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1.
Oncotarget ; 6(4): 1920-41, 2015 Feb 10.
Article in English | MEDLINE | ID: mdl-25605240

ABSTRACT

The biochemistry of cancer cells diverges significantly from normal cells as a result of a comprehensive reprogramming of metabolic pathways. A major factor influencing cancer metabolism is hypoxia, which is mediated by HIF1α and HIF2α. HIF1α represents one of the principal regulators of metabolism and energetic balance in cancer cells through its regulation of glycolysis, glycogen synthesis, Krebs cycle and the pentose phosphate shunt. However, less is known about the role of HIF1α in modulating lipid metabolism. Lipids serve cancer cells to provide molecules acting as oncogenic signals, energetic reserve, precursors for new membrane synthesis and to balance redox biological reactions. To study the role of HIF1α in these processes, we used HCT116 colorectal cancer cells expressing endogenous HIF1α and cells in which the hif1α gene was deleted to characterize HIF1α-dependent and independent effects on hypoxia regulated lipid metabolites. Untargeted metabolomics integrated with proteomics revealed that hypoxia induced many changes in lipids metabolites. Enzymatic steps in fatty acid synthesis and the Kennedy pathway were modified in a HIF1α-dependent fashion. Palmitate, stearate, PLD3 and PAFC16 were regulated in a HIF-independent manner. Our results demonstrate the impact of hypoxia on lipid metabolites, of which a distinct subset is regulated by HIF1α.


Subject(s)
Hypoxia-Inducible Factor 1, alpha Subunit/metabolism , Lipid Metabolism , Lipids/biosynthesis , Signal Transduction , Acetyl-CoA C-Acyltransferase/genetics , Acetyl-CoA C-Acyltransferase/metabolism , Acetyl-CoA Carboxylase/genetics , Acetyl-CoA Carboxylase/metabolism , Aged , Basic Helix-Loop-Helix Transcription Factors/genetics , Basic Helix-Loop-Helix Transcription Factors/metabolism , Blotting, Western , Cell Hypoxia , Cell Line, Tumor , Colorectal Neoplasms/genetics , Colorectal Neoplasms/metabolism , Colorectal Neoplasms/pathology , Fatty Acids/biosynthesis , Female , Genomics/methods , HCT116 Cells , Humans , Hypoxia-Inducible Factor 1, alpha Subunit/genetics , Male , Metabolomics/methods , Middle Aged , Platelet Activating Factor/genetics , Platelet Activating Factor/metabolism , Proteomics/methods , RNA Interference
2.
Mol Pain ; 4: 33, 2008 Aug 12.
Article in English | MEDLINE | ID: mdl-18700027

ABSTRACT

Neuropathic pain may arise following peripheral nerve injury though the molecular mechanisms associated with this are unclear. We used proteomic profiling to examine changes in protein expression associated with the formation of hyper-excitable neuromas derived from rodent saphenous nerves. A two-dimensional difference gel electrophoresis (2D-DIGE) profiling strategy was employed to examine protein expression changes between developing neuromas and normal nerves in whole tissue lysates. We found around 200 proteins which displayed a >1.75-fold change in expression between neuroma and normal nerve and identified 55 of these proteins using mass spectrometry. We also used immunoblotting to examine the expression of low-abundance ion channels Nav1.3, Nav1.8 and calcium channel alpha2delta-1 subunit in this model, since they have previously been implicated in neuronal hyperexcitability associated with neuropathic pain. Finally, S35methionine in vitro labelling of neuroma and control samples was used to demonstrate local protein synthesis of neuron-specific genes. A number of cytoskeletal proteins, enzymes and proteins associated with oxidative stress were up-regulated in neuromas, whilst overall levels of voltage-gated ion channel proteins were unaffected. We conclude that altered mRNA levels reported in the somata of damaged DRG neurons do not necessarily reflect levels of altered proteins in hyper-excitable damaged nerve endings. An altered repertoire of protein expression, local protein synthesis and topological re-arrangements of ion channels may all play important roles in neuroma hyper-excitability.


Subject(s)
Neuroma/metabolism , Peripheral Nerves/metabolism , Protein Biosynthesis/physiology , Proteome/metabolism , Animals , Electrophoresis, Gel, Two-Dimensional , Gene Expression Profiling , Mice , Mice, Inbred C57BL , Protein Biosynthesis/genetics , Proteome/genetics , Psychomotor Agitation/genetics , Psychomotor Agitation/metabolism , Rats , Rats, Sprague-Dawley
3.
J Proteome Res ; 6(1): 376-81, 2007 Jan.
Article in English | MEDLINE | ID: mdl-17203981

ABSTRACT

Silicone has been used in medical practice as a paradigmatic implant material for decades despite significant detrimental side effects. Our targeted proteomics approach was aimed at identification of the proteins adsorbed to the surface of silicone because they have been characterized as key components in the onset and perpetuation of local immune reactions to silicone. The composition of the proteinacious film, the dynamics of protein deposition, and protein modifications after adsorption were analyzed both in vivo and in vitro. Differential analysis of protein deposition was performed, followed by protein identification with mass spectrometry, database matching, and Western blots. Thus far, we have identified the 30 most abundant proteins deposited on the surface of silicone, the largest known inventory of such proteins so far. Structural and extracellular matrix proteins predominated, followed by mediators of host defense, metabolism, transport, and stress related proteins. In addition, several biochemical modifications of fibronectin, vitronectin, and heat shock protein 60 were detected. Our analyses also revealed previously undetected proteins deposited on the surface of silicone. As tentative initiators and/or modulators of the response to silicone, they are therefore valuable candidates for prognosis and therapy.


Subject(s)
Biocompatible Materials/chemistry , Breast Implants , Proteins/chemistry , Proteomics/methods , Silicone Gels/chemistry , Adsorption , Adult , Blotting, Western , Case-Control Studies , Female , Fibrosis , Humans , Immune System , In Vitro Techniques , Middle Aged , Time Factors , Tissue Adhesions
4.
J Drug Target ; 14(3): 137-46, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16753827

ABSTRACT

Within this study, the potential of three clinically relevant microproteins (SE-AG-AZ, SE-EM and SE-EP) with cystine-knot architecture as pharmacophoric scaffolds for oral peptide delivery was investigated. Cystine-knot microproteins (CKM) were analysed regarding their stability towards the most important gastrointestinal secreted and membrane bound proteases in physiological concentrations. In addition, their permeation behaviour through freshly excised rat intestinal mucosa as well as important parameters such as aggregation behaviour, stability in rat plasma and isoelectric point were evaluated and compared to the properties of the model peptide drugs bacitracin and insulin. Aggregation studies indicate that under physiological conditions between 25 and 70% of the CKMs occur as monomers, whereas the rest forms di- and trimers. Pepsin and elastase cause no or only minor degradation to CKMs, whereas trypsin and chymotrypsin degrade CKMs extensively. Removing the theoretical chymotrypsin cleavage site from a CKM, however, led to stabilization towards this protease. Two of the three evaluated CKMs are stable against membrane bound proteases. P(app) values were determined to be 5.96 +/- 0.98 x 10(-6) and 6.63 +/- 0.47 x 10(-6) cm/s. In conclusion, this study indicates that CKM are promising novel pharmacophoric scaffolds for oral peptide delivery.


Subject(s)
Cystine/chemistry , Peptides/administration & dosage , Proteins/chemistry , Administration, Oral , Amino Acid Sequence , Animals , Chromatography, High Pressure Liquid , Isoelectric Point , Molecular Sequence Data , Peptides/chemistry , Rats
5.
Electrophoresis ; 27(8): 1641-50, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16550499

ABSTRACT

In the present study, we used 2-D differential gel electrophoresis (2-D DIGE) and MS to screen biomarker candidates in serum samples obtained from 39 patients with breast cancer and 35 controls. First, we pooled the serum samples matched with age and menopausal status. Then, we depleted the two most abundant proteins albumin and IgG by immunoaffinity chromatography under partly denaturing conditions in order to enrich low-abundance proteins and proteins with low molecular weight. Concentrated and desalted samples were labeled with three different CyDyes including one internal standard, pooled from all the samples, and separated with 2-D DIGE in triplicate experiments. Biological variations of the protein expression level were analyzed with DeCyder software and evaluated for reproducibility and statistical significance. The profile of differentially expressed protein spots between patients and controls revealed proapolipoprotein A-I, transferrin, and hemoglobin as up-regulated and three spots, apolipoprotein A-I, apolipoprotein C-III, and haptoglobin alpha2 as down-regulated in patients. Finally, routine clinical immunochemical reactions were used to validate selected candidate biomarkers by quantitative determination of specific proteins in all individual serum samples. The serum level of transferrin correlated well with the 2-D-DIGE results. However, the serum levels of apolipoprotein A-I and haptoglobin could not be detected with the clinical routine diagnostic tests. This demonstrated an advantage 2-D DIGE still has over other techniques. 2-D DIGE can distinguish between isoforms of proteins, where the overall immunochemical quantification does fail due to a lack of isoform-special antibodies.


Subject(s)
Biomarkers/blood , Breast Neoplasms/blood , Electrophoresis, Gel, Two-Dimensional/methods , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization/methods , Adult , Apolipoprotein A-I/analysis , Apolipoprotein C-III , Apolipoproteins A/blood , Apolipoproteins C/blood , Down-Regulation , Female , Haptoglobins/analysis , Hemoglobins/analysis , Humans , Middle Aged , Postmenopause , Premenopause , Protein Precursors/blood , Transferrin/analysis , Up-Regulation
6.
J Proteome Res ; 4(6): 2312-9, 2005.
Article in English | MEDLINE | ID: mdl-16335980

ABSTRACT

The study of protein phosphorylation has grown exponentially in recent years, as it became evident that important cellular functions are regulated by phosphorylation and dephosphorylation of proteins on serine, threonine and tyrosine residues. The use of immobilized metal affinity chromatography (IMAC) to enrich phosphopeptides from peptide mixtures has been shown to be useful especially prior to mass spectrometric analysis. For the selective enrichment applying solid-phase extraction (SPE) of phosphorylated peptides, we introduce poly(glycidyl methacrylate/divinylbenzene) (GMD) derivatized with imino-diacetic acid (IDA) and bound Fe(III) as a material. GMD is rapidly synthesized and the resulting free epoxy groups enable an easy access to further derivatization with, e.g., IDA. Electron microscopy showed that the synthesized GMD-IDA-Fe(III) for SPE has irregular agglomerates of spherical particles. Inductively coupled plasma (ICP) analysis resulted in a metal capacity of Fe(III) being 25.4 micromol/mL. To enable on-line preconcentration and desalting in one single step, GMD-IDA-Fe(III) and Silica C18 were united in one cartridge. Methyl esterification (ME) of free carboxyl groups was carried out to prevent binding of nonphosphorylated peptides to the IMAC function. The recovery for a standard phosphopeptide using this SPE method was determined to be 92%. The suitability of the established system for the selective enrichment and analysis of model proteins phosphorylated at different amino acid residues was evaluated stepwise. After successful enrichment of beta-casein deriving phosphopeptides, the established system was extended to the analysis of in vitro phosphorylated proteins, e.g. deriving from glutathione-S-transferase tagged extracellular signal regulated kinase 2 (GST-ERK2).


Subject(s)
Iron/analysis , Phosphoproteins/chemistry , Proteomics/methods , Amino Acid Sequence , Caseins/chemistry , Chromatography, Affinity , Epoxy Compounds/chemistry , Glutathione Transferase/metabolism , Imino Acids/chemistry , Iron/chemistry , Mass Spectrometry , Methacrylates/chemistry , Microscopy, Electron , Mitogen-Activated Protein Kinase 1/metabolism , Models, Chemical , Molecular Sequence Data , Myoglobin/chemistry , Peptides/chemistry , Phosphopeptides/chemistry , Phosphorylation , Polymers/chemistry , Proteome , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization , Time Factors , Trypsin/pharmacology , Vinyl Compounds/chemistry
7.
Electrophoresis ; 26(14): 2843-9, 2005 Jul.
Article in English | MEDLINE | ID: mdl-15971195

ABSTRACT

We present a simple protocol for affinity depletion to remove the two most abundant serum proteins, albumin and immunoglobulin G (IgG). Under native conditions, albumin/IgG were efficiently removed and several proteins were enriched as shown by two-dimensional electrophoresis (2-DE). Besides that, partly denaturing conditions were established by adding 5 or 20% acetonitrile (ACN) in order to disrupt the binding of low-molecular-weight (LMW) proteins to the carrier proteins albumin/IgG. 2-DE results showed that the total number of detected LMW proteins increased under denaturing conditions when compared to native conditions. Interestingly, the presence of 5% ACN in serum revealed better enrichment of LMW proteins when compared to 20% ACN condition. Seven randomly distributed spots in albumin/IgG depleted serum samples under 5% ACN condition were picked from the 2-DE gels and identified by mass spectrometry (MS). The intensity of five LMW protein spots increased under denaturing conditions when compared to native conditions. Three of the seven identified spots (serum amyloid P, vitamin D-binding protein, and transthyretin) belong to a group of relatively low-abundant proteins, which make up only 1% of all serum proteins. The method presented here improves the resolution of the serum proteome by increasing the number of visualized spots on 2-D gels and allowing the detection and MS identification of LMW proteins and proteins of lower abundance.


Subject(s)
Albumins/isolation & purification , Blood Proteins/analysis , Chromatography, Affinity/methods , Immunoglobulin G/isolation & purification , Proteome/analysis , Acetonitriles/chemistry , Albumins/chemistry , Electrophoresis, Gel, Two-Dimensional , Humans , Immunoglobulin G/chemistry , Protein Denaturation
8.
Proteomics ; 5(1): 46-54, 2005 Jan.
Article in English | MEDLINE | ID: mdl-15744834

ABSTRACT

Detailed characterization of phosphoproteins as well as other post-translationally modified proteins such as glycoproteins, is required to fully understand protein function and regulatory events in cells and organisms. Therefore, an experimental strategy for the isolation of phosphoproteins using a new immobilized metal ion affinity chromatograph (IMAC) material on the basis of cellulose has been developed and characterized. Different approaches have been used to test the material. Recovery rates were determined by 32P labelling of a myelin basic protein fragment and by reversed-phase high-performance liquid chromatography-electrospray ionization mass spectrometry using a tryptic digest of the model protein bovine beta-casein. Selectivity was demonstrated by enrichment and separation of phosphopeptides from different samples, such as from a digest of horse myoglobin as well as from a digest of in vitro phosphorylated extracellular signal regulates kinase 2 (ERK2) mixed with synthetic phosphopeptides, phosphorylated on different amino acid residues. Furthermore, simplification and optimization of sample pretreatment was achieved by combining the separating (IMAC) and desalting (C18) step during preparative high performance liquid chromatography. The comparison between our material and a commercially available IMAC system (POROS 20 MC; Perspective BioSystems) emphasizes the competitiveness of the cellulose. Confirmed by the obtained data, the cellulose material performed as well as the commercially available sorbent, however with the advantage, that it can be produced rather easily and at very low cost.


Subject(s)
Metals/chemistry , Phosphopeptides/chemistry , Animals , Caseins/chemistry , Cattle , Cellulose/chemistry , Chromatography, Affinity , Chromatography, High Pressure Liquid , Horses , Imino Acids/chemistry , Mitogen-Activated Protein Kinase 1/chemistry , Myoglobin/chemistry , Phosphorylation , Phosphotyrosine/chemistry , Polystyrenes/chemistry , Spectrometry, Mass, Electrospray Ionization
9.
Nature ; 422(6934): 888-93, 2003 Apr 24.
Article in English | MEDLINE | ID: mdl-12712204

ABSTRACT

Leptospirosis is a widely spread disease of global concern. Infection causes flu-like episodes with frequent severe renal and hepatic damage, such as haemorrhage and jaundice. In more severe cases, massive pulmonary haemorrhages, including fatal sudden haemoptysis, can occur. Here we report the complete genomic sequence of a representative virulent serovar type strain (Lai) of Leptospira interrogans serogroup Icterohaemorrhagiae consisting of a 4.33-megabase large chromosome and a 359-kilobase small chromosome, with a total of 4,768 predicted genes. In terms of the genetic determinants of physiological characteristics, the facultatively parasitic L. interrogans differs extensively from two other strictly parasitic pathogenic spirochaetes, Treponema pallidum and Borrelia burgdorferi, although similarities exist in the genes that govern their unique morphological features. A comprehensive analysis of the L. interrogans genes for chemotaxis/motility and lipopolysaccharide synthesis provides a basis for in-depth studies of virulence and pathogenesis. The discovery of a series of genes possibly related to adhesion, invasion and the haematological changes that characterize leptospirosis has provided clues about how an environmental organism might evolve into an important human pathogen.


Subject(s)
Genes, Bacterial/genetics , Genome, Bacterial , Leptospira interrogans/genetics , Leptospira interrogans/pathogenicity , Bacterial Adhesion/genetics , Chemotaxis , Chromosomes, Bacterial/genetics , Humans , Leptospira interrogans/cytology , Leptospira interrogans/metabolism , Lipopolysaccharides/biosynthesis , Molecular Sequence Data , Open Reading Frames/genetics , Sequence Analysis, DNA , Sequence Homology, Amino Acid , Virulence/genetics
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