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1.
《Molecular & cellular proteomics : MCP》2019,18(5):936-953
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- •In-depth proteome profiling of primary human myeloma cells
- •Characteristics of myeloma cells are related to hypoxic bone marrow conditions
- •Myeloma cells show specific immune evasion strategies
- •Metabolic adaptations involve tumor and stroma cells
2.
《Molecular & cellular proteomics : MCP》2019,18(12):2516-2523
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- •Open source software for comprehensive HDX-MS data analysis.
- •Automatic back-exchange correction options.
- •Rigorous statistical analysis of the significance of uptake differences.
- •High quality visualization tools.
3.
《Molecular & cellular proteomics : MCP》2019,18(6):1183-1196
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- •Atlantic salmon O-glycome expanded to 169 structures in three epithelia.
- •Low interindividual variation amongst all populations and geographical regions.
- •Small variations in glycosylation between geographical locations and fish size.
- •Prominent fucosylation in gastrointestinal mucins from Tasmanian fish.
4.
《Molecular & cellular proteomics : MCP》2019,18(4):669-685
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- •quantitative phosphoproteome analysis of TDM-activated macrophages.
- •distinct Mincle-dependent and independent phosphorylation and gene regulations.
- •Mincle-dependent activation of PI3K/AKT signaling by TDM.
- •Mincle-independent macrophage response is linked to cell cycle regulation.
5.
《Molecular & cellular proteomics : MCP》2019,18(12):2348-2358
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- •Glycosylation is not currently considered in flu vaccine design.
- •Glycosylation influences on immunodominance are not well understood.
- •Identification of site-specific glycosylation using mass spectrometry has matured.
- •New methods are needed to quantify site-specific glycosylation for vaccine design.
6.
《Molecular & cellular proteomics : MCP》2019,18(10):2121-2137
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- •Endogenous plasma/serum QC marker that quantifies cumulative sample thawed time.
- •Mechanism of marker change known, and rate law established.
- •Data interpretation based on documented population averages and rate law.
- •Blind-challenge verified; utility proven via exposure of undisclosed freezer outage.
7.
《Molecular & cellular proteomics : MCP》2019,18(4):735-743
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- •HPV is being introduced as the primary test in cervical cancer screening programs.
- •New biomarkers are needed for co-testing of women HPV positive in screening.
- •Analysis of plasma from women with invasive cervical cancer identified a 11-marker panel.
- •This signature shows high sensitivity and specificity to identify women with cancer.
8.
《Molecular & cellular proteomics : MCP》2019,18(9):1705-1720
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- •Quantitative changes in global proteome and ubiquitinome in Huntington's disease.
- •Differential ubiquitination of wild-type and mutant Htt in mice brain.
- •Enriched pathways include vesicle transport and mRNA processing.
- •Correlation between protein and diGly site fold changes.
9.
《Molecular & cellular proteomics : MCP》2019,18(4):806-817
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- •Retention time shift can lead to inversion of elution order of peptides.
- •Global alignment methods are suboptimal for alignment of distant runs.
- •DIAlignR employs hybrid (global + local) RT alignment approach.
- •DIAlignR can align swapped peaks accurately across distant runs.
10.
《Molecular & cellular proteomics : MCP》2019,18(9):1796-1806
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- •iTRAQ-based analysis of saliva samples from oral cancer patients.
- •Proteome profiling of saliva samples from patients with oral premalignant lesions.
- •Verification of salivary biomarker candidates with MRM-MS and immunoassays.
- •Identification of salivary proteins as potential biomarkers of oral cancer.
11.
《Molecular & cellular proteomics : MCP》2019,18(11):2298-2309
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- •HLA-B*40:02 and ERAP2 are risk factors for ankylosing spondylitis.
- •The effects of ERAP2 on the B*40:02 peptidome are defined.
- •ERAP2 has a major influence mainly due to alterations of N-terminal residues.
- •These effects provide a basis for the association of ERAP2 with disease.
12.
《Molecular & cellular proteomics : MCP》2019,18(2):308-319
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- •Over 1700 Arabidopsis proteins with thermal models in multiple replicates.
- •Melting temperature correlates with 1°, 2°, and 3° protein characteristics.
- •Ligand-induced thermal shifts are evident in complex protein extracts.
13.
《Molecular & cellular proteomics : MCP》2019,18(3):477-489
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- •Developed a data processing pipeline to format phosphopeptide identifications.
- •Identified the preferred substrate motif for FLT3 and mutant kinases.
- •Designed and validated a panel of pan-FTL3 artificial substrates.
- •Monitored FLT3 and mutant kinase activity through FAStide phosphorylation.
14.
《Molecular & cellular proteomics : MCP》2018,17(12):2496-2507
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- •Quantitative (phospho)proteome analysis of antibiotic treatment in E. coli.
- •Largest bacterial phosphorylation catalogue.
- •Specific phosphorylation motifs changes during resistance development.
- •Phosphorylation mediated signaling could be a potential target for drug design.
15.
《Molecular & cellular proteomics : MCP》2018,17(12):2518-2533
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- •Chromobodies are stabilized by antigen binding in live cells.
- •Monitoring changes of endogenous protein levels in living cells with chromobodies.
- •Broadly applicable system to generate turnover-accelerated chromobodies.
- •Quantification of time- and dose-dependent compound effects.
16.
《Molecular & cellular proteomics : MCP》2019,18(8):1491-1510
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- •HLA-B*51 and ERAP1, but not ERAP2, are risk factors for Behçet's disease.
- •The HLA-B*51 peptidome and the effects of ERAP1 and ERAP2 on it are analyzed.
- •ERAP1 and ERAP2 alter multiple features of the HLA-B*51 peptidome in distinct ways.
- •Both enzymes act independently with complementary and partially redundant functions.
17.
《Molecular & cellular proteomics : MCP》2019,18(6):1085-1095
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- •Rapamycin and zinc induce moderate but significant mitochondrial proteome changes.
- •The mitochondrial proteins processing system is robust under subtoxic conditions.
- •Rapamycin and zinc perturb the mitochondrial proteins processing system.
- •Rapamycin and zinc perturb the mitochondrial proteins homeostasis.
18.
《Molecular & cellular proteomics : MCP》2019,18(11):2285-2297
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- •BioID with Golgi fractions identified C10orf76 as proximal to GBF1.
- •Tagged C10orf76 overlaps with Golgi markers.
- •C10orf76 binds GBF1 and exchanges rapidly between free and bound forms.
- •C10orf76 is essential for maintenance of the Golgi and for secretion.
19.
《Molecular & cellular proteomics : MCP》2019,18(12):2524-2531
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- •Efficient sample preparation workflow for deep N-glycomics analysis from serum.
- •Temperature gradient denaturing protocol to prevent protein precipitation.
- •Decrease of free sugar content in serum enhanced PNGase F digestion efficiency.
- •Modified evaporative labeling method increased fluorophore labeling yield.
20.
《Molecular & cellular proteomics : MCP》2019,18(11):2149-2164
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- •Enrichment of methyl peptides using two orthogonal techniques.
- •Knockdown of PRMT1 leads to substantial changes in protein arginine “methylome”.
- •Discrimination of ADMA and SDMA using characteristic neutral losses.
- •Identification of PRMT1 targets and substrate scavenged by other PRMTs in the absence of PRMT1 activity.