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1.
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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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2.
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Highlights
  • •Two-step cross-linking coupled with affinity purification to facilitate structural analysis of protein complexes.
  • •Integrated QXL-MS workflow for studying condition-dependent structural changes of protein complexes.
  • •Mechanistic insights on in vivo H2O2-induced conformational dynamics of proteasome complexes.
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3.
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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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4.
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Highlights
  • •Protein interaction screen of SETD1A/COMPASS complex subunits.
  • •Unexpected interaction with DNA damage protein RAD18 was confirmed for SETD1A, but not for other subunits.
  • •SETD1A and/or RAD18 influence each other's mRNA and protein expression levels, and disruption of either gene elicits a similar DNA damage sensitivity phenotype.
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5.
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Highlights
  • •mRNA-seq, miRNA-seq, proteomes of P. fulvidraco, P. vachelli, hybrid Huangyou-1.
  • •Predicted miRNA-mRNA-protein pairs were found and validated by qRT-PCR and PRM.
  • •Immune, metabolism, digestion, absorption, proliferation, development generate heterosis.
  • •High parental gene/protein with low parental miRNAs inherit from the mother or father.
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6.
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Highlights
  • •Open source software for comprehensive HDX-MS data analysis.
  • •Automatic back-exchange correction options.
  • •Rigorous statistical analysis of the significance of uptake differences.
  • •High quality visualization tools.
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7.
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Highlights
  • •Over 1700 Arabidopsis proteins with thermal models in multiple replicates.
  • •Melting temperature correlates with 1°, 2°, and 3° protein characteristics.
  • •Ligand-induced thermal shifts are evident in complex protein extracts.
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8.
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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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9.
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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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10.
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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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11.
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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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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
  • •Quantitative proteomes and epigenetic regulation of T. gondii.
  • •Protein crotonylation and 2-hydroxyisobutylation in phenotypically different T. gondii parasites.
  • •Regulation of invasion regulation of T. gondii by protein modification.
  • •Lysine crotonylation and 2-hydroxyisobutylation regulated in multiple biological processes in phenotypically different T. gondii parasites.
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14.
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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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15.
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Highlights
  • •The developed Ac-LysargiNase showed higher stability and activity than before.
  • •The merged spectra of the mirror peptides achieved nearly complete ion coverage.
  • •pNovoM obviously increased the efficiency and accuracy of peptide sequencing.
  • •The mirror enzymatic strategy achieved precision de novo sequencing on proteome scales.
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16.
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Highlights
  • •Our search identifies 2,134 kinase-substrate phosphosite pairs in breast cancer.
  • •CDKs and MAPKs are dominant regulators of trans substrate-phosphorylation.
  • •Druggability, outcomes, and immune signatures related to kinase-substrates.
  • •Experimentally validated activated phosphosites of ERBB2, EIF4EBP1, and EGFR.
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17.
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Highlights
  • •Proteome of mature boar spermatozoa from cauda epididymal and ejaculated sources were analyzed by iTRAQ-based LC-MS/MS.
  • •1,723 sperm proteins identified (974 of Sus scrofa taxonomy).
  • •1,602 sperm proteins quantified (960 of Sus scrofa taxonomy).
  • •32 Sus scrofa sperm proteins were differentially expressed among sperm sources.
  • •The proteome of boar spermatozoa is remodelled during ejaculation.
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18.
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Highlights
  • •Proteomic landscapes of Drosophila somatic and reproductive tissues during aging.
  • •Pulsed metabolic labeling determines a decline in protein synthesis with age.
  • Drosophila model of human Parkinson's disease signifies an early-onset decline in protein synthesis.
  • •Collapse of proteostasis and mitochondria are early signals for normal aging.
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19.
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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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20.
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Highlights
  • •Identification of the substrates profile of the endothelial phosphatase VE-PTP.
  • •A large fraction of VE-PTP substrate candidates (29%) is cell junction related.
  • •Tie-2 and EPHB are substrates which associate as ternary complex with VE-PTP.
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