共查询到20条相似文献,搜索用时 15 毫秒
1.
《Molecular & cellular proteomics : MCP》2019,18(6):1183-1196
Highlights
- •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.
2.
《Molecular & cellular proteomics : MCP》2019,18(4):657-668
Highlights
- •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.
3.
《Molecular & cellular proteomics : MCP》2019,18(6):1171-1182
Highlights
- •First report on the quantitative proteomic profiling of Drosophila lymph glands.
- •Comparative proteomic analysis under conditions of perturbed blood cell homeostasis.
- •Resource for identifying new regulators of insect and vertebrate hematopoiesis.
4.
《Molecular & cellular proteomics : MCP》2019,18(7):1396-1409
Highlights
- •A panel of HEK293 isogenic cell lines with knockout of GALNT genes.
- •Identification of nonredundant O-glycosylation sites regulated by specific GalNAc-T isoforms.
- •GalNAc-T7 and T10 contribute to follow-up activity in regions of high density O-glycosylation.
- •GalNAc-T11 specifically controls O-glycosylation of specific linker regions in the low-density lipoprotein receptor related proteins.
5.
《Molecular & cellular proteomics : MCP》2019,18(8):1630-1650
Highlights
- •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.
6.
《Molecular & cellular proteomics : MCP》2019,18(6):1110-1122
Highlights
- •Comprehensive analysis of inter-individual variation of normal urinary proteome.
- •Significant gender differences were observed.
- •Proteins increased in female urine are enriched in immunological pathways.
- •Estimated reference intervals of proteins as the baseline for biomarker discovery.
7.
《Molecular & cellular proteomics : MCP》2019,18(7):1437-1453
Highlights
- •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.
8.
《Molecular & cellular proteomics : MCP》2019,18(4):773-785
Highlights
- •The developed Ac-LysargiNase showed higher stability and activity than before.
- •The merged spectra of the mirror peptides achieved nearly complete ion coverage.
- •pNovoM obviously increased the efficiency and accuracy of peptide sequencing.
- •The mirror enzymatic strategy achieved precision de novo sequencing on proteome scales.
9.
《Molecular & cellular proteomics : MCP》2019,18(6):1085-1095
Highlights
- •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.
10.
《Molecular & cellular proteomics : MCP》2019,18(10):2089-2098
Highlights
- •Cathepsin-L is introduced as a novel protease for HX-MS studies.
- •Cathepsin-L improves resolution of traditionally challenging histone tails.
- •Cathepsin-L can be readily combined with pepsin for improved protein coverage.
- •In-solution dynamics of the H3.1 and H4 monomers reveal extensive EX1 kinetics.
11.
《Molecular & cellular proteomics : MCP》2019,18(3):594-605
Highlights
- •A new strategy for simultaneous quantification of protein expression and modification.
- •This top-down LC/MS-based method shows high reproducibility and high throughput.
- •Quantification at the intact protein level with results comparable to Western blot.
- •This top-down proteomics method is applicable to different species and tissues.
12.
《Molecular & cellular proteomics : MCP》2019,18(5):936-953
Highlights
- •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
13.
Posttranslational Modifications Drive Protein Stability to Control the Dynamic Beer Brewing Proteome
《Molecular & cellular proteomics : MCP》2019,18(9):1721-1731
Highlights
- •SWATH-MS profiles protein abundance and modification during mashing in beer brewing.
- •Proteolysis due to barley proteases leads to extreme proteoform diversity.
- •Sequence-specific proteolytic clipping of proteins controls their stability.
14.
《Molecular & cellular proteomics : MCP》2019,18(5):854-864
Highlights
- •Zero-length chemical cross-linking of APOA1 peptides in HDL.
- •Cross-links match antiparallel isomers of APOA dimers in molecular modeling.
- •Identical MS/MS spectra of native and synthetic cross-linked peptides.
- •First biochemical evidence of LL5/5 and LL5/4 isomers in human HDL.
15.
《Molecular & cellular proteomics : MCP》2019,18(3):490-503
Highlights
- •MHC-II-bound peptide repertoires from DO-sufficient and DO-deficient cells.
- •Fewer unique peptides and core epitopes were presented in the absence of DO.
- •Immunopeptidome differences appeared to result from reduced DM editing.
- •DO-dependent self-epitopes elicited CD4 T cell responses in mice.
16.
17.
《Molecular & cellular proteomics : MCP》2019,18(5):968-981
Highlights
- •Quantitative substrate profiling method for characterizing peptidase specificity.
- •Applicable to both purified peptidases and peptidases in complex biological samples.
- •TMT labeling improves throughput, accuracy and reproducibility of the assay.
- •Design of fluorescent probes to monitor peptidase activity based on substrate data.
18.
《Molecular & cellular proteomics : MCP》2019,18(6):1157-1170
Highlights
- •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.
19.
《Molecular & cellular proteomics : MCP》2019,18(8):1669-1682
Highlights
- •Spatiotemporal microproteomics analysis of TBI.
- •Injury site microproteomics reveal distinct phases in 10-day frame post TBI.
- •Uninjured proteomic profile is restored in TBI at 10 days post injury.
- •Substantia nigra protein post 3 days suggest link to Parkinson's disease.
20.
《Molecular & cellular proteomics : MCP》2019,18(5):818-836
Highlights
- •Kallikrein-related peptidase 7 is over expressed in ovarian cancer.
- •Quantitative PROTOMAP and TAILS approaches identified putative substrates of KLK7.
- •Pro-MMP10 is activated by KLK7.
- •KLK7 cleaves thrombospondin 1 and IGFBP6 in vitro.