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1.
Nucleic Acids Res ; 45(W1): W300-W306, 2017 07 03.
Article in English | MEDLINE | ID: mdl-28520987

ABSTRACT

Profiling of proteome dynamics is crucial for understanding cellular behavior in response to intrinsic and extrinsic stimuli and maintenance of homeostasis. Over the last 20 years, mass spectrometry (MS) has emerged as the most powerful tool for large-scale identification and characterization of proteins. Bottom-up proteomics, the most common MS-based proteomics approach, has always been challenging in terms of data management, processing, analysis and visualization, with modern instruments capable of producing several gigabytes of data out of a single experiment. Here, we present ProteoSign, a freely available web application, dedicated in allowing users to perform proteomics differential expression/abundance analysis in a user-friendly and self-explanatory way. Although several non-commercial standalone tools have been developed for post-quantification statistical analysis of proteomics data, most of them are not end-user appealing as they often require very stringent installation of programming environments, third-party software packages and sometimes further scripting or computer programming. To avoid this bottleneck, we have developed a user-friendly software platform accessible via a web interface in order to enable proteomics laboratories and core facilities to statistically analyse quantitative proteomics data sets in a resource-efficient manner. ProteoSign is available at http://bioinformatics.med.uoc.gr/ProteoSign and the source code at https://github.com/yorgodillo/ProteoSign.


Subject(s)
Proteomics/methods , Software , Data Interpretation, Statistical , Internet , Mass Spectrometry
2.
Elife ; 4: e09545, 2015 Oct 29.
Article in English | MEDLINE | ID: mdl-26512888

ABSTRACT

Cholera toxin (CT) enters and intoxicates host cells after binding cell surface receptors using its B subunit (CTB). The ganglioside (glycolipid) GM1 is thought to be the sole CT receptor; however, the mechanism by which CTB binding to GM1 mediates internalization of CT remains enigmatic. Here we report that CTB binds cell surface glycoproteins. Relative contributions of gangliosides and glycoproteins to CTB binding depend on cell type, and CTB binds primarily to glycoproteins in colonic epithelial cell lines. Using a metabolically incorporated photocrosslinking sugar, we identified one CTB-binding glycoprotein and demonstrated that the glycan portion of the molecule, not the protein, provides the CTB interaction motif. We further show that fucosylated structures promote CTB entry into a colonic epithelial cell line and subsequent host cell intoxication. CTB-binding fucosylated glycoproteins are present in normal human intestinal epithelia and could play a role in cholera.


Subject(s)
Cholera Toxin/metabolism , Membrane Proteins/metabolism , Protein Processing, Post-Translational , Receptors, Cell Surface/metabolism , Cell Line , Epithelial Cells/metabolism , G(M1) Ganglioside/metabolism , Glycosylation , Humans , Protein Binding
3.
PLoS Pathog ; 11(8): e1005128, 2015 Aug.
Article in English | MEDLINE | ID: mdl-26305100

ABSTRACT

The type VI secretion system (T6SS) is a widespread protein secretion apparatus used by Gram-negative bacteria to deliver toxic effector proteins into adjacent bacterial or host cells. Here, we uncovered a role in interbacterial competition for the two T6SSs encoded by the marine pathogen Vibrio alginolyticus. Using comparative proteomics and genetics, we identified their effector repertoires. In addition to the previously described effector V12G01_02265, we identified three new effectors secreted by T6SS1, indicating that the T6SS1 secretes at least four antibacterial effectors, of which three are members of the MIX-effector class. We also showed that the T6SS2 secretes at least three antibacterial effectors. Our findings revealed that many MIX-effectors belonging to clan V are "orphan" effectors that neighbor mobile elements and are shared between marine bacteria via horizontal gene transfer. We demonstrated that a MIX V-effector from V. alginolyticus is a functional T6SS effector when ectopically expressed in another Vibrio species. We propose that mobile MIX V-effectors serve as an environmental reservoir of T6SS effectors that are shared and used to diversify antibacterial toxin repertoires in marine bacteria, resulting in enhanced competitive fitness.


Subject(s)
Bacterial Toxins/genetics , Genes, Bacterial/genetics , Type VI Secretion Systems/genetics , Vibrio alginolyticus/genetics , Amino Acid Sequence , Base Sequence , Gene Transfer, Horizontal , Genetic Fitness/genetics , Mass Spectrometry , Molecular Sequence Data
4.
Nat Commun ; 6: 6758, 2015 Apr 07.
Article in English | MEDLINE | ID: mdl-25849564

ABSTRACT

The impact of protein arginine methylation on the regulation of immune functions is virtually unknown. Here, we apply a novel method­isomethionine methyl-SILAC­coupled with antibody-mediated arginine-methylated peptide enrichment to identify methylated peptides in human T cells by mass spectrometry. This approach allowed the identification of 2,502 arginine methylation sites from 1,257 tissue-specific and housekeeping proteins. We find that components of T cell antigen receptor signal machinery and several key transcription factors that regulate T cell fate determination are methylated on arginine. Moreover, we demonstrate changes in arginine methylation stoichiometry during cellular stimulation in a subset of proteins critical to T cell differentiation. Our data suggest that protein arginine methyltransferases exert key regulatory roles in T cell activation and differentiation, opening a new field of investigation in T cell biology.


Subject(s)
Arginine/metabolism , Cell Differentiation , Lymphocyte Activation , Protein-Arginine N-Methyltransferases/metabolism , Receptors, Antigen, T-Cell/metabolism , T-Lymphocytes/metabolism , Transcription Factors/metabolism , Humans , Mass Spectrometry , Methylation , Protein Processing, Post-Translational
6.
Nat Commun ; 5: 4816, 2014 Sep 16.
Article in English | MEDLINE | ID: mdl-25226414

ABSTRACT

Viruses use virions to spread between hosts, and virion composition is therefore the primary determinant of viral transmissibility and immunogenicity. However, the virions of many viruses are complex and pleomorphic, making them difficult to analyse in detail. Here we address this by identifying and quantifying virion proteins with mass spectrometry, producing a complete and quantified model of the hundreds of host-encoded and viral proteins that make up the pleomorphic virions of influenza viruses. We show that a conserved influenza virion architecture is maintained across diverse combinations of virus and host. This 'core' architecture, which includes substantial quantities of host proteins as well as the viral protein NS1, is elaborated with abundant host-dependent features. As a result, influenza virions produced by mammalian and avian hosts have distinct protein compositions. Finally, we note that influenza virions share an underlying protein composition with exosomes, suggesting that influenza virions form by subverting microvesicle production.


Subject(s)
Host Specificity/genetics , Influenza A Virus, H1N1 Subtype/ultrastructure , Influenza A Virus, H3N2 Subtype/ultrastructure , Viral Nonstructural Proteins/genetics , Virion/ultrastructure , Amino Acid Sequence , Animals , Cattle , Chickens , Dogs , Epithelial Cells/virology , Gene Expression , Influenza A Virus, H1N1 Subtype/genetics , Influenza A Virus, H1N1 Subtype/growth & development , Influenza A Virus, H3N2 Subtype/genetics , Influenza A Virus, H3N2 Subtype/growth & development , Madin Darby Canine Kidney Cells , Models, Molecular , Molecular Sequence Data , Ovum/virology , Sequence Alignment , Viral Load , Virion/genetics , Virion/growth & development
7.
Proc Natl Acad Sci U S A ; 111(25): 9271-6, 2014 Jun 24.
Article in English | MEDLINE | ID: mdl-24927539

ABSTRACT

Bacteria use diverse mechanisms to kill, manipulate, and compete with other cells. The recently discovered type VI secretion system (T6SS) is widespread in bacterial pathogens and used to deliver virulence effector proteins into target cells. Using comparative proteomics, we identified two previously unidentified T6SS effectors that contained a conserved motif. Bioinformatic analyses revealed that this N-terminal motif, named MIX (marker for type six effectors), is found in numerous polymorphic bacterial proteins that are primarily located in the T6SS genome neighborhood. We demonstrate that several MIX-containing proteins are T6SS effectors and that they are not required for T6SS activity. Thus, we propose that MIX-containing proteins are T6SS effectors. Our findings allow for the identification of numerous uncharacterized T6SS effectors that will undoubtedly lead to the discovery of new biological mechanisms.


Subject(s)
Bacteria/genetics , Bacterial Proteins/genetics , Bacterial Secretion Systems/genetics , Genome, Bacterial/physiology , Amino Acid Motifs , Bacteria/metabolism , Bacteria/pathogenicity , Bacterial Proteins/metabolism , Genome-Wide Association Study
8.
Mol Cell Proteomics ; 13(6): 1573-84, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24696503

ABSTRACT

Bottom-up proteomics largely relies on tryptic peptides for protein identification and quantification. Tryptic digestion often provides limited coverage of protein sequence because of issues such as peptide length, ionization efficiency, and post-translational modification colocalization. Unfortunately, a region of interest in a protein, for example, because of proximity to an active site or the presence of important post-translational modifications, may not be covered by tryptic peptides. Detection limits, quantification accuracy, and isoform differentiation can also be improved with greater sequence coverage. Selected reaction monitoring (SRM) would also greatly benefit from being able to identify additional targetable sequences. In an attempt to improve protein sequence coverage and to target regions of proteins that do not generate useful tryptic peptides, we deployed a multiprotease strategy on the HeLa proteome. First, we used seven commercially available enzymes in single, double, and triple enzyme combinations. A total of 48 digests were performed. 5223 proteins were detected by analyzing the unfractionated cell lysate digest directly; with 42% mean sequence coverage. Additional strong-anion exchange fractionation of the most complementary digests permitted identification of over 3000 more proteins, with improved mean sequence coverage. We then constructed a web application (https://proteomics.swmed.edu/confetti) that allows the community to examine a target protein or protein isoform in order to discover the enzyme or combination of enzymes that would yield peptides spanning a certain region of interest in the sequence. Finally, we examined the use of nontryptic digests for SRM. From our strong-anion exchange fractionation data, we were able to identify three or more proteotypic SRM candidates within a single digest for 6056 genes. Surprisingly, in 25% of these cases the digest producing the most observable proteotypic peptides was neither trypsin nor Lys-C. SRM analysis of Asp-N versus tryptic peptides for eight proteins determined that Asp-N yielded higher signal in five of eight cases.


Subject(s)
Peptide Fragments/genetics , Peptides/genetics , Proteomics , Trypsin , Gene Expression Regulation, Neoplastic , HeLa Cells , Humans , Mass Spectrometry , Peptide Fragments/biosynthesis , Peptide Fragments/isolation & purification , Peptides/isolation & purification , Protein Processing, Post-Translational
9.
Proteomics ; 14(12): 1467-71, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24723505

ABSTRACT

Modern nano-HPLC systems are capable of extremely precise control of solvent gradients, allowing high-resolution separation of peptides. Most proteomics laboratories use a simple linear analytical gradient for nano-LC-MS/MS experiments, though recent evidence indicates that optimized non-linear gradients result in increased peptide and protein identifications from cell lysates. In concurrent work, we examined non-linear gradients for the analysis of samples fractionated at the peptide level, where the distribution of peptide retention times often varies by fraction. We hypothesized that greater coverage of these samples could be achieved using per-fraction optimized gradients. We demonstrate that the optimized gradients improve the distribution of peptides throughout the analysis. Using previous generation MS instrumentation, a considerable gain in peptide and protein identifications can be realized. With current MS platforms that have faster electronics and achieve shorter duty cycle, the improvement in identifications is smaller. Our gradient optimization method has been implemented in a simple graphical tool (GOAT) that is MS-vendor independent, does not require peptide ID input, and is freely available for non-commercial use at http://proteomics.swmed.edu/goat/


Subject(s)
Chromatography, Liquid/methods , Computational Biology , Peptide Fragments/analysis , Proteins/analysis , Proteomics/methods , Software , Tandem Mass Spectrometry/methods , Humans
10.
Mol Cell ; 53(4): 645-54, 2014 Feb 20.
Article in English | MEDLINE | ID: mdl-24486019

ABSTRACT

Efficient stop codon recognition and peptidyl-tRNA hydrolysis are essential in order to terminate translational elongation and maintain protein sequence fidelity. Eukaryotic translational termination is mediated by a release factor complex that includes eukaryotic release factor 1 (eRF1) and eRF3. The N terminus of eRF1 contains highly conserved sequence motifs that couple stop codon recognition at the ribosomal A site to peptidyl-tRNA hydrolysis. We reveal that Jumonji domain-containing 4 (Jmjd4), a 2-oxoglutarate- and Fe(II)-dependent oxygenase, catalyzes carbon 4 (C4) lysyl hydroxylation of eRF1. This posttranslational modification takes place at an invariant lysine within the eRF1 NIKS motif and is required for optimal translational termination efficiency. These findings further highlight the role of 2-oxoglutarate/Fe(II) oxygenases in fundamental cellular processes and provide additional evidence that ensuring fidelity of protein translation is a major role of hydroxylation.


Subject(s)
Gene Expression Regulation , Histone Demethylases/metabolism , Mixed Function Oxygenases/chemistry , Peptide Chain Termination, Translational/genetics , Peptide Termination Factors/chemistry , Protein Biosynthesis , Amino Acid Sequence , Animals , Catalysis , Cell Line, Tumor , Codon, Terminator , HeLa Cells , Humans , Hydrolysis , Hydroxylation , Jumonji Domain-Containing Histone Demethylases , Models, Molecular , Molecular Sequence Data , Protein Processing, Post-Translational , Protein Structure, Tertiary , Sequence Homology, Amino Acid
11.
PLoS One ; 8(10): e77423, 2013.
Article in English | MEDLINE | ID: mdl-24204825

ABSTRACT

Signaling through the T cell receptor (TCR) initiates adaptive immunity and its perturbation may results in autoimmunity. The plasma membrane scaffolding protein LAT acts as a central organizer of the TCR signaling machinery to activate many functional pathways. LAT-deficient mice develop an autoimmune syndrome but the mechanism of this pathology is unknown. In this work we have compared global dynamics of TCR signaling by MS-based quantitative phosphoproteomics in LAT-sufficient and LAT-defective Jurkat T cells. Surprisingly, we found that many TCR-induced phosphorylation events persist in the absence of LAT, despite ERK and PLCγ1 phosphorylation being repressed. Most importantly, the absence of LAT resulted in augmented and persistent tyrosine phosphorylation of CD3ζ and ZAP70. This indicates that LAT signaling hub is also implicated in negative feedback signals to modulate upstream phosphorylation events. Phosphorylation kinetics data resulting from this investigation is documented in a database (phosphoTCR) accessible online. The MS data have been deposited to the ProteomeXchange with identifier PXD000341.


Subject(s)
Adaptor Proteins, Signal Transducing/genetics , CD3 Complex/genetics , Membrane Proteins/genetics , Phosphoproteins/genetics , Signal Transduction/genetics , ZAP-70 Protein-Tyrosine Kinase/genetics , Adaptor Proteins, Signal Transducing/deficiency , CD3 Complex/metabolism , Chromatography, Liquid , Databases, Protein , Feedback, Physiological , Gene Expression Regulation , Humans , Jurkat Cells , Mass Spectrometry , Membrane Proteins/deficiency , Phospholipase C gamma/genetics , Phospholipase C gamma/metabolism , Phosphoproteins/metabolism , Phosphorylation , Protein Interaction Mapping , Receptors, Antigen, T-Cell/genetics , Receptors, Antigen, T-Cell/metabolism , Tyrosine/metabolism , ZAP-70 Protein-Tyrosine Kinase/metabolism
12.
Proc Natl Acad Sci U S A ; 110(47): 18826-31, 2013 Nov 19.
Article in English | MEDLINE | ID: mdl-24191005

ABSTRACT

The Ste20 family protein kinases oxidative stress-responsive 1 (OSR1) and the STE20/SPS1-related proline-, alanine-rich kinase directly regulate the solute carrier 12 family of cation-chloride cotransporters and thereby modulate a range of processes including cell volume homeostasis, blood pressure, hearing, and kidney function. OSR1 and STE20/SPS1-related proline-, alanine-rich kinase are activated by with no lysine [K] protein kinases that phosphorylate the essential activation loop regulatory site on these kinases. We found that inhibition of phosphoinositide 3-kinase (PI3K) reduced OSR1 activation by osmotic stress. Inhibition of the PI3K target pathway, the mammalian target of rapamycin complex 2 (mTORC2), by depletion of Sin1, one of its components, decreased activation of OSR1 by sorbitol and reduced activity of the OSR1 substrate, the sodium, potassium, two chloride cotransporter, in HeLa cells. OSR1 activity was also reduced with a pharmacological inhibitor of mTOR. mTORC2 phosphorylated OSR1 on S339 in vitro, and mutation of this residue eliminated OSR1 phosphorylation by mTORC2. Thus, we identify a previously unrecognized connection of the PI3K pathway through mTORC2 to a Ste20 protein kinase and ion homeostasis.


Subject(s)
Intracellular Signaling Peptides and Proteins/metabolism , Osmotic Pressure/physiology , Protein Serine-Threonine Kinases/metabolism , Signal Transduction/physiology , Sodium-Potassium-Chloride Symporters/metabolism , Adaptor Proteins, Signal Transducing/deficiency , Analysis of Variance , HeLa Cells , Humans , Immunoblotting , Immunoprecipitation , Mechanistic Target of Rapamycin Complex 2 , Minor Histocompatibility Antigens , Multiprotein Complexes/metabolism , Oligonucleotides/genetics , Phosphoinositide-3 Kinase Inhibitors , Phosphorylation , RNA, Small Interfering/genetics , Sorbitol , TOR Serine-Threonine Kinases/metabolism , WNK Lysine-Deficient Protein Kinase 1
13.
Cell ; 154(2): 416-29, 2013 Jul 18.
Article in English | MEDLINE | ID: mdl-23870129

ABSTRACT

Protein translation is an energetically demanding process that must be regulated in response to changes in nutrient availability. Herein, we report that intracellular methionine and cysteine availability directly controls the thiolation status of wobble-uridine (U34) nucleotides present on lysine, glutamine, or glutamate tRNAs to regulate cellular translational capacity and metabolic homeostasis. tRNA thiolation is important for growth under nutritionally challenging environments and required for efficient translation of genes enriched in lysine, glutamine, and glutamate codons, which are enriched in proteins important for translation and growth-specific processes. tRNA thiolation is downregulated during sulfur starvation in order to decrease sulfur consumption and growth, and its absence leads to a compensatory increase in enzymes involved in methionine, cysteine, and lysine biosynthesis. Thus, tRNA thiolation enables cells to modulate translational capacity according to the availability of sulfur amino acids, establishing a functional significance for this conserved tRNA nucleotide modification in cell growth control.


Subject(s)
Amino Acids, Sulfur/metabolism , Protein Biosynthesis , RNA, Transfer/metabolism , Saccharomyces cerevisiae Proteins/metabolism , Saccharomyces cerevisiae/metabolism , Uridine/metabolism , Down-Regulation , RNA, Transfer/chemistry , Saccharomyces cerevisiae/growth & development
14.
Nat Methods ; 10(4): 343-6, 2013 Apr.
Article in English | MEDLINE | ID: mdl-23474466

ABSTRACT

Here we demonstrate quantitation of stimuli-induced proteome dynamics in primary cells by combining the power of bio-orthogonal noncanonical amino acid tagging (BONCAT) and stable-isotope labeling of amino acids in cell culture (SILAC). In conjunction with nanoscale liquid chromatography-tandem mass spectrometry (nanoLC-MS/MS), quantitative noncanonical amino acid tagging (QuaNCAT) allowed us to monitor the early expression changes of >600 proteins in primary resting T cells subjected to activation stimuli.


Subject(s)
CD4-Positive T-Lymphocytes/metabolism , Gene Expression Regulation/physiology , Proteomics/methods , Amino Acids , CD4-Positive T-Lymphocytes/drug effects , Calcium Ionophores/pharmacology , Carcinogens/pharmacology , Chromatography, Liquid/methods , Humans , Ionomycin/pharmacology , Isotope Labeling , Phorbol Esters/pharmacology , Sensitivity and Specificity , Tandem Mass Spectrometry/methods
15.
PLoS Pathog ; 8(11): e1002993, 2012.
Article in English | MEDLINE | ID: mdl-23144613

ABSTRACT

Protein phosphorylation is a common post-translational modification in eukaryotic cells and has a wide range of functional effects. Here, we used mass spectrometry to search for phosphorylated residues in all the proteins of influenza A and B viruses--to the best of our knowledge, the first time such a comprehensive approach has been applied to a virus. We identified 36 novel phosphorylation sites, as well as confirming 3 previously-identified sites. N-terminal processing and ubiquitination of viral proteins was also detected. Phosphorylation was detected in the polymerase proteins (PB2, PB1 and PA), glycoproteins (HA and NA), nucleoprotein (NP), matrix protein (M1), ion channel (M2), non-structural protein (NS1) and nuclear export protein (NEP). Many of the phosphorylation sites detected were conserved between influenza virus genera, indicating the fundamental importance of phosphorylation for all influenza viruses. Their structural context indicates roles for phosphorylation in regulating viral entry and exit (HA and NA); nuclear localisation (PB2, M1, NP, NS1 and, through NP and NEP, of the viral RNA genome); and protein multimerisation (NS1 dimers, M2 tetramers and NP oligomers). Using reverse genetics we show that for NP of influenza A viruses phosphorylation sites in the N-terminal NLS are important for viral growth, whereas mutating sites in the C-terminus has little or no effect. Mutating phosphorylation sites in the oligomerisation domains of NP inhibits viral growth and in some cases transcription and replication of the viral RNA genome. However, constitutive phosphorylation of these sites is not optimal. Taken together, the conservation, structural context and functional significance of phosphorylation sites implies a key role for phosphorylation in influenza biology. By identifying phosphorylation sites throughout the proteomes of influenza A and B viruses we provide a framework for further study of phosphorylation events in the viral life cycle and suggest a range of potential antiviral targets.


Subject(s)
Influenza A virus/metabolism , Influenza B virus/metabolism , Orthomyxoviridae Infections/metabolism , Proteome/metabolism , Viral Proteins/metabolism , Animals , Cell Line , Dogs , Influenza A virus/chemistry , Influenza B virus/chemistry , Phosphorylation , Proteome/chemistry , Viral Proteins/chemistry
16.
Nat Chem Biol ; 8(12): 960-962, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23103944

ABSTRACT

The finding that oxygenase-catalyzed protein hydroxylation regulates animal transcription raises questions as to whether the translation machinery and prokaryotic proteins are analogously modified. Escherichia coli ycfD is a growth-regulating 2-oxoglutarate oxygenase catalyzing arginyl hydroxylation of the ribosomal protein Rpl16. Human ycfD homologs, Myc-induced nuclear antigen (MINA53) and NO66, are also linked to growth and catalyze histidyl hydroxylation of Rpl27a and Rpl8, respectively. This work reveals new therapeutic possibilities via oxygenase inhibition and by targeting modified over unmodified ribosomes.


Subject(s)
Escherichia coli Proteins/metabolism , Mixed Function Oxygenases/metabolism , Oxygenases/metabolism , Prokaryotic Cells/metabolism , Ribosomes/metabolism , Animals , Arginine/metabolism , Chromosomal Proteins, Non-Histone/metabolism , Dioxygenases , Enzyme Inhibitors/pharmacology , Escherichia coli/metabolism , Escherichia coli Proteins/antagonists & inhibitors , Histidine/metabolism , Histone Demethylases , Humans , Hydroxylation , Magnetic Resonance Spectroscopy , Mixed Function Oxygenases/antagonists & inhibitors , Nuclear Proteins/metabolism , Oxygenases/antagonists & inhibitors , Ribosomal Proteins/metabolism
17.
J Proteome Res ; 11(12): 6282-90, 2012 Dec 07.
Article in English | MEDLINE | ID: mdl-23088505

ABSTRACT

We have extended the functionality of the Central Proteomics Facilities Pipeline (CPFP) to allow use of remote cloud and high performance computing (HPC) resources for shotgun proteomics data processing. CPFP has been modified to include modular local and remote scheduling for data processing jobs. The pipeline can now be run on a single PC or server, a local cluster, a remote HPC cluster, and/or the Amazon Web Services (AWS) cloud. We provide public images that allow easy deployment of CPFP in its entirety in the AWS cloud. This significantly reduces the effort necessary to use the software, and allows proteomics laboratories to pay for compute time ad hoc, rather than obtaining and maintaining expensive local server clusters. Alternatively the Amazon cloud can be used to increase the throughput of a local installation of CPFP as necessary. We demonstrate that cloud CPFP allows users to process data at higher speed than local installations but with similar cost and lower staff requirements. In addition to the computational improvements, the web interface to CPFP is simplified, and other functionalities are enhanced. The software is under active development at two leading institutions and continues to be released under an open-source license at http://cpfp.sourceforge.net.


Subject(s)
Computational Biology/methods , Proteomics/methods , Software , Cell Line , Computational Biology/economics , Databases, Protein , Electronic Data Processing/methods , Humans , Internet , Proteomics/economics , Reproducibility of Results , Search Engine , Time Factors
18.
Mol Cell Proteomics ; 11(11): 1489-99, 2012 Nov.
Article in English | MEDLINE | ID: mdl-22865923

ABSTRACT

The lack of methods for proteome-scale detection of arginine methylation restricts our knowledge of its relevance in physiological and pathological processes. Here we show that most tryptic peptides containing methylated arginine(s) are highly basic and hydrophilic. Consequently, they could be considerably enriched from total cell extracts by simple protocols using either one of strong cation exchange chromatography, isoelectric focusing, or hydrophilic interaction liquid chromatography, the latter being by far the most effective of all. These methods, coupled with heavy methyl-stable isotope labeling by amino acids in cell culture and mass spectrometry, enabled in T cells the identification of 249 arginine methylation sites in 131 proteins, including 190 new sites and 93 proteins not previously known to be arginine methylated. By extending considerably the number of known arginine methylation sites, our data reveal a novel proline-rich consensus motif and identify for the first time arginine methylation in proteins involved in cytoskeleton rearrangement at the immunological synapse and in endosomal trafficking.


Subject(s)
Arginine/metabolism , Proteins/metabolism , Proteomics/methods , Amino Acid Sequence , CD4-Positive T-Lymphocytes/metabolism , Cell Compartmentation , Chromatography, Ion Exchange , Chromatography, Liquid , Computational Biology , Humans , Hydrophobic and Hydrophilic Interactions , Isoelectric Focusing , Isotope Labeling , Jurkat Cells , Methylation , Models, Biological , Molecular Sequence Data , Peptides/metabolism , Proteins/chemistry
19.
Mol Cell Proteomics ; 11(2): M9.00384, 2012 Feb.
Article in English | MEDLINE | ID: mdl-22311593

ABSTRACT

Ankylosing spondylitis (AS) is a common, inflammatory rheumatic disease that primarily affects the axial skeleton and is associated with sacroiliitis, uveitis, and enthesitis. Unlike other autoimmune rheumatic diseases, such as rheumatoid arthritis or systemic lupus erythematosus, autoantibodies have not yet been reported to be a feature of AS. We therefore wished to determine whether plasma from patients with AS contained autoantibodies and, if so, characterize and quantify this response in comparison to patients with rheumatoid arthritis (RA) and healthy controls. Two high density nucleic acid programmable protein arrays expressing a total of 3498 proteins were screened with plasma from 25 patients with AS, 17 with RA, and 25 healthy controls. Autoantigens identified were subjected to Ingenuity Pathway Analysis to determine the patterns of signaling cascades or tissue origin. 44% of patients with ankylosing spondylitis demonstrated a broad autoantibody response, as compared with 33% of patients with RA and only 8% of healthy controls. Individuals with AS demonstrated autoantibody responses to shared autoantigens, and 60% of autoantigens identified in the AS cohort were restricted to that group. The autoantibody responses in the AS patients were targeted toward connective, skeletal, and muscular tissue, unlike those of RA patients or healthy controls. Thus, patients with AS show evidence of systemic humoral autoimmunity and multispecific autoantibody production. Nucleic acid programmable protein arrays constitute a powerful tool to study autoimmune diseases.


Subject(s)
Autoantibodies/blood , Autoantigens/immunology , Nucleic Acids/chemistry , Protein Array Analysis , Spondylitis, Ankylosing/diagnosis , Spondylitis, Ankylosing/immunology , Adolescent , Adult , Aged , Autoantibodies/immunology , Case-Control Studies , Female , Humans , Male , Middle Aged , Prognosis , Proteome/analysis , Spondylitis, Ankylosing/blood , Young Adult
20.
EMBO Rep ; 13(3): 251-7, 2012 Mar 01.
Article in English | MEDLINE | ID: mdl-22310300

ABSTRACT

Hypoxic and oxidant stresses can coexist in biological systems, and oxidant stress has been proposed to activate hypoxia pathways through the inactivation of the 'oxygen-sensing' hypoxia-inducible factor (HIF) prolyl and asparaginyl hydroxylases. Here, we show that despite reduced sensitivity to cellular hypoxia, the HIF asparaginyl hydroxylase--known as FIH, factor inhibiting HIF--is strikingly more sensitive to peroxide than the HIF prolyl hydroxylases. These contrasting sensitivities indicate that oxidant stress is unlikely to signal hypoxia directly to the HIF system, but that hypoxia and oxidant stress can interact functionally as distinct regulators of HIF transcriptional output.


Subject(s)
Hypoxia-Inducible Factor 1, alpha Subunit/metabolism , Mixed Function Oxygenases/metabolism , Peroxides/metabolism , Repressor Proteins/metabolism , Cell Hypoxia/genetics , Cell Line , Cysteine/metabolism , Gene Expression Regulation/drug effects , Humans , Hydroxylation/drug effects , Mixed Function Oxygenases/antagonists & inhibitors , Peroxides/pharmacology , Repressor Proteins/antagonists & inhibitors , Transcription, Genetic
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