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1.
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Highlights
  • •Cross-linked peptides are physically separated from mono-linked peptides in the gas-phase by TIMS ion mobility.
  • •Development of a novel data acquisition routine that a-priori distinguishes cross-linked from mono-linked peptides called caps-PASEF.
  • •First application of PhoX-driven cross-linking mass spectrometry on the timsTOF Pro.
  • •Application of cross-linking mass spectrometry to medium to high complexity samples.
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2.
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Highlights
  • •Brain membrane protein extraction.
  • •Protein prenylation.
  • •Prenyl peptide capture and characterization by LC-MS/MS.
  • •HCD and EThcD peptide fragmentation.
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3.
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Highlights
  • •Curation of 2066 phosphorylated HLA class I peptides from immunopeptidomics data.
  • •Determination of 22 HLA class I binding motifs for phosphorylated peptides.
  • •Observation of a higher frequency of phosphorylated ligands binding HLA-C molecules.
  • •Development of a predictor of phosphorylated peptide interactions with HLA class I.
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4.
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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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5.
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Highlights
  • •Comprehensive sialiomics of isolated rat synaptosomes.
  • •Site-specific modulation of sialic acids on surface glycoproteins after brief depolarization.
  • •Sialylation as dynamic modification important for synaptic depolarization-dependent processes.
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6.
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Highlights
  • •Laser microdissection of highly vulnerable hippocampal region.
  • •Proteomic analysis of postmortem human brain tissue of AD and control cases.
  • •Decreased levels of presynaptic proteins, but not postsynaptic proteins, in AD.
  • •Immunohistochemistry verifies decreased levels of selected presynaptic proteins.
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7.
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Highlights
  • •EGFR-TKI molecular response profiling covering 10138 proteins and 13486 mRNAs.
  • •EGFR-TKI combination therapy screen using a library of 528 compounds.
  • •Several new candidate EGFR-TKI escape mechanisms and combination therapy targets.
  • •Combined targeting of the oncogene BCL6 and EGFR results in synergy in NSCLC cells.
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8.
9.
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Highlights
  • •Comprehensive molecular profiling of cutaneous and cerebellar metastasis variants.
  • •Identification of differentially regulated metastasis-associated molecules.
  • •Evidence for individually distinct patterns of metastasis-associated molecules.
  • •Highlighting the evident need for establishing meta-analyses strategies.
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10.
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Highlights
  • •DEqMS is a method for statistical analysis of quantitative MS-data.
  • •Variance estimates based on the actual MS-data structure.
  • •Improved statistical power and accuracy in protein differential analysis.
  • •DEqMS is available as a user-friendly R package in Bioconductor.
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11.
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Highlights
  • •Epitope-tagging of a proteasome subunit allows for facile immuno-isolation.
  • •An engineered yeast strain permits capture of proteasome-associated substrates.
  • •MS/MS identified all 33 resident proteasome subunits in the 20S and 19S particles.
  • •Analysis of associated proteins and characterization of newly identified ERAD substrate.
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12.
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Highlights
  • •Guidelines for studying protein complexes via co-fractionation mass spectrometry.
  • •A novel procedure for profiling gold standard protein complexes in CF-MS data.
  • •Recommendations for efficient CF-MS fractionation collection.
  • •Scoring metric recommendations for precise and sensitive CF-MS data analysis.
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13.
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Highlights
  • •NCMR is crucial for substrate recognition and activity regulation.
  • •MASTL conserves a cryptic C-Lobe in the non-conserved middle region.
  • •MASTL450 containing the cryptic C-lobe is observed in cancer cell lines.
  • •Key phosphorylation sites for MASTL provide an activation model.
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14.
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Highlights
  • •Quantitative mass spectrometric method to monitor PTM stability.
  • •Pulse labeling reveals dehydroxylation of several asparagine hydroxylation sites.
  • •Reversal of TNKS2, TRPV3 and HIF1a asparagine hydroxylation sites.
  • •Protein dehydroxylation is an additional level of control for cellular signaling networks.
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15.
16.
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Highlights
  • •Proximity-dependent biotinylation (PDB) approaches involve fusion of a bait with an enzyme.
  • •BioID (biotin protein ligase) and APEX (peroxidase) are distinct enzymes used in PDB.
  • •Past, present and future development and applications of PDB are discussed.
  • •We review labeling mechanisms and kinetics to provide guidance for experimental design.
  • •We discuss controls and considerations for data interpretation.
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17.
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Highlights
  • •Label-free and dimethyl labeling MS analysis of 6 RBPs from Drosophila ovaries.
  • •Functionally related RBPs show overlapping proteomes.
  • •Selective co-purification of splicing factors and translational regulators.
  • •Validation of 26 novel interactions by co-immunoprecipitation.
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18.
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Highlights
  • •In-depth proteomes of 4 SARS-CoV-2 cell line models (Vero E6, Calu-3, Caco-2, A549).
  • •Proteomic evidence for thousands of Chlorocebus sabaeus proteins.
  • •Proteomic response of Vero E6 cells to SARS-CoV-2 infection.
  • •Synthetic peptides, spectral libraries, and targeted assays for SARS-CoV-2 proteins.
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19.
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Highlights
  • •Highly parallelizable 4D feature detection in ion mobility enhanced shotgun proteomics.
  • •Multidimensional non-linear mass, retention time and ion mobility recalibration.
  • •Collision cross section aware matching between runs.
  • •Label-free quantification of ion mobility MS data.
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20.
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Highlights
  • •SILAC-based protein quantification of OA hBMSCs undergoing chondrogenesis.
  • •Spatially-resolved metabolomics by MSI of hBMSCs in chondrogenic differentiation.
  • •Differential metabolic pathways involved in OA compared to control hBMSCs.
  • •UDP-glucuronic acid/UDP-GlcNAc synthesis is decreased in chondrogenic OA hBMSCs.
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