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1.
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Highlights
  • •Quantitative proteomics of mitotic chromosome scaffold isolated from chicken DT40 cells.
  • •BAZ1B identified in the isolated mitotic chromosome scaffold localizes to mitotic chromosome axes.
  • •BAZ1B knockout caused prophase delay because of altered chromosome condensation timing and impaired mitosis progression.
  • •BAZ1B knockout did not affect prometaphase chromosome structure.
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2.
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Highlights
  • •MEEC are a reliable endocardial in vitro model.
  • •Quantitative proteomics to characterize the NOTCH-driven endocardial secretome.
  • •NOTCH pathway status underlies different paracrine biological functions.
  • •New insights into secreted factors involved in cardiac valve development.
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3.
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Highlights
  • •OMICS distinguish cancer cells from resistant or cancer stem cells.
  • •Bactericidal antibiotics and mitochondria.
  • •Linezolid and anticancer therapy.
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4.
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Highlights
  • •microRNA-222 attenuates TGEV-induced mitochondrial dysfunction.
  • •microRNA-222 downregulates THBS1 and CD47.
  • •THBS1 is the target of microRNA-222 during TGEV infection.
  • •THBS1 and CD47 increase mitochondrial Ca2+ level and reduced mitochondrial membrane potential (MMP).
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5.
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Highlights
  • •Surface loops play an essential role in SH2 domain specificity.
  • •Diverse specificities may be obtained from a single SH2 domain by combinatorial mutations in the EF and BG loops.
  • •The specificity of a loop mutant correlates with the sequence characteristics of the bait peptide used in its isolation.
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6.
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Highlights
  • •This study reports the first proteomic characterization of a type II hemidesmosomal complex.
  • •This study characterizes the interactome of β4-integrin in the presence and absence of α6-integrin in a simple epithelial cell model.
  • •The assembly of the β4-integrin interacting complex was largely independent of α6-integrin expression.
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7.
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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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8.
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Highlights
  • •Definition of early systemin-responsive phosphorylation time course.
  • •Reconstruction of kinase-substrate relationships from phosphorylation time profiles.
  • •Phosphatase PLL5 rapidly dephosphorylated H+-ATPase LHA1 inducing alkalinization of the medium.
  • •MAP-Kinase MPK2 re-phosphorylated LHA1 after 15 minutes.
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9.
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Highlights
  • •In-depth proteome profiling of primary human myeloma cells
  • •Characteristics of myeloma cells are related to hypoxic bone marrow conditions
  • •Myeloma cells show specific immune evasion strategies
  • •Metabolic adaptations involve tumor and stroma cells
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10.
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Highlights
  • •Mice lacking Wip1 display spermatogenesis defects at the late-stage germ cell types.
  • •Proteome and phosphoproteome profiling reveals impaired dynamics of testis junction.
  • •Elevated levels of cytokines may lead to abnormal BTB structure and spermatogenesis.
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11.
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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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12.
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Highlights
  • •Anticancer activity of midostaurin but not other PKC inhibitors in NSCLC cells.
  • •Mechanism of action by network-based integration of chemo- and phosphoproteomics.
  • •Midostaurin polypharmacology by simultaneous inhibition of TBK1, PDPK1 and AURKA.
  • •Design of synergistic drug combination with PLK1 inhibitor by pathway validation.
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13.
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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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14.
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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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15.
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Highlights
  • •Support for mass spectrometry-based proteomics in cBioPortal.
  • •User-friendly web interface, a web API, and an R client to query proteogenomic data.
  • •Integration of Clinical Proteomics Tumor Analysis Consortium data with cBioPortal.
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16.
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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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17.
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Highlights
  • •Novel PTMs detected in native yeast exosome, RNA polymerase II and proteasome.
  • •MD based approach outperforms published tools in predicting PTMs stability effect.
  • •Dynamical approach reveals long range effects of PTMs on subunits binding.
  • •Acetylations may have a role in local stabilization of protein complex formation.
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18.
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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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19.
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Highlights
  • •MaxQuant.Live controls Orbitrap mass analyzers in real-time.
  • •Freely available apps enable advanced data acquisition strategies.
  • •On-the-fly mass, retention time and intensity recalibration.
  • •Global targeting unifies shotgun and targeted proteomics.
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20.
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