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1.
《Molecular & cellular proteomics : MCP》2019,18(2):352-371
Highlights
- •H. pylori dysregulates the in vivo gastric proteome of gerbils in a strain-specific manner.
- •H. pylori increases RABEP2 and G3BP2 levels in cell culture.
- •H. pylori upregulates RABEP2 and G3BP2 in gerbil and human gastric epithelium.
- •Levels of RABEP2 and G3BP2 increase with severity of malignant lesions in vivo.
2.
《Molecular & cellular proteomics : MCP》2019,18(11):2298-2309
Highlights
- •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.
3.
《Molecular & cellular proteomics : MCP》2019,18(10):1981-2002
Highlights
- •R-10G is a mono-sulfated glycan antigen of human iPS and ES cells on podocalyxin.
- •R-10G and nonsulfated i are reciprocal antigens on type 2 glycan backbones.
- •TRA-1–60 and -81 and FC10.2 are antigens expressed on unsulfated type 1 backbones.
- •These assignments open the way to probing their roles in podocalyxin-signaling.
4.
《Molecular & cellular proteomics : MCP》2019,18(12):2516-2523
Highlights
- •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.
5.
《Molecular & cellular proteomics : MCP》2019,18(8):1491-1510
Highlights
- •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.
6.
《Molecular & cellular proteomics : MCP》2019,18(2):245-262
Highlights
- •AP-DIA/SWATH analysis to identify TCTP-interacting proteins in NF1 tumor cells.
- •A highly specific TCTP–EF1A2 interaction but rather than TCTP–EF1A1 interaction.
- •TCTP–EF1A2 interaction mediating formation of EF1A2-elogation factor complex.
- •TCTP–EF1A2 dependent translation machinery regulating NF1 tumor cell growth.
7.
《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
8.
《Molecular & cellular proteomics : MCP》2019,18(7):1410-1427
Highlights
- •Quantitative (phoshpo)proteome of primary cell cultures of patient-matched prostate CAF and NPF.
- •Key CAF-associated proteins validated using orthogonal methodologies.
- •LOXL2 inhibitors D-penicillamine and PXS-S2A impaired CAF migration and ECM alignment.
- •Pre-treatment with LOXL2 inhibitors impaired migratory capacity of RWPE-2 cells in co-culture.
9.
《Molecular & cellular proteomics : MCP》2019,18(5):876-891
Highlights
- •Three novel Conodipines P1-3 in the injected venom of Conus purpurascens.
- •Conodipines P1-3 have consensus catalytic characteristics of sPLA2.
- •We determined multiple modification sites in Conodipines P1-3.
- •Evaluated the activity of Conohyal-P1 by a MS-based method.
10.
11.
《Molecular & cellular proteomics : MCP》2019,18(4):686-703
Highlights
- •nLC-MS/MS method to analyze immunoglobulin (Ig) N-glycopeptides from human serum.
- •Multi-isotype, site-specific characterization of immunoglobulin N-glycosylation.
- •IgA2 sequence and glycosylation-site variant analyses.
- •Platform to define disease-specific N-glycan signatures for different Ig isotypes.
12.
《Molecular & cellular proteomics : MCP》2019,18(1):51-64
Highlights
- •microRNA-222 attenuates TGEV-induced mitochondrial dysfunction.
- •microRNA-222 downregulates THBS1 and CD47.
- •THBS1 is the target of microRNA-222 during TGEV infection.
- •THBS1 and CD47 increase mitochondrial Ca2+ level and reduced mitochondrial membrane potential (MMP).
13.
《Molecular & cellular proteomics : MCP》2019,18(4):669-685
Highlights
- •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.
14.
《Molecular & cellular proteomics : MCP》2019,18(12):2348-2358
Highlights
- •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.
15.
《Molecular & cellular proteomics : MCP》2019,18(3):520-533
Highlights
- •1. Celastrol alleviated cholestatic liver injury.
- •2. Celastrol inhibited the decrease of SIRT1 induced by deoxycholic acid.
- •3. SIRT1-FXR signaling pathway mediated the effect of celastrol.
16.
《Molecular & cellular proteomics : MCP》2019,18(8):1526-1542
Highlights
- •Definition of early systemin-responsive phosphorylation time course.
- •Reconstruction of kinase-substrate relationships from phosphorylation time profiles.
- •Phosphatase PLL5 rapidly dephosphorylated H+-ATPase LHA1 inducing alkalinization of the medium.
- •MAP-Kinase MPK2 re-phosphorylated LHA1 after 15 minutes.
17.
《Molecular & cellular proteomics : MCP》2019,18(4):704-714
Highlights
- •The proteomes of L. lactis MG1363 and phage p2 at different stages of infection were characterized.
- •16% (226/1412) of the bacterial proteins detected were unique to infected cultures.
- •A targeted approach using synthetic peptides improved the coverage of phage p2 proteome.
- •By means of proteogenomics, we uncovered a conserved phage protein coded by a previously unannotated gene.
- •Deletion of the bacterial gene llmg_0219 (unknown function) impedes phage p2 infection.
18.
《Molecular & cellular proteomics : MCP》2019,18(3):571-575
Highlights
- •Incrementally build mzML 1.1, and mzIdentML 1.2 files in Python over a file stream.
- •Traverse controlled vocabularies using common mapping patterns.
- •Generate byte offset index as the document streams.
- •Manage referential integrity on-the-fly.
19.
《Molecular & cellular proteomics : MCP》2019,18(5):982-994
Highlights
- •MaxQuant.Live controls Orbitrap mass analyzers in real-time.
- •Freely available apps enable advanced data acquisition strategies.
- •On-the-fly mass, retention time and intensity recalibration.
- •Global targeting unifies shotgun and targeted proteomics.
20.
《Molecular & cellular proteomics : MCP》2019,18(2):231-244
Highlights
- •OMICS distinguish cancer cells from resistant or cancer stem cells.
- •Bactericidal antibiotics and mitochondria.
- •Linezolid and anticancer therapy.