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1.
《Molecular & cellular proteomics : MCP》2019,18(6):1036-1053
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- •Establishment of a flow system allowing multi-omics analysis of S. aureus biofilms.
- •Biofilm proteome profiling (intracellular and ECM) plus metabolic footprint analysis.
- •Virulence factors and ribosomal proteins stabilize the ECM as moonlighting proteins.
- •They act as electrostatic bridges between anionic cell surfaces, eDNA and metabolites.
2.
《Molecular & cellular proteomics : MCP》2019,18(5):892-908
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- •Interplay of epithelial cells and internalized S. aureus was dissected over 96 h.
- •Surviving host cells contain nonreplicating bacteria that persists in the cytoplasm.
- •Competition over resources triggers temporal metabolic changes.
- •Metabolic adaptation of host and bacteria determines the outcome of infection.
3.
《Molecular & cellular proteomics : MCP》2019,18(6):1157-1170
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- •Auxin responsive proteins in Arabidopsis roots were identified from 3,514 detected proteins.
- •All six auxin receptors are stable in response to hormone via novel MRM assays.
- •The >100 differentially expressed proteins exhibit dynamic and transient responses to auxin.
- •Phenotypic screening of the top responsive proteins uncovered several novel root mutants.
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5.
《Molecular & cellular proteomics : MCP》2019,18(1):41-50
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- •Proteome of mature boar spermatozoa from cauda epididymal and ejaculated sources were analyzed by iTRAQ-based LC-MS/MS.
- •1,723 sperm proteins identified (974 of Sus scrofa taxonomy).
- •1,602 sperm proteins quantified (960 of Sus scrofa taxonomy).
- •32 Sus scrofa sperm proteins were differentially expressed among sperm sources.
- •The proteome of boar spermatozoa is remodelled during ejaculation.
6.
《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.
7.
《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.
8.
《Molecular & cellular proteomics : MCP》2019,18(1):28-40
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- •Method to probe the isomeric variants of the glycans attached to purified proteins.
- •Uses multiple rounds of glycosidase cleavage and lectin profiling.
- •Computation integration of lectin-binding, glycan-array, and mass spectrometry data.
- •Applied to microspots for compatibility with analyzing low-abundance proteins.
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10.
《Molecular & cellular proteomics : MCP》2019,18(2):200-215
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- •A global lysine succinylome was investigated in A. hydrophila.
- •The lysine succinylation modifications play crucial role on various metabolic pathways.
- •Reversible succinylation on Lys23 and Lys30 regulates the activity of S-ribosylhomocysteine lyase LuxS.
- •Lysine succinylation modifications of LuxS affect quorum sensing and metabolism.
11.
《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.
12.
《Molecular & cellular proteomics : MCP》2019,18(4):657-668
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- •Global proteomic remodeling alters antibiotic susceptibility in K. pneumoniae.
- •Drug specific transport, sugar utilization, central metabolism, capsule synthesis.
- •Common pathways of reactive oxygen scavenging, turnover of misfolded proteins.
- •Integrated adjustments and unique drug-specific features for drug combinations.
13.
《Molecular & cellular proteomics : MCP》2019,18(10):2078-2088
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- •Proteomic landscapes of Drosophila somatic and reproductive tissues during aging.
- •Pulsed metabolic labeling determines a decline in protein synthesis with age.
- •Drosophila model of human Parkinson's disease signifies an early-onset decline in protein synthesis.
- •Collapse of proteostasis and mitochondria are early signals for normal aging.
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》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
16.
《Molecular & cellular proteomics : MCP》2019,18(8):1630-1650
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- •Our search identifies 2,134 kinase-substrate phosphosite pairs in breast cancer.
- •CDKs and MAPKs are dominant regulators of trans substrate-phosphorylation.
- •Druggability, outcomes, and immune signatures related to kinase-substrates.
- •Experimentally validated activated phosphosites of ERBB2, EIF4EBP1, and EGFR.
17.
《Molecular & cellular proteomics : MCP》2019,18(11):2138-2148
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- •Highly glycosylated matrisome proteins and their binding partners comprise extracellular networks that mediate tissue-specific cellular microenvironments.
- •Elucidation of roles of matrisome molecules in disease mechanisms requires detailed mapping of matrisome glycosylation and other post-translational modifications.
- •We review tissue workup methods for matrisome proteomics, glycomics and glycoproteomics.
- •The combination of proteomics, glycomics and glycoproteomics profiles matrisome protein modifications distinct from those studied by immunohistochemistry.
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(1):115-126
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- •Application of Sortase A to label protein N-termini across the whole proteome.
- •Novel gel, proteomic and ELISA-based methods to determine N-myristoylation of proteins in cells, without metabolic labelling.
- •Side by side mass spectrometric quantification of changes in protein N-myristoylation by two complementary methods.
- •Improved Biotin-Neutravidin affinity enrichment protocol.
20.
《Molecular & cellular proteomics : MCP》2019,18(7):1437-1453
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- •mRNA-seq, miRNA-seq, proteomes of P. fulvidraco, P. vachelli, hybrid Huangyou-1.
- •Predicted miRNA-mRNA-protein pairs were found and validated by qRT-PCR and PRM.
- •Immune, metabolism, digestion, absorption, proliferation, development generate heterosis.
- •High parental gene/protein with low parental miRNAs inherit from the mother or father.