共查询到20条相似文献,搜索用时 31 毫秒
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《Molecular & cellular proteomics : MCP》2020,19(1):181-197
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- •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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《Molecular & cellular proteomics : MCP》2020,19(6):944-959
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- •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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《Structure (London, England : 1993)》2021,29(10):1192-1199.e4
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《Developmental cell》2022,57(7):930-944.e6
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《Molecular & cellular proteomics : MCP》2020,19(1):1-10
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- •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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《Cell reports》2023,42(3):112140
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《Molecular & cellular proteomics : MCP》2020,19(3):540-553
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- •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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《Molecular & cellular proteomics : MCP》2020,19(4):574-588
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- •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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Halogenases: diverse structures mediating distinctive chemistries. 相似文献
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《Molecular & cellular proteomics : MCP》2020,19(7):1132-1144
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- •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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《Molecular & cellular proteomics : MCP》2020,19(6):1058-1069
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- •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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Tirsa L. E. van Westering Henrik J. Johansson Britt Hanson Anna M. L. Coenen-Stass Yulia Lomonosova Jun Tanihata Norio Motohashi Toshifumi Yokota Shin'ichi Takeda Janne Lehti Matthew J. A. Wood Samir EL Andaloussi Yoshitsugu Aoki Thomas C. Roberts 《Molecular & cellular proteomics : MCP》2020,19(12):2047-2068
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- •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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Fengchao Yu Sarah E. Haynes Guo Ci Teo Dmitry M. Avtonomov Daniel A. Polasky Alexey I. Nesvizhskii 《Molecular & cellular proteomics : MCP》2020,19(9):1575-1585
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- •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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A Quantitative Tri-fluorescent Yeast Two-hybrid System: From Flow Cytometry to In cellula Affinities
《Molecular & cellular proteomics : MCP》2020,19(4):701-715
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- •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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