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1.
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Highlights
  • •Lectins and glycan-binding antibodies are valuable as probe of glycans.
  • •Advanced bioinformatics tools enable the mining of glycan-array data.
  • •New insights into protein-glycan interactions have value in biological research.
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2.
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Highlights
  • •A broad-based interlaboratory study of the glycosylation of a reference antibody: NISTmAb.
  • •103 reports were received from 76 diverse laboratories worldwide.
  • •Analysis involved two samples, the NISTmAb and an enzymatically modified sample, enabling within-lab separation of random and systematic errors using the “Youden two-sample” method.
  • •Consensus values were derived and similar performance across all experimental methods was noted.
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3.
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Highlights
  • •Changes in N-linked glycosylation in influenza A virus affect antigenicity of the virus.
  • •Glycosylation similarity can be quantified, even in heterogeneously glycosylated proteins.
  • •Glycosylation is measurably and site-specifically distinct in influenza from related strains.
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4.
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Highlights
  • •Rapid DIA-only library building with gas-phase fractionation.
  • •Recommended DIA acquisition strategies with staggered windows and forbidden zones.
  • •Optimized DIA instrument settings for several Thermo Orbitrap instruments.
  • •Data analysis tutorial using open source DIA software.
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5.
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Highlights
  • •MSFragger now supports raw timsTOF PASEF data.
  • •IonQuant performs fast and accurate feature detection and quantification.
  • •MSFragger and IonQuant provide excellent performance for timsTOF PASEF data.
  • •Flexibility allows for complex analyses, such as semi-enzymatic and open search.
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6.
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Highlights
  • •OpenPepXL is a new XL-MS identification tool with a high sensitivity.
  • •It is available for all common operating systems and remote computing environments.
  • •OpenPepXL is open source and supports open OpenPepXL is available as part of OpenMS data formats like mzML and mzIdentML.
  • •at https://www.openms.de/openpepxl.
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7.
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Highlights
  • •Co-elution stands out as a global interactome mapping method.
  • •Benefits include all-to-all protein analysis and measurement of interactome perturbations.
  • •Different separation, quantification and bioinformatic strategies are available.
  • •Design considerations depend largely on system under study.
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8.
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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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9.
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Highlights
  • •cGAS acetylations and phosphorylations under basal and immune-stimulated states.
  • •K384 and K414 acetylations and S305 phosphorylation inhibit cGAS-mediated apoptosis.
  • •Acetylation at K198 stimulates cGAS-dependent interferon signaling.
  • •K198 acetylation is decreased upon herpesvirus infection.
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10.
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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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11.
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Highlights
  • •Modern DIA methods contain high quality MS1 and MS2.
  • •We developed a statistical procedure incorporating MS1 and MS2.
  • •Benchmarking, the combined method outperformed the individual use of MS1 or MS2.
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12.
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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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13.
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Highlights
  • P. aeruginosa grown with exosiderophores and analyzed by proteomic and RT-qPCR.
  • •Catechol-type exosiderophores strongly induce the expression of their transporters.
  • •Repression of the endogenous iron uptake pathways.
  • •Complex phenotypic plasticity in the expression of the various iron-uptake pathways.
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14.
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Highlights
  • •Two molecular groups in anal squamous carcinoma according proteomic profile.
  • •Differences in possible targeted processes such as metabolism or immune response.
  • •Different percentage of tumor lymphocyte infiltration.
  • •Difference in the frequency of ATM variants, related to PPAR inhibitors.
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15.
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Highlights
  • •Acute inhibition of growth-regulatory AGC-kinases Sch9, PKA and Ypk1.
  • •Phospho-proteomic profiling of 6373 phsopho-sites.
  • •Ypk1 regulates phospho-sites in RRxS/T-context and functionally overlaps with PKA.
  • •Ypk1 and PKA activate trehalase activity of Nth1.
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16.
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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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17.
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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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18.
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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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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
  • •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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