US20080249083A1 - Novel genes related to glutaminyl cyclase - Google Patents

Novel genes related to glutaminyl cyclase Download PDF

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US20080249083A1
US20080249083A1 US11/859,217 US85921707A US2008249083A1 US 20080249083 A1 US20080249083 A1 US 20080249083A1 US 85921707 A US85921707 A US 85921707A US 2008249083 A1 US2008249083 A1 US 2008249083A1
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seq
qpctl
polypeptide
nucleic acid
isoqc
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Stephan Schilling
Holger Cynis
Jens-Ulrich Rahfeld
Hans-Ulrich Demuth
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Vivoryon Therapeutics AG
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Probiodrug AG
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Priority to US11/859,217 priority Critical patent/US20080249083A1/en
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Priority to US12/497,082 priority patent/US8129160B2/en
Priority to US12/554,584 priority patent/US8889709B2/en
Priority to US13/325,015 priority patent/US8647834B2/en
Priority to US13/888,239 priority patent/US9277737B2/en
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Definitions

  • the present invention relates to novel glutaminyl-peptide cyclotransferase-like proteins (QPCTLs), which are isoenzymes of glutaminyl cyclase (QC, EC 2.3.2.5), and to isolated nucleic acids coding for these isoenzymes, all of which are useful for the discovery of new therapeutic agents, for measuring cyclase activity, and for determining the inhibitory activity of compounds against these glutaminyl cyclase isoenzymes.
  • QPCTLs novel glutaminyl-peptide cyclotransferase-like proteins
  • Glutaminyl cyclase catalyzes the intramolecular cyclization of N-terminal glutamine residues into pyroglutamic acid (pGlu*) liberating ammonia.
  • pGlu* pyroglutamic acid
  • EP 02 011 349.4 discloses polynucleotides encoding insect glutaminyl cyclase, as well as polypeptides encoded thereby.
  • This application further provides host cells comprising expression vectors comprising polynucleotides of the invention. Isolated polypeptides and host cells comprising insect QC are useful in methods of screening for agents that reduce glutaminyl cyclase activity. Such agents are useful as pesticides.
  • Inhibitors of QC which also could be useful as inhibitors of QC isoenzymes, are described in WO 2004/098625, WO 2004/098591, WO 2005/039548 and WO 2005/075436, which are incorporated herein in their entirety, especially with regard to the structure of the inhibitors, their use and their production.
  • Reversible enzyme inhibitors comprise competitive inhibitors, non-competitive reversible inhibitors, slow-binding or tight-binding inhibitors, transition state analogs and multisubstrate analogs.
  • a competitive inhibitor or transition state analog can be designed which contains structural characteristics resembling two or more of the substrates.
  • Irreversible enzyme inhibitors drive the equilibrium between the unbound enzyme and inhibitor and enzyme inhibitor complex (E+I ⁇ - - - >E-I) all the way to the right with a covalent bond ( ⁇ 100 kcal/mole), making the inhibition irreversible.
  • Uncompetitive enzyme inhibitors From the definition of uncompetitive inhibitor (an inhibitor which binds only to ES complexes) the following equilibria can be written:
  • the ES complex dissociates the substrate with a dissociation constant equal to Ks, whereas the ESI complex does not dissociate it (i.e has a Ks value equal to zero).
  • the K m 's of Michaelis-Menten type enzymes are expected to be reduced.
  • Increasing substrate concentration leads to increasing ESI concentration (a complex incapable of progressing to reaction products), therefore the inhibition can not be removed.
  • Preferred according to the present invention are competitive enzyme inhibitors. Most preferred are competitive reversible enzyme inhibitors.
  • k i or “K I ” and “K D ” are binding constants, which describe the binding of an inhibitor to and the subsequent release from an enzyme. Another measure is the “IC 50 ” value, which reflects the inhibitor concentration, which at a given substrate concentration results in 50% enzyme activity.
  • QC comprises glutaminyl cyclase (QC), which is synonymous to glutaminyl-peptide cyclotransferase (QPCT); and QC-like enzymes, which are synonymous to glutaminyl-peptide cyclotransferase-like proteins (QPCTLs).
  • QC and QC-like enzymes have identical or similar enzymatic activity, further defined as QC activity.
  • QC-like enzymes can fundamentally differ in their molecular structure from QC.
  • QC-activity is defined as the catalytic activity of glutaminyl cyclase (QC, QPCT) and QC-like enzymes (QPCTLs). These enzymes are found in various tissues of the body of a mammal including kidney, liver, intestine, brain and body fluids such as CSF, where they cyclize glutamine or glutamate at the N-terminus of biologically active peptides with a high specificity.
  • QC activity is defined as intramolecular cyclization of N-terminal glutamine residues into pyroglutamic acid (pGlu*) or of N-terminal L-homoglutamine or L- ⁇ -homoglutamine to a cyclic pyro-homoglutamine derivative under liberation of ammonia. See therefore schemes 1 and 2.
  • EC as used herein comprises the side activity of glutaminyl cyclase (QC, QPCT) and QC-like enzymes (QPCTLs) as glutamate cyclase (EC), further defined as EC activity.
  • EC activity is defined as intramolecular cyclization of N-terminal glutamate residues into pyroglutamic acid (pGlu*) by glutaminyl cyclase (QC, QPCT) and QC-like enzymes (QPCTLs). See therefore scheme 3 .
  • QC-inhibitor or “glutaminyl cyclase inhibitor” is generally known to a person skilled in the art and means enzyme inhibitors, which inhibit the catalytic activity of glutaminyl cyclase (QC, QPCT) or QC-like enzymes (QPCTLs) or their glutamyl cyclase (EC) activity, preferably by direct interaction of the inhibitor with the enzyme.
  • selective QC-inhibitor as defined herein means enzyme inhibitors, which inhibit the catalytic activity of glutaminyl cyclase (QC, QPCT) but do not or with a lower potency inhibit at least one QC-like enzymes (QPCTLs).
  • selective QC-inhibitors which inhibit glutaminyl cyclase (QC, QPCT) with an ki-value, which is one order of magnitude lower than its ki-value for the inhibition of at least one QC-like enzyme (QPCTL).
  • the ki-value of said selective QC-inhibitor for the inhibition of glutaminyl cyclase is two orders of magnitude lower than its ki-value for the inhibition of at least one QC-like enzyme (QPCTL).
  • selective QC-inhibitors wherein their ki-value for the inhibition of glutaminyl cyclase (QC, QPCT) is three orders of magnitude lower than their ki-value for the inhibition of at least one QC-like enzyme (QPCTL).
  • selective QPCTL-inhibitor as defined herein means enzyme inhibitors, which inhibit the catalytic activity of at least one QC-like enzyme (QPCTL), but do not or with a lower potency inhibit the activity of glutaminyl cyclase (QC, QPCT).
  • QPCTL QC-like enzyme
  • the ki-value of said selective QPCTL-inhibitor for the inhibition of at least one QC-like enzyme is two orders of magnitude lower than its ki-value for the inhibition of of of glutaminyl cyclase (QC, QPCT).
  • selective QPCTL-inhibitors wherein their ki-value for the inhibition of at least one QC-like enzyme (QPCTL) is three orders of magnitude lower than their ki-value for the inhibition of glutaminyl cyclase (QC, QPCT).
  • the subject method and medical use utilize an agent with a K i for QC inhibition of 10 ⁇ M or less, more preferably of 1 ⁇ M or less, even more preferably of 0.1 ⁇ M or less or 0.01 ⁇ M or less, or most preferably 0.01 ⁇ M or less.
  • K i for QC inhibition
  • 10 ⁇ M or less more preferably of 1 ⁇ M or less, even more preferably of 0.1 ⁇ M or less or 0.01 ⁇ M or less, or most preferably 0.01 ⁇ M or less.
  • the QC inhibitors of the subject method or medical use will be small molecules, e.g., with molecular weights of 1000 g/mole or less, 500 g/mole or less, preferably of 400 g/mole or less, and even more preferably of 350 g/mole or less and even of 300 g/mole or less.
  • subject refers to an animal, preferably a mammal, most preferably a human, who has been the object of treatment, observation or experiment.
  • terapéuticaally effective amount means that amount of active compound or pharmaceutical agent that elicits the biological or medicinal response in a tissue system, animal or human being sought by a researcher, veterinarian, medical doctor or other clinician, which includes alleviation of the symptoms of the disease or disorder being treated.
  • the term “pharmaceutically acceptable” embraces both human and veterinary use: for example the term “pharmaceutically acceptable” embraces a veterinarily acceptable compound or a compound acceptable in human medicine and health care.
  • Guillain-Barré syndrome is a serious disorder that occurs when the body's defense (immune) system mistakenly attacks part of the nervous system. This leads to nerve inflammation that causes muscle weakness, which continues to get worse.
  • Guillain-Barré syndrome is an autoimmune disorder. The exact cause of Guillain-Barré syndrome is unknown. The syndrome may occur at any age, but is most common in people of both sexes between the ages 30 and 50. It often follows a minor infection, usually a respiratory (lung) infection or gastrointestinal (gut) infection. Usually, signs of the original infection have disappeared before the symptoms of Guillain-Barré begin. Guillain-Barré syndrome causes inflammation that damages parts of nerves. This nerve damage causes tingling, muscle weakness, and paralysis. The inflammation usually affects the nerve's covering (myelin sheath). Such damage is called demyelination. Demyelination slows nerve signaling. Damage to other parts of the nerve can cause the nerve to stop working.
  • Symptoms of Guillain-Barré get worse very quickly. It may take only a few hours to reach the most severe symptoms. Muscle weakness or the loss of muscle function (paralysis) affects both sides of the body. If the muscle weakness starts in the legs and then spreads to the arms, it is called ascending paralysis.
  • Patients may notice tingling, foot or hand pain, and clumsiness. As the loss of muscle function gets worse, the patient may need breathing assistance.
  • Guillain-Barré syndrome There is no cure for Guillain-Barré syndrome.
  • many treatments are available to help reduce symptoms, treat complications, and speed up recovery. When symptoms are severe, the patient will need to go to the hospital for breathing help, treatment, and physical therapy.
  • a method called plasmaphoresis is used to remove a person's blood and replace it with intravenous fluids or donated blood that is free of antibodies.
  • High-dose immunoglobulin therapy is another procedure used to reduce the severity and length of Guillain-Barré symptoms. Other treatments are directed at preventing complications.
  • CIDP Chronic Inflammatory Demyelinizing Polyradiculoneuropathy
  • CIDP chronic inflammatory demyelinizing polyradiculoneuropathy
  • the process of demyelinization, especially in the region of the nerve roots, is currently regarded as the decisive mechanism in the development of nerve conduction block.
  • One theory is based on a disorder of the blood/cerebrospinal fluid (CSF) barrier as a relatively early important step in the development of the disease.
  • Another theory claims that leaks develop in the blood/CSF barrier as a consequence of the disease and cause the increased protein content in the CSF.
  • non-specific serum constituents without direct reference to the immune system could penetrate into the CSF from the blood, cause neuronal or glial dysfunctions and/or modify neuronal activity.
  • An alternative mechanism is a reduced flow rate of the CSF, which could explain the increased protein content of the CSF.
  • MS Multiple Sclerosis
  • Multiple sclerosis is an autoimmune disease that affects the central nervous system (the brain and spinal cord). Multiple sclerosis usually affects woman more than men. The disorder most commonly begins between ages 20 and 40, but can strike at any age. The exact cause is not known, but MS is believed to result from damage to the myelin sheath, the protective material, which surrounds nerve cells. It is a progressive disease, meaning the damage gets worse over time. Inflammation destroys the myelin, leaving multiple areas of scar tissue (sclerosis). The inflammation occurs when the body's own immune cells attack the nervous system. The inflammation causes nerve impulses to slow down or become blocked, leading to the symptoms of MS. Repeated episodes, or flare ups, of inflammation can occur along any area of the brain and spinal cord. Symptoms vary because the location and extent of each attack varies. Usually episodes that last days, weeks, or months alternate with times of reduced or no symptoms (remission). Recurrence (relapse) is common although non-stop progression without periods of remission may also occur.
  • MS is more likely to occur in northern Europe, the northern United States, southern Australia, and New Zealand than in other areas. Geographic studies indicate there may be an environmental factor involved. People with a family history of MS and those who live in a geographical area with a higher incidence rate for MS have a higher risk of the disease.
  • the present invention provides proteins with glutaminyl cyclase activities that constitute novel members of a family of proteins related to glutaminyl cyclase, including the full-length proteins, alternative splice forms, subunits, and mutants, as well as nucleotide sequences encoding the same.
  • the present invention also provides methods of screening for substrates, interacting proteins, agonists, antagonists or inhibitors of the above proteins, and furthermore to pharmaceutical compositions comprising the proteins and/or mutants, derivatives and/or analogues thereof and/or ligands thereto.
  • proteins having significant sequence similarity to glutaminyl cyclase are proteins (QPCTLs) from human (further named as human isoQC) (GenBank accession no. NM — 017659), mouse (GenBank accession no. NM — 027455), Macaca fascicularis (GenBank accession no. AB168255), Macaca mulatta (GenBank accession no. XM — 001110995), cat (GenBank accession no. XM — 541552), rat (GenBank accession no. XM — 001066591), cow (GenBank accession no. BT026254) or an analogue thereof having at least 50%/75% sequence identity/similarity, preferably 70%/85% sequence identity/similarity, more preferably 90%/95% sequence identity/similarity, most preferably 99% sequence identity/similarity.
  • the protein sequences are given in SEQ. ID NOS: 11 to 18. Further disclosed are nucleic acid sequences coding for these proteins (SEQ. ID NOS: 2 to 9). Table 1 illustrates the similarity between the novel proteins and the known glutaminyl cyclase. Table 2 illustrates the identity between the novel proteins and the known glutaminyl cyclase.
  • the expression pattern of the QPCTLs in brain, prostate and lung tissue is consistent with a role in the diseases described below.
  • the enzymatic activity as glutaminyl cyclase demonstrates that QPCTLs-activating or inhibiting molecules will have numerous therapeutic applications as described below.
  • QPCTL activities described herein and their expression patterns are compatible with their functional roles as physiological regulators of the immune and neuroendocrine systems through the enzymatic modification of biochemical mediators like hormones, peptides and chemokines.
  • biochemical mediators like hormones, peptides and chemokines.
  • the numerous functions previously described for QC based upon the use of inhibitors may be due in part to its action and that of similar proteins, like the QPCTLs. Therefore, the discovery of selective and potent inhibitors of QC, of the QPCTLs and of other related enzymes is considered central to achieving effective and safe pharmaceutical use of these and any newly identified glutaminyl-peptide cyclotransferases, as well as other active compounds that modify the function(s) of such proteins.
  • the invention thus provides novel proteins or polypeptides, the nucleic acids coding therefore, cells which have been modified with the nucleic acid so as to express these proteins, antibodies to these proteins, a screening method for the discovery of new therapeutic agents which are inhibitors of the activity of these proteins (or which are inhibitors of QC and not of the proteins), and therapeutic agents discovered by such screening methods.
  • the novel proteins and the nucleic acids coding therefore can be used to discover new therapeutic agents for the treatment of certain diseases, such as for example, neurodegenerative, reproductive, inflammatory and metabolic disorders and also in the preparation of antibodies with therapeutic or diagnostic value.
  • novel, mature, biologically active proteins preferably of human origin.
  • Such proteins may be isolated in small quantities from suitable animal (including human) tissue or biological fluids by standard techniques; however, larger quantities are more conveniently prepared in cultures of cells genetically modified so as to express the protein.
  • isolated nucleic acid molecules encoding polypeptides of the present invention including mRNAs, DNAs, cDNAs, genomic DNAs thereof.
  • nucleic acid probes are also provided comprising nucleic acid molecules of sufficient length to specifically hybridize to a nucleic acid sequence of the present invention.
  • processes utilizing recombinant techniques are provided for producing such polypeptides useful for in vitro scientific research, for example, synthesis of DNA and manufacture of DNA vectors.
  • Processes for producing such polypeptides include culturing recombinant prokaryotic and/or eukaryotic host cells that have been transfected with DNA vectors containing a nucleic acid sequence encoding such a polypeptide and/or the mature protein under conditions promoting expression of such protein and subsequent recovery of such protein or a fragment of the expressed product.
  • the invention provides methods for using QPCTL polypeptides and polynucleotides for the treatment of diseases.
  • the invention provides an isolated nucleic acid which encodes (a) a QPCTL polypeptide, selected from SEQ ID NOS: 11 to 18, or (b) having an amino acid sequence that is at least about 75% similar thereto and exhibits the same biological function, or which is an alternative splice variant of one of SEQ ID NOS: 2 to 9, or which is a probe comprising at least 14 contiguous nucleotides from said nucleic acid encoding (a) or (b), or which is complementary to any one of the foregoing.
  • a QPCTL polypeptide selected from SEQ ID NOS: 11 to 18, or (b) having an amino acid sequence that is at least about 75% similar thereto and exhibits the same biological function, or which is an alternative splice variant of one of SEQ ID NOS: 2 to 9, or which is a probe comprising at least 14 contiguous nucleotides from said nucleic acid encoding (a) or (b), or which is complementary to any one of the foregoing.
  • the invention provides a polypeptide which may be optionally glycosylated, and which (a) has the amino acid sequence of a mature protein set forth in any one of SEQ ID NOS: 10 to 18; preferably of a mature protein set forth in any one of SEQ ID NOS: 11 to 18 (b) has the amino acid sequence of a mature protein having at least about 75% similarity to one of the mature proteins of (a) and which exhibits the same biological function; (c) has the amino acid sequence of a mature protein having at least about 50% identity with a mature protein of any of SEQ ID NOS: 10 to 18; preferably of a mature protein set forth in any one of SEQ ID NOS: 11 to 18 or (d) is an immunologically reactive fragment of (a).
  • the invention provides a method of screening for a compound capable of inhibiting the enzymatic activity of at least one mature protein according to the present invention, preferably selected from the proteins of SEQ ID NOS: 11 to 18, which method comprises incubating said mature protein and a suitable substrate for said mature protein in the presence of one or more test compounds or salts thereof, measuring the enzymatic activity of said mature protein, comparing said activity with comparable activity determined in the absence of a test compound, and selecting the test compound or compounds that reduce the enzymatic activity.
  • the present invention pertains to diagnostic kits and methods based on the use of a QC-inhibitor, selective QC-inhibitor or selective QPCTL-inhibitor.
  • FIG. 1 shows the sequence alignment of human QC (hQC), human isoQC (hisoQC), murine QC (mQC) and murine isoQC (misoQC). Multiple sequence alignment was performed using ClustalW at PBIL (Pole Bioposition Lyonnais) (http://npsa-pbil.ibcp.fr) with default settings.
  • PBIL Poly Bioposition Lyonnais
  • FIG. 2 shows the sequence alignment of isoQC from Homo sapiens (hisoQC, GenBank NM — 017659, SEQ ID NO: 11), Macaca fascicularis ( M — fascicularis, GenBank AB168255, SEQ ID NO: 13), Macaca mulatta ( M — mulatta, GenBank XM — 001110995, SEQ ID NO: 14), Canis familiaris ( C — familiaris, GenBank XM — 541552, SEQ ID NO: 15), Rattus norvegicus ( R — norvegicus, GenBank XM — 001066591, SEQ ID NO: 16), Mus musculus ( M — musculus, GenBank BC058181, SEQ ID NO: 17) and Bos taurus ( B — taurus, GenBank BT026254, SEQ ID NO: 18).
  • FIG. 3 shows the sequence alignment of human QC (hQC, SEQ ID NO: 10) and human isoQC (hisoQC, SEQ ID NO: 12) and other M28 family members of the metallopeptidase Clan MH. Multiple sequence alignment was performed using ClustalW at ch.EMBnet.org with default settings.
  • FIG. 4 shows the sequence alignment of human QC (hQC, SEQ ID NO: 10) and human isoQC (hisoQC, SEQ ID NO: 11), showing two putative tranlational starts (methionine I—bold, underlined; methionine II—bold).
  • Multiple sequence alignment was performed using ClustalW at PBIL (Preferred Bioposition Lyonnais) http://npsa-pbil.ibcp.fr with default settings.
  • the transmembrane domain, present in human isoQC, is indicated by the black bar.
  • FIG. 5 shows the sequence alignment of human QC (hQC, SEQ ID NO: 10) and human isoQC (hisoQC, SEQ ID NO: 12), starting with methionine II (bold). Multiple sequence alignment was performed using ClustalW at ch.EMBnet.org with default settings. The amino acids involved in metal binding are underlined and typed in bold. The transmembrane domain, present in human isoQC, is indicated by the black bar.
  • FIG. 6 shows the analysis of isoQC expression by RT-PCR. Detection in SH-SY5Y, LN405, HaCaT and Hep-G2.
  • FIG. 7 shows the analysis of isoQC (Met I, SEQ ID NO: 11) subcellular localization by immunhistochemistry.
  • Human isoQC starting at methionine I was expressed as a fusion protein with EGFP (isoQC (MetI) EGFP) in LN 405.
  • Mannosidase II counterstaining was performed using AB3712 (Chemicon). Merge represents the overlay of isoQC (MetI)-EGFP and Mannosidase II staining.
  • FIG. 8 shows the analysis of isoQC (Met I, SEQ ID NO: 11) subcellular localization by immunhistochemistry.
  • Human isoQC starting at methionine I was expressed as a fusion protein with EGFP (isoQC (MetI) EGFP) in LN 405.
  • Mitochondrial counterstaining was performed using MAB1273 (Chemicon).
  • Merge represents the overlay of isoQC (MetI)-EGFP and mitochondrial staining.
  • FIG. 9 shows the analysis of isoQC (Met II, SEQ ID NO: 12) subcellular localization by immunhistochemistry.
  • Human isoQC starting at methionine Ii was expressed as a fusion protein with EGFP (isoQC (MetII) EGFP) in LN 405.
  • Mannosidase II counterstaining was performed using AB3712 (Chemicon). Merge represents the overlay of isoQC (MetII)-EGFP and Mannosidase II staining.
  • FIG. 10 shows the analysis of isoQC (Met II, SEQ ID NO: 12) subcellular localization by immunhistochemistry.
  • Human isoQC starting at methionine II was expressed as a fusion protein with EGFP (isoQC (MetII) EGFP) in LN 405 .
  • Mitochondrial counterstaining was performed using MAB1273 (Chemicon).
  • Merge represents the overlay of isoQC (MetII)-EGFP and mitochondrial staining.
  • FIG. 11 shows the analysis of the subcellular localization of isoQC (Met I, SEQ ID NO: 11) by immunhistochemistry.
  • Human isoQC starting at methionine I was expressed as a fusion protein with EGFP (isoQC (MetI) EGFP) in COS-7.
  • Mannosidase II counterstaining was performed using AB3712 (Chemicon). Merge represents the overlay of isoQC (MetI)-EGFP and Mannosidase II staining.
  • FIG. 12 shows the analysis of isoQC (Met I, SEQ ID NO: 11) subcellular localization by immunhistochemistry.
  • Human isoQC starting at methionine I was expressed as a fusion protein with EGFP (isoQC (MetI) EGFP) in COS-7.
  • Mitochondrial counterstaining was performed using MAB1273 (Chemicon).
  • Merge represents the overlay of isoQC (MetI)-EGFP and mitochondrial staining.
  • FIG. 13 shows the analysis of isoQC (Met II, SEQ ID NO: 12) subcellular localization by immunhistochemistry.
  • Human isoQC starting at methionine II was expressed as a fusion protein with EGFP (isoQC (MetII) EGFP) in COS-7.
  • Mannosidase II counterstaining was performed using AB3712 (Chemicon). Merge represents the overlay of isoQC (MetII)-EGFP and Mannosidase II staining.
  • FIG. 14 shows the analysis of isoQC (Met II, SEQ ID NO: 12) subcellular localization by immunhistochemistry. Expression of human isoQC starting at methionine II as a fusion protein with EGFP (isoQC (MetII) EGFP) in COS-7. Mitochondrial counterstaining was performed using MAB1273 (Chemicon). Merge represents the overlay of isoQC (MetII)-EGFP and mitochondrial staining.
  • FIG. 15 shows the inhibition of human isoQC-catalyzed conversion of H-Gln-AMC into pGlu-AMC by the inhibitor P150/03.
  • the data were evaluated according to the Michaelis-Menten kinetic model considering linear competitive inhibition.
  • Inhibitor concentrations were as follows:
  • FIG. 16 shows the human isoQC-catalyzed conversion of H-Gln-Ala-OH into pGlu-Ala-OH determined using a spectrophotometric assay.
  • the data were evaluated according to Michaelis-Menten kinetics.
  • the kinetic parameters were 324 ⁇ 28 ⁇ M and 7.4 ⁇ 0.2 nM/min for the K M and V max -value, respectively.
  • FIG. 17 provides a schematic representation of the human isoQC protein constructs that were expressed hetereologously in the yeast P. pastoris. Two mutations were introduced in some proteins, leading to a glycosylation site at position 55 (I55N) and a mutated cystein residue at position 351 (C351A). For expression, the N-terminus including the transmembrane domain was replaced by a secretion signal of yeast (YSS). The constructs containing the N-terminal secretion signal should be efficiently secreted into the medium.
  • YSS secretion signal of yeast
  • FIG. 18 shows the QC activity, which was determined in the medium of expressing yeast cells. Due to the transmembrane domain, the native constructs were not secreted into the medium (not implemented). Caused by glycosylation (I55N), proteins are most efficiently secreted. The mutation C351A resulted also in higher QC activity detected in the medium. The constructs are described in FIG. 17 .
  • FIG. 19 shows the purification of the human isoQC, based on construct YSShisoQCI55NC351A C-His, from the medium of a transgenic P.pastoris strain.
  • the QC was purified by a combination of IMAC (immobilized metal affinity chromatography, lane 3), HIC (hydrophobic interaction chromatography, lane 4) and desalting (lane 5).
  • the glycosylation of the enzyme was evidence by enzymatic deglycosalytion, which results in a shift in migration of the protein (lane 6).
  • Lane 1 protein standard: Lane 2, medium prior to purification.
  • FIG. 20 shows the purification of the human isoQC, based on construct GST-hisoQC C-His, from the cell homogenate of transformed E. coli.
  • the isoQC was purified by a combination of IMAC (immobilized metal affinity chromatography, lane 3), GST-affinity (lane 4), desalting (lane 5) and ion exchange chromatography (lane 6).
  • Lane 1 protein standard: Lane 2, cell homogenate prior to purification.
  • the difference in the molecular mass between the hisoQC which was expressed in yeast and E. coli is caused by the N-terminal GST-tag fusion.
  • the expressed construct is provided schematically in the upper part of the figure.
  • FIG. 21 shows the specificity constants for conversion of dipeptide-surrogates, dipeptides and oligopeptides by human isoQC (YSShisoQCI55NC351A C-His; compare FIG. 17 ), GST-hisoQC and human QC.
  • the specificity of GST-hisoQC was the lowest, followed by YSShisoQCI55NC351A C-His.
  • FIG. 22 shows the pH-dependency of catalysis, investigated with human isoQC (hisoQC), which was expressed in yeast, and human QC (hQC). Both proteins display a pH-optimum between pH 7 and 8.
  • the fitted curve is based on three dissociating groups that influence catalysis, one at acidic pH, two at basic pH.
  • FIG. 23 shows the analysis of conversion of glutamic acid, which is present at the N-terminus of the amyloid- ⁇ related peptide AP(3-11).
  • the analysis was performed using Maldi-Tof mass spectrometry, the substrate and product differ in their molecular mass/charge ratio of the single chared molecule by about 18 Da, which is the mass of the released water. In both cases, the same protein concentration was present in the samples, clearly suggesting that human isoQC also converts N-terminal glutamic acid, but slower than the human QC.
  • FIG. 24 shows the tissue distribution of murine QC (mQC, SEQ ID NO: 79) and its isoenzyme misoQC (SEQ ID NO: 17), analyzed using real-time PCR. Bothe enzymes are expressed in the tested organs. However, the expression level of mQC was higher in the brain compared with the peripheral organs. In contrats, misoQC was expressed in all tested organs and tisssues at a more similar level, indicating a ubiquitous, “house-keeping” protein.
  • FIG. 25 shows the time-dependent inhibition of human isoQC (hisoQC) by metal-chelating compounds 1,10-phenanthroline (circles) and EDTA (squares). Residual hisoQC activity was determined directly after addition (closed symbols) or preincubation of hisoQC with respective reagent for 15 min at 30° C. (open symbols).
  • FIG. 26 shows the biochemical analysis of the subcellular localization of QC activity after expression of pcDNA and the native enzymes hisoQC (Met I, SEQ ID NO: 11), hisoQC (Met II, SEQ ID NO: 12) and hQC (SEQ ID NO: 10) in HEK293 cells.
  • HisoQC Metal I, SEQ ID NO: 11
  • hisoQC Metal II, SEQ ID NO: 12
  • hQC hQC
  • h-isoQC (Met I, SEQ ID NO: 11), h-isoQC (Met II, SEQ ID NO: 12) and hQC (SEQ ID NO: 10) possessing a C-terminal FLAG-tag in HEK293 in comparison to vector-transfected control (pcDNA), followed by Western Blot analysis applying specific antibodies detecting either the FLAG-epitope (anti-DYKDDDDK-antibody, Cell Signaling), a 65 kDa protein of human mitochondria (anti-human mitochondria, Chemicon) or human Sialyltransferase ST1GAL3 (Abnova).
  • FIG. 27 shows the subcellular localization of human isoQC (hisoQC) signal sequences (A) methionine I—serine 53 and (B) methionine II—serine 53, fused to EGFP.
  • Golgi complex was stained using an anti-mannosidase II antibody and mitochondria were stained using an antibody detecting a 65 kDA protein of human mitochondria.
  • Co-localization is shown by superimposition of EGFP fluorescence and Red X fluorescence (Merge).
  • FIG. 28 shows the domain structure of human isoQC (hisoQC) and murine isoQC (misoQC ) in comparison to published sequences of human glycosyltransferases: alpha-N-acetylgalactosaminide alpha-2,6-sialyl transferase 1 (ST6GaINAC1; E.C. 2.4.99.3); beta-1,4-galactosyltransferase 1 (b 4 Gal-T1, E.C. 2.4.1.-); Galactoside 3(4)-L-fucosyltransferase (FucT-III; E.C.
  • FIG. 29 shows the quantification of human isoQC (QPCTL) mRNA in different carcinoma cell lines.
  • the QPCTL expression was normalized to 50 ng total-RNA.
  • the black bar within the boxes represents the respective median.
  • FIG. 30 shows the quantification of human isoQC (QPCTL) mRNA expression in different melanoma cell lines.
  • the QPCTL expression was normalized to 50 ng total-RNA.
  • FIG. 31 shows the quantification of human isoQC (QPCTL) mRNA expression in samples from soft tissue carcinoma, gastric carcinoma and thyroid carcinoma from different patients.
  • the QPCTL expression was normalized to 50 ng total-RNA.
  • the black bar within the boxes represents the respective median.
  • FIG. 32 shows the human isoQC (QPCTL) mRNA expression in different gastric carcinomas against their stage of differentiation. QPCTL expression was normalized to 50 ng total-RNA. The black bar within the boxes represents the respective median.
  • FIG. 33 shows a comparison of human QC (QPCT) mRNA expression in different thyroid carcinomas.
  • QPCT expression was normalized to 50 ng total-RNA.
  • the black bar within the boxes represents the respective median.
  • FTC folicular thyroid carcinoma
  • PTC papillary thyroid carcinoma
  • UTC undifferentiated thyroid carcinoma
  • FIG. 34 shows a comparison of human isoQC (QPCTL) mRNA expression in different thyroid carcinomas.
  • QPCTL expression was normalized to 50 ng total-RNA.
  • the black bar within the boxes represents the respective median.
  • FTC folicular thyroid carcinoma
  • PTC papillary thyroid carcinoma
  • UTC undifferentiated thyroid carcinoma
  • FIG. 35 shows the influence of different stimuli on mRNA expression of human QC (QPCT), human isoQC (QPCTL) and CCL2 in HEK293 cells.
  • the amount of transcripts is depicted relating to basal expression without stimulus.
  • the used concentration of stimulus is stated on the x-axis drawing.
  • FIG. 36 shows the influence of different stimuli on mRNA expression of human QC (QPCT), human isoQC (QPCTL) and CCL2 in FTC-133 cells.
  • QPCT human QC
  • QPCTL human isoQC
  • CCL2 CCL2 in FTC-133 cells.
  • the amount of transcripts is depicted relating to basal expression without stimulus.
  • the used concentration of stimulus is stated on the x-axis drawing.
  • FIG. 37 shows the influence of different stimuli on mRNA expression of human QC (QPCT), human isoQC (QPCTL) and CCL2 in THP-1 cells.
  • the amount of transcripts is depicted relating to basal expression without stimulus.
  • the used concentration of stimulus is stated on the x-axis drawing.
  • FIG. 38 shows the influence of different stimuli on mRNA expression of human QC (QPCT), CCL2, CCL7, CCL8 and CCL13 in THP-1 cells.
  • QPCT human QC
  • CCL2 CCL2
  • CCL7 CCL8
  • CCL13 THP-1 cells.
  • the amount of transcripts is depicted relating to basal expression without stimulus.
  • the used concentration of stimulus is stated on the x-axis drawing.
  • FIG. 39 shows the influence of hypoxia on the mRNA level of human QC (QPCT), human isoQC (QPCTL) and HIF1 ⁇ in HEK293 (A), FTC-133 (b) and THP-1 (C).
  • isolated nucleic acid sequences of SEQ ID NOS: 2 to 9, 19 and 20, which encode the mature polypeptides having the deduced amino acid sequences of the QPCTLs from different sources (SEQ ID NOS: 11 to 18, 21 and 22).
  • Preferred according to the present invention are isolated nucleic acid sequences (polynucleotides) of SEQ ID NOS: 2 and 3, 19 and 20, which encode the mature polypeptides having the deduced amino acid sequences of the QPCTLs from human (SEQ ID NOS: 11 and 12, 21 and 22).
  • nucleic acid sequences of SEQ ID NOS: 2 and 3, which encode the mature polypeptides having the deduced amino acid sequences of the human QPCTLs of SEQ ID NOS: 11 and 12.
  • nucleic acid sequences of SEQ ID NOS: 19 and 20, which encode the mature polypeptides having the deduced amino acid sequences of alternative spliceforms of human QPCTLs of SEQ ID NOS: 21 and 22.
  • nucleic acid sequence of SEQ ID NO: 2, which encodes the mature polypeptide having the deduced amino acid sequence of the human QPCTL of SEQ ID NOS: 11.
  • nucleic acid sequence of SEQ ID NO: 3, which encodes the mature polypeptide having the deduced amino acid sequence of the human QPCTL of SEQ ID NOS: 12.
  • the polynucleotides of this invention were discovered by similarity search using Nucleotide BLAST at NCBI (http://www.ncbi.nlm.nih.gov/BLAST/) applying human QC as template.
  • the search resulted in discovery of a putative QPCTL on chromosome 19, which is encoded in region 19q13.32.
  • primers for a cell line screening of human isoQC were designed (Table 4).
  • the isolated cDNA for human QPCTL contains an open reading frame encoding a protein of 382 amino acids in length, which is related to human QC displaying 45.24% sequence identity, and 71.98% similarity.
  • Applying different bioinformatic algorithms (www.expasy.ch) for prediction of the subcellular localization did not result in a reliable result.
  • the prognosis depending on the prediction program, was transfer to golgi-apparatus or mitochondria.
  • the human isoQC gene contains at least 8 exons.
  • the sequence coding for the human isoQC protein is located on exons 1 to 7.
  • Human isoQC maps to chromosome 19 at position 19q13.32.
  • a cell line screening for human isoQC revealed transcripts in cells origin from liver (Hep-G2, hepatocellular carcinoma), skin (HaCaT, keratinocyte) and neuronal tissues (LN405, astrocytoma; SH-SY5Y, neuroblastoma) ( FIG. 6 ).
  • the isolated QPCTL-cDNA was tested on functional expression in several expression hosts.
  • Expression in P. pastoris which was successfully applied for human QC, did not result in an enzymatically active protein.
  • Expression in mammalian cells resulted in detection of activity, however, expression levels were very low.
  • Enzymatically active protein was isolated only following expression of a GST-QPCTL fusion protein in E. coli, applying very unusual expression conditions: Expression for 4 h at 37° C. in presence of 1% Glucose, induction of expression using 20 ⁇ M IPTG. The expression conditions result in a low-level expression in E. coli, which is necessary for functional folding of the peptide chain.
  • the present invention relates to QPCTL knockout animals, preferably rats or mice.
  • QPCTL knockout animals preferably rats or mice.
  • the use of knockout mice in further analysis of the function of QPCTL genes is a valuable tool.
  • the polynucleotides of the present invention may be in the form of RNA or in the form of DNA; DNA should be understood to include cDNA, genomic DNA, and synthetic DNA.
  • the DNA may be double-stranded or single-stranded and, if single stranded, may be the coding strand or non-coding (antisense) strand.
  • the coding sequence, which encodes the mature polypeptide may be identical to the coding sequence shown in SEQ ID NOS 2 to 9, or it may be a different coding sequence encoding the same mature polypeptide, as a result of the redundancy or degeneracy of the genetic code or a single nucleotide polymorphism. For example, it may also be an RNA transcript which includes the entire length of any one of SEQ ID NOS 11 to 18.
  • the polynucleotides which encode the mature proteins of SEQ ID NOS 2 to 9 may include but are not limited to the coding sequence for the mature protein alone; the coding sequence for the mature polypeptide plus additional coding sequence, such as a leader or secretory sequence or a proprotein sequence; and the coding sequence for the mature protein (and optionally additional coding sequence) plus non-coding sequence, such as introns or a non-coding sequence 5′ and/or 3′ of the coding sequence for the mature protein.
  • polynucleotide encoding a polypeptide or the term “nucleic acid encoding a polypeptide” should be understood to encompass a polynucleotide or nucleic acid which includes only coding sequence for the mature protein as well as one which includes additional coding and/or non-coding sequence.
  • polynucleotides and nucleic acid are used interchangeably.
  • the present invention also includes polynucleotides where the coding sequence for the mature protein may be fused in the same reading frame to a polynucleotide sequence which aids in expression and secretion of a polypeptide from a host cell; for example, a leader sequence which functions as a secretory sequence for controlling transport of a polypeptide from the cell may be so fused.
  • the polypeptide having such a leader sequence is termed a preprotein or a preproprotein and may have the leader sequence cleaved, by the host cell to form the mature form of the protein.
  • These polynucleotides may have a 5′ extended region so that it encodes a proprotein, which is the mature protein plus additional amino acid residues at the N-terminus.
  • polynucleotides of the present invention may encode mature proteins, or proteins having a prosequence, or proteins having both a prosequence and a presequence (leader sequence).
  • the polynucleotides of the present invention may also have the coding sequence fused in frame to a marker sequence which allows for purification of the polypeptides of the present invention.
  • the marker sequence may be a polyhistidine tag, a hemagglutinin (HA) tag, a c-myc tag or a V5 tag when a mammalian host, e.g. COS-1 cells, is used.
  • the HA tag would correspond to an epitope derived from the influenza hemagglutinin protein (Wilson, I., etal., Cell, 37: 767 (1984)), and the c-myc tag may be an epitope from human Myc protein (Evans, G. I. et al., Mol. Cell. Biol. 5: 3610-3616(1985)).
  • gene means the segment of DNA involved in producing a polypeptide chain; it includes regions preceding and following the coding region (leader and trailer) as well as intervening sequences (introns) between individual coding segments (exons).
  • significant sequence homology is intended to denote that at least 25%, preferably at least 40%, of the amino acid residues are conserved, and that, of the nonconserved residues, at least 40% are conservative substitutions.
  • Fragments of the full-length genes of the present invention may be used as a hybridization probe for a cDNA library to isolate full-length cDNA as well as to isolate other cDNAs, which have significant sequence homology to the gene and will encode proteins or polypeptides having similar biological activity or function.
  • similar biological activity or function for purposes of this application, is meant the ability to form pyroglutamate from a N-terminal glutamine or glutamic acid of peptides, proteins, hormones or other substrates, defined as QC- and EC-activity, respectively.
  • Such a probe of this type has at least 14 bases (at least 14 contiguous nucleotides from one of SEQ ID NOS: 2 to 9), preferably at least 30 bases, and such may contain, for example, 50 or more bases. Preferred are the probes of SEQ ID NOS 53 to 61. Such probe may also be used to identify a cDNA clone corresponding to a full-length transcript and/or a genomic clone or clones that contains the complete gene, including regulatory and promoter regions, exons, and introns.
  • Labelled oligonucleotides having a sequence complementary to that of the gene of the present invention are useful to screen a library of human cDNA, genomic DNA or mRNA or similar libraries from other sources or animals to locate members of the library to which the probe hybridizes.
  • a known DNA sequence may be used to synthesize an oligonucleotide probe, which is then used in screening a library to isolate the coding region of a gene of interest.
  • the present invention is considered to further provide polynucleotides which hybridize to the hereinabove-described sequences wherein there is at least about 70%, preferably at least about 90%, more preferably at least about 95%, and most preferably at least about 99% identity or similarity between the sequences, and thus encode proteins having similar biological activity.
  • identity between two polypeptides when the amino acid sequences contain the same or conserved amino acid substitutes for each individual residue in the sequence. Identity and similarity may be measured using sequence analysis software (e.g., ClustalW at PBIL (Pused Bioposition Lyonnais) http://npsa-pbil.ibcp.fr).
  • the present invention particularly provides such polynucleotides, which hybridize under stringent conditions to the hereinabove-described polynucleotides.
  • stringent conditions means conditions which permit hybridization between polynucleotides sequences and the polynucleotide sequences of SEQ ID NOS: 2 to 9 where there is at least about 70% identity.
  • stringent conditions can be defined by, e.g., the concentrations of salt or formamide in the prehybridization and hybridization solutions, or by the hybridization temperature, and are well known in the art.
  • stringency can be increased by reducing the concentration of salt, by increasing the concentration of formamide, and/or by raising the hybridization temperature.
  • hybridization under high stringency conditions may employ about 50% formamide at about 37° C. to 42° C.
  • hybridization under reduced stringency conditions might employ about 35% to 25% formamide at about 30° C. to 35° C.
  • One particular set of conditions for hybridization under high stringency conditions employs 42° C., 50% formamide, 5 ⁇ SSPE, 0.3% SDS, and 200 ⁇ g/ml sheared and denatured salmon sperm DNA.
  • similar conditions as described above may be used in 35% formamide at a reduced temperature of 35° C.
  • the temperature range corresponding to a particular level of stringency can be further narrowed by calculating the purine to pyrimidine ratio of the nucleic acid of interest and adjusting the temperature accordingly.
  • hybridization should occur only if there is at least 95%, and more preferably at least 97%, identity between the sequences.
  • the polynucleotides which hybridize to the hereinabove described polynucleotides in a preferred embodiment encode polypeptides which exhibit substantially the same biological function or activity as the mature protein encoded by one of the cDNAs of SEQ ID NOS: 2 to 9.
  • a suitable polynucleotide probe may have at least 14 bases, preferably 30 bases, and more preferably at least 50 bases, and will hybridize to a polynucleotide of the present invention, which has an identity thereto, as hereinabove described, and which may or may not retain activity.
  • such polynucleotides may be employed as a probe for hybridizing to the polynucleotides of SEQ ID NOS: 2 to 9 respectively, for example, for recovery of such a polynucleotide, or as a diagnostic probe, or as a PCR primer.
  • the present invention includes polynucleotides having at least about a 70% identity, preferably at least about a 90% identity, and more preferably at least about a 95% identity, and most preferably at least about a 99% identity to a polynucleotide which encodes the polypeptides of SEQ ID NOS: 11 to 18 respectively, as well as fragments thereof, which fragments preferably have at least 30 bases and more preferably at least 50 bases, and to polypeptides encoded by such polynucleotides.
  • the genetic code is redundant in that certain amino acids are coded for by more than one nucleotide triplet (codon), and the invention includes those polynucleotide sequences which encode the same amino acids using a different codon from that specifically exemplified in the sequences herein.
  • Such a polynucleotide sequence is referred to herein as an “equivalent” polynucleotide sequence.
  • the present invention further includes variants of the hereinabove described polynucleotides which encode for fragments, such as part or all of the mature protein, analogs and derivatives of one of the polypeptides having the deduced amino acid sequence of any one of SEQ ID NOS: 11 to 18.
  • the variant forms of the polynucleotides may be a naturally occurring allelic variant of the polynucleotides or a non-naturally occurring variant of the polynucleotides.
  • the variant in the nucleic acid may simply be a difference in codon sequence for the amino acid resulting from the degeneracy of the genetic code, or there may be deletion variants, substitution variants and addition or insertion variants.
  • an allelic variant is an alternative form of a polynucleotide sequence, which may have a substitution, deletion or addition of one or more nucleotides that does not substantially alter the biological function of the encoded polypeptide.
  • the present invention further includes polypeptides, which have the deduced amino acid sequence of SEQ ID NOS: 11 to 18, as well as fragments, analogs and derivatives of such polypeptides.
  • fragment when referring to the polypeptides of SEQ ID NOS: 11 to 18, means polypeptides that retain essentially the same biological function or activity as such polypeptides.
  • An analog might, for example, include a proprotein, which can be activated by cleavage of the proprotein portion to produce an active mature protein.
  • the polypeptides of the present invention may be recombinant polypeptides, natural polypeptides or synthetic polypeptide; however, they are preferably recombinant polypeptides, glycosylated or unglycosylated.
  • the fragment, derivative or analog of a polypeptide of any one of SEQ ID NOS 11 to 18, may be (i) one in which one or more of the amino acid residues is substituted with a conserved or non-conserved amino acid residue (preferably a conserved amino acid residue) and such substituted amino acid residue may or may not be one encoded by the genetic code, or (ii) one in which one or more of the amino acid residues includes a substituent group, or (iii) one in which additional amino acids are fused to the mature protein, such as a leader or secretory sequence or a sequence which is employed for purification of the mature polypeptide or a proprotein sequence.
  • Such fragments, derivatives and analogs are deemed to be within the scope of those skilled in the art to provide upon the basis of the teachings herein.
  • polypeptides and polynucleotides of the present invention should be in an isolated form, and preferably they are purified to substantial homogeneity or purity.
  • substantial homogeneity is meant a purity of at least about 85%.
  • isolated is used to mean that the material has been removed from its original environment (e.g., the natural environment if it is naturally occurring).
  • a naturally occurring polynucleotide or polypeptide present in a living animal is not considered to be isolated, but the same polynucleotide or polypeptide, when separated from substantially all of the coexisting materials in the natural system, is considered isolated.
  • the term includes, for example, a recombinant DNA which is incorporated into a vector, into an autonomously replicating plasmid or virus, or into the genomic DNA of a prokaryote or eukaryote; or which exists as a separate molecule (e.g., a cDNA or a genomic or cDNA fragment produced by polymerase chain reaction (PCR) or restriction endonuclease digestion) independent of other sequences. It also includes a recombinant DNA, which is part of a hybrid gene encoding additional polypeptide sequence, e.g., a fusion protein.
  • recombinant DNA which includes a portion of the nucleotides shown in one of SEQ ID NOS 2 to 9 which encodes an alternative splice variant of the QPCTLs.
  • SEQ ID NOS 2 to 9 which encodes an alternative splice variant of the QPCTLs.
  • Various alternative splice variants are exemplified in SEQ ID NOS: 19-22.
  • polypeptides of the present invention include any one of the polypeptides of SEQ ID NOS 11 to 18 (in particular the mature proteins), as well as polypeptides which have at least 75% similarity (e.g. preferably at least 50% and more preferably at least 70% identity) to one of the polypeptides of SEQ ID NOS 11 to 18, more preferably at least 85% similarity (e.g. preferably at least 70% identity) to one of the polypeptides of SEQ ID NOS 11 to 18, and most preferably at least 95% similarity (e.g. preferably at least 90% identity) to any one of the polypeptides of SEQ ID NOS 11 to 18.
  • at least 75% similarity e.g. preferably at least 50% and more preferably at least 70% identity
  • polypeptides of SEQ ID NOS 11 to 18 more preferably at least 85% similarity (e.g. preferably at least 70% identity) to one of the polypeptides of SEQ ID NOS 11 to 18, and most preferably at least 95% similarity (e.
  • Certain preferred embodiments can have at least about 95% sequence identity or more, including, for example, at least about 96% sequence identity, at least about 97% sequence identity, at least about 98% sequence identity, or at least about 99% sequence identity. Moreover, they should preferably include exact portions of such polypeptides containing a sequence of at least 30 amino acids, and more preferably at least 50 amino acids.
  • Fragments or portions of the polypeptides of the present invention may be employed as intermediates for producing the corresponding full-length polypeptides by peptide synthesis. Fragments or portions of the polynucleotides of the present invention may also be used to synthesize full-length polynucleotides of the present invention.
  • the present invention also includes vectors, which include such polynucleotides, host cells which are genetically engineered with such vectors and the production of polypeptides by recombinant techniques using the foregoing.
  • Host cells are genetically engineered (transduced or transformed or transfected) with such vectors, which may be, for example, a cloning vector or an expression vector.
  • the vector may be, for example, in the form of a plasmid, a viral particle, a phage, etc.
  • the engineered host cells can be cultured in conventional nutrient media modified as appropriate for activating promoters, selecting transformants or amplifying the genes of the present invention.
  • the culture conditions such as temperature, pH and the like, are those commonly used with the host cell selected for expression, as well known to the ordinarily skilled artisan.
  • the polynucleotides of the present invention may be employed for producing polypeptides by recombinant techniques.
  • the polynucleotides may be included in any one of a variety of expression vectors for expressing polypeptides.
  • Such vectors include chromosomal, nonchromosomal and synthetic DNA sequences, e.g., derivatives of SV40; bacterial plasmids; phage DNA; baculovirus; yeast plasmids; vectors derived from combinations of plasmids and phage DNA, viral DNA such as vaccinia, adenovirus, fowl pox virus, and pseudorabies.
  • any other vector may be used as long as it is replicable and viable in the host.
  • the appropriate DNA sequence may be inserted into the vector by any of a variety of procedures.
  • the DNA sequence is inserted into an appropriate restriction endonuclease site (s) by procedures well known in the art, which procedures are deemed to be within the scope of those skilled in this art.
  • the DNA sequence in the expression vector is operatively linked to an appropriate expression control sequence (s) (promoter) to direct mRNA synthesis.
  • s expression control sequence
  • promoters there may be mentioned: LTR or SV40 promoter, the E. coli lac or trp, the phage lambda P.sub.L promoter and other promoters known to control expression of genes in prokaryotic or eukaryotic cells or their viruses.
  • the expression vector should also contain a ribosome binding site for translation initiation and a transcription terminator.
  • the vector may also include appropriate sequences for amplifying expression.
  • the expression vectors preferably contain one or more selectable marker genes to provide a phenotypic trait for selection of transformed host cells, such as dihydrofolate reductase or neomycin-resistance for eukaryotic cell culture, or such as tetracycline-or ampicillin-resistance in E. coli.
  • the vector containing the appropriate DNA sequence as hereinabove described, as well as an appropriate promoter or control sequence, may be employed to transform an appropriate host to permit the host to express the protein.
  • appropriate hosts there may be mentioned: bacterial cells, such as E. coli, Streptomyces, Salmonella typhimurium; fungal cells, such as yeast; insect cells, such as Drosophila S2 and Spodoptera Sf9; animal cells, such as CHO, COS or Bowes melanoma; adenoviruses; plant cells, etc.
  • bacterial cells such as E. coli, Streptomyces, Salmonella typhimurium
  • fungal cells such as yeast
  • insect cells such as Drosophila S2 and Spodoptera Sf9
  • animal cells such as CHO, COS or Bowes melanoma
  • adenoviruses adenoviruses
  • plant cells etc.
  • the selection of an appropriate host is deemed to be within the scope of those skilled in the
  • the present invention also includes expression vectors useful for the production of the proteins of the present invention.
  • the present invention further includes recombinant constructs comprising one or more of the sequences as broadly described above.
  • the constructs may comprise a vector, such as a plasmid or viral vector, into which a sequence of the invention has been inserted, in a forward or reverse orientation.
  • the construct further comprises regulatory sequences, including, for example, a promoter, operably linked to the sequence.
  • vectors and promoters are known to those of skill in the art, and are commercially available.
  • the following vectors are provided by way of example: Bacterial: pQE70, pQE60, pQE-9 (Qiagen), pBS, pD10, phagescript, psiX174, pbluescript SK, pbsks, pNH8A, pNH16a, pNHI8A, pNH46A (Stratagene), ptrc99a, pKK223-3, pKK233-3, pDR540 and pRIT5 (Pharmacia); and Eukaryotic: pWLNEO, pSV2CAT, pOG44, pXTI, pSG (Stratagene), pSVK3, pBPV, pMSG, and pSVL (Pharmacia).
  • any other suitable plasmid or vector may be used as long as it is replicable and viable in the
  • Promoter regions can be selected from any desired gene using CAT (chloramphenicol acetyl transferase) vectors or other vectors with selectable markers.
  • CAT chloramphenicol acetyl transferase
  • Two appropriate vectors are pKK232-8 and pCM7.
  • Particular named bacterial promoters include lacl, lacZ, T3, T7, gpt, lambda P.sub.R, P.sub.L and trp.
  • Eukaryotic promoters include CMV immediate early, HSV thymidine kinase, early and late SV40, LTRs from retrovirus, and mouse metallothionein-I. Selection of the appropriate vector and promoter is well within the level of ordinary skill in the art.
  • Components of the expression vector may generally include: 1) a neomycin phosphotransferase (G418), or hygromycin B phosphotransferase (hyg) gene as a selection marker, 2) an E. coli origin of replication, 3) a T7 and SP6 phage promoter sequence, 4) lac operator sequences, 5) the lactose operon repressor gene (lacIq) and 6) a multiple cloning site linker region.
  • G408 neomycin phosphotransferase
  • hyg hygromycin B phosphotransferase
  • lacIq lactose operon repressor gene
  • a multiple cloning site linker region Such an origin of replication (oriC) may be derived from pUC19 (LTI, Gaithersburg, Md.).
  • a nucleotide sequence encoding one of the polypeptides of SEQ ID NOS: 2 to 9 having the appropriate restriction sites is generated, for example, according to the PCR protocol described in Examples 1 and 2 hereinafter, using PCR primers having restriction sites for EcoR I (as the 5′ primer) and Sal I (as the 3′primer) for cloning of isoQC Met I and Met II into vector EGFP-N3, or sites for Spe I (as the 5′ primer) and EcoR I (as the 3′ primer) for cloning of isoQC into vector pET41a.
  • the PCR inserts are gel-purified and digested with compatible restriction enzymes.
  • the insert and vector are ligated according to standard protocols.
  • the present invention provides host cells containing the above-described constructs.
  • the host cell can be a higher eukaryotic cell, such as a mammalian cell, or a lower eukaryotic cell, such as a yeast cell, or the host cell can be a prokaryotic cell, such as a bacterial cell.
  • Introduction of the construct into the host cell can be effected by calcium phosphate transfection, DEAE-Dextran mediated transfection, lipofection or electroporation (Davis, L., Dibner, M., Battey, I., Basic Methods in Molecular Biology, (1986)).
  • polypeptides of the invention can be synthetically produced by conventional peptide synthesizers or by chemical ligation of suitable fragments thus prepared.
  • Mature proteins can be expressed in mammalian cells, yeast, bacteria, or other cells under the control of appropriate promoters. Cell-free translation systems can also be employed to produce such proteins using RNAs derived from the DNA constructs of the present invention. Appropriate cloning and expression vectors for use with prokaryotic and eukaryotic hosts are described by Sambrook, et al., Molecular Cloning: A Laboratory Manual, Second Edition, Cold Spring Harbor, N. Y., (1989).
  • Enhancers include cis-acting elements of DNA, usually about from 10 to 300 bp, that act on a promoter to increase its transcription. Examples include the SV40 enhancer on the late side of the replication origin bp 100 to 270, acytomegalovirus early promoter enhancer, the polyoma enhancer on the late side of the replication origin, and adenovirus enhancers.
  • recombinant expression vectors will include origins of replication and selectable markers permitting transformation of the host cell, e.g., the ampicillin resistance gene of E. coli and S. cerevisiae TRP1 gene, and a promoter derived from a highly expressed gene to direct transcription of a downstream structural sequence.
  • promoters can be derived from operons encoding glycolytic enzymes, such as 3-phosphoglycerate kinase (PGK), alpha-factor, acid phosphatase, or heat shock proteins, among others.
  • the heterologous structural sequence is assembled in appropriate phase with translation initiation and termination sequences, and preferably, a leader sequence capable of directing secretion of translated protein into the periplasmic space or extracellular medium.
  • the heterologous sequence can encode a fusion protein including an N-terminal identification peptide imparting desired characteristics, e.g., stabilization or simplified purification of expressed recombinant product.
  • Useful expression vectors for bacterial use are constructed by inserting a structural DNA sequence encoding a desired protein together with suitable translation initiation and termination signals in operable reading phase with a functional promoter.
  • the vector will comprise one or more phenotypic selectable markers and an origin of replication to ensure maintenance of the vector and to, if desired, provide amplification within the host.
  • Suitable prokaryotic hosts for transformation include E. coli, Bacillus subtilis, Salmonella typhimurium and various species within the genera Pseudomonas, Streptomyces and Staphylococcus, although others may also be employed as a matter of choice.
  • useful expression vectors for bacterial use can comprise a selectable marker and bacterial origin of replication derived from commercially available plasmids comprising genetic elements of the well known cloning vector pBR322 (ATCC 37017).
  • cloning vector pBR322 ATCC 37017
  • Such commercial vectors include, for example, pKK223-3 (Pharmacia Fine Chemicals, Uppsala, Sweden) and GEM1 (Promega Biotec, Madison, Wis., U.S.A.). These pBR322 “backbone” sections are combined with an appropriate promoter and the structural sequence to be expressed.
  • the selected promoter is induced by appropriate means (e.g., temperature shift or chemical induction), and cells are cultured for an additional period.
  • Cells are typically harvested by centrifugation and then disrupted by physical or chemical means, with the resulting crude extract being retained for further purification.
  • Microbial cells employed in expression of proteins can be disrupted by any convenient method, including freeze-thaw cycling, sonication, mechanical disruption and use of cell-lysing agents; such methods are well known to those skilled in the art.
  • mammalian cell culture systems can also be employed to express a recombinant protein.
  • mammalian expression systems include the COS-7 lines of monkey kidney fibroblasts, described by Gluzman, Cell, 23: 175 (1981).
  • Other cell lines capable of expressing a compatible vector include, for example, the C127, 3T3, CHO, HeLa and BHK cell lines.
  • Mammalian expression vectors will generally comprise an origin of replication, a suitable promoter and enhancer, and also any necessary ribosome binding sites, polyadenylation site, splice donor and acceptor sites, transcriptional termination sequences, and 5′ flanking nontranscribed sequences. DNA sequences derived from the SV40 splice, and polyadenylation sites may be used to provide required nontranscribed genetic elements.
  • the polypeptides can be recovered and purified from recombinant cell cultures by methods including ammonium sulfate or ethanol precipitation, acid extraction, anion or cation exchange chromatography, phosphocellulose chromatography, hydrophobic interaction chromatography, affinity chromatography, hydroxylapatite chromatography and lectin chromatography. Recovery can be facilitated if the polypeptide is expressed at the surface of the cells, but such is not a prerequisite. Recovery may also be desirable of cleavage products that are cleaved following expression of a longer form of the polypeptide. Protein refolding steps as known in this art can be used, as necessary, to complete configuration of the mature protein. High performance liquid chromatography (HPLC) can be employed for final purification steps.
  • HPLC high performance liquid chromatography
  • polypeptides of the present invention may be purified natural products, or produced by recombinant techniques from a prokaryotic or eukaryotic host (for example, by bacterial, yeast, higher plant, insect or mammalian cells in culture). Depending upon the host employed in a recombinant production procedure, the polypeptides of the present invention may be glycosylated or may be non-glycosylated. Polypeptides of the invention may also include an initial methionine amino acid residue.
  • the proteins of the invention are isolated and purified so as to be substantially free of contamination from other proteins.
  • the proteins of the invention should constitute at least 80% by weight of the total protein present in a sample, more preferably at least 90%, even more preferably at least 95%, and most preferably at least 98% by weight of the total protein.
  • These proteins may be in the form of a solution in water, another suitable solvent, such as dimethyl sulphoxide (DMSO) or ethanol, or a mixture of suitable solvents.
  • DMSO dimethyl sulphoxide
  • ethanol a mixture of suitable solvents.
  • mixtures of solvents include 10% (by weight) ethanol in water and 2% (by weight) DMSO in water.
  • a solution may further comprise salts, buffering agents, chaotropic agents, detergents, preservatives and the like.
  • the proteins may be in the form of a solid, such as a lyophilised powder or a crystalline solid, which may also comprise a residual solvent, a salt or the like.
  • antibodies includes polyclonal antibodies, affinity-purified polyclonal antibodies, monoclonal antibodies, and antigen-binding fragments, such as F (ab′)2 and Fab′ proteolytic fragments. Genetically engineered intact antibodies or fragments, such as chimeric antibodies, Fv fragments, single chain antibodies and the like, as well as synthetic antigen-binding peptides and polypeptides, are also included.
  • Non-human antibodies may be humanized by grafting non-human CDRs onto human framework and constant regions, or by incorporating the entire non-human variable domains (optionally “cloaking” them with a human-like surface by replacement of exposed residues, wherein the result is a “veneered” antibody). In some instances, humanized antibodies may retain non-human residues within the human variable region framework domains to enhance proper binding characteristics. Through humanizing antibodies, biological half-life may be increased, and the potential for adverse immune reactions upon administration to humans should be reduced.
  • Alternative techniques for generating or selecting antibodies useful herein include in vitro exposure of lymphocytes to human isoQC protein or a peptide therefrom, and selection of antibody display libraries in phage or similar vectors (for instance, through use of immobilized or labeled human isoQC protein or peptide).
  • Genes encoding polypeptides having potential human isoQC polypeptide binding domains can be obtained by screening random peptide libraries displayed on phage (phage display) or on bacteria, such as E. coli. Nucleotide sequences encoding such polypeptides can be obtained in a number of ways well known in the art.
  • polyclonal antibodies can be generated from inoculating a variety of warm-blooded animals, such as horses, cows, goats, sheep, dogs, chickens, rabbits, mice and rats, with a human isoQC polypeptide or a fragment thereof.
  • the immunogenicity of a human isoQC polypeptide may be increased through the use of an adjuvant, such as alum (aluminum hydroxide) or Freund's complete or incomplete adjuvant, or surface active substances, such as lysolecithin, pluronic polyols, polyanions, peptides, oil emulsions, KLH or dinitrophenol.
  • an adjuvant such as alum (aluminum hydroxide) or Freund's complete or incomplete adjuvant
  • surface active substances such as lysolecithin, pluronic polyols, polyanions, peptides, oil emulsions, KLH or dinitrophenol.
  • Polypeptides useful for immunization also include fusion polypeptides, such as fusions of isoQC or a portion thereof with an immunoglobulin polypeptide or with maltose binding protein.
  • the polypeptide immunogen may be a full-length molecule or a portion thereof. If the polypeptide portion is “hapten-like”, such portion may be advantageously joined or linked to a macromolecular carrier, such as keyhole limpet hemocyanin (KLH), bovine serum albumin (BSA) or tetanus toxoid, for immunization.
  • KLH keyhole limpet hemocyanin
  • BSA bovine serum albumin
  • Antibodies to isoQC may also be generated using methods that are well known in the art. Such antibodies may include, but are not limited to, polyclonal, monoclonal, chimeric, and single chain antibodies, Fab fragments, and fragments produced by a Fab expression library.
  • Neutralizing antibodies i.e., those which block or modify interactions at the active sites are especially preferred for therapeutic use.
  • libraries of single chain antibodies, Fab fragments, other antibody fragments, non-antibody protein domains, or peptides may be screened.
  • the libraries could be generated using phage display, other recombinant DNA methods, or peptide synthesis (Vaughan, T. J. et al. Nature Biotechnology 14: 309-314 (1966)).
  • Such libraries would commonly be screened using methods, which are well known in the art to identify sequences which demonstrate specific binding to QPCTL.
  • the oligopeptides, peptides, or fragments used to induce antibodies to QPCTL have an amino acid sequence consisting of at least about 5 amino acids and, more preferably, of at least about 10 amino acids. It is also preferable that these oligopeptides, peptides, or fragments are identical to a portion of the amino acid sequence of the natural protein. Short stretches of QPCTL amino acids may also be fused with those of another protein, such as KLH, and antibodies to the chimeric molecule may be produced.
  • Monoclonal antibodies to QPCTL may be prepared using any well known technique which provides for the production of antibody molecules by continuous cell lines in culture. These include, but are not limited to, the hybridoma technique, the human B-cell hybridoma technique, and the EBV-hybridoma technique, although monoclonal antibodies produced by hybridoma cells may be preferred.
  • chimeric antibodies such as the splicing of mouse antibody genes to human antibody genes to obtain a molecule with appropriate antigen specificity and biological activity, can be used, see Neuberger, M. S. et al. Nature 312: 604-608 (1984).
  • techniques described for the production of single chain antibodies may be adapted, using methods known in the art, to produce QPCTL-specific single chain antibodies.
  • Antibodies with related specificity, but of distinct idiotypic composition may be generated by chain shuffling from random combinatorial immunoglobulin libraries. (Burton D. R. Proc. Natl. Acad. Sci. 88: 11120-11123 (1991)).
  • Antibodies may also be produced by inducing in vivo production in the lymphocyte population or by screening immunoglobulin libraries or panels of highly specific binding reagents as disclosed in the literature. (Orlandi, R. et al. Proc. Natl. Acad. Sci. 86: 3833-3837 (1989)).
  • Antibody fragments which contain specific binding sites for QPCTL may also be generated.
  • fragments include, but are not limited to, F(ab′) 2 fragments produced by pepsin digestion of the antibody molecule and Fab fragments generated by reducing the disulfide bridges of the F(ab′) 2 fragments.
  • Fab expression libraries may be constructed to allow rapid and easy identification of monoclonal Fab fragments with the desired specificity. (Huse, W. D. et al. Science 254: 1275-1281(1989)).
  • immunoassays may be used to identify antibodies having the desired specificity.
  • Numerous protocols for competitive binding or immunoradiometric assays using either polyclonal or monoclonal antibodies with established specificities are well known in the art.
  • Such immunoassays typically involve the measurement of complex formation between QPCTL and its specific antibody.
  • a two-site, monoclonal-based immunoassay utilizing monoclonal antibodies reactive to two non-interfering QPCTL epitopes is preferred, but a competitive binding assay may also be employed.
  • the QPCTLs can be used in treatment of the Diseases.
  • compositions suitable for use in this aspect of the invention include compositions wherein the active ingredients are contained in an effective amount to achieve the intended purpose relating to one of the Diseases.
  • the determination of a therapeutically effective dose is well within the capability of those skilled in the art and can be estimated initially either in cell culture assays, e.g. of neoplastic cells, or in animal models, usually mice, rats, rabbits, dogs, or pigs.
  • An animal model may also be used to determine the appropriate concentration range and route of administration, which information is then commonly used to determine useful doses and routes for administration in humans.
  • a therapeutically effective dose refers to that amount of active ingredient, e.g. a QPCTL or fragment thereof, antibodies of DPRP, or an agonist, antagonist or inhibitor of QPCTL, which ameliorates particular symptoms or conditions of the disease.
  • the amount to be administered may be effective to cyclise N-terminal Glu or Gln of a desired target substrate upon contact therewith.
  • Therapeutic efficacy and toxicity may likewise be determined by standard pharmaceutical procedures in cell cultures or with experimental animals, such as by calculating the ED50 (the dose therapeutically effective in 50% of the population) or LD50 (the dose lethal to 50% of the population) statistics.
  • the dose ratio of toxic to therapeutic effects is the therapeutic index, and it can be expressed as the LD50/ED50 ratio.
  • compositions which exhibit large therapeutic indices, are preferred.
  • the data obtained from cell culture assays and animal studies is used in formulating a range of dosage for human use.
  • the dosage contained in such compositions is preferably within a range of circulating concentrations that include the ED50 with little or no toxicity.
  • the dosage varies within this range depending upon the dosage form employed, the sensitivity of the patient, and the route of administration.
  • An exact dosage will normally be determined by the medical practitioner in light of factors related to the subject requiring treatment, with dosage and administration being adjusted to provide a sufficient level of the active moiety or to maintain a desired effect. Factors to be taken into account include the severity of the disease state, the general health of the subject, the age, weight, and gender of the subject, diet, time and frequency of administration, drug combination (s), reaction sensitivities, and tolerance/response to therapy. Long-acting pharmaceutical compositions may be administered every 3 to 4 days, every week, or even once every two weeks, depending on the half-life and clearance rate of the particular formulation.
  • Yet another aspect of the invention provides polynucleotide molecules having sequences that are antisense to mRNA transcripts of a polynucleotide of SEQ ID NOS 2 to 9.
  • Administration of an antisense polynucleotide molecule can block the production of the protein encoded by the QPCTL genes of SEQ ID NOS 2 to 9.
  • the techniques for preparing antisense polynucleotide molecules and administering such molecules are known in the art.
  • antisense polynucleotide molecules can be encapsulated into liposomes for fusion with cells.
  • the expression of the QPCTL genes of SEQ ID NOS 2 to 9 in brain, prostate, lung, heart, liver, spleen and kidney tissue provides evidence for a potential role in the pathophysiology of the diseases described below. Therefore in a further aspect, the invention relates to diagnostic assays for detecting diseases associated with inappropriate QPCTL activity or expression levels.
  • Antibodies that specifically bind QPCTL may be used for the diagnosis of disorders characterized by expression of QPCTL, or in assays to monitor patients being treated with QPCTL or with agonists or antagonists (inhibitors) of QPCTL.
  • Antibodies useful for diagnostic purposes may be prepared in the same manner as those described above for therapeutics.
  • Diagnostic assays for QPCTL include methods that utilize the antibody and a label to detect QPCTL in human body fluids or in extracts of cells or tissues.
  • the antibodies may be used with or without modification, and they may be labeled by covalent or non-covalent joining with a reporter molecule.
  • reporter molecules A wide variety of reporter molecules are known in the art.
  • Recombinant QPCTL proteins that have been modified so as to be catalytically inactive can also be used as dominant negative inhibitors. Such modifications include, for example, mutation of the active site.
  • a variety of protocols for measuring QPCTL are known in the art and provide a basis for diagnosing altered or abnormal levels of QPCTL expression.
  • Normal or standard values for QPCTL expression are established by combining body fluids or cell extracts taken from normal mammalian subjects, preferably human, with antibody to QPCTL under conditions suitable for complex formation.
  • the method for detecting QPCTL in a biological sample would comprise the steps of a) providing a biological sample; b) combining the biological sample and an anti-QPCTL antibody under conditions which are suitable for complex formation to occur between QPCTL and the antibody; and c) detecting complex formation between QPCTL and the antibody, thereby establishing the presence of QPCTL in the biological sample.
  • the amount of complex formation then may be quantified by various methods, preferably by photometric means. Quantities of QPCTL expressed in a subject, control, and disease samples from biopsied tissues are compared with the standard values. Deviation between standard and subject values establishes the parameters for diagnosing disease.
  • the polynucleotides encoding QPCTL are used for diagnostic purposes, which polynucleotides may include oligonucleotide sequences, complementary RNA and DNA molecules, and PNAs. These polynucleotides may be used to detect and quantitate gene expression in biopsied tissues in which expression of QPCTL may be correlated with one of the diseases.
  • the diagnostic assay may be used to distinguish between absence, presence, and excess expression of QPCTL and to monitor regulation of QPCTL levels during therapeutic intervention.
  • pharmacogenomic, single nucleotide polymorphisms (SNP) analysis of the QPCTL genes can be used as a method to screen for mutations that indicate predisposition to disease or modified response to drugs.
  • QPCTL polynucleotide and polypeptide sequences, fragments thereof, antibodies of QPCTLs, and agonists, antagonists or inhibitors of QPCTLs can be used as discovery tools to identify molecular recognition events and therefore proteins, polypeptides and peptides that interact with QPCTL proteins.
  • a specific example is phage display peptide libraries where greater than 108 peptide sequences can be screened in a single round of panning. Such methods as well as others are known within the art and can be utilized to identify compounds that inhibit or enhance the activity of any one of the QPCTLs of SEQ ID NOS 11-18.
  • Coupled links represent functional interactions such as complexes or pathways, and proteins that interact with QPCTLs can be identified by a yeast two-hybrid system, proteomics (differential 2D gel analysis and mass spectrometry) and genomics (differential gene expression by microarray or serial analysis of gene expression SAGE).
  • Proteins identified as functionally linked to QPCTLs and the process of interaction form the basis of methods of screening for inhibitors, agonists and antagonists and modulators of these QPCTL-protein interactions.
  • Antagonist refers to an inhibitor molecule which, when bound to QPCTL, decreases the amount or the duration of the effect of the biological or immunological activity of QPCTL, e.g. decreasing the enzymatic activity of the peptidase to cyclise Glu- or Gln-residues at the N-termini of the QPCTL substrates.
  • Antagonists may include proteins, nucleic acids, carbohydrates, antibodies, or any other molecules which decrease the effect of QPCTL; for example, they may include small molecules and organic compounds that bind to and inactivate QPCTLs by a competitive or non-competitive type mechanism.
  • Preferred are small molecule inhibitors of QPCTL. Most preferred are competitive small molecule inhibitors of QPCTL.
  • Inhibitors can be, for example, inhibitors of the QPCTL cyclase activity, or alternatively inhibitors of the binding activity of the QPCTL to proteins with which they interact.
  • Specific examples of such inhibitors can include, for example, anti-QPCTL antibodies, peptides, protein fragments, or small peptidyl protease inhibitors, or small non-peptide, organic molecule inhibitors which are formulated in a medium that allows introduction into the desired cell type.
  • such inhibitors can be attached to targeting ligands for introduction by cell-mediated endocytosis and other receptor mediated events.
  • Such methods are described further below and can be practiced by those skilled in the art given the QPCTL nucleotide and amino acid sequences described herein.
  • QPCTLs are for the screening of potential antagonists for use as therapeutic agents, for example, for inhibiting binding to QPCTL, as well as for screening for agonists.
  • QPCTL, its immunogenic fragments, or oligopeptides thereof can be used for screening libraries of compoundswhich are prospective agonists or antagonists in any of a variety of drug screening techniques.
  • the fragment employed in such screening may be free in solution, affixed to a solid support, borne on a cell surface, or located intracellularly. The formation of binding complexes between QPCTL and the agent being tested is then measured.
  • Other assays to discover antagonists that will inhibit QPCTL are apparent from the disclosures of Patents Nos.
  • a method provided for screening a library of small molecules to identify a molecule which binds QPCTL generally comprises: a) providing a library of small molecules; b) combining the library of small molecules with the polypeptide of either SEQ ID NOS 11 to 18, or with a fragment thereof, under conditions which are suitable for complex formation; and c) detecting complex formation, wherein the presence of such a complex identifies a small molecule, which binds to the QPCTL.
  • One method for identifying an antagonist comprises delivering a small molecule which binds QPCTL into extracts from cells transformed with a vector expressing QPCTL along with a chromogenic substrate (e.g. Ala-Pro-AFC or Ala-Pro-AMC) under conditions where cleavage would normally occur, and then assaying for inhibition of cleavage by the enzyme by monitoring changes in fluorescence, or UV light absorption, by spectrophotometry to identify molecules that inhibit cleavage.
  • a reduced rate of reaction or total amount of fluorescence or UV light absorption, in the presence of the molecule establishes that the small molecule is an antagonist, which reduces QPCTL catalytic/enzymatic activity.
  • Once such molecules are identified they may be administered to reduce or inhibit cyclisation of N-terminal Glu- or Gln-residues by a QPCTL.
  • the invention provides a method of screening for a compound capable of inhibiting the enzymatic activity of at least one mature protein according to the present invention, preferably selected from the proteins of SEQ ID NOS: 11 to 18, which method comprises incubating said mature protein and a suitable substrate for said mature protein in the presence of one or more test compounds or salts thereof, measuring the enzymatic activity of said mature protein, comparing said activity with comparable activity determined in the absence of a test compound, and selecting the test compound or compounds that reduce the enzymatic activity.
  • the invention also provides a method of screening for a selective QC-inhibitor, i.e. a compound capable of inhibiting the enzymatic activity of QC, wherein said QC is preferably the protein of SQ ID NO: 10, that does not inhibit the enzymatic activity of at least one mature protein according to the present invention, preferably selected from the proteins of SEQ ID NOS: 11 to 18, which method comprises incubating said mature protein and a suitable substrate in the presence of one or more inhibitors or salts thereof of QC, measuring the enzymatic activity of said mature protein, comparing said activity with comparable activity determined in the absence of the QC inhibitor, and selecting a compound that does not reduce the enzymatic activity of said mature protein.
  • a selective QC-inhibitor i.e. a compound capable of inhibiting the enzymatic activity of QC
  • said QC is preferably the protein of SQ ID NO: 10
  • that does not inhibit the enzymatic activity of at least one mature protein according to the present invention preferably selected
  • the invention also provides a method of screening for a selective QPCTL-inhibitor, i.e. a compound capable of inhibiting the enzymatic activity of at least one QPCTL protein, which is preferably selected from the proteins of SEQ ID NOS: 11 to 18; that does not inhibit the enzymatic activity of QC, wherein said QC is preferably the protein of SQ ID NO: 10, which method comprises incubating said QC in the presence of one or more inhibitors or salts thereof of a QPCTL, measuring the enzymatic activity of QC, comparing said activity with comparable activity determined in the absence of the QPCTL inhibitor, and selecting a compound that does not reduce the enzymatic activity of said QPCTL protein.
  • a selective QPCTL-inhibitor i.e. a compound capable of inhibiting the enzymatic activity of at least one QPCTL protein, which is preferably selected from the proteins of SEQ ID NOS: 11 to 18; that does not inhibit the enzymatic activity of QC, wherein
  • QPCTL-inhibitors which are suitable for uses and methods according to the present invention are disclosed in WO 2005/075436, which is incorporated herein in its entirety with regard to the structure, synthesis and methods of use of the QC-inhibitors.
  • a suitable compound is that of formula 1*:
  • inhibitors of QPCTL may be those of formula 1a,
  • R is defined in examples 1 to 53.
  • inhibitors of QPCTL may be those of formula 1b,
  • R 1 and R 2 are defined in examples 54 to 95.
  • inhibitors of QPCTL may be those of formula 1c,
  • R 3 is defined in examples 96 to 102.
  • inhibitors of QPCTL may be those of formula 1d,
  • inhibitors of QPCTL may be those of formula 1e,
  • R 4 and R 5 are defined in examples 106 to 109.
  • inhibitors of QPCTL may be those of formula 1f,
  • R 6 is defined in examples 110 to 112.
  • inhibitors of QPCTL may be those of formula 1g,
  • R 7 , R 8 and R 9 are defined in examples 113 to 132.
  • inhibitors of QPCTL may be are those of formula 1h,
  • n is defined in examples 133 to 135.
  • inhibitors of QPCTL may be those of formula 1i,
  • m is defined in examples 136 and 137.
  • inhibitors of QPCTL may be those of formula 138 to 141.
  • agonist refers to a molecule which, when bound to QPCTL, increases or prolongs the duration of the effect of QPCTL.
  • Agonists may include proteins, nucleic acids, carbohydrates, or any other molecules that bind to and modulate the effect of QPCTL.
  • a method for identifying such a small molecule, which binds QPCTL as an agonist comprises delivering a chromogenic form of a small molecule that binds QPCTL into cells transformed with a vector expressing QPCTL and assaying for fluorescence or UV light absorption changes by spectrophotometry. An increased amount of UV absorption or fluorescence would establish that the small molecule is an agonist that increases QPCTL activity.
  • Another technique for drug screening which may be used provides for high throughput screening of compounds having suitable binding affinity to the protein of interest as described in published PCT application WO 84/03564.
  • large numbers of different small test compounds are synthesized on a solid substrate, such as plastic pins or some other surface.
  • the test compounds are reacted with QPCTL, or with fragments thereof, and then washed. Bound QPCTL is then detected by methods well known in the art.
  • Purified QPCTL can also be coated directly onto plates for use in the aforementioned drug screening techniques.
  • non-neutralizing antibodies can be used to capture the peptide and immobilize it on a solid support.
  • ligands may be designed that, for example, have more interactions with QPCTL than do its natural ligands. Such antagonist ligands will bind to QPCTL with higher affinity and so function as competitive ligands.
  • synthetic or recombinant proteins homologous or analogous to the ligand binding site of native QPCTL may be designed, as may other molecules having high affinity for QPCTL. Such molecules should also be capable of displacing QPCTL and provide a protective effect.
  • QPCTL knowledge of the structures of QPCTL enables synthetic binding site homologues and analogues to be designed. Such molecules will facilitate greatly the use of the binding properties to target potential therapeutic agents, and they may also be used to screen potential therapeutic agents. Furthermore, they may be used as immunogens in the production of monoclonal antibodies, which antibodies may themselves be used in diagnosis and/or therapy as described hereinbefore.
  • amyloid peptides e.g. Abeta 1-42 (SEQ ID NO 23) and Abeta 1-40 (SEQ ID NO 24) become N-terminally truncated by proteolytic enzymes such as for example aminopeptidases or dipeptidyl aminopeptidases, resulting in the Abeta-peptides 3-42 (SEQ ID NO 25), 3-40 (SEQ ID NO 26), 11-42 (SEQ ID NO 27) and 11-40 (SEQ ID NO 28).
  • proteolytic enzymes such as for example aminopeptidases or dipeptidyl aminopeptidases
  • Abeta-peptides of SED ID NOS 29-32 are much more hydrophobic than the non-pyroglutamted peptides, are much more prone to form A-beta peptide aggregates, such as oligomers and fibrills, and were shown to by highly neurotoxic.
  • the Abeta-peptides of SEQ ID NOS 29-32 play a crucial role in the development of Alzheimer's disease and Down Syndrome.
  • inhibitors of the QPCTLs of SEQ ID NOS 11-18, 21 and 22, preferably the human isoQCs of SEQ ID NOS 11, 12, 21 and 22, most preferably the human isoQCs of SEQ ID NOS 11 and 12, may be used for the treatment of amyloid peptide related diseases, especially neurodegenerative diseases, in particular Alzheimer's disease and Down Syndrome.
  • QPTCLs Other potential physiological substrates of QPTCLs in mammals are selected from the group consisting of Glu 1 -ABri (SEQ ID NO 33), Glu 1 -ADan (SEQ ID NO 34), and Gln 1 -Gastrins (17 and 34) (SEQ ID NOS 35 and 36).
  • Their pyroglutamated forms SEQ ID NOS 37-40) cause pathologies such as those selected from the group consisting of duodenal cancer with or w/o Helicobacter pylori infections, colorectal cancer, Zolliger-Ellison syndrome, Familial British Dementia (FBD) and Familial Danish Dementia (FDD). Accordingly, inhibitors of QPCTLs can be used to treat these pathologies.
  • FPP QEP amide A tripeptide related to thyrotrophin releasing hormone (TRH), is found in seminal plasma. Recent evidence obtained in vitro and in vivo showed that FPP plays an important role in regulating sperm fertility.
  • TRH QHP amide TRH functions as a regulator Swiss-Prot: P20396 of the biosynthesis of TSH in the anterior pituitary gland and as a neurotransmitter/ neuromodulator in the central and peripheral nervous systems.
  • GnRH QHWSYGL RP(G) amide Stimulates the secretion of (SEQ ID NO 42) gonadotropins; it stimulates Swiss-Prot: P01148 the secretion of both luteinizing and follicle- stimulating hormones.
  • CCL16 small QPKVPEW VNTPSTCCLK Shows chemotactic activity inducible cytokine YYEKVLPRRL VVGYRKALNC for lymphocytes and A16
  • Recombinant SCYA16 shows chemotactic activity for monocytes and THP-1 monocytes, but not for resting lymphocytes and neutrophils.
  • CCL8 small QPDSVSI PITCCFNVIN Chemotactic factor that inducible cytokine RKIPIQRLES YTRITNIQCP attracts monocytes, A8) KEAVIFKTKR GKEVCADPKE lymphocytes, basophils and (SEQ ID NO 44) RWVRDSMKHL DQIFQNLKP eosinophils. May play a role Swiss-Prot: P80075 in neoplasia and inflammatory host responses. This protein can bind heparin.
  • CCL2 small QPDAINA PVTCCYNFTN Chemotactic factor that inducible cytokine RKISVQRLAS YRRITSSKCP attracts monocytes and A2
  • KEAVIFKTIV AKEICADPKQ basophils but not neutrophils SEQ ID NO 45
  • KWVQDSMDHL DKQTQTPKT or eosinophils Augments Swiss-Prot: P13500 monocyte anti-tumor activity.
  • CCL18 small QVGTNKELC CLVYTSWQIP Chemotactic factor that inducible cytokine QKFIVDYSET SPQCPKPGVI attracts lymphocytes but not A18
  • LLTKRGRQIC ADPNKKWVQK monocytes or granulocytes.
  • SEQ ID NO 46 YISDLKLNA May be involved in B cell Swiss-Prot: P55774 migration into B cell follicles in lymph nodes.
  • naive T lymphocytes toward dendritic cells and activated macrophages in lymph nodes has chemotactic activity for naive T cells, CD4+ and CD8+ T cells and thus may play a role in both humoral and cell-mediated immunity responses.
  • Fractalkine QHHGVT KCNITCSKMT The soluble form is (neurotactin) SKIPVALLIH YQQNQASCGK chemotactic for T cells and (SEQ ID NO 47) RAIILETRQH RLFCADPKEQ monocytes, but not for Swiss-Prot: P78423 WVKDAMQHLD RQAAALTRNG neutrophils.
  • the membrane- GTFEKQIGEV KPRTTPAAGG bound form promotes MDESVVLEPE ATGESSSLEP adhesion of those leukocytes TPSSQEAQRA LGTSPELPTG to endothelial cells. May play VTGSSGTRLP PTPKAQDGGP a role in regulating leukocyte VGTELFRVPP VSTAATWQSS adhesion and migration APHQPGPSLW AEAKTSEAPS processes at the TQDPSTQAST ASSPAPEENA endothelium. Binds to PSEGQRVWGQ GQSPRPENSL cx3cr1.
  • Augments Swiss-Prot P80098 monocyte anti-tumor activity. Also induces the release of gelatinase B.
  • This protein can bind heparin. Binds to CCR1, CCR2 and CCR3.
  • Orexin A QPLPDCCRQK TCSCRLYELL Neuropeptide that plays a (Hypocretin-1) HGAGNHAAGI LTL significant role in the (SEQ ID NO 49) regulation of food intake and Swiss-Prot O43612 sleep-wakefulness, possibly by coordinating the complex behavioral and physiologic responses of these complementary homeostatic functions. It plays also a broader role in the homeostatic regulation of energy metabolism, autonomic function, hormonal balance and the regulation of body fluids.
  • Orexin-A binds to both OX1R and OX2R with a high 7affinity.
  • Substance P RPK PQQFFGLM Belongs to the tachykinins.
  • Tachykinins are active peptides which excite neurons, evoke behavioral responses, are potent vasodilators and secretagogues, and contract (directly or indirectly) many smooth muscles.
  • the peptides Gln 1 -Gastrin (17 and 34 amino acids in length), Gln 1 -Neurotensin and Gln 1 -FPP were identified as new physiological substrates of QPCTLs.
  • Gastrin, Neurotensin and FPP comprise a pGlu residue in their N-terminal position.
  • This N-terminal pGlu residue may be formed from N-terminal glutamine by QPCTL catalysis for all peptides. As a result, these peptides are activated in terms of their biological function upon conversion of the N-terminal glutamine residue to pGlu.
  • Transepithelial transducing cells particularly the gastrin (G) cell, co-ordinate gastric acid secretion with the arrival of food in the stomach.
  • G gastrin
  • Biosynthetic precursors and intermediates are putative growth factors; their products, the amidated gastrins, regulate epithelial cell proliferation, the differentiation of acid-producing parietal cells and histamine-secreting enterochromaffin-like (ECL) cells, and the expression of genes associated with histamine synthesis and storage in ECL cells, as well as acutely stimulating acid secretion.
  • Gastrin also stimulates the production of members of the epidermal growth factor (EGF) family, which in turn inhibit parietal cell function but stimulate the growth of surface epithelial cells.
  • EGF epidermal growth factor
  • Plasma gastrin concentrations are elevated in subjects with Helicobacter pylori, who are known to have increased risk of duodenal ulcer disease and gastric cancer (Dockray, G. J. 1999 J Physiol 15 315-324).
  • the peptide hormone gastrin released from antral G cells, is known to stimulate the synthesis and release of histamine from ECL cells in the oxyntic mucosa via CCK-2 receptors.
  • the mobilized histamine induces acid secretion by binding to the H(2) receptors located on parietal cells.
  • gastrin in both its fully amidated and less processed forms (progastrin and glycine-extended gastrin), is also a growth factor for the gastrointestinal tract. It has been established that the major trophic effect of amidated gastrin is for the oxyntic mucosa of stomach, where it causes increased proliferation of gastric stem cells and ECL cells, resulting in increased parietal and ECL cell mass.
  • the major trophic target of the less processed gastrin e.g. glycine-extended gastrin
  • the colonic mucosa Kelman, T. J. and Chen, D. 2000 Regul Pept 9337-44.
  • the present invention provides the use of activity increasing effectors of QPCTLs for the stimulation of gastrointestinal tract cell proliferation, especially gastric mucosal cell proliferation, epithelial cell proliferation, the differentiation of acid-producing parietal cells and histamine-secreting enterochromaffin-like (ECL) cells, and the expression of genes associated with histamine synthesis and storage in ECL cells, as well as for the stimulation of acute acid secretion in mammals by maintaining or increasing the concentration of active pGlu 1 -Gastrin (SEQ ID NOS 39 and 40).
  • ECL enterochromaffin-like
  • the present invention provides the use of inhibitors of QPCTLs for the treatment of duodenal ulcer disease and gastric cancer with or w/o Helicobacter pylori infections in mammals by decreasing the conversion rate of inactive Gln 1 -Gastrin (SEQ ID NOS 35 and 36) to active pGlu 1 -Gastrin (SEQ ID NOS 39 and 40).
  • Neurotensin (SEQ ID NO 41) is a neuropeptide implicated in the pathophysiology of schizophrenia that specifically modulates neurotransmitter systems previously demonstrated to be misregulated in this disorder.
  • Clinical studies in which cerebrospinal fluid (CSF) NT concentrations have been measured revealed a subset of schizophrenic patients with decreased CSF NT concentrations that are restored by effective antipsychotic drug treatment.
  • CSF cerebrospinal fluid
  • NT cerebrospinal fluid
  • the behavioral and biochemical effects of centrally administered NT remarkably resemble those of systemically administered antipsychotic drugs, and antipsychotic drugs increase NT neurotransmission. This concatenation of findings led to the hypothesis that NT functions as an endogenous antipsychotic.
  • the present invention provides the use of activity increasing effectors of QPCTLs for the preparation of antipsychotic drugs and/or for the treatment of schizophrenia in mammals.
  • the effectors of QPCTLs either maintain or increase the concentration of active pGlu 1 -neurotensin.
  • FPP Fertilization promoting peptide
  • TRH thyrotrophin releasing hormone
  • FPP and adenosine have been shown to stimulate cAMP production in uncapacitated cells but inhibit it in capacitated cells, with FPP receptors somehow interacting with adenosine receptors and G proteins to achieve regulation of AC. These events affect the tyrosine phosphorylation state of various proteins, some being important in the initial “switching on,” others possibly being involved in the acrosome reaction itself.
  • Calcitonin and angiotensin II also found in seminal plasma, have similar effects in vitro on uncapacitated spermatozoa and can augment responses to FPP. These molecules have similar effects in vivo, affecting fertility by stimulating and then maintaining fertilizing potential.
  • the present invention provides the use of inhibitors of QPCTLs for the preparation of fertilization prohibitive drugs and/or to reduce the fertility in mammals.
  • the inhibitors of QPCTLs decrease the concentration of active pGlu 1 -FPP, leading to a prevention of sperm capacitation and deactivation of sperm cells.
  • activity increasing effectors of QC are able to stimulate fertility in males and to treat infertility.
  • further physiological substrates of QPCTLs were identified within the present invention. These are Gln 1 -CCL2 (SEQ ID NO 45), Gln 1 -CCL7 (SEQ ID NO 48), Gln 1 -CCL8 (SEQ ID NO 44), Gln 1 -CCL16 (SEQ ID NO 43), Gln 1 -CCL18 (SEQ ID NO 46) and Gln 1 -fractalkine (SEQ ID NO 47). For details see Table 3.
  • polypeptides play an important role in pathophysiological conditions, such as suppression of proliferation of myeloid progenitor cells, neoplasia, inflammatory host responses, cancer, psoriasis, rheumatoid arthritis, atherosclerosis, humoral and cell-mediated immunity responses, leukocyte adhesion and migration processes at the endothelium.
  • cytotoxic T lymphocyte peptide-based vaccines against hepatitis B, human immunodeficiency virus and melanoma were recently studied in clinical trials.
  • This peptide is a Melan-A/MART-1 antigen immunodominant peptide analog, with an N-terminal glutamic acid. It has been reported that the amino group and gamma-carboxylic group of glutamic acids, as well as the amino group and gamma-carboxamide group of glutamines, condense easily to form pyroglutamic derivatives.
  • the present invention provides the use of inhibitors of QPCTLs for the preparation of a medicament for the treatment of pathophysiological conditions, such as suppression of proliferation of myeloid progenitor cells, neoplasia, inflammatory host responses, cancer, malign metastasis, melanoma, psoriasis, rheumatoid arthritis, atherosclerosis, impaired humoral and cell-mediated immunity responses, leukocyte adhesion and migration processes at the endothelium.
  • pathophysiological conditions such as suppression of proliferation of myeloid progenitor cells, neoplasia, inflammatory host responses, cancer, malign metastasis, melanoma, psoriasis, rheumatoid arthritis, atherosclerosis, impaired humoral and cell-mediated immunity responses, leukocyte adhesion and migration processes at the endothelium.
  • Gln 1 -orexin A (SEQ ID NO 49) was identified as a physiological substrate of QPCTLs within the present invention.
  • Orexin A is a neuropeptide that plays a significant role in the regulation of food intake and sleep-wakefulness, possibly by coordinating the complex behavioral and physiologic responses of these complementary homeostatic functions. It plays also a role in the homeostatic regulation of energy metabolism, autonomic function, hormonal balance and the regulation of body fluids.
  • the present invention provides the use of inhibitors of QPCTLs for the preparation of a medicament for the treatment of impaired food intake and sleep-wakefulness, impaired homeostatic regulation of energy metabolism, impaired autonomic function, impaired hormonal balance and impaired regulation of body fluids.
  • the biochemical properties of polyglutamine repeats suggest one possible explanation: endolytic cleavage at a glutaminyl-glutaminyl bond followed by pyroglutamate formation may contribute to the pathogenesis through augmenting the catabolic stability, hydrophobicity, amyloidogenicity, and neurotoxicity of the polyglutaminyl proteins (Saido, T; Med Hypotheses (2000) March;54(3):427-9). Accordingly, the present invention provides therefore the use of inhibitors of QPCTLs for the preparation of a medicament for the treatment of Parkinson disease and Huntington's disease.
  • a further substrate of QPTCLs is the peptide QYNAD (SEQ ID NO 51). Its pyroglutamated form pGlu-Tyr-Asn-Ala-Asp (PEYNAD) (SEQ ID NO 52) is the effective agent with blocking activity of voltage-gated sodium channels. Sodium channels are expressed at high density in myelinated axons and play an obligatory role in conducting action potentials along axons within the mammalian brain and spinal cord. Therefore, it is speculated that they are involved in several aspects of the pathophysiology of multiple sclerosis (MS), the Guillain-Barré syndrome and chronic inflammatory demyelinizing polyradiculoneuropathy.
  • MS multiple sclerosis
  • Guillain-Barré syndrome chronic inflammatory demyelinizing polyradiculoneuropathy
  • the present invention provides the use of inhibitors of QPCTLs for the preparation of a medicament for the treatment of inflammatory autoimmune diseases, especially for multiple sclerosis, the Guillain-Barré syndrome and chronic inflammatory demyelinizing polyradiculoneuropathy, wherein the formation of the voltage-gated sodium channel blocking peptide pEYNAD is inhibited.
  • the present invention provides a diagnostic assay, comprising a QC-inhibitor.
  • the present invention provides a method of diagnosing any one of the aforementioned diseases and/or conditions, comprising the steps of
  • the sample in said diagnosing method is a blood sample, a serum sample, a sample of cerebrospinal liquor or a urine sample.
  • the subject in said diagnosing method is a human being.
  • the QC inhibitor in said diagnosing method is a selective QC inhibitor.
  • the present invention further pertains to a diagnostic kit for carrying out the dignosing method comprising as detection means the aforementioned diagnostic assay and a determination means.
  • African green monkey kidney cell line COS-7, human neuroblastoma cell line SH-SY5Y, human asatrocytoma cell line LN405, human keratinocytoma cell line HaCaT and human hepatocellular carcinoma cell line Hep-G2 were cultured in appropriate cell culture media (DMEM, 10% FBS for Cos-7, SH-SY5Y, LN405, HaCaT), (RPM11640, 10% FBS for Hep-G2), in a humidified atmosphere of 5% CO 2 (HaCaT, Hep-G2, COS-7) or 10% CO 2 (SH-SY5Y, LN405) at 37° C.
  • DMEM 10% FBS for Cos-7
  • SH-SY5Y, LN405, HaCaT human hepatocellular carcinoma cell line Hep-G2
  • cDNA of human isoQC was isolated from Hep-G2 cells using RT-PCR. Briefly, total RNA of Hep-G2 cells was reversely transcribed by SuperScript II (Invitrogen). Subsequently, human isoQC was amplified on a 1:12,5 dilution of generated cDNA product in a 25 ⁇ l reaction with Herculase Enhanced DNA-Polymerase (Stratagene) using primers isoQChu-1 (sense, SEQ ID NO: 55) and isoQChu-2 (antisense, SEQ ID NO: 56). The resulting PCR-product was subcloned into vector pPCRScript CAM SK (+) (Stratagene) and confirmed by sequencing.
  • the primers isoQC EGFP-1 Met I (SEQ ID NO: 57) and isoQC EGFP-3 (SEQ ID NO: 59) were used for amplification of human isoQC starting with methionine I and primers isoQC EGFP-2 Met II (SEQ ID NO: 58) and isoQC EGFP-3 (SEQ ID NO: 59) were used for amplification of human isoQC starting with methionine II.
  • the fragments were inserted into vector pEGFP-N3 (Invitrogen) employing the restriction sites of EcoRI and Sall and the correct insertion was confirmed by sequencing. Subsequently, the vectors were isolated for cell culture purposes using the EndoFree Maxi Kit (Qiagen).
  • vector pEGFP-N3 Invitrogen
  • vector pcDNA 3.1 Invitrogen
  • EGFP-1 sense
  • EGFP-2 antisense
  • the N-terminal sequences of hisoQC beginning with methionine I and II each ending at serine 53 were fused C-terminally with EGFP in vector pcDNA 3.1 using isoQC EGFP-1 Met I (sense, SEQ ID NO: 57) and hisoQC SS EGFP pcDNA as (antisense) (SEQ ID NO: 87) for the N-terminal fragment of hisoQC beginning with methionine I and isoQC EGFP-2 Met II (sense, SEQ ID NO: 58) and hisoQC SS EGFP pcDNA as (antisense) (SEQ ID NO: 87) for the N-terminal fragment of hisoQC beginning with methionine II. Fragments were inserted into EcoRI and NotI restrictione sites of vector pcDNA 3.1. Subsequently, the vectors were isolated for cell culture purposes using the EndoFree Maxi Kit (Qiagen).
  • Native hQC was inserted into HindIII and NotI restriction sites and native hisoQC was inserted into EcoRI and NotI restriction sites of vector pcDNA 3.1 (+) (Invitrogen) after amplification utilizing primers hQC-1 (sense) (SEQ ID NO: 82) and hQC-2 (antisense) (SEQ ID NO: 83) for hQC, isoQC EGFP-1 Met I (sense) (SEQ ID NO: 57) and hisoQC pcDNA as (antisense) (SEQ ID NO: 84) for hisoQC starting with methionine I and isoQC EGFP-2 Met II (sense) (SEQ ID NO: 58) and hisoQC pcDNA as (antisense) (SEQ ID NO: 84) for hisoQC starting with methionine II.
  • Human QC was cloned with a C-terminal FLAG-tag after amplification applying primers hQC-1 (sense) (SEQ ID NO: 82) and hQC C-FLAG pcDNA as (antisense) (SEQ ID NO: 88) into HindIII and NotI restriction sits of vector pcDNA 3.1.
  • Human isoQC was inserted with a C-terminal FLAG-tag into pcDNA 3.1 after amplification using primers isoQC EGFP-1 Met I (sense) (SEQ ID NO: 57) and hisoQC C-FLAG pcDNA as (antisense) (SEQ ID NO: 89) for hisoQC starting with methionine I and primers isoQC EGFP-2 Met II (sense) (SEQ ID NO: 58) and hisoQC C-FLAG pcDNA as (antisense) (SEQ ID NO: 89) for hisoQC starting with methionine 2.
  • COS-7 and LN405 were cultured in 6-well dishes containing a cover slip. Cells were grown until 80% confluency, transfected using Lipofectamin2000 (Invitrogen) according to manufacturer's manual and incubated in the transfection solution for 5 hours. Afterwards, the solution was replaced by appropriate growth media and cells were grown over night.
  • Lipofectamin2000 Invitrogen
  • the cells were washed 3 times with D-PBS for 10 min.
  • Cells stained for golgi-zone were incubated with goat anti-rabbit IgG secondary antibody conjugated with Rhodamin-RedX (Dianova) for 45 min at room temperature in the dark.
  • Cells stained for mitochondria were incubated with goat anti-mouse IgG secondary antibody conjugated with Rhodamin-RedX (Dianova) for 45 min at room temperature in the dark.
  • cells were washed 3 times with D-PBS for 5 min at room temperature and at least, the cover slips were mounted on a microscope slide with citiflour. Cells were observed under a fluorescence microscope (Carl-Zeiss).
  • human isoQC-EGFP fusion protein starting with methionine I and methionine II in cell line LN405 leads to a compartmentalization of the resulting protein.
  • Counterstaining of the golgi-zone of LN405 using mannosidase II antibody (red fluorescence) and subsequent superimposition of human isoQC-EGFP with mannosidase II suggests a localization of human isoQC-EGFP fusion protein within the golgi-compartment (yellow coloration of the merged images) (FIG. 7 , 9 ).
  • human isoQC starting at methionine 11 is sufficient to generate a golgi-localization of the human isoQC fusion protein.
  • Escherichia coli strain DH5 ⁇ was used for propagation of plasmids and E. coli strain BL21 was used for the expression of human isoQC. E. coli strains were grown, transformed and analyzed according to the manufacturer's instructions (Qiagen(DH5 ⁇ ) Stratagene (BL21)). The media required for E. coli, i.e. Luria-Bertani (LB) medium, was prepared according to the manufacturer's recommendations.
  • LB Luria-Bertani
  • the construct encoding the human isoQC was transformed into BL21 cells (Stratagene) and grown on selective LB agar plates at 37° C. Protein expression was carried out in LB medium containing 1% glucose at 37° C. After reaching an OD 600 of approximately 0.8, isoQC expression was induced with 20 ⁇ M IPTG for 4 h at 37° C. Cells were separated from the medium by centrigugation (4000 ⁇ g, 20 min), resuspended in PBS (140 mM NaCl, 2.7 mM KCl, 10 mM Na 2 HPO 4 , 1.8 mM KH 2 PO 4 , pH 7.3) and lysed by one cycle of freezing and thawing followed by one cycle of French Press.
  • PBS 140 mM NaCl, 2.7 mM KCl, 10 mM Na 2 HPO 4 , 1.8 mM KH 2 PO 4 , pH 7.3
  • the cell lysate was diluted to a final volume of 1.5 l using phosphate-containing buffer (50 mM Na 2 HPO 4 , 500 mM NaCl. pH 7.3) and centrifuged at 13.400 ⁇ g at 4° C. for 1 h. After centrifugation, the protein concentration of the resulting supernatant was determined using the mothod of Bradford. If necessary, the solution was diluted again to obtain a final total protein concentration of 0.6 mg/ml.
  • the GST-isoQC fusion protein was purified utilizing a 4-step protocol (Table 5). The purfication is illustrated by SDS-PAGE analysis in FIG. 20 .
  • QC was activity was determined using H-Gln-AMC as substrate. Reactions were carried out at 30° C. utilizing the NOVOStar reader for microplates (BMG Labtechnologies). The samples consisted of varying concentrations of the fluorogenic substrate, 0.1 U pyroglutamyl aminopeptidase (Qiagen) in 0.05 M Tris/HCl, pH 8.0 and an appropriately diluted aliquot of QC in a final volume of 250 ⁇ l. Excitation/emission wavelengths were 380/460 nm. The assay reactions were initiated by addition of glutaminyl cyclase. QC activity was determined from a standard curve of 7-amino-4-methylcoumarin under assay conditions. The kinetic data were evaluated using GraFit sofware.
  • This assay was used to determine the kinetic parameters for most of the QC substrates.
  • QC activity was analyzed spectrophotometrically using a continuous method (Schilling, S. et al., 2003 Biol Chem 384, 1583-1592) utilizing glutamic dehydrogenase as auxiliary enzyme.
  • Samples consisted of the respective QC substrate, 0.3 mM NADH, 14 mM ⁇ -Ketoglutaric acid and 30 U/ml glutamic dehydrogenase in a final volume of 250 ⁇ l. Reactions were started by addition of QC and pursued by monitoring of the decrease in absorbance at 340 nm for 8-15 min. The initial velocities were evaluated and the enzymatic activity was determined from a standard curve of ammonia under assay conditions. All samples were measured at 30° C., using the Sunrise reader for microplates. Kinetic data were evaluated using GraFit software.
  • the sample composition was the same as described above, except of the putative inhibitory compound added.
  • samples contained 4 mM of the respective inhibitor and a substrate concentration at 1 K M .
  • influence of the inhibitor on the auxiliary enzymes was investigated first. In every case, there was no influence on either enzyme detected, thus enabling the reliable determination of the QC inhibition.
  • the inhibitory constant was evaluated by fitting the set of progress curves to the general equation for competitive inhibition using GraFit software.
  • Human isoQC was expressed in E. coli BL21 (hisoQCdt) or P. pastoris (YSShisoQC). The substrates are displayed in the one-letter code of amino acids.
  • Escherichia coli strain DH5 ⁇ was used for propagation of plasmids and P. pastoris strain X-33 was used for the expression of human isoQC in yeast.
  • E. coli and P. pastoris strains were grown, transformed and analyzed according to the manufacturer's instructions (Qiagen (DH5 ⁇ ), invitrogen (X-33)).
  • the media required for E. coli, i.e. Luria-Bertani (LB) medium was prepared according to the manufacturer's recommendations.
  • the media required for Pichia pastoris, i.e. BMMY, BMGY, YPD, YPDS and the concentration of the antibiotics, i.e. Zeocin were prepared as described in the Pichia manual (invitrogen, catalog. No. K1740-01). The manual also includes all relevant descriptions for the handling of yeast.
  • the mutagenesis was performed according to standard PCR techniques followed by digestion of the parent DNA using DpnI (quik-change II site-directed mutagenesis kit, Stratagene, Catalog No. 200524). The generated constructs are illustrated schematically in FIG. 17 .
  • plasmid DNA 1-2 ⁇ g were applied for transformation of competent P. pastoris cells by electroporation according to the manufacturer's instructions (BioRad). Selection was done on plates containing 100 ⁇ g/ml Zeocin.
  • recombinants were grown for 24 h in 10 ml conical tubes containing 2 ml BMGY. Afterwards, the yeast was centrifuged and resuspended in 2 ml BMMY containing 0.5% methanol. This concentration was maintained by addition of methanol every 24 h for about 72 h. Subsequently, QC activity in the supernatant was determined. Clones that displayed the highest activity were chosen for further experiments and fermentation. Depending on the expressed construct, the isoQC-activity in the medium differed ( FIG. 18 ).
  • the fluorometric assay using H-Gln- ⁇ NA was applied to investigate the pH-dependence of the catalytic specificity.
  • the reactions were carried out at substarte concentrations of 7 ⁇ M, i.e. at [S] ⁇ K M . Therefore, the the observed specificity constants could be directly deduced from the initial velocity of the progress curves of substrate conversion.
  • the reaction buffer consisted of 0.075 M acetic acid, 0.075 M Mes and 0.15 M Tris, adjusted to the desired pH using HCl or NaOH. The buffer assures a constant ionic strength over a very broad pH-range. Evaluation of the acquired enzyme kinetic data was performed using the following equation:
  • k cat /K M ( pH ) k cat /K M (limit)*1/(1+[ H + ]/K HS +K E1 /[H + ]+K E1 /[H + ]*K E2 /[H + ]),
  • k cat /K M denotes the pH-dependent (observed) kinetic parameter.
  • k cat /K M limit denotes the pH-independent (“limiting”) value.
  • K HS , K E1 and K E2 denote the dissociation constants of an dissociating group in the acidic pH-range, and two dissociating groups of the enzyme, respectively. Evaluation of all kinetic data was performed using GraFit software (version 5.0.4. for windows, ERITHACUS SOFTWARE Ltd., Horley, UK).
  • the hisoQC displays a pH-optimum of specificity at pH 7-8.
  • the pH-optimum of catalysis is very similar to human QC. Fitting of the data according to a model which is based on three dissociating groups resulted in a well interpretation of the pH-dependence of hisoQC and hQC ( FIG. 22 ).
  • the catalysis of both enzymatic reactions is influenced by similar dissociating groups, suggesting a similar catalytic mechanism in general.
  • the determined pKa-values are displayed in Table 8. It is obvious, that only one pKa differs between hisoQC and hQC significantly. In hQC, the pKa corresponds to the pKa of the dissociation constant of the substrate. Possibly, the subtle difference between hQC and hisoQC is caused by structural changes occurring in isoQC catalysis (induced fit), influencing the pH-dependence.
  • human QC and human isoQC catalyze the conversion of A ⁇ (3-11) into pGlu-A ⁇ (3-11).
  • hisoQC catalyzes the conversion of A ⁇ (3-11) into pGlu-A ⁇ (3-11).
  • the conversion of N-terminal glutamic acid by hisoQC is much slower compared with hQC.
  • the lower specificity constants for conversion of glutaminyl substrates is also observed with glutamyl substrates. No cyclization was observed under these conditions with inactivated enzyme (Schilling, S. et al., 2004 FEBS Lett. 563, 191-196).
  • the tissue distribution of murine QC and murine isoQC was investigated using quantitative real time PCR techniques. Prior to analysis of cDNA from several different organs and tissues, the murine isoQC open reading frame was isolated applying specific primers (isoQCm MetI s (SEQ ID NO: 68), isoQCm MetI as (SEQ ID NO: 69) (table 4), which were deduced from the chromosomal coding region of murine isoQC.
  • the open reading frame was cloned into vector pPCR-Script CAM SK (+) (PCR-Script CAM Cloning Kit, Stratagene) and used as a positive control in the real-time PCR determinations and for preparation of a standard curve under assay conditions.
  • RNA-isolation kit II Macherey and Nagel. The RNA concentration and purity was assessed by gelelectrophoresis (agarose gel) and spectrophotometry. For synthesis of cDNA, 1 ⁇ g of RNA was used. The reaction was done applying the reverse Transcriptase Superscript II RT (Invitrogen) according to the recommendations of the supplier, the cDNA was stored at ⁇ 80° C.
  • the quantitative analysis of the transcript concentration in different tissues was analysed using the “Light Cycler” (Corbett research), applying the “QuantiTect SYBR Green PCR” (Qiagen).
  • the DNA standard contained 4 concentrations in the range of 10 7 -10 1 Molecules / ⁇ l , and an limiting concentration (10 0 ).
  • the reaction protocoll is displayed in Table 8. The results are displayed in FIG. 24 .
  • murine QC and murine isoQC are expressed in all organs tested.
  • the variances in expression of murine isoQC between different organs are smaller, indicating a lower stringency of regulation of transcription.
  • the data for expression of mQC correspond to previous analyses of bovine QC, which was analyzed using Northern-Blot (Pohl, T. et al. 1991 Proc Natl Acad Sci USA 88, 10059-10063). Highest expression of QC was observed in Thalamus, Hippocampus and Cortex. Thus, QC-expression is primarily detected in neuronal tissue. Little QC-expression is detected in peripheral organs as spleen and kidney. Also misoQC is expressed in neuronal tissue, but at lower levels compared with mQC. In contrast, expresssion levels in peripheral organs is very similar between isoQC and QC.
  • the combined activity should be highest in brain.
  • highest QC-protein levels are present in organs that are afflicted by amyloidoses like Alzheimers Disease, familial british dementia and familial danish dementia.
  • h-isoQC is also time-dependently inactivated by the heterocyclic chelators 1,10-phenanthroline ( FIG. 25 ) and dipicolinic acid (not shown), clearly pointing to a metal-dependent activity.
  • EDTA also inhibited h-isoQC ( FIG. 25 ). This is in sharp contrast to QCs, since neither human QC, porcine QC nor murine QC has shown discernible inhibition by EDTA. However, inhibition of hisoQC by EDTA even stronger suggests a metal-dependent catalysis.
  • HEK293 cells were washed with D-PBS and collected by centrifugation at 500 ⁇ g for 5 min at 4° C. Subsequently, D-PBS was discarded and the cells were resuspended in 1 ml of disruption buffer (50 mM Tris, 50 mM KCl, 5 mM EDTA, 2 mM MgCl 2 , pH 7.6 adjusted with HCl) and cracked by 30 crushes in a Potter cell homogenisator. The suspension was centrifuged at 700 ⁇ g for 10 min at 4° C. The obtained pellet was resuspended in 300 ⁇ l disruption buffer and designated as debris fraction (D).
  • disruption buffer 50 mM Tris, 50 mM KCl, 5 mM EDTA, 2 mM MgCl 2 , pH 7.6 adjusted with HCl
  • the resulting supernatant was further centrifuged at 20.000 ⁇ g for 30 min at 4° C.
  • the pellet illustrated the heavy membrane fraction (HM) and was resuspended in 200 ⁇ l disruption buffer.
  • the resulting supernatant was centrifuged at 100.000 ⁇ g for 1 h at 4° C. using an ultracentrifuge (Beckmann).
  • the obtained pellet was resuspended in 200 ⁇ l disruption buffer and was termed as light membrane fraction (LM).
  • the supernatant was designated as soluble fraction (S).
  • Debris, heavy membrane and light membrane fractions were sonicated for 10 sec and. the protein content of all fractions was determined using the method of Bradford. Subsequently, fractions were analyzed for QC activity and stained for marker proteins using Western Blot.
  • biochemical analysis of QC activity distribution derived from hisoQC and hQC expression were performed.
  • the native hisoQC beginning with methionine I and II and hQC were expressed in HEK293 cells, respectively.
  • the QC activity in the each fraction was determined using the fluorescence assay applying H-Gln-PNA as substrate. In cells, transfected with the empty vector (pcDNA), specific QC activity is hardly measurable.
  • QC activity When expressing native hisoQC (MetI) and hisoQC (MetII), QC activity was readily detectable with the highest specific activity in the heavy membrane fraction (MetI: 40 ⁇ 2 ⁇ mole/min/g; MetII: 36 ⁇ 1.5 ⁇ mole/min/g) and the medium (MetI: 30 ⁇ 2 ⁇ mole/min/g; MetII: 54 ⁇ 3 ⁇ mole/min/g).
  • hQC shows the highest specific QC activity within the medium (1339 ⁇ 76 ⁇ mole/min/g) followed by the heavy membrane fraction (251 ⁇ 21 ⁇ mole/min/g) ( FIG. 26A ).
  • QC activity deduced by hQC expression shows high activity within the medium (1138 ⁇ 65 nM/min) and within intracellular compartements (debris: 1089 ⁇ 14 nM/min; heavy membrane fraction: 583 ⁇ 38 nM/min) supporting an Golgi localization of hisoQC as shown by histochemical analysis ( FIG. 26B ).
  • the data obtained by the expression of the native enzymes was further supported by expression of hisoQC (MetI and MetII) and hQC possessing a C-terminal FLAG-tag ( FIG. 26C ).
  • Western Blot analysis of the resulting FLAG-tagged proteins in comparison to marker proteins of the Golgi complex and mitochondria revealed a mainly intracellular localization of hisoQC(MetI) and hisoQC (MetII) within the debris and heavy membrane fraction, whereas hQC is enriched within the medium but also found within the debris and heavy membrane fraction.
  • Visualization of marker proteins of the Golgi complex (ST1GAL3) and mitochondria revealed the presence of these compartments within the debris and heavy membrane fraction.
  • the 65 kDa mitochondrial protein was also found to a smaller portion within the soluble fraction.
  • the signal peptides starting at MetI and MetII, including the transmembrane helix were cloned in frame with EGFP.
  • the resulting vectors hisoQC (MetI) SS EGFP and hisoQC (MetII) SS EGFP were expressed in LN405 cells and examined in analogy to the full-length hisoQC EGFP fusion proteins using confocal laserscanning microscopy.
  • hisoQC (MetI) SS EGFP led to the same Golgi complex localization observed for the full-length hisoQC (MetI) EGFP fusion protein. Again, a transport of hisoQC (MetI) SS EGFP to the mitochondria was not observed ( FIG. 27A ). In addition, the expression of the N-terminal truncated peptide hisoQC (MetII) SS EGFP also led to a enrichment of the protein within the Golgi complex. In analogy to hisoQC (MetI) SS EGFP, no mitochondrial EGFP fluorescence could be recorded ( FIG. 27B ).
  • Glycosyltransferases are type II transmembrane proteins, possessing a short cytoplasmatic sequence, followed by the transmembrane helix and a large luminal catalytic domain. Clearly, this is essentially the same domain structure as found for misoQC and hisoQC ( FIG. 28 ). For a number of glycosyltransferases, the Golgi retention signal was identified to reside within the transmembrane domain. Furthermore, for some of these enzymes truncation of the cytoplasmatic sequence was found to have no influence on the activity or the localization of the protein. In summary, evidence was provided, that hisoQC is a type II transmembrane protein showing a retention within the Golgi complex similar to glycosyltransferases.
  • the quantitative analysis of the transcript concentration in different tissues was analysed using the “Light Cycler” (Corbett research), applying the “QuantiTect SYBR Green PCR” (Qiagen).
  • the DNA standard (cloned cDNA isoQC human) was used for quantification.
  • the DNA standard contained 4 concentrations in the range of 10 7 -10 1 Molecules / ⁇ l , and an limiting concentration (10 0 ).
  • human melanoma cells show the highest expression of QPCTL transcripts (approx. 7000 copies/50 ng total-RNA), whereas the human soft tissue sarcoma cell lines show the lowest expression of QPCTL (365 copies/50 ng total-RNA).
  • Pancreas carcinoma shows 2100 copies, thyroid carcinoma 3500 copies and gastric carcinoma possesses 4100 copies in the median ( FIG. 29 ).
  • melanoma-specific tumor-associated antigens were selected by data base mining and published results.
  • AIM1 and AIM2 abent in melanoma
  • MAGEA1, -A2, -A1 and MAGEB2 melanoma antigen familiy A and B
  • MART1 melanoma antigen recognized by T-cells
  • TYR tyrosinase
  • TYRP1 and TYRP2 tyrosinase related protein
  • MCL-1 myeloid cell leukemia
  • FTC follicular thyroid carcinoma
  • PTC papillary thyroid carcinoma
  • UTC undifferentiated thyroid carcinoma
  • UTC possesses 5400 copies/50 ng total-RNA and is 2.5 times higher than observed in goiter.
  • the QPCTL mRNA level in thyroid carcinoma is homogeneous.
  • the samples from FTC (2600 copies/50 ng total-RNA) and UTC (2500 copies/50 ng total-RNA) are similar to goiter (2500 copies/50 ng total-RNA).
  • the expression of QPCTL in PTC is slightly decreased to 1900 copies/50 ng total-RNA ( FIG. 34 ).
  • QPCT and QPCTL are equally expressed in goiter. However, in tumor tissues the expression of QPCT increases, whereas the expression of QPCTL remains stable.
  • the stimulation experiments were performed using the human embryonal kidney cell line HEK293, human acute monocytic leukemia cell line THP-1 and the follicular thyroid carcinoma cell line FTC-133.
  • Cells were grown in appropriate culture media (DMEM, 10% FBS for HEK293, RPMI1640, 10% FBS for THP-1 and DMEM/F12, 10% FBS for FTC-133) in a humidified atmosphere at 37° C. and 5% CO 2 .
  • HEK293 and FTC-133 cells were cultivated as adherent cultures and THP-1 cells were grown in suspension.
  • 2 ⁇ 10 6 cells of THP-1 were grown in 24 well suspension plates. All stimulation experiments were applied under serum-free conditions. FTC-133 was grown over night. Afterwards, cells were adapted to serum-free media for another 24 h and the stimulation was started by replacing the conditioned media by fresh serum-free media.
  • HEK293 cells were grown over night and afterwards the stimulation using respective agents was started without an adaption to serum-free conditions due to morphological changes in case of cultivation of HEK293 under serum-free conditions for more than 24 h.
  • THP-1 cells were plated in serum-free media together with respective agent. The applied stimuli and final concentrations are listed in Table 12.
  • THP-1, HEK293 and FTC-133 cells were plated into two 25 cm 2 tissue culture flasks, respectively. Thereby, one flask of each cell line served as negative control, cultivated under normal growth conditions for 24 h. The other flasks were placed in a anaerobic bag together with an anaerobic reagent (Anaeroculte P, Merck) and an indicator. The bag was sealed to ensure air tight conditions. Cells were also grown for 24 h and subsequently, total-RNA was isolated using the Nucleo-Spin® RNA II Kit (Macherey-Nagel) and stored until qPCR assay.
  • the basal expression in the used cell lines HEK293, FTC-133 and THP-1 was evaluated in preparation for the following stimulation experiments.
  • the copy number of QPCT and QPCTL transcripts is summarized in Table 13.
  • FTC-133 was stimulated using LPS and TGF- ⁇ and the regulation of QPCT, QPCTL and CCL2 was monitored.
  • LPS and TGF- ⁇ stimulated the expression of QPCT mRNA, but failed to induce QPCTL and CCL2 expression ( FIG. 36 ).
  • TGF- ⁇ was less effective as stimulus and induced the expression of QPCT, CCL2, CCL7 and CCL8 maximum 2 fold.
  • CCL13 was repressed by TGF- ⁇ stimulation ( FIG. 38 ).
  • QPCTL expression could not be regulated by chemical agents, bioactive pepitides or LPS. Therefore, we tested, whether QPCTL expression is regulated by hypoxia. As summarized in FIG. 39 . Hypoxia selectively induced the expression of QPCTL but not of QPCT. In comparison, hypoxia induced factor 1a (HIF1a) was repressed by 15% ( FIG. 39A ) and 45% ( FIG. 39C ). The data suggest a connection of QPCTL to hypoxia.
  • hypoxia induced factor 1a HIF1a
  • Reagents and conditions (a) NaH, DMF, 4 h, rt.; (b), 8 h, 100° C.; (c) H 2 N—NH 2 ,EtOH, 8 h, reflux then 4N HCl, 6 h, reflux, (d) R 3 —NCO, EtOH, 6 h, reflux, (e) 3,4 dimethoxy-phenyl-isothiocyanate,
  • Reagents and conditions (a) R—NCS, EtOH, 6 h, reflux; (b) WSCD, 1H-imidazole-1-propanamine, DMF, 2 h, r.t.
  • Reagents and conditions (a) NaH, DMF, rt., 3 h; (b) LiAlH 4 , dioxane, reflux, 1 h; (c) R—NCS, EtOH, reflux 6 h,
  • Reagents and conditions (a) NaH, DMF, 4 h, rt.; (b), 8 h, 100° C.; (c) H 2 N—NH 2 ,EtOH, 8 h, reflux then 4 N HCl, 6 h, reflux, (d) 3,4 dimethoxy-phenyl-isothiocyanate, EtOH, 6 h, reflux
  • the 1H-imidazole-1-alkylamines were prepared according to the literature from ⁇ -brom-alkyl-phtalimides and imidazolium salt and subsequent hydrazinolysis. The resulting products were transformed into the thioureas according to example 1-53 giving a 88% (example 136) and 95% (example 137) yield.
  • 1H-imidazole-1-propanamine was reacted with the corresponding 2-phenyl acetic acid in dry dioxane by adding one equivalent of CAIBE and N-methylmorpholine at a temperature of 0° C. After 2 h the mixture was allowed to warm to r.t. and the mixture was stirred for 12 h. After removing the solvent the resulting oil was redissolved in methylene chloride and the organic layer was washed by means of an aqueous solution of NaHCO 3 and water, dried and the solvent was evaporated. The remaining oil was dissolved in dioxane adding Laweson's Reagent. After stirring for 12 h a saturated solution of NaHCO 3 was added.
  • Dioxane was evaporated and the aqueous layer was extracted by means of ethyl acetate. The organic layer was separated, dried and the solvent was evaporated. The remainig solid was crystallized from acetyl acetate/ether, giving 113-118, 120-124 and 126-132 with total yields of 62-85%.
  • the organic solution was dried, filtered, and the solvent was removed under reduced pressure. After redissolving in 50 mL of dry dioxane 2.2 mmol of Lawesson's reagent was added, and the mixture was heated to 90° C. and stirred for 8 h. The solvent was removed by reduced pressure, and the residue was redissolved in 50 mL of dichloromethane. The organic layer was washed three times by means of a saturated aqueous solution of NaHCO 3 , followed three times by water, dried, filtered, and then the organic solvent was removed.
  • the compound was purified by chromatography using a centrifugal-force-chromatography device, (Harrison Research Ltd.) utilizing silica plates of a layer thickness of 2 mm, and a CHCl 3 /MeOH gradient as eluting system.
  • the compound was purified by chromatography using a centrifugal-force-chromatography device, (Harrison Research Ltd.) utilizing silica plates of a layer thickness of 2 mm, and a CHCl 3 /MeOH gradient as eluting system.
  • GnRH gonadotropin-releasing hormone gonadotropin-releasing hormone (gonadoliberin)
  • glutaminyl cyclase glutaminyl-peptide cyclotransferase
  • VpAP Vibrio proteolytica amino peptidase

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