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1.
《Molecular & cellular proteomics : MCP》2020,19(7):1145-1160
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- •Quantitative proteomics reveals HIGD2A is required for assembly of the COX3 module.
- •Pulse-SILAC demonstrates that HIGD2A is involved in COX3 biogenesis.
- •Supercomplexes in HIGD2A knockout cells are depleted of COX3.
- •HIGD2A is the first assembly factor identified for the COX3 module of Complex IV.
2.
《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.
3.
《Molecular & cellular proteomics : MCP》2020,19(3):467-477
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- •Each component of the AMPK trimeric complex was profiled by interaction proteomics.
- •The subunit composition of the AMPK complex directs interactions to distinct proteins.
- •AMPK interacts with Artemis and plays a role in Non-Homologous End Joining.
4.
《Molecular & cellular proteomics : MCP》2020,19(7):1076-1087
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- •Organelle profiling maps capture localizations of 1000s of proteins in one experiment.
- •Comparing maps +/− perturbation reveals disease mechanisms & cellular responses.
- •A conceptual guide to planning and interpreting organellar profiling experiments.
- •A cross-study consensus set of human organellar marker proteins.
5.
《Molecular & cellular proteomics : MCP》2020,19(4):624-639
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- •Used affinity-enrichable, isotopically coded, and MS-cleavable crosslinker.
- •Targeted acquisition strategy based on isotopic-coding described and evaluated.
- •Novel data analysis pipeline developed provides improved crosslink identification.
- •Large dataset reveals hundreds of mitochondrial protein-protein interactions.
6.
《Molecular & cellular proteomics : MCP》2020,19(5):900-912
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- •Affinity-based proteomics of infected macrophage cells.
- •Salmonella-modified membranes exhibit host-specific composition.
- •Proteome differences explain some host-dependent pathophysiological differences.
7.
《Molecular & cellular proteomics : MCP》2020,19(7):1120-1131
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- •Quantitative proteomics of isolated lysosomes, autophagosomes and proteasomes.
- •Pharmacological inhibition of proteasomes leads to their accumulation within lysosomes.
- •Inhibition of classical autophagy pathways cannot completely block this process.
- •Known autophagy adaptor proteins are not involved.
8.
《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.
9.
《Molecular & cellular proteomics : MCP》2020,19(1):114-127
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- •Quantitative proteomics and machine learning to study plasma biomarkers in HCM.
- •Six peptides are increased in plasma of LVH+ HCM compared to controls.
- •Peptide biomarkers correlate with imaging markers of phenotype severity.
- •Peptide biomarkers correlate with the estimated sudden cardiac death risk.
10.
11.
《Molecular & cellular proteomics : MCP》2020,19(7):1161-1178
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- •XL-MS reveals new PPIs in yeast mitochondria under glycerol and glucose condition.
- •Significant but limited results from quantitative XL-MS experiments.
- •Ndi1 participates in a CIII2CIV2 respiratory supercomplex.
- •Min8 promotes assembly of Cox12 into an intermediate complex IV.
12.
Anatte Margalit James C. Carolan David Sheehan Kevin Kavanagh 《Molecular & cellular proteomics : MCP》2020,19(8):1346-1359
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- •Pseudomonas aeruginosa growth increases in Aspergillus fumigatus culture filtrates.
- •A. fumigatus culture filtrates are characterized by a range of peptidases and proteases.
- •LFQ proteomics characterizes the response of P. aeruginosa to A. fumigatus culture filtrates.
- •A. fumigatus creates an environment for P. aeruginosa to proliferate.
13.
《Molecular & cellular proteomics : MCP》2020,19(11):1777-1789
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- •Quantitative mass spectrometric method to monitor PTM stability.
- •Pulse labeling reveals dehydroxylation of several asparagine hydroxylation sites.
- •Reversal of TNKS2, TRPV3 and HIF1a asparagine hydroxylation sites.
- •Protein dehydroxylation is an additional level of control for cellular signaling networks.
14.
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.
15.
《Molecular & cellular proteomics : MCP》2020,19(1):50-64
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- •BioID reveals the proximity partners of RSK family members.
- •All RSK isoforms associate with and phosphorylate p120ctn on Ser320.
- •RSK negatively regulates adherens junctions and reduces cell-cell adhesion.
- •p120ctn phosphorylation plays a role in the reorganization of proximity partners.
16.
《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.
17.
《Molecular & cellular proteomics : MCP》2020,19(11):1826-1849
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- •Identification of subcellular protein interactomes via proximity labeling and quantitative multiplexed proteomics.
- •SEC61β and RPN1 interactomes overlap with translocon-associated protein networks.
- •SEC62 interacts with redox-linked proteins and ER luminal chaperones.
- •LRRC59 directly interacts with mRNA translation factors and SRP machinery on the ER.
18.
《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.
19.
Prashali Bansal Johannes Madlung Kristina Schaaf Boris Macek Fulvia Bono 《Molecular & cellular proteomics : MCP》2020,19(9):1485-1502
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- •Label-free and dimethyl labeling MS analysis of 6 RBPs from Drosophila ovaries.
- •Functionally related RBPs show overlapping proteomes.
- •Selective co-purification of splicing factors and translational regulators.
- •Validation of 26 novel interactions by co-immunoprecipitation.
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.