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1.
2.
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Highlights
  • •In-depth proteome underpins the gland ontogeny and age-specific activity of the HGs.
  • •The well-developed acini in the HGs of NBs promote the RJ secretary activities.
  • •The enhanced protein and energy metabolism in the HGs boost the stronger RJ secretion of RJBs.
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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
  • •Dimethyl fumarate covalently modifies cysteine residues in neurons and astrocytes.
  • •Cofilin-1, tubulin and collapsin response mediator protein 2 (CRMP2) are targets.
  • •DMF-modified cofilin-1 reduces actin-severing ability, preserving filamentous actin.
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5.
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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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6.
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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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7.
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Highlights
  • •Three novel Conodipines P1-3 in the injected venom of Conus purpurascens.
  • •Conodipines P1-3 have consensus catalytic characteristics of sPLA2.
  • •We determined multiple modification sites in Conodipines P1-3.
  • •Evaluated the activity of Conohyal-P1 by a MS-based method.
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8.
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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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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
  • •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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11.
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Highlights
  • •Multiplex epitope mapping/antigenic determinant identification in the gas phase.
  • •Intact transition and controlled dissociation of immune complexes by MS.
  • •Simultaneous identification and amino acid sequence determination of epitopes.
  • •Simplified in-solution sample handling because of ion manipulation and filtering by MS.
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12.
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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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14.
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Highlights
  • •Kallikrein-related peptidase 7 is over expressed in ovarian cancer.
  • •Quantitative PROTOMAP and TAILS approaches identified putative substrates of KLK7.
  • •Pro-MMP10 is activated by KLK7.
  • •KLK7 cleaves thrombospondin 1 and IGFBP6 in vitro.
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15.
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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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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
  • •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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18.
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Highlights
  • •Intensive investigation of dynamic interactions in MyD88, TRAF6, and NEMO complexes.
  • •Mechanistic insights into IRAKs proteins' assembly.
  • •A signal amplification mechanism for MyD99-denpendent TLR signaling disclosed by stoichiometry of complexes.
  • •Quantitative measurement of multiple phosphorylation sites on the key components in TLR signaling pathway.
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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
  • •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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