Highlights
  • •EGFR-TKI molecular response profiling covering 10138 proteins and 13486 mRNAs.
  • •EGFR-TKI combination therapy screen using a library of 528 compounds.
  • •Several new candidate EGFR-TKI escape mechanisms and combination therapy targets.
  • •Combined targeting of the oncogene BCL6 and EGFR results in synergy in NSCLC cells.
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14.
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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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15.
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Highlights
  • •Urinary peptide profiling of youths with type 1 diabetes before clinical injury.
  • •Internal validation of uromodulin peptides by parallel reaction monitoring.
  • •Discovery of novel bioactivity of uromodulin peptides in vitro.
  • In silico prediction of proteases involved in uromodulin processing.
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16.
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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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17.
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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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18.
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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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19.
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Highlights
  • •Several proteins were found to be unique to each male type.
  • •Expression levels of seven proteins trended downward in teratospermic males.
  • •Several proteins were related to sperm motility and subsequent oocyte binding.
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20.
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Highlights
  • •In-depth proteomes of 4 SARS-CoV-2 cell line models (Vero E6, Calu-3, Caco-2, A549).
  • •Proteomic evidence for thousands of Chlorocebus sabaeus proteins.
  • •Proteomic response of Vero E6 cells to SARS-CoV-2 infection.
  • •Synthetic peptides, spectral libraries, and targeted assays for SARS-CoV-2 proteins.
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