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1.
《Molecular & cellular proteomics : MCP》2020,19(2):233-244
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- •Mapping kinase-substrate relationships is vital in discovering new tuberculosis drug targets.
- •LC-MS/MS-based phosphoproteomics expand mycobacterial STPK substrate catalogues.
- •We review and integrate MS-generated datasets on novel candidate substrates.
- •Validation studies are necessary to confirm true physiological substrates of STPKs.
2.
Litong Nie Chao Wang Nan Li Xu Feng Namsoo Lee Dan Su Mengfan Tang Fan Yao Junjie Chen 《Molecular & cellular proteomics : MCP》2020,19(12):2015-2030
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- •Proteome analyses reveal RNF146 and TNKS1/2 substrates targeted for degradation.
- •RNF146 KO and TNKS1/2 DKO cells display significantly different proteomes.
- •RNF146 has both TNKS-dependent and -independent substrates.
3.
《Molecular & cellular proteomics : MCP》2020,19(11):1896-1909
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- •Epitope-tagging of a proteasome subunit allows for facile immuno-isolation.
- •An engineered yeast strain permits capture of proteasome-associated substrates.
- •MS/MS identified all 33 resident proteasome subunits in the 20S and 19S particles.
- •Analysis of associated proteins and characterization of newly identified ERAD substrate.
4.
《Molecular & cellular proteomics : MCP》2020,19(3):501-517
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- •Urinary peptide profiling of youths with type 1 diabetes before clinical injury.
- •Internal validation of uromodulin peptides by parallel reaction monitoring.
- •Discovery of novel bioactivity of uromodulin peptides in vitro.
- •In silico prediction of proteases involved in uromodulin processing.
5.
《Molecular & cellular proteomics : MCP》2020,19(11):1739-1748
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- •Label-free and isobaric labeling approaches for in-depth profiling of single cells.
- •Miniaturization and simplification of sample processing reduce surface losses.
- •Nanoflow separations enhance ionization efficiency and reduced chemical noise.
- •Ultrasensitive mass spectrometry and gas-phase separation add selectivity.
6.
《Molecular & cellular proteomics : MCP》2020,19(6):1005-1016
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- •Brain membrane protein extraction.
- •Protein prenylation.
- •Prenyl peptide capture and characterization by LC-MS/MS.
- •HCD and EThcD peptide fragmentation.
7.
Svenja Wiechmann Elena Saupp Daniela Schilling Stephanie Heinzlmeir Günter Schneider Roland M. Schmid Stephanie E. Combs Bernhard Kuster Sophie Dobiasch 《Molecular & cellular proteomics : MCP》2020,19(10):1649-1663
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- •Proteomes and phosphoproteomes of radiosensitive and radioresistant PDAC cell lines.
- •Common activation of DDR is proven by ATM activity on known and novel substrates.
- •Resistant cells bear raised NQO1 expression, actin dynamics including FAK activity.
- •Inhibitors of CHEK Rabusertib and FAK Defactinib radiosensitize PDAC cells.
8.
Ting Huang Meena Choi Manuel Tzouros Sabrina Golling Nikhil Janak Pandya Balazs Banfai Tom Dunkley Olga Vitek 《Molecular & cellular proteomics : MCP》2020,19(10):1706-1723
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- •Statistical approach for differential abundance analysis for proteomic experiments with TMT labeling.
- •Applicable to large-scale experiments with complex or unbalanced design.
- •An open-source R/Bioconductor package compatible with popular data processing tools.
9.
《Molecular & cellular proteomics : MCP》2020,19(4):655-671
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- •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.
10.
《Molecular & cellular proteomics : MCP》2020,19(11):1910-1920
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- •PRMT5 glutathionylation is increased in aged mice or under oxidative stress.
- •Deglutathionylation of PRMT5 is catalyzed by glutaredoxin-1.
- •PRMT5 glutathionylation decreases its methyltransferase activity.
- •PRMT5 glutathionylation results in G2/M arrest and inhibits cell proliferation.
11.
《Molecular & cellular proteomics : MCP》2020,19(7):1179-1192
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- •Proteomics uncovers the flow-induced remodeling of the endothelial basement membrane.
- •Flow alters the composition and localization of the laminin-integrin network.
- •Flow induces proteolytic processing of LAMA4, resulting in shedding of LG4–5 region.
- •TNFα- and flow-exposure induce a distinct proteomic signature with limited interplay.
12.
《Molecular & cellular proteomics : MCP》2020,19(5):828-838
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- •Higher AGC significantly improves quantitation quality in single-cell analysis.
- •The boosting-to-sample ratio should be carefully evaluated and optimized.
- •iBASIL allows for precise quantitation of 1,500 proteins from 104 AML single cells.
- •iBASIL recapitulates major biological differences in different AML single cells.
13.
《Molecular & cellular proteomics : MCP》2020,19(3):456-466
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- •Urinary proteomes of patients with recurrent UTI, renal scarring, and VUR.
- •80 proteins differentially expressed, compared to healthy controls.
- •62 proteins may be indicative of susceptibility for UTI.
- •Altered acute phase response, extracellular matrix and carbohydrate metabolism.
14.
《Molecular & cellular proteomics : MCP》2020,19(11):1767-1776
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- •N-glycan patterns are distinct in pediatric and adult urine.
- •Sex differences of N-glycans are much larger in adults.
- •Pediatric urine has almost no sex differences in N-glycan levels.
- •In adults, the majority of N-glycans were more abundant in males.
15.
《Molecular & cellular proteomics : MCP》2020,19(3):444-455
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- •Human spermatozoa possess cells of poor morphology that lack nuclear integrity.
- •These cells can be isolated by density separation.
- •Mass spectrometry reveals their nuclei contain excess protein.
- •TOP2A is a promising marker of this poor nuclear development.
16.
Nataly Mancette Rijensky Netta R. Blondheim Shraga Eilon Barnea Nir Peled Eli Rosenbaum Aron Popovtzer Solomon M. Stemmer Alejandro Livoff Mark Shlapobersky Neta Moskovits Dafna Perry Eitan Rubin Itzhak Haviv Arie Admon 《Molecular & cellular proteomics : MCP》2020,19(8):1360-1374
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- •Sufficient tumor tissues are often unavailable large HLA peptidome discovery.
- •Using patient derived xenograft (PDX) tumors can overcome this limitation.
- •The large PDX HLA peptidomes expand significantly those of the original biopsies.
- •The HLA peptidomes of the PDX tumors included many tumor antigens.
17.
Sandhya Manohar Qing Yu Steven P. Gygi Randall W. King 《Molecular & cellular proteomics : MCP》2020,19(9):1450-1467
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- •Chemical proteomics in G1 cells treated with small molecule APC/C inhibitors reveals novel putative APC/C substrates.
- •The insulin receptor adaptor IRS2 is an APC/C substrate that is targeted for degradation by APC/CCdh1.
- •Quantitative proteomics in IRS2 knockout cells reveals a deficiency in cell cycle related protein expression.
- •IRS2 promotes a robust spindle assembly checkpoint (SAC) during M-phase.
18.
《Molecular & cellular proteomics : MCP》2020,19(4):589-607
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- •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.
19.
《Molecular & cellular proteomics : MCP》2020,19(7):1193-1208
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- •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.
20.
《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.