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1.
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Highlights
  • •First report on the quantitative proteomic profiling of Drosophila lymph glands.
  • •Comparative proteomic analysis under conditions of perturbed blood cell homeostasis.
  • •Resource for identifying new regulators of insect and vertebrate hematopoiesis.
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2.
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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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3.
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Highlights
  • •Quantitative global proteome, acetylome and succinylome of phytoplasma-infected Paulownia tomentosa seedlings.
  • •Acetylation may be more important than succinylation in response to phytoplasma infection.
  • •Acetylation modified the activities of POR and RuBisCO.
  • •Possible model to elucidate the molecular mechanism responses to PaWB from proteome and PTMs.
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4.
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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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5.
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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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6.
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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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7.
8.
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Highlights
  • •nLC-MS/MS method to analyze immunoglobulin (Ig) N-glycopeptides from human serum.
  • •Multi-isotype, site-specific characterization of immunoglobulin N-glycosylation.
  • •IgA2 sequence and glycosylation-site variant analyses.
  • •Platform to define disease-specific N-glycan signatures for different Ig isotypes.
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9.
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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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10.
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Highlights
  • •Plant mitoribosomes contain several pentatricopeptide repeat proteins.
  • •The small mitoribosomal subunit is of an exceptionally large size.
  • •Protein units not directly related to translation may be attached to plant mitoribosomes to confer additional functions to these molecular machines.
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11.
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Highlights
  • •A panel of HEK293 isogenic cell lines with knockout of GALNT genes.
  • •Identification of nonredundant O-glycosylation sites regulated by specific GalNAc-T isoforms.
  • •GalNAc-T7 and T10 contribute to follow-up activity in regions of high density O-glycosylation.
  • •GalNAc-T11 specifically controls O-glycosylation of specific linker regions in the low-density lipoprotein receptor related proteins.
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12.
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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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13.
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Highlights
  • •Auxin responsive proteins in Arabidopsis roots were identified from 3,514 detected proteins.
  • •All six auxin receptors are stable in response to hormone via novel MRM assays.
  • •The >100 differentially expressed proteins exhibit dynamic and transient responses to auxin.
  • •Phenotypic screening of the top responsive proteins uncovered several novel root mutants.
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14.
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Highlights
  • •Atlantic salmon O-glycome expanded to 169 structures in three epithelia.
  • •Low interindividual variation amongst all populations and geographical regions.
  • •Small variations in glycosylation between geographical locations and fish size.
  • •Prominent fucosylation in gastrointestinal mucins from Tasmanian fish.
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15.
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Highlights
  • •Cts L−/− cells proliferate faster than wild types and shift to aerobic glycolysis.
  • •LDHA is a key glycolytic enzyme controlling Cts L−/− cell proliferation.
  • •Cts L regulates LDHA expression and function.
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16.
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Highlights
  • •Identification of previously undetected chloroplast envelope proteins.
  • •Up to date manual annotation of genuine (or shared) envelope components.
  • •New hypotheses for localizations, functions, interactions among cell compartments.
  • •A new resource of significant value to the broader plant science community.
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17.
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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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18.
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Highlights
  • •SWATH-MS profiles protein abundance and modification during mashing in beer brewing.
  • •Proteolysis due to barley proteases leads to extreme proteoform diversity.
  • •Sequence-specific proteolytic clipping of proteins controls their stability.
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19.
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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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20.
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Highlights
  • •Rapamycin and zinc induce moderate but significant mitochondrial proteome changes.
  • •The mitochondrial proteins processing system is robust under subtoxic conditions.
  • •Rapamycin and zinc perturb the mitochondrial proteins processing system.
  • •Rapamycin and zinc perturb the mitochondrial proteins homeostasis.
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