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1.
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2.
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Highlights
  • •Provision of data generated on the basis of a gold standard spike-in sample set.
  • •Choice of spectral library has great impact on identification and quantification.
  • •DIA is superior to DDA in quantification reproducibility, specificity and accuracy.
  • •DIA outperforms DDA in the quantification of low protein amounts.
  • •Quantification on peptide level is generally preferable.
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3.
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4.
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Highlights
  • •Automated statistical approach for detecting uninformative features and outliers.
  • •Improved performance on relative protein quantification.
  • •An option in the open-source R-based software MSstats.
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5.
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6.
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7.
《Developmental cell》2022,57(7):930-944.e6
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8.
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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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9.
《Cell reports》2023,42(3):112140
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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
  • •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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12.
《Cell》2021,184(25):6022-6036.e18
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13.
Halogenases: diverse structures mediating distinctive chemistries.
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14.
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Highlights
  • •Proteomes measured from human heart biopsies collected in-vivo covers >7000 cardiac proteins and highlight hundreds of chamber-specific molecular signatures that meaningfully reflect the specialized functions of the respective chambers.
  • •Protein quantification from freshly collected biopsies is preferential to necropsy samples because of unspecific post-mortem protein degradation in the latter.
  • •Increased abundances of proteins associated with sustained atrial fibrillation are not a sufficient condition to generate the disease state.
  • •Protein abundance differences between atria and ventricle primarily originate at the level of gene regulation and reflect a functional need.
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15.
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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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16.
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Highlights
  • •Proteomics analysis was performed in two murine models of Duchenne muscular dystrophy (mdx and mdx52) at three ages (8, 16 and 80 weeks) and compared with wild-type controls.
  • •High-resolution isoelectric focusing liquid chromatography-tandem mass spectrometry enabled the quantification of 4974 proteins in all samples.
  • •This study has revealed protein signatures of dystrophin deficiency and the progression of dystrophic pathology.
  • •In contrast, the proteomes of the mdx and mdx52 mice were highly similar.
  • •Pathway analysis revealed crosstalk between inflammatory, metabolic and muscle growth processes in dystrophic muscle.
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17.
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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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18.
19.
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Highlights
  • •Simultaneous quantification of Bait, Prey and Reporter at the single cell level.
  • •Two hours of reaction are enough instead of 24–48 h for conventional assays.
  • •Potential expression problems of the Bait and Prey can be easily detected.
  • •True positive PPIs feature a distinct pattern of Reporter level versus Bait/Prey level.
  • •PPIs with unknown affinities can be ranked using an affinity ladder.
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20.
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