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1.
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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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3.
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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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4.
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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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5.
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Highlights
  • •Signaling networks can be highly heterogeneous across cells in a tissue.
  • •Various technologies allow analyzing signaling networks at single-cell resolution.
  • •The advantages and limitations of each single-cell approach are summarized.
  • •Confounding factors in single-cell signaling network analysis are discussed.
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6.
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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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7.
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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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8.
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Highlights
  • •Modern DIA methods contain high quality MS1 and MS2.
  • •We developed a statistical procedure incorporating MS1 and MS2.
  • •Benchmarking, the combined method outperformed the individual use of MS1 or MS2.
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9.
10.
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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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11.
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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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12.
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Highlights
  • •Rapid DIA-only library building with gas-phase fractionation.
  • •Recommended DIA acquisition strategies with staggered windows and forbidden zones.
  • •Optimized DIA instrument settings for several Thermo Orbitrap instruments.
  • •Data analysis tutorial using open source DIA software.
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13.
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Highlights
  • •ProAlanase is a powerful protease for efficient low pH disulfide bond mapping.
  • •High suitability for analysis of histone family members and their PTMs.
  • •Accurate phosphorylation profiling in proline-rich proteins.
  • •Sequence coverage increase and full de novo sequencing in combination with trypsin.
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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
  • •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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16.
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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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17.
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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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18.
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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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19.
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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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20.
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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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