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1.
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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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2.
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Highlights
  • •Summarize the development of functional protein microarray.
  • •Application of functional proteome microarray in basic research.
  • •Application of functional proteome microarray in translational research.
  • •Fabrication of functional membrane protein array using virion display method.
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3.
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Highlights
  • •Increased proteome coverage with Orbitrap Exploris 480 MS and FAIMS using single compensation voltages and short LC gradients.
  • •Towards single-cell proteomics with high-sensitivity analysis of 5 ng HeLa with more than 1,000 proteins identified in 5 minutes using FAIMS and DIA.
  • •Deep proteome profiling across twelve rat organs tissues by label-free quantitation using DIA compared to TMT-multiplexing and turboTMT acquisition using phi-SDM.
  • •Rapid and sensitive phosphoproteomics with automated enrichment using Ti-IMAC magnetic beads and direct DIA analysis.
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4.
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Highlights
  • •Mutant Tau dysregulates exosome cargo generated by human iPSC neurons.
  • •Expression of P301L and V337M mutations of Tau in human iPSC neurons result in recruitment of distinct proteins to exosomes, and absence of control proteins to exosomes.
  • •Tau mutations of FTDP-17 result in up- and downregulation of exosome proteins.
  • •Altered proteome cargo of mTau exosomes may be involved in Tau pathogenesis in vivo in brain.
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7.
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Highlights
  • •Quantitative proteome interactions with 5 different C9ORF72 dipolypeptides (DPRs).
  • •The arg-rich DPRs promiscuously bound to the proteome compared with the other DPRs.
  • •Long repeat lengths of arg-rich DPRs, but not short lengths, stalled ribosomes.
  • •The arg-rich DPRs also reduced arginine methylation and actin cytoskeleton assembly.
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8.
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Highlights
  • •A detailed investigation of the protein extraction step from FFPE tissue is shown.
  • •Acidification during peptide wash increased peptide recovery of the SP3 method.
  • •LCM of substantia nigra enriched neuron-specific proteins including TH.
  • •>5,600 proteins were quantified using 3000 cells per sample from substantia nigra.
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9.
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Highlights
  • •Urinary proteomes of patients with recurrent UTI, renal scarring, and VUR.
  • •80 proteins differentially expressed, compared to healthy controls.
  • •62 proteins may be indicative of susceptibility for UTI.
  • •Altered acute phase response, extracellular matrix and carbohydrate metabolism.
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10.
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Highlights
  • •Cecal Ligation Puncture (CLP) mouse model to study sepsis-induced kidney disease.
  • •Quantitative global proteome and phosphoproteome profiling of mouse kidneys.
  • •Highly significant candidate markers for onset and progression of AKI to CKD.
  • •Mechanistic insights into sepsis-associated kidney injuries.
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11.
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Highlights
  • •Repeatable quantification of 200 proteins in dried blood spots.
  • •Determined lower limit of quantification, repeatability, parallelism and stability.
  • •Protein stability in DBS stored at ambient temperatures for up to 2 months.
  • •Concentration ranges for 200 proteins in 20 healthy individuals.
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12.
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Highlights
  • •Salivary secretion was increased by mouth rinsing with TRP channel agonists.
  • •The salivary proteome varied over time and was changed by TRP channel stimulation.
  • •Immunoreactive Cystatin S was increased in saliva after TRPV1 stimulation.
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13.
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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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14.
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Highlights
  • •TOP: robust, bio-friendly FFPE proteome extraction method with less fixation bias.
  • •Proteome of MSI-H colorectal cancer identifies immunobiology key elements.
  • •MSI-H tumor displays an “INFg-STAT1 centric signature”.
  • •Long-term IFNg induction In-vitro mimicks MSI-H signature.
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15.
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Highlights
  • •Organelle profiling maps capture localizations of 1000s of proteins in one experiment.
  • •Comparing maps +/− perturbation reveals disease mechanisms & cellular responses.
  • •A conceptual guide to planning and interpreting organellar profiling experiments.
  • •A cross-study consensus set of human organellar marker proteins.
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16.
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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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17.
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Highlights
  • •In-depth profiling of the serum proteome in early-stage COVID-19 patients.
  • •A landscape of inflammation and immune signaling related to the SARS-CoV-2 infection.
  • •CCL2 and CXCL10 medicated cytokine signaling pathways may correlate with neutrophil and lymphocyte respectively.
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18.
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Highlights
  • •TOF-SIMS allows to visualize normal brain and tumor border.
  • •Glioma samples can be subdivided into clinically relevant groups by TOF-SIMS data.
  • •TOF-SIMS allows to simultaneously detect proteins and metabolites in clinical samples.
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19.
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Highlights
  • •Quantitative proteomics of isolated lysosomes, autophagosomes and proteasomes.
  • •Pharmacological inhibition of proteasomes leads to their accumulation within lysosomes.
  • •Inhibition of classical autophagy pathways cannot completely block this process.
  • •Known autophagy adaptor proteins are not involved.
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20.
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Highlights
  • •Affinity-based proteomics of infected macrophage cells.
  • Salmonella-modified membranes exhibit host-specific composition.
  • •Proteome differences explain some host-dependent pathophysiological differences.
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