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1.
Oncotarget ; 4(7): 1008-18, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23900284

ABSTRACT

Multiple myeloma (MM) is characterized by recurrent chromosomal translocations. MMSET, identified by its fusion to the IgH locus in t(4;14) MM, is universally overexpressed in t(4;14) MM. In order to identify cell surface biomarkers associated with t(4;14) MM for small molecule or antibody based therapies, we knocked down MMSET expression with shRNA and generated a cell line pair from KMS11, a t(4;14) MM cell line. We used quantitative mass spectrometry to identify plasma membrane proteins associated with MMSET overexpression. Using this approach, 50 cell surface proteins were identified as differentially expressed between KMS11 and KMS11/shMMSET. Western blot and flow cytometry analysis indicated SLAMF7 was over-expressed in t(4;14) MM cell lines and down-regulated by MMSET shRNAs. SLAMF7 expression was also confirmed in primary t(4;14) MM samples by flow cytometry analysis. Quantitative RT-PCR and ChIP analysis indicated MMSET might regulate the transcription level of SLAMF7 and be an important functional element for SLAMF7 promoter activity. Furthermore, SLAMF7 shRNA could induce G1 arrest or apoptosis and reduce clonogenetic capacity in t(4;14) MM cells. Overall, these results illustrated SLAMF7 might be a novel cell surface protein associated with t(4;14) MM. It is potential to develop t(4;14) MM targeted therapy by SLAMF7 antibody mediated drug delivery.


Subject(s)
Biomarkers, Tumor/metabolism , Histone-Lysine N-Methyltransferase/biosynthesis , Multiple Myeloma/metabolism , Repressor Proteins/biosynthesis , Cell Line, Tumor , Cell Membrane/genetics , Cell Membrane/metabolism , Chromosomes, Human, Pair 14 , Chromosomes, Human, Pair 4 , Down-Regulation , Gene Expression Regulation, Neoplastic , HEK293 Cells , Histone-Lysine N-Methyltransferase/genetics , Histone-Lysine N-Methyltransferase/metabolism , Humans , Multiple Myeloma/genetics , Proteomics/methods , Receptors, Immunologic/biosynthesis , Receptors, Immunologic/genetics , Repressor Proteins/genetics , Repressor Proteins/metabolism , Signaling Lymphocytic Activation Molecule Family , Transfection , Translocation, Genetic
2.
EMBO Rep ; 13(7): 638-44, 2012 Jun 29.
Article in English | MEDLINE | ID: mdl-22653443

ABSTRACT

The invasiveness of tumour cells depends on changes in cell shape, polarity and migration. Mutant p53 induces enhanced tumour metastasis in mice, and human cells overexpressing p53R273H have aberrant polarity and increased invasiveness, demonstrating the 'gain of function' of mutant p53 in carcinogenesis. We hypothesize that p53R273H interacts with mutant p53-specific binding partners that control polarity, migration or invasion. Here we analyze the p53R273H interactome using stable isotope labelling by amino acids in cell culture and quantitative mass spectrometry, and identify at least 15 new potential mutant p53-specific binding partners. The interaction of p53R273H with one of them--nardilysin (NRD1)--promotes an invasive response to heparin binding-epidermal growth factor-like growth factor that is p53R273H-dependant but does not require Rab coupling protein or p63. Advanced proteomics has thus allowed the detection of a new mechanism of p53-driven invasion.


Subject(s)
Metalloendopeptidases/metabolism , Neoplasm Invasiveness , Tumor Suppressor Protein p53/genetics , Tumor Suppressor Protein p53/metabolism , Animals , Cell Line, Tumor , Cell Movement , Cell Polarity , Epidermal Growth Factor/metabolism , Histidine , Mass Spectrometry/methods , Mice , Mutation, Missense , Protein Binding , Proteomics
3.
Mol Cell Proteomics ; 11(8): 381-93, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22511458

ABSTRACT

Annexin 1 (ANXA1), the first characterized member of the annexin superfamily, is known to bind or annex to cellular membranes in a calcium-dependent manner. Besides mediating inflammation, ANXA1 has also been reported to be involved in important physiopathological implications including cell proliferation, differentiation, apoptosis, cancer, and metastasis. However, with controversies in ANXA1 expression in breast carcinomas, its role in breast cancer initiation and progression remains unclear. To elucidate how ANXA1 plays a role in breast cancer initiation, we performed stable isotope labeling of amino acids in cell culture analysis on normal mammary gland epithelial cells from ANXA1-heterozygous (ANXA1(+/-)) and ANXA1-null (ANXA1(-/-)) mice. Among over 4000 quantified proteins, we observed 214 up-regulated and 169 down-regulated with ANXA1(-/-). Bioinformatics analysis of the down-regulated proteins revealed that ANXA1 is potentially implicated in DNA damage response, whereas the analysis of up-regulated proteins showed the possible roles of ANXA1 in cell adhesion and migration pathways. These observations were supported by relevant functional assays. The assays for DNA damage response demonstrated an accumulation of more DNA damage with slower recovery on heat stress and an impaired oxidative damage response in ANXA1(-/-) cells in comparison with ANXA1(+/-) cells. Overexpressing Yes-associated protein 1 or Yap1, the most down-regulated protein in DNA damage response pathway cluster, rescued the proliferative response in ANXA1(-/-) cells exposed to oxidative damage. Both migration and wound healing assays showed that ANXA1(+/-) cells possess higher motility with better wound closure capability than ANXA1(-/-) cells. Knocking down of ß-parvin, the protein with the highest fold change in the cell adhesion protein cluster, indicated an increased cell migration in ANXA1(-/-) cells. Altogether our quantitative proteomics study on ANXA1 suggests that ANXA1 plays a protective role in DNA damage and modulates cell adhesion and motility, indicating its potential role in cancer initiation as well as progression in breast carcinoma.


Subject(s)
Annexin A1/physiology , Cell Movement/physiology , DNA Damage , Mammary Glands, Animal/metabolism , Proteomics/methods , Animals , Annexin A1/analysis , Annexin A1/genetics , Blotting, Western , Cell Adhesion/genetics , Cell Adhesion/physiology , Cell Movement/genetics , Cells, Cultured , Comet Assay , Epithelial Cells/drug effects , Epithelial Cells/metabolism , Epithelial Cells/physiology , Female , Humans , Hydrogen Peroxide/pharmacology , Isotope Labeling/methods , Mammary Glands, Animal/cytology , Mass Spectrometry , Mice , Mice, Inbred C57BL , Mice, Knockout , Oxidants/pharmacology , Peptides/analysis , Peptides/genetics , Proteome/analysis , Proteome/genetics , Reverse Transcriptase Polymerase Chain Reaction
4.
J Biol Chem ; 286(20): 18093-103, 2011 May 20.
Article in English | MEDLINE | ID: mdl-21454687

ABSTRACT

The tumor suppressor PTEN (phosphatase and tensin homologue) negatively regulates the PI3K pathway through its lipid phosphatase activity and is one of the most commonly lost tumor suppressors in human cancers. Though the tumor suppressive function involves the lipid phosphatase-dependent and -independent activities of PTEN, the mechanism leading to the phosphatase-independent function of PTEN is understood poorly. Some PTEN mutants have lipid phosphatase activity but fail to suppress cell growth. Here, we use a cancer-associated mutant, G20E, to gain insight into the phosphatase-independent function of PTEN by investigating protein-protein interactions using MS-based stable isotope labeling by amino acids in cell culture (SILAC). A strategy named parallel affinity purification (PAP) and SILAC has been developed to prioritize interactors and to compare the interactions between wild-type and G20E PTEN. Clustering of the prioritized interactors acquired by the PAP-SILAC approach shows three distinct clusters: 1) wild-type-specific interactors, 2) interactors unique to the G20E mutant, and 3) proteins common to wild-type and mutant. These interactors are involved mainly in cell migration and apoptosis pathways. We further demonstrate that the wild-type-specific interactor, NUDTL16L1, is required for the regulatory function of wild-type PTEN in cell migration. These findings contribute to a better understanding of the mechanisms of the phosphatase-dependent and -independent functions of PTEN.


Subject(s)
Mutation, Missense , Neoplasm Proteins/metabolism , Neoplasms/enzymology , PTEN Phosphohydrolase/metabolism , Amino Acids/pharmacology , Cell Line, Tumor , Humans , Isotope Labeling/methods , Neoplasm Proteins/genetics , Neoplasms/genetics , PTEN Phosphohydrolase/genetics
5.
J Neurochem ; 97 Suppl 1: 16-23, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16635246

ABSTRACT

Characterization of the composition of the postsynaptic proteome (PSP) provides a framework for understanding the overall organization and function of the synapse in normal and pathological conditions. We have identified 698 proteins from the postsynaptic terminal of mouse CNS synapses using a series of purification strategies and analysis by liquid chromatography tandem mass spectrometry and large-scale immunoblotting. Some 620 proteins were found in purified postsynaptic densities (PSDs), nine in AMPA-receptor immuno-purifications, 100 in isolates using an antibody against the NMDA receptor subunit NR1, and 170 by peptide-affinity purification of complexes with the C-terminus of NR2B. Together, the NR1 and NR2B complexes contain 186 proteins, collectively referred to as membrane-associated guanylate kinase-associated signalling complexes. We extracted data from six other synapse proteome experiments and combined these with our data to provide a consensus on the composition of the PSP. In total, 1124 proteins are present in the PSP, of which 466 were validated by their detection in two or more studies, forming what we have designated the Consensus PSD. These synapse proteome data sets offer a basis for future research in synaptic biology and will provide useful information in brain disease and mental disorder studies.


Subject(s)
Multiprotein Complexes/analysis , Nerve Tissue Proteins/analysis , Proteome/chemistry , Synapses/chemistry , Animals , Brain Chemistry , Chromatography, Liquid , Guanylate Kinases/analysis , Guanylate Kinases/metabolism , Mass Spectrometry , Mice , Nerve Tissue Proteins/classification , Proteome/analysis
6.
Sci STKE ; 2005(298): pl6, 2005 Aug 23.
Article in English | MEDLINE | ID: mdl-16118397

ABSTRACT

Reversible protein phosphorylation mediated by kinases, phosphatases, and regulatory molecules is an essential mechanism of signal transduction in living cells. Although phosphorylation is the most intensively studied of the several hundred known posttranslational modifications on proteins, until recently the rate of identification of phosphorylation sites has remained low. The use of tandem mass spectrometry has greatly accelerated the identification of phosphorylation sites, although progress was limited by difficulties in phosphoresidue enrichment techniques. We have improved upon existing immobilized metal-affinity chromatography (IMAC) techniques for capturing phosphopeptides, to selectively purify phosphoproteins from complex mixtures. Combinations of phosphoprotein and phosphopeptide enrichment were more effective than current single phosphopeptide purification approaches. We have also implemented iterative mass spectrometry-based scanning techniques to improve detection of phosphorylated peptides in these enriched samples. Here, we provide detailed instructions for implementing and validating these methods together with analysis by tandem mass spectrometry for the study of phosphorylation at the mammalian synapse. This strategy should be widely applicable to the characterization of protein phosphorylation in diverse tissues, organelles, and in cell culture.


Subject(s)
Chromatography, Affinity/methods , Chromatography, Agarose/methods , Mass Spectrometry/methods , Phosphoproteins/isolation & purification , Animals , Buffers , Cell Fractionation/methods , Chromatography, Affinity/instrumentation , Chromatography, Agarose/instrumentation , Indicators and Reagents , Mass Spectrometry/instrumentation , Metals , Nerve Tissue Proteins/analysis , Nerve Tissue Proteins/isolation & purification , Peptides/analysis , Peptides/isolation & purification , Phosphoproteins/analysis , Phosphorylation , Protein Processing, Post-Translational , Proteomics/methods , Specimen Handling/methods , Spectrometry, Mass, Electrospray Ionization/instrumentation , Spectrometry, Mass, Electrospray Ionization/methods , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization/instrumentation , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization/methods , Subcellular Fractions/chemistry , Synaptosomes/chemistry
7.
J Biol Chem ; 280(7): 5972-82, 2005 Feb 18.
Article in English | MEDLINE | ID: mdl-15572359

ABSTRACT

In the nervous system, protein phosphorylation is an essential feature of synaptic function. Although protein phosphorylation is known to be important for many synaptic processes and in disease, little is known about global phosphorylation of synaptic proteins. Heterogeneity and low abundance make protein phosphorylation analysis difficult, particularly for mammalian tissue samples. Using a new approach, combining both protein and peptide immobilized metal affinity chromatography and mass spectrometry data acquisition strategies, we have produced the first large scale map of the mouse synapse phosphoproteome. We report over 650 phosphorylation events corresponding to 331 sites (289 have been unambiguously assigned), 92% of which are novel. These represent 79 proteins, half of which are novel phosphoproteins, and include several highly phosphorylated proteins such as MAP1B (33 sites) and Bassoon (30 sites). An additional 149 candidate phosphoproteins were identified by profiling the composition of the protein immobilized metal affinity chromatography enrichment. All major synaptic protein classes were observed, including components of important pre- and postsynaptic complexes as well as low abundance signaling proteins. Bioinformatic and in vitro phosphorylation assays of peptide arrays suggest that a small number of kinases phosphorylate many proteins and that each substrate is phosphorylated by many kinases. These data substantially increase existing knowledge of synapse protein phosphorylation and support a model where the synapse phosphoproteome is functionally organized into a highly interconnected signaling network.


Subject(s)
Phosphoproteins/analysis , Proteomics , Synapses/chemistry , Animals , Cell Membrane/chemistry , Computational Biology , Mice , Phosphoproteins/chemistry , Phosphoproteins/metabolism , Phosphorylation , Protein Array Analysis , Protein Binding , Protein Kinases/metabolism , Solubility/drug effects , Synapses/metabolism , Synaptosomes/chemistry , Urea/pharmacology
8.
Structure ; 12(6): 1015-25, 2004 Jun.
Article in English | MEDLINE | ID: mdl-15274921

ABSTRACT

Trichomaglin is a protein isolated from root tuber of the plant Maganlin (Trichosanthes Lepiniate, Cucurbitaceae). The crystal structure of trichomaglin has been determined by multiple-isomorphous replacement and refined at 2.2 A resolution. The X-ray sequence was established, based on electron density combined with the experimentally determined N-terminal sequence, and the sequence information derived from mass spectroscopic analysis. X-ray sequence-based homolog search and the three-dimensional structure reveal that trichomaglin is a novel S-like RNase, which was confirmed by biological assay. Trichomaglin molecule contains an additional beta sheet in the HV(b) region, compared with the known plant RNase structures. Fourteen cystein residues form seven disulfide bridges, more than those in the other known structures of S- and S-like RNases. His43 and His105 are expected to be the catalytic acid and base, respectively. Four hydrosulfate ions are bound in the active site pocket, three of them mimicking the substrate binding sites.


Subject(s)
N-Glycosyl Hydrolases/chemistry , Plant Proteins/chemistry , Ribonucleases/chemistry , Amino Acid Sequence , Binding Sites , Catalysis , Crystallography, X-Ray , Cysteine/chemistry , Disulfides , Electrons , Histidine/chemistry , Hydrogen-Ion Concentration , Ions , Mass Spectrometry , Models, Molecular , Molecular Sequence Data , Protein Conformation , Protein Structure, Secondary , Protein Structure, Tertiary , Ribosome Inactivating Proteins, Type 1 , Sequence Homology, Amino Acid , Software
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