JP2002233368A - New protein and its dna - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a new protein having a K+ channel activity and a DNA capable of encoding the protein, a method for screening a compound capable of promoting or inhibiting the activity of the protein, and the compound obtained by the screening method. SOLUTION: This protein has the same or substantially the same amino acid sequence as a specific amino acid sequence derived from a human. The protein is useful as a diagnostic marker, etc., for myonosus, central nervous system disease or heart disease and the compound capable of promoting or inhibiting the activity of the protein and available by the method for screening sing the protein can be used as a prophylactic or a therapeutic agent for diseases, e.g. the myonosus, central nervous system disease or heart disease.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

TECHNICAL FIELD The present invention relates to a novel K ⁺ channel protein, a DNA encoding the protein, a method for screening a compound that promotes or inhibits the activity of the protein,
A compound or the like obtained by the screening method is provided.

[0002]

2. Description of the Related Art K ⁺ channels, which are membrane proteins that selectively allow K ⁺ ions to permeate, are ubiquitous from prokaryotes to humans, and are composed of an extremely large number of families. In the living body, it is distributed in a wide range of tissues, and is closely related to important physiological functions such as formation of resting membrane potential of cells, repolarization, and regulation of action potential generation frequency. The structure of the K ⁺ channel is diverse, and in addition to a six-transmembrane type, a two-transmembrane type, a one-transmembrane type, and the like, there is also a connection type channel molecule in which two of these basic structures are connected. Among them, the potential difference-dependent K ⁺
The channel (Kv) has a six-transmembrane structure, and a pore region exists between the fifth and sixth transmembrane regions.

[0003]

The K ⁺ channel has a very large number of molecular species, and their expression sites are also diverse. In addition, one cell often expresses a plurality of K ⁺ channels. Although the characteristics of K ⁺ currents due to the opening of individual K ⁺ channels have become fairly clear, the nature of the signal when multiple K ⁺ channels work and the mutual regulatory action between each K ⁺ channel are discussed. Little knowledge. Although K ⁺ channel plays a number of important functions for cell, to clarify the relationship between the specific features and each molecular species, muscular disorders, central nervous system disorders, the K ⁺ channels in such heart diseases It leads to clarifying the role.

[0004]

Means for Solving the Problems The present inventors have set forth the above section.
As a result of intensive research to solve the problem, a new potential difference
Dependency K⁺See channel protein (human Kv2.2 homolog)
Issued. The human KV2.2 homolog is at the amino acid level,
Showing 38% homology partially with human Kv2.2, ⁺Channel
Can function as a file. Suppress KV2.2 homolog
As a method of controlling, for example, K⁺Inhibits ion transmission
Or suppress the transcription of KV2.2 homologue
Can be reduced. KV2.2 homolog
As an activation method, for example, K⁺Enhances ion penetration
Or activated the promoter of the KV2.2 homolog
Enhances expression levels by stabilizing mRNA
It is possible. The present inventors based on these findings.
As a result of further studies, the present invention was completed.
Was.

That is, the present invention relates to (1) SEQ ID NO: 1.
A protein or a salt thereof containing the same or substantially the same amino acid sequence as the amino acid sequence represented by
(2) a partial peptide of the protein of (1) or a salt thereof; (3) a DNA encoding the protein of (1) or the partial peptide of (2)
(4) a DNA according to the above (3) having a base sequence represented by SEQ ID NO: 2, (5) a recombinant vector containing the DNA according to the above (4),
(6) A transformant transformed with the recombinant vector according to the above (5), (7) A transformant described in the above (6) is cultured, and the protein according to the above (1) or the above ( (2) a method for producing the protein according to the above (1), the partial peptide according to the above (2) or a salt thereof, wherein the partial peptide according to the above (2) is produced, accumulated, and collected. A pharmaceutical comprising the protein according to the above (1) or the partial peptide according to the above (2) or a salt thereof; (9) a pharmaceutical comprising the DNA according to the above (3); (1) An antibody against the protein described in (1) or the partial peptide described in (2) or a salt thereof, (11) Use of the protein described in (1) or the partial peptide described in (2) or a salt thereof To A method for screening a compound or a salt thereof that promotes or inhibits the activity of the protein according to the above (1) or the partial peptide or the salt thereof according to the above (2), and (12) the method according to the above (1). A compound that promotes or inhibits the activity of the protein of (1) or the partial peptide of (2) or a salt thereof, comprising the protein or the partial peptide of (2) or a salt thereof; (13) The protein according to (1) or (2) above, which is obtained using the screening kit for a salt thereof, (13) the screening method according to (11) or the screening kit according to (12). A compound or a salt thereof, which promotes or inhibits the activity of the partial peptide or a salt thereof according to the above (14); Or a compound that promotes or inhibits the activity of the protein of (1) or the partial peptide of (2) or a salt thereof obtained by using the screening method of (1) or the screening kit of (12). (15) a medicament comprising a salt, (15) a medicament according to the above (8) or (9), which is a prophylactic / therapeutic agent for a muscular disease, a central nervous system disease or a heart disease, (16) a muscular disease, a central nervous system The present invention provides the medicament according to the above (14), which is a preventive / therapeutic agent for systemic diseases and heart diseases.

[0006]

BEST MODE FOR CARRYING OUT THE INVENTION SEQ ID NO: 1 used in the present invention
A protein containing the same or substantially the same amino acid sequence as the amino acid sequence represented by (hereinafter, sometimes referred to as the protein of the present invention or the protein used in the present invention) is a human or a warm-blooded animal (for example, Cells of guinea pigs, rats, mice, chickens, rabbits, pigs, sheep, cows, monkeys, etc. (eg, hepatocytes, spleen cells, nerve cells, glial cells, pancreatic β cells, bone marrow cells, mesangial cells, Langerhans cells, epidermis) Cell, epithelial cell, goblet cell, endothelial cell, smooth muscle cell, fibroblast, fiber cell, muscle cell, adipocyte, immune cell (eg, macrophage, T cell, B cell, natural killer cell, mast cell, neutrophil Spheres, basophils, eosinophils, monocytes), megakaryocytes, synovial cells, chondrocytes, osteocytes, osteoblasts, osteoclasts, breast cells, hepatocytes or stroma Vesicles, or precursor cells of these cells, stem cells or cancer cells) or any tissue in which these cells are present, such as the brain, various parts of the brain (eg, olfactory bulb, amygdala, basal sphere, hippocampus, thalamus, thalamus) Lower, cerebral cortex, medulla, cerebellum), spinal cord, pituitary, stomach, pancreas, kidney, liver, gonads, thyroid, gall bladder, bone marrow, adrenal gland, skin, muscle, lung, digestive tract (eg, large intestine, small intestine), blood vessels Or a protein derived from the heart, thymus, spleen, submandibular gland, peripheral blood, prostate, testis, ovary, placenta, uterus, bone, joint, skeletal muscle, or the like, or may be a synthetic protein.

The amino acid sequence substantially identical to the amino acid sequence represented by SEQ ID NO: 1 is about 50% or more, preferably about 60%, of the amino acid sequence represented by SEQ ID NO: 1.
Or more, more preferably about 70% or more, particularly preferably about 80%
%, And most preferably about 90% or more homology. Examples of the protein having an amino acid sequence substantially the same as the amino acid sequence represented by SEQ ID NO: 1 include, for example, a protein having the same amino acid sequence as the amino acid sequence represented by SEQ ID NO: 1. And a protein having substantially the same activity as the protein having the amino acid sequence represented by SEQ ID NO: 1. Examples of substantially equivalent activities include, for example, K
⁺ Ion permeation activity and the like. Substantially homogenous indicates that the properties are homogenous (eg, physiologically or pharmacologically). Therefore, K ⁺
It is preferable that the ion permeation activity is the same (eg, about 0.01 to 100 times, preferably about 0.1 to 10 times, more preferably 0.5 to 2 times), but the degree of these activities and the amount of protein such as molecular weight The target element may be different. Activity such as K ⁺ ion permeation activity can be measured according to a known method. For example, J. Biol. Chem. 275: 2839
It can be measured according to the method described in 8-28405, 2000 or a method analogous thereto.

The protein used in the present invention may be, for example, one or two or more (preferably about 1 to 30, preferably about 1 to 10) of the amino acid sequence represented by SEQ ID NO: 1. , More preferably a number (1-5)
Amino acid sequence), SEQ ID NO:
An amino acid sequence in which one or more (preferably about 1 to 30, preferably about 1 to 10, and more preferably number (1 to 5)) amino acids have been added to the amino acid sequence represented by 1, 1 is added to the amino acid sequence represented by SEQ ID NO: 1.
Or an amino acid sequence into which two or more (preferably about 1 to 30, preferably about 1 to 10, and more preferably a number (1 to 5)) amino acids have been inserted, represented by SEQ ID NO: 1 An amino acid sequence in which one or more (preferably about 1 to 30, preferably about 1 to 10, and more preferably a number (1 to 5)) amino acids in the amino acid sequence have been substituted with other amino acids Or so-called muteins such as proteins containing an amino acid sequence obtained by combining them. The amino acid sequence is inserted as described above,
When deleted or substituted, the position of the insertion, deletion or substitution is not particularly limited.

The protein in the present specification is a peptide
The left end is the N-terminus (amino terminus) and the right end is according to the convention
Is the C-terminus (carboxyl terminus). SEQ ID NO: 1
Including proteins containing the amino acid sequence represented
The protein used in the present invention has a C-terminal
Ordinary carboxyl group (-COOH) or carboxyl
G (-COO^-), But the C-terminal is an amide (—CONH
_Two) Or an ester (—COOR). This
Here, R in the ester includes, for example, methyl,
Butyl, n-propyl, isopropyl, n-butyl, etc.
C_1-6Alkyl groups such as cyclopentyl, cyclohexyl
C such as kishiru_3-8Cycloalkyl groups such as phenyl
And C such as α-naphthyl_6-12Aryl groups, e.g.
Phenyl-C such as benzyl and phenethyl_1-2Alkyl group
Or α-naphthyl-C such as α-naphthylmethyl
_1-2C such as an alkyl group_7-14Aralkyl group, pivaloyl
An oxymethyl group is used. Used in the present invention
If the protein has a carboxyl group (or
Carboxyl group).
Those that are imidized or esterified are also used in the present invention.
Included in the protein to be obtained. In this case, the ester
For example, the above-mentioned C-terminal ester or the like is used
You. Further, the proteins used in the present invention include N-terminal.
The amino group at the terminal amino acid residue (eg, methionine residue)
Protecting groups (for example, C such as formyl group and acetyl group) _1-6
C such as alkanoyl_1-6Protected by an acyl group, etc.)
N-terminal gluta produced by cleavage in vivo
Pyroglutamine oxidized min residue, amino acid in the molecule
Substituents on the side chain of the acid (e.g., -OH, -SH, amino
Group, imidazole group, indole group, guanidino group
Are suitable protecting groups (eg, formyl group, acetyl group)
Such as C_1-6C such as alkanoyl group_1-6Acyl group, etc.)
Protected with sugar chains or sugar chains
Complex proteins such as glycoproteins.
Specific examples of the protein used in the present invention include, for example,
For example, a human containing the amino acid sequence represented by SEQ ID NO: 1
And liver-derived proteins.

[0010] The partial peptide of the protein used in the present invention is a partial peptide of the protein used in the present invention described above, and preferably has the same properties as the protein used in the present invention described above. Any one may be used. For example, at least 20 or more, preferably 50 or more, more preferably 70 or more, more preferably 100 or more, most preferably 200 or more amino acid sequences of the constituent amino acid sequences of the protein used in the present invention. Peptides and the like are used.
In the partial peptide used in the present invention, one or more (preferably about 1 to 10, more preferably a number (1 to 5)) amino acids in the amino acid sequence are deleted, or One or more (preferably about 1 to 20, more preferably about 1 to 10, and still more preferably, about 1 to 5) amino acids are added to the amino acid sequence, or the amino acid One or two or more (preferably about 1 to 20, more preferably about 1 to 10, and still more preferably, about 1 to 5) amino acids are inserted into the sequence, or One or two or more (preferably about 1 to 10, more preferably several, and still more preferably about 1 to 5) amino acids may be substituted with another amino acid. The partial peptide of the present invention is preferably, for example, the amino acid sequence at positions 176 to 201 and 471 to 491 in the amino acid sequence represented by SEQ ID NO: 1.

The partial peptide used in the present invention usually has a carboxyl group (—COOH) or a carboxylate (—COO ⁻ ) at the C-terminus. (-
CONH ₂ ) or an ester (—COOR). Further, the partial peptide used in the present invention includes
Similar to the protein used in the present invention described above, those having a carboxyl group (or carboxylate) other than the C-terminus, and the amino group of the N-terminal amino acid residue (eg, methionine residue) is a protecting group. Protected, N
Glutamine residue generated by cleavage at the end in vivo is pyroglutamine-oxidized, substituent on the side chain of amino acid in the molecule is protected by an appropriate protecting group, or so-called sugar to which sugar chain is bonded Complex peptides such as peptides are also included. The partial peptide used in the present invention can also be used as an antigen for producing an antibody. For example, to prepare the antibody of the present invention described below, for example, the amino acid sequence represented by SEQ ID NO:
Peptides having the amino acid sequence at positions 417-500 and 500-649.

The salt of the protein or partial peptide used in the present invention may be a physiologically acceptable acid (eg,
Salts with inorganic acids, organic acids) and bases (eg, alkali metal salts) are used, and physiologically acceptable acid addition salts are particularly preferable. Examples of such salts include salts with inorganic acids (eg, hydrochloric acid, phosphoric acid, hydrobromic acid, sulfuric acid),
Alternatively, organic acids (eg, acetic acid, formic acid, propionic acid,
Fumaric acid, maleic acid, succinic acid, tartaric acid, citric acid,
For example, salts with malic acid, oxalic acid, benzoic acid, methanesulfonic acid, and benzenesulfonic acid) are used. The protein or its partial peptide or a salt thereof used in the present invention can be produced from the above-mentioned method for purifying a protein from human or warm-blooded animal cells or tissues. It can also be produced by culturing the transformant.
Further, it can be produced according to the peptide synthesis method described later. When producing from human or mammalian tissues or cells, the homogenized human or mammalian tissues or cells are extracted with an acid or the like, and the extract is subjected to chromatography such as reverse phase chromatography or ion exchange chromatography. Can be purified and isolated.

For the synthesis of the protein or partial peptide or a salt thereof or an amide thereof used in the present invention, a commercially available resin for protein synthesis can be usually used. Such resins include, for example, chloromethyl resin, hydroxymethyl resin, benzhydrylamine resin, aminomethyl resin, 4-benzyloxybenzyl alcohol resin, 4-methylbenzhydrylamine resin,
PAM resin, 4-hydroxymethylmethylphenylacetamidomethyl resin, polyacrylamide resin, 4-
(2 ', 4'-dimethoxyphenyl-hydroxymethyl) phenoxy resin, 4- (2', 4'-dimethoxyphenyl-F
(moc aminoethyl) phenoxy resin. Using such a resin, an amino acid having an α-amino group and a side chain functional group appropriately protected is condensed on the resin in accordance with the sequence of the target protein according to various known condensation methods. At the end of the reaction, a protein or partial peptide is cleaved from the resin, and at the same time, various protecting groups are removed.
Further, an intramolecular disulfide bond formation reaction is carried out in a highly diluted solution to obtain a target protein or partial peptide or an amide thereof. For the condensation of the above protected amino acids, various activating reagents that can be used for protein synthesis can be used, and carbodiimides are particularly preferable. Carbodiimides include DCC, N,
N'-diisopropylcarbodiimide, N-ethyl-N'-
(3-Dimethylaminoprolyl) carbodiimide and the like are used. For activation by these, the protected amino acid was directly added to the resin together with a racemization inhibitor additive (eg, HOBt, HOOBt), or the protected amino acid was previously activated as a symmetric acid anhydride or HOBt ester or HOOBt ester. It can be added later to the resin.

The solvent used for activating the protected amino acid or condensing with the resin can be appropriately selected from solvents known to be usable for the protein condensation reaction. For example, acid amides such as N, N-dimethylformamide, N, N-dimethylacetamide, N-methylpyrrolidone, halogenated hydrocarbons such as methylene chloride and chloroform, alcohols such as trifluoroethanol,
Sulfoxides such as dimethyl sulfoxide, ethers such as pyridine, dioxane, and tetrahydrofuran; nitriles such as acetonitrile and propionitrile; esters such as methyl acetate and ethyl acetate; and an appropriate mixture thereof are used. The reaction temperature is appropriately selected from a range known to be usable for a protein bond formation reaction, and is usually appropriately selected from a range of about -20 ° C to 50 ° C. Activated amino acid derivatives are usually
Used in 1.5 to 4 fold excess. As a result of the test using the ninhydrin reaction, when the condensation is insufficient, sufficient condensation can be carried out by repeating the condensation reaction without removing the protecting group. When a sufficient condensation cannot be obtained by repeating the reaction, the unreacted amino acid can be acetylated using acetic anhydride or acetylimidazole so as not to affect the subsequent reaction.

Examples of the protecting group for the amino group of the starting material include Z, Boc, t-pentyloxycarbonyl, isobornyloxycarbonyl, 4-methoxybenzyloxycarbonyl, Cl-Z, Br-Z, adamantyloxycarbonyl, Trifluoroacetyl, phthaloyl, formyl, 2
-Nitrophenylsulfenyl, diphenylphosphinothioyl, Fmoc and the like are used. The carboxyl group may be, for example, a linear, branched or cyclic alkyl ester such as an alkyl esterified ester (eg, methyl, ethyl, propyl, butyl, t-butyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, 2-adamantyl). Aralkyl esterification (eg, benzyl ester, 4-nitrobenzyl ester,
4-methoxybenzyl ester, 4-chlorobenzyl ester, benzhydryl esterification), phenacyl esterification, benzyloxycarbonyl hydrazide, t-
It can be protected by butoxycarbonyl hydrazide, trityl hydrazide and the like. The hydroxyl group of serine can be protected, for example, by esterification or etherification. Examples of groups suitable for the esterification include lower (C _1-6 ) alkanoyl groups such as acetyl group, aroyl groups such as benzoyl group, and groups derived from carbonic acid such as benzyloxycarbonyl group and ethoxycarbonyl group. Used. Further, groups suitable for etherification include, for example, a benzyl group, a tetrahydropyranyl group, a t-butyl group and the like. Examples of the protecting group for the phenolic hydroxyl group of tyrosine include, for example, Bzl, Cl ₂ -Bz
l, 2-nitrobenzyl, Br-Z, t-butyl and the like are used. As a protecting group for imidazole of histidine,
For example, Tos, 4-methoxy-2,3,6-trimethylbenzenesulfonyl, DNP, benzyloxymethyl, Bu
m, Boc, Trt, Fmoc, etc. are used.

Examples of the activated carboxyl group of the raw material include, for example, a corresponding acid anhydride, azide, active ester [alcohol (eg, pentachlorophenol, 2,4,5-trichlorophenol, 2,4- Dinitrophenol, cyanomethyl alcohol, paranitrophenol, HONB, N-hydroxysuccinimide, N-hydroxyphthalimide, and esters with HOBt). As the activated amino group of the raw material, for example, a corresponding phosphoric amide is used. As a method for removing (eliminating) the protecting group, for example, Pd-black or Pd
-Catalytic reduction in a stream of hydrogen in the presence of a catalyst such as carbon, acid treatment with anhydrous hydrogen fluoride, methanesulfonic acid, trifluoromethanesulfonic acid, trifluoroacetic acid or a mixture thereof, diisopropyl Base treatment with ethylamine, triethylamine, piperidine, piperazine and the like, reduction with sodium in liquid ammonia, and the like are also used. The elimination reaction by the above acid treatment is generally performed at a temperature of about -20 ° C to 40 ° C. In the acid treatment, for example, anisole, phenol, thioanisole, metacresol, paracresol, dimethylsulfide, 1,4 -Addition of a cation scavenger such as butanedithiol, 1,2-ethanedithiol and the like is effective. In addition, the 2,4-dinitrophenyl group used as an imidazole protecting group of histidine is removed by thiophenol treatment, and the formyl group used as an indole protecting group of tryptophan is 1,2-ethanedithiol, 1,4-butane described above. In addition to deprotection by acid treatment in the presence of dithiol or the like, it is also removed by alkali treatment with dilute sodium hydroxide solution, dilute ammonia or the like.

The protection of the functional group which should not be involved in the reaction of the raw materials, the protecting group, the elimination of the protective group, the activation of the functional group involved in the reaction, and the like can be appropriately selected from known groups or known means. . As another method for obtaining an amide form of a protein or partial peptide, for example, first, after amidating and protecting the α-carboxyl group of the carboxy terminal amino acid, a peptide (protein) chain is added to the amino group side to a desired chain length. After the elongation, a protein or partial peptide from which only the protecting group for the N-terminal α-amino group of the peptide chain has been removed, and a protein or partial peptide from which only the protecting group for the C-terminal carboxyl group has been removed, are produced. The protein or peptide is condensed in a mixed solvent as described above. Details of the condensation reaction are the same as described above. After purifying the protected protein or peptide obtained by the condensation, all the protecting groups are removed by the above-mentioned method to obtain a desired crude protein or peptide. This crude protein or peptide is purified by various known purification means, and the main fraction is lyophilized to obtain an amide of the desired protein or peptide. To obtain an ester of a protein or peptide, for example, α-
After condensing the carboxyl group with a desired alcohol to form an amino acid ester, the desired protein or peptide ester can be obtained in the same manner as the protein or peptide amide.

The partial peptide used in the present invention or a salt thereof can be produced according to a known peptide synthesis method or by cleaving the protein used in the present invention with an appropriate peptidase. As a method for synthesizing a peptide, for example, any of a solid phase synthesis method and a liquid phase synthesis method may be used. That is, the target peptide can be produced by condensing a partial peptide or amino acid capable of constituting the partial peptide used in the present invention with the remaining portion, and removing the protecting group when the product has a protecting group. it can. Known methods for condensation and elimination of protecting groups include, for example, the methods described in (1) to (4) below. M. Bodanszky and MA Ondetti, Peptide Synthesis, Interscience Publisher
s, New York (1966) Schroeder and Luebke, The Peptid
e), Academic Press, NewYork (1965) Nobuo Izumiya et al., Fundamentals and experiments of peptide synthesis, Maruzen Co., Ltd.
(1975) Haruaki Yajima and Shunpei Sakakibara, Laboratory of Biochemistry 1, Protein Chemistry IV, 205, (1977) Supervised by Haruaki Yajima, Development of Continuing Pharmaceuticals, Vol. 14, Peptide Synthesis, Hirokawa Shoten Thereafter, the partial peptide used in the present invention can be purified and isolated by a combination of ordinary purification methods such as solvent extraction, distillation, column chromatography, liquid chromatography, and recrystallization. When the partial peptide obtained by the above method is a free form, it can be converted to an appropriate salt by a known method or a method analogous thereto, and conversely, when the partial peptide is obtained as a salt, a known method or analogous method It can be converted into a free form or another salt by a method.

The DNA encoding the protein used in the present invention may be any DNA containing the above-described nucleotide sequence encoding the protein used in the present invention. In addition, genomic DNA, genomic DNA library, cDN derived from the above-described cells and tissues
A, a cDNA library derived from the cells and tissues described above,
Any of synthetic DNAs may be used. The vector used for the library may be any of bacteriophage, plasmid, cosmid, phagemid and the like. In addition, Reverse Transcriptase Polyme
It can also be amplified by the rase Chain Reaction (hereinafter abbreviated as RT-PCR method). As the DNA encoding the protein used in the present invention, for example, a DNA containing the nucleotide sequence represented by SEQ ID NO: 2 or a nucleotide sequence hybridized with the nucleotide sequence represented by SEQ ID NO: 2 under high stringency conditions Any DNA may be used as long as it has a soybean base sequence and encodes a protein having substantially the same properties as the protein used in the present invention.

DNA capable of hybridizing with the base sequence represented by SEQ ID NO: 2 under high stringent conditions
For example, about 50% or more, preferably about 60% or more, more preferably about 70% or more, particularly preferably about 80% or more, most preferably about 90% or more of the nucleotide sequence represented by SEQ ID NO: 2 DN containing a base sequence having the above homology
A or the like is used. Hybridization is performed by a known method or a method analogous thereto, for example, molecular cloning (Molecular Cloning) 2nd (J. Samb.
rook et al., Cold Spring Harbor Lab. Press, 1989)
And the like. Also,
When a commercially available library is used, it can be performed according to the method described in the attached instruction manual. More preferably, it can be performed under high stringency conditions. High stringency conditions include, for example,
Sodium concentration of about 19 to 40 mM, preferably about 19 to 20 m
M indicates conditions at a temperature of about 50-70 ° C, preferably about 60-65 ° C. In particular, a sodium concentration of about 19 mM and a temperature of about 65
C is most preferred. More specifically, SEQ ID NO:
As the DNA encoding the protein containing the amino acid sequence represented by 1, a DNA containing the base sequence represented by SEQ ID NO: 2 or the like is used.

The DNA encoding the partial peptide used in the present invention may be any DNA containing the above-described nucleotide sequence encoding the partial peptide used in the present invention. In addition, genomic DNA, genomic DNA library, c
It may be any of DNA, cDNA library derived from the above-mentioned cells and tissues, and synthetic DNA. Examples of the DNA encoding the partial peptide used in the present invention include a DNA having a part of the DNA having the nucleotide sequence represented by SEQ ID NO: 2, or a DNA having the nucleotide sequence represented by SEQ ID NO: 2 and high stringency For example, DNAs containing a part of DNA encoding a protein having a base sequence that hybridizes under a simple condition and having substantially the same activity as the protein of the present invention can be used. The DNA hybridizable to the base sequence represented by SEQ ID NO: 2 has the same significance as described above. The same hybridization method and high stringency conditions as described above are used.

The protein and partial peptide used in the present invention (hereinafter, in the description of the cloning and expression of DNAs encoding them, these may be simply abbreviated as the protein of the present invention) are completely encoded by D
As a means for cloning NA, the DNA may be amplified by a PCR method using a synthetic DNA primer having a part of the nucleotide sequence encoding the protein of the present invention, or the DNA incorporated into an appropriate vector may be a part of the protein of the present invention. Alternatively, selection can be carried out by hybridization with a DNA fragment encoding the entire region or labeled with a synthetic DNA. Hybridization methods are described, for example, in Molecular Cloning 2nd (J. Sambrook et al.,
Cold Spring Harbor Lab. Press, 1989). When a commercially available library is used, it can be performed according to the method described in the attached instruction manual. Conversion of the base sequence of DNA can be performed by PCR or a known kit, for example, Mutan ^™ -superExp.
ress Km (Takara Shuzo Co., Ltd.), Mutan ^TM -K (Takara Shuzo Co., Ltd.)
The method can be performed according to a known method such as the ODA-LAPCR method, the gapped duplex method, the Kunkel method, or a method analogous thereto. The DNA encoding the cloned protein can be used as it is depending on the purpose, or it can be used after digesting with a restriction enzyme or adding a linker, if desired. The DNA may have ATG as a translation initiation codon at the 5 'end and TAA, TGA or TAG as a translation stop codon at the 3' end. These translation initiation codon and translation termination codon can also be added using a suitable synthetic DNA adapter. The expression vector of the protein of the present invention is
For example, (a) DNA encoding the protein of the present invention
From (b) the DNA
It can be produced by ligating the fragment downstream of the promoter in an appropriate expression vector.

As a vector, a plasmid derived from Escherichia coli (eg, pBR322, pBR325, pUC12,
UC13), a plasmid derived from Bacillus subtilis (eg, pUB11)
0, pTP5, pC194), yeast-derived plasmids (eg, pSH19, pSH15), bacteriophages such as phage λ, animal viruses such as retrovirus, vaccinia virus, baculovirus, etc.
A1-11, pXT1, pRc / CMV, pRc / RS
V, pcDNAI / Neo, etc. are used. The promoter used in the present invention may be any promoter as long as it is appropriate for the host used for gene expression. For example, when animal cells are used as hosts, SRα promoter, SV40 promoter, L
TR promoter, CMV promoter, HSV-TK
Promoters and the like. Of these, CMV
(Cytomegalovirus) promoter, SRα promoter and the like are preferably used. When the host is Escherichia, trp promoter, lac promoter, recA promoter, λPL promoter,
When the host is a bacterium of the genus Bacillus, the SPO1 promoter, the S7 promoter,
When the host is yeast, such as a PO2 promoter and a penP promoter, a PHO5 promoter, a PGK promoter, a GAP promoter, an ADH promoter, and the like are preferable. When the host is an insect cell, a polyhedrin promoter, a P10 promoter and the like are preferable.

[0024] In addition to the above, an expression vector optionally containing an enhancer, a splicing signal, a poly-A addition signal, a selection marker, an SV40 replication origin (hereinafter sometimes abbreviated as SV40 ori) and the like may be used. Can be used. As a selection marker, for example, dihydrofolate reductase (hereinafter, dhfr)
Gene (sometimes abbreviated as “methotrexate (M
TX) resistance], an ampicillin resistance gene (hereinafter referred to as Amp
^r ), a neomycin resistance gene (hereinafter sometimes referred to as Neo ^r , G418 resistance) and the like. In particular, when the dhfr gene is used as a selection marker using dhfr gene-deficient Chinese hamster cells, the target gene can be selected using a thymidine-free medium. If necessary, a signal sequence suitable for the host is added to the N-terminal side of the protein of the present invention. When the host is a bacterium belonging to the genus Escherichia, a PhoA signal sequence, an OmpA signal sequence, and the like. When the host is a bacterium belonging to the genus Bacillus, an α-amylase signal sequence, a subtilisin signal sequence, and the like,
When the host is yeast, the MFα signal sequence, SUC
When the host is an animal cell, such as a 2 signal sequence,
Insulin signal sequence, α-interferon signal sequence, antibody molecule signal sequence, etc. can be used, respectively. A transformant can be produced using the vector containing the DNA encoding the protein of the present invention thus constructed.

As the host, for example, Escherichia, Bacillus, yeast, insect cells, insects, animal cells and the like are used. Specific examples of Escherichia bacteria include
For example, Escherichia coli K1
2. DH1 [Procedures of the National Academy of Sciences of the USA (Proc. Natl. Acad. Sci. USA), 60]
Vol. 160 (1968)], JM103 [Nukuirek
Acids Research, (Nucleic Acids Research), 9
309 (1981)], JA 221 [Journal of Molecule Biology (Journal of Molecul)
ar Biology)], 120, 517 (1978)], HB
101 [Journal of Molecular Biology, Vol. 41, 459 (1969)], C600 [Genetics, Vol. 39, 440 (1954)] and the like are used. Examples of Bacillus spp. Include, for example, Bacillus subtilis MI114
[Gene, 24, 255 (1983)], 207-21
[Journal of Biochemistry
Biochemistry), 95, 87 (1984)]. As yeast, for example, Saccharomyces
Saccharomyces cerevisiae AH22, A
^{H22R -, NA87-11A, DKD-5D} , 20B
-12, Schizosacchamyces pombe
romyces pombe) NCYC1913, NCYC203
6. Pichia pastoris KM71
Are used.

As insect cells, for example, virus is A
In the case of cNPV, a cell line derived from night larvae of moth (Spodop
tera frugiperda cell (Sf cell), Trichoplusia ni
MG1 cells from the midgut, H from the eggs of Trichoplusia ni
igh FiveTM cells, cells from Mamestra brassicae or
Estigmena acrea-derived cells and the like are used. When the virus is BmNPV, a silkworm-derived cell line (Bombyx mor
iN cells; BmN cells) and the like. As the Sf cells, for example, Sf9 cells (ATCC CRL1711), Sf9
21 cells (Vaughn, JL et al., In Vivo
ivo), 13, 213-217, (1977)). As insects, for example, silkworm larvae are used [Maeda et al., Nature, 315, 592 (198).
5)]. As animal cells, for example, monkey cells COS-
7, Vero, Chinese hamster cell CHO (hereinafter abbreviated as CHO cell), dhfr gene-deficient Chinese hamster cell CHO (hereinafter, CHO (dhf)
r ⁻ ) cells), mouse L cells, mouse AtT-2
0, mouse myeloma cells, rat GH3, human FL cells, and the like. In order to transform Escherichia, for example, Processings of the National Academy of Sciences of the USA (Proc. Natl. Acad. Sci. USA), 69
Vol. 2110 (1972) and Gene, Vol. 17, 1
07 (1982).

For transformation of Bacillus sp., For example, Molecular & General Genetics, Vol.
111 (1979). To transform yeast, for example, Methods in Enzymolog
y), 194, 182-187 (1991), Processings of the National Academy of Sciences of the USA (Proc. Na)
Acad. Sci. USA), 75, 1929 (197).
8) and the like. In order to transform insect cells or insects, for example, Bio / Technology, 6, 47-55 (1988))
And the like. To transform animal cells, for example, see Cell Engineering Separate Volume 8, New Cell Engineering Experiment Protocol. 263-267 (1995) (published by Shujunsha), Virology, 52, 456 (1973). Thus, a transformant transformed with the expression vector containing the DNA encoding the protein can be obtained.
When culturing a transformant whose host is a genus Escherichia or Bacillus, a liquid medium is suitable as a medium used for the culturing, and a carbon source necessary for growth of the transformant is used therein. Nitrogen sources, inorganic substances, etc. are contained.
As the carbon source, for example, glucose, dextrin,
Nitrogen sources such as soluble starch and sucrose include, for example, ammonium salts, nitrates, corn steep liquor,
Inorganic or organic substances such as peptone, casein, meat extract, soybean meal, potato extract, and inorganic substances include, for example, calcium chloride, sodium dihydrogen phosphate, and magnesium chloride. In addition, yeast extract, vitamins, growth promoting factors and the like may be added. Medium p
H is preferably about 5 to 8.

As a medium for culturing the genus Escherichia, for example, M9 medium containing glucose and casamino acid [Miller, Journal of Experiments in Molecular Genetics (Journa)
l of Experiments in Molecular Genetics), 431-43
3, Cold Spring Harbor Laboratory, New York 1972]
Is preferred. If necessary, an agent such as 3β-indolylacrylic acid can be added in order to make the promoter work efficiently. When the host is a bacterium belonging to the genus Escherichia, the cultivation is usually performed at about 15 to 43 ° C. for about 3 to 24 hours, and if necessary, aeration and stirring can be added.
When the host is a bacterium belonging to the genus Bacillus, the cultivation is usually performed at about 30 to 40 ° C. for about 6 to 24 hours, and if necessary, aeration and stirring can be added. When culturing a transformant whose host is yeast,
As a medium, for example, Burkholde (Burkholde)
r) Minimal medium [Bostian, KL et al., Processings.
Proc. Natl. Acad. Sc of the National Academy of Sciences of the USA
USA, 77, 4505 (1980)] and SD medium containing 0.5% casamino acid [Bitter, GA, et al., Proceedings of the National Academy of Sciences of the USA]. (Proc. Natl. Acad.
Sci. USA), 81, 5330 (1984)].
Preferably, the pH of the medium is adjusted to about 5-8. The cultivation is usually performed at about 20 ° C. to 35 ° C. for about 24 to 72 hours, and aeration and stirring are added as necessary. When culturing a transformant in which the host is an insect cell or an insect, the medium used is Grace's Inse
ct Medium (Grace, TCC, Nature, 195,
788 (1962)) to which an additive such as immobilized 10% bovine serum is appropriately added. PH of the medium is about 6.2 ~
Preferably adjusted to 6.4. Culture is usually performed at about 27 ° C for about 3
５5 days, with aeration and / or agitation as needed. When culturing a transformant in which the host is an animal cell, examples of the medium include MEM medium containing about 5 to 20% fetal bovine serum [Science, 122, 501 (1952)], D
MEM medium [Virology, 8, 396 (19
59)], RPMI 1640 medium [Journal of the American Medical Association (The Jo
urnal of the American Medical Association) Volume 199,
519 (1967)], 199 medium [Proceeding of the Society for the Biological Medicine (Proceeding of the Society for the Biological Medicine)]
Medicine, 73, 1 (1950)]. pH
Is preferably about 6-8. Culture is usually about 30 ° C-40
C. for about 15-60 hours, adding aeration and agitation as needed. As described above, the protein of the present invention can be produced in the cell, in the cell membrane, or outside the cell of the transformant.

The protein of the present invention can be separated and purified from the above culture by, for example, the following method. When the protein of the present invention is extracted from cultured cells or cells, after culturing, the cells or cells are collected by a known method, suspended in an appropriate buffer, and subjected to sonication, lysozyme, and / or freeze-thawing. After the cells or cells are destroyed by the method, a method of obtaining a crude extract of the protein by centrifugation or filtration is used as appropriate. The buffer may contain a protein denaturant such as urea or guanidine hydrochloride, or a surfactant such as Triton X-100 ^™ . When the protein is secreted into the culture solution, after the culture is completed, the supernatant is separated from the cells or cells by a known method, and the supernatant is collected. The protein contained in the thus obtained culture supernatant or extract can be purified by appropriately combining known separation and purification methods. These known separation and purification methods include methods using solubility such as salting out and solvent precipitation, dialysis, ultrafiltration, gel filtration, and SDS-polyacrylamide gel electrophoresis, mainly molecular weight. Method using difference in charge, method using charge difference such as ion exchange chromatography, method using specific affinity such as affinity chromatography, and use of difference in hydrophobicity such as reverse phase high performance liquid chromatography A method utilizing a difference between isoelectric points, such as an isoelectric focusing method, is used.

When the protein thus obtained is obtained in a free form, it can be converted into a salt by a known method or a method analogous thereto, and conversely, when the protein is obtained as a salt, a known method or analogous method Depending on the method, it can be converted into a free form or other salts. The protein produced by the recombinant can be arbitrarily modified or the polypeptide can be partially removed by applying an appropriate protein modifying enzyme before or after purification. As the protein modifying enzyme, for example, trypsin, chymotrypsin, arginyl endopeptidase, protein kinase, glycosidase and the like are used. The presence of the protein of the present invention thus produced can be measured by an enzyme immunoassay using a specific antibody, Western blotting, or the like.

The antibody against the protein or partial peptide or a salt thereof used in the present invention may be a polyclonal antibody or a monoclonal antibody as long as it can recognize the protein or partial peptide or a salt thereof used in the present invention. Is also good. Antibodies against the protein or partial peptide used in the present invention or a salt thereof (hereinafter, these may be simply abbreviated to the protein of the present invention in the description of the antibody) can be obtained by using the protein of the present invention as an antigen and a known antibody. It can be produced according to a method for producing an antibody or antiserum. [Preparation of Monoclonal Antibody] (a) Preparation of Monoclonal Antibody-Producing Cell The protein of the present invention is administered to a warm-blooded animal by itself or together with a carrier or a diluent at a site where the antibody can be produced by administration. Complete Freund's adjuvant or incomplete Freund's adjuvant may be administered in order to enhance the antibody-producing ability upon administration. Administration is usually performed once every 2 to 6 weeks, for a total of about 2 to 10 times. Examples of the warm-blooded animal to be used include monkeys, rabbits, dogs, guinea pigs, mice, rats, sheep, goats and chickens, and mice and rats are preferably used. When preparing monoclonal antibody-producing cells, a warm-blooded animal immunized with an antigen, for example, an individual having an antibody titer is selected from a mouse, and the spleen or lymph node is collected 2 to 5 days after the final immunization and contained in the spleen or lymph node. By fusing the antibody-producing cells thus obtained with myeloma cells of the same or different species, a monoclonal antibody-producing hybridoma can be prepared. The antibody titer in the antiserum can be measured, for example, by reacting a labeled protein described below with the antiserum, and then measuring the activity of a labeling agent bound to the antibody. The fusion operation is performed by known methods, for example, the method of Kohler and Milstein [Nature, 256, 495 (1
975)]. Examples of the fusion promoter include polyethylene glycol (PEG) and Sendai virus, but PEG is preferably used.

Examples of myeloma cells include NS-1,
Examples include warm-blooded animal myeloma cells such as P3U1, SP2 / 0, and AP-1, but P3U1 is preferably used. The preferred ratio between the number of antibody-producing cells (spleen cells) and the number of myeloma cells used is about 1: 1 to 20: 1.
EG (preferably PEG1000-PEG6000)
Added at a concentration of about 10 to 80%, preferably at 20 to 40 ° C, preferably
By incubating at 30 to 37 ° C for 1 to 10 minutes, cell fusion can be carried out efficiently. Various methods can be used to screen for monoclonal antibody-producing hybridomas. For example, a hybridoma culture supernatant is added to a solid phase (eg, a microplate) on which a protein antigen is adsorbed directly or together with a carrier, and then radioactive substances or A method for detecting a monoclonal antibody bound to a solid phase by adding an anti-immunoglobulin antibody labeled with an enzyme or the like (an anti-mouse immunoglobulin antibody is used when cells used for cell fusion are mice) or protein A; A method in which a hybridoma culture supernatant is added to a solid phase to which globulin antibodies or protein A is adsorbed, a protein labeled with a radioactive substance, an enzyme, or the like is added, and a monoclonal antibody bound to the solid phase is detected. Selection of the monoclonal antibody can be performed according to a known method or a method analogous thereto. Usually, it can be carried out in a medium for animal cells supplemented with HAT (hypoxanthine, aminopterin, thymidine). As a selection and breeding medium, any medium can be used as long as a hybridoma can grow. For example, 1-20%, preferably
RPMI 1640 medium containing 10-20% fetal calf serum,
GIT medium containing 1-10% fetal calf serum (Wako Pure Chemical Industries, Ltd.) or serum-free medium for hybridoma culture (S
FM-101, Nissui Pharmaceutical Co., Ltd.) can be used. The culturing temperature is usually 20 to 40 ° C, preferably about 37 ° C. The culturing time is usually 5 days to 3 weeks, preferably 1 week to 2 weeks. The culture can be usually performed under 5% carbon dioxide. The antibody titer of the hybridoma culture supernatant is
The measurement can be performed in the same manner as the measurement of the antibody titer in the antiserum described above.

(B) Purification of Monoclonal Antibody Separation and purification of monoclonal antibodies can be performed by known methods, for example, immunoglobulin separation and purification methods (eg, salting out method, alcohol precipitation method, isoelectric point precipitation method, electrophoresis method). , Ion-exchanger (eg, DEAE) adsorption / desorption method, ultracentrifugation method, gel filtration method, antigen-bound solid phase or active adsorbent such as protein A or protein G to collect only antibody and dissociate the antibody Specific purification method for obtaining

[Preparation of Polyclonal Antibody] The polyclonal antibody of the present invention can be produced according to known methods or modifications thereof. For example, an immunizing antigen (protein antigen) itself or a complex thereof with a carrier protein is formed, and immunization is performed on a warm-blooded animal in the same manner as in the above-described method for producing a monoclonal antibody. It can be produced by collecting a substance and separating and purifying the antibody. With respect to the complex of the immunizing antigen and the carrier protein used for immunizing a warm-blooded animal, the type of the carrier protein and the mixing ratio of the carrier and the hapten are such that the antibody is efficiently cross-linked to the hapten immunized by crosslinking the carrier. If possible, any material may be cross-linked at any ratio. For example, bovine serum albumin, bovine thyroglobulin, hemocyanin, etc. may be used in a weight ratio of about 1 to hapten.
A method of coupling at a rate of 0.1 to 20, preferably about 1 to 5 is used. Various coupling agents can be used for coupling the hapten and the carrier, and glutaraldehyde, carbodiimide, a maleimide active ester, an active ester reagent containing a thiol group or a dithioviridyl group, or the like is used. The condensation product is administered to a warm-blooded animal itself or together with a carrier or diluent at a site where antibody production is possible. Complete Freund's adjuvant or incomplete Freund's adjuvant may be administered in order to enhance the antibody-producing ability upon administration. The administration is usually performed once every about 2 to 6 weeks, about 3 to 10 times in total. The polyclonal antibody can be collected from the blood, ascites, etc., preferably from the blood of a warm-blooded animal immunized by the above method. The measurement of the polyclonal antibody titer in the antiserum can be performed in the same manner as the measurement of the antibody titer in the antiserum described above. The polyclonal antibody can be separated and purified according to the same method for separating and purifying immunoglobulins as in the above-described method for separating and purifying a monoclonal antibody.

A DNA that is complementary to the base sequence of DNA encoding the protein or partial peptide used in the present invention (hereinafter, these DNAs may be abbreviated to the DNA of the present invention in the description of antisense nucleotides).
Alternatively, the antisense nucleotide having a substantially complementary nucleotide sequence includes a nucleotide sequence complementary to or substantially complementary to the nucleotide sequence of the DNA of the present invention.
Any antisense nucleotide may be used as long as it has an effect of suppressing the expression of NA, but antisense DNA is preferable. The base sequence substantially complementary to the DNA of the present invention is, for example, a base sequence complementary to the DNA of the present invention (that is, a complementary strand of the DNA of the present invention).
And a base sequence having about 70% or more, preferably about 80% or more, more preferably about 90% or more, and most preferably about 95% or more homology with the entire base sequence or partial base sequence. In particular, out of the entire base sequence of the complementary strand of the DNA of the present invention, the base sequence of the portion encoding the N-terminal portion of the protein of the present invention (for example, the base sequence near the start codon and the like) is at least about 70% or more. Antisense nucleotides having preferably at least about 80%, more preferably at least about 90%, most preferably at least about 95% homology are suitable. Specifically, a base sequence complementary to or substantially complementary to the base sequence of DNA having the base sequence represented by SEQ ID NO: 2, or an antisense nucleotide having a part thereof, preferably, for example, SEQ ID NO: : 2, a base sequence complementary to the base sequence of the DNA having the base sequence represented by 2, or an antisense nucleotide having a part thereof. The antisense nucleotide is usually composed of about 10 to 40, preferably about 15 to 30 bases. In order to prevent degradation by a hydrolase such as nuclease, the phosphate residue (phosphate) of each nucleotide constituting the antisense DNA is replaced with a chemically modified phosphate residue such as phosphorothioate, methylphosphonate or phosphorodithionate. It may be substituted. These antisense nucleotides can be produced using a known DNA synthesizer or the like.

Hereinafter, the protein or partial peptide of the present invention or a salt thereof (hereinafter sometimes abbreviated as the protein of the present invention), the DNA encoding the protein or partial peptide of the present invention (hereinafter referred to as the DNA of the present invention) Abbreviated), antibodies against the protein or partial peptide of the present invention or a salt thereof (hereinafter sometimes abbreviated as the antibody of the present invention), and antisense nucleotides of the DNA of the present invention (hereinafter referred to as the antisense nucleotide of the present invention). (May be abbreviated as sense nucleotide).

A drug containing a compound that inhibits the activity of the protein of the present invention or a salt thereof can suppress the generation of a membrane potential based on the K ⁺ current by suppressing the K ⁺ channel activity. It can be used as a therapeutic / prophylactic agent for muscle diseases, central nervous system diseases, heart diseases and the like. On the other hand, a medicament containing a compound or a salt thereof that promotes the activity of the protein of the present invention, for example, can promote K ⁺ channel activity and promote the generation of membrane potential based on K ⁺ current. Leads to improvement,
For example, it can be used as a therapeutic / prophylactic agent for muscular diseases, central nervous system diseases, heart diseases and the like.

[1] Therapeutic / prophylactic agent for various diseases related to the protein of the present invention The protein of the present invention has K ⁺ channel activity, contributes to the permeation of K ⁺ ions, and contributes to the generation of membrane potential of cells. Plays a central role. In addition, generation of a membrane potential by the protein of the present invention plays an important role in expressing cell functions such as nerve transmission, muscle contraction, and secretion of a physiologically active substance. Therefore, when the DNA encoding the protein of the present invention is abnormal or defective, or when the expression level of the protein of the present invention is reduced, for example, muscular disease, central nervous system disease, heart disease And various diseases develop. Therefore, the protein of the present invention and the DNA of the present invention can be used as medicaments such as agents for treating or preventing diseases such as muscular diseases, central nervous system diseases, and heart diseases. For example, since the protein of the present invention is reduced or deleted in vivo, K ⁺
When there is a patient in which the permeation of ions is not sufficiently or normally not exerted, (a) administering the DNA of the present invention to the patient and expressing the protein of the present invention in a living body, After inserting the DNA of the present invention and expressing the protein of the present invention, the cells are transplanted into the patient, or (c) administering the protein of the present invention to the patient. The role of the protein of the present invention can be sufficiently or normally exerted. When the DNA of the present invention is used as the above-mentioned therapeutic / prophylactic agent, the DNA is inserted alone or into a suitable vector such as a retrovirus vector, an adenovirus vector, an adenovirus associated virus vector, and the like. It can be administered to humans or warm-blooded animals. The DNA of the present invention
It can be administered as it is or in the form of a formulation together with a physiologically acceptable carrier such as an adjuvant for promoting uptake, and administered by a gene gun or a catheter such as a hydrogel catheter. When the protein of the present invention is used as the above-mentioned therapeutic / prophylactic agent, at least 90%, preferably 95%
Or more, more preferably 98% or more, still more preferably 99%
It is preferable to use those purified as described above.

The protein and the like of the present invention include, for example, tablets, capsules, elixirs,
It can be used orally as microcapsules or the like, or parenterally in the form of injections such as sterile solutions or suspensions with water or other pharmaceutically acceptable liquids. For example, the protein or the like of the present invention is mixed with physiologically acceptable carriers, flavors, excipients, vehicles, preservatives, stabilizers, binders, and the like in the unit dosage form generally required for the practice of the formulation. Can be manufactured. The amount of the active ingredient in these preparations is such that a proper dosage in the specified range can be obtained. Examples of additives that can be mixed with tablets, capsules, and the like include binders such as gelatin, corn starch, tragacanth, and acacia, excipients such as crystalline cellulose, corn starch, gelatin, and alginic acid. Useful bulking agents, lubricants such as magnesium stearate, sweeteners such as sucrose, lactose or saccharin, flavoring agents such as peppermint, reddish oil or cherry and the like are used. When the preparation unit form is a capsule, a liquid carrier such as oil and fat can be further contained in the above-mentioned type of material. Sterile compositions for injection can be formulated according to normal pharmaceutical practice such as dissolving or suspending the active substance in vehicles such as water for injection, and naturally occurring vegetable oils such as sesame oil, coconut oil and the like. Aqueous liquids for injection include, for example, physiological saline, isotonic solutions containing glucose and other adjuvants (eg, D-sorbitol, D-mannitol, sodium chloride, etc.), and suitable solubilizing agents. For example, it may be used in combination with an alcohol (eg, ethanol or the like), a polyalcohol (eg, propylene glycol, polyethylene glycol, or the like), a nonionic surfactant (eg, polysorbate 80 ^™ , HCO-50, or the like). Examples of the oily liquid include sesame oil and soybean oil, and may be used in combination with a solubilizing agent such as benzyl benzoate or benzyl alcohol. In addition, buffers (eg, phosphate buffer, sodium acetate buffer, etc.), soothing agents (eg, benzalkonium chloride, procaine hydrochloride, etc.), stabilizers (eg, human serum albumin, polyethylene glycol, etc.), Preservatives (for example,
Benzyl alcohol, phenol, etc.), antioxidants and the like. The prepared injection is usually filled in a suitable ampoule. The vector into which the DNA of the present invention has been inserted is also formulated in the same manner as described above, and is usually used parenterally.

Since the preparation thus obtained is safe and has low toxicity, for example, warm-blooded animals (eg, human, rat, mouse, guinea pig, rabbit, bird, sheep, pig, cow, horse, cat, Dogs, monkeys, chimpanzees, etc.). The dose of the protein or the like of the present invention varies depending on the target disease, the administration subject, the administration route, and the like. )), About 0.1 mg to 100 mg, preferably about 1.0 to 50 mg of the protein or the like per day.
g, more preferably about 1.0-20 mg. When administered parenterally, the single dose of the protein or the like varies depending on the administration subject, target disease, and the like. (As a body weight of 60 kg), about 0.01 to 30 mg, preferably about 0.
It is convenient to administer about 1 to 20 mg, more preferably about 0.1 to 10 mg by injecting into the affected area. In the case of other animals, the amount can be administered in terms of 60 kg.

[2] Screening of Candidate Drug Compounds for Disease The protein of the present invention is useful as a reagent for screening a compound or a salt thereof that promotes or inhibits the activity of the protein of the present invention. That is, the present invention
(1) A compound or a salt thereof that promotes or inhibits the activity of the protein of the present invention (for example, K ⁺ ion permeation activity and the like) characterized by using the protein of the present invention (hereinafter referred to as a promoter and an inhibitor, respectively) (May be abbreviated in some cases), more specifically, for example, (2) (i) K ⁺ ion permeability of a cell capable of producing the protein of the present invention and (ii) There is provided a method for screening for an accelerator or an inhibitor, which comprises comparing the K ⁺ ion permeability of a mixture of cells having the ability to produce the protein of the invention and a test compound. Specifically, in the above screening method, for example, in the cases (i) and (ii), the K ⁺ ion current is measured by the patch clamp method and compared as an index of the K ⁺ ion permeation activity. It is a feature.

As the test compound, for example, peptide,
Examples include proteins, non-peptidic compounds, synthetic compounds, fermentation products, cell extracts, plant extracts, animal tissue extracts, and the like.These compounds may be novel compounds or known compounds. Is also good. To carry out the above screening method, cells having the ability to produce the protein of the present invention are prepared by suspending them in a buffer suitable for screening. The buffer has a pH of about 4-10.
Any buffer that does not inhibit the K ⁺ ion permeation activity of the protein of the present invention, such as a phosphate buffer (preferably about 6 to 8) and a borate buffer, may be used. As a cell having the ability to produce the protein of the present invention, for example, a host (transformant) transformed with a vector containing the DNA encoding the protein of the present invention described above is used. As a host, for example, animal cells such as CHO cells are preferably used.
For the screening, for example, a transformant in which the protein of the present invention is expressed on a cell membrane by culturing by the method described above is preferably used.

The K ⁺ ion permeation activity of the protein of the present invention can be determined by a known method, for example, J. Biol. Chem. 275: 2839.
It can be measured according to the method described in 8-28405, 2000 or a method analogous thereto. For example, a test compound that promotes the K ⁺ ion permeation activity in the case (ii) above by about 20% or more, preferably 30% or more, more preferably about 50% or more as compared with the case (i) above It can be selected as a compound or a salt thereof that promotes the activity of the protein of the present invention. In addition, for example, the K ⁺ ion permeation activity in the case (ii) is inhibited by about 20% or more, preferably 30% or more, more preferably about 50% or more as compared with the case (i). The test compound to be inhibited) can be selected as a compound that inhibits the activity of the protein of the present invention or a salt thereof. Also, the protein of the present invention
A gene such as secreted alkaline phosphatase or luciferase is inserted downstream of the promoter of the KV2.2 homolog gene, expressed in the above various cells, and activates or inhibits the enzyme activity when the test compound is brought into contact with the cells. By searching for a compound or a salt thereof, a compound or a salt thereof that promotes or suppresses the expression of the protein of the present invention (KV2.2 homolog) (that is, promotes or inhibits the activity of the protein of the present invention) can be screened. .

The screening kit of the present invention contains the protein or partial peptide used in the present invention or a salt thereof, or a cell capable of producing the protein or partial peptide used in the present invention.

The compound obtained by using the screening method or the screening kit of the present invention or a salt thereof may be a test compound such as a peptide, protein, non-peptide compound, synthetic compound, fermentation product, cell extract, Compounds or salts thereof selected from plant extracts, animal tissue extracts, plasma, and the like, and compounds or salts thereof that promote or inhibit the activity of the protein of the present invention (eg, K ⁺ ion permeability). . As the salt of the compound, those similar to the aforementioned salts of the protein of the present invention are used. The compound or its salt that promotes the activity of the protein of the present invention is useful, for example, as a medicament such as a therapeutic / prophylactic agent for muscle diseases, central nervous system diseases, and heart diseases. Further, the compound or a salt thereof that inhibits the activity of the protein of the present invention is useful as a medicament such as a therapeutic / prophylactic agent for muscle disease, central nervous system disease, and heart disease.

When a compound or a salt thereof obtained by using the screening method or the screening kit of the present invention is used as the above-mentioned therapeutic or prophylactic agent, it can be formulated into a preparation according to a conventional method. For example, tablets, capsules, elixirs, microcapsules, sterile solutions, suspensions and the like can be used. The preparations obtained in this way are safe and low toxic, for example, human or warm-blooded animals (eg, mouse, rat, rabbit, sheep, pig, cow, horse, bird, cat, dog, monkey, chimpanzee, etc.) ) Can be administered orally or parenterally. The dose of the compound or a salt thereof varies depending on its action, a target disease, an administration subject, an administration route and the like. For oral administration, generally adults (weight 60kg)
In about, the compound or a salt thereof is added in an amount of about 0.1 per day.
-100 mg, preferably about 1.0-50 mg, more preferably about 1.0-20 mg. If administered parenterally,
The single dose of the compound or a salt thereof varies depending on the administration subject, target disease and the like. When administered to an adult (assuming a body weight of 60 kg), the compound or a salt thereof is added in an amount of about 0.5 mg / day.
It is convenient to administer about 01 to 30 mg, preferably about 0.1 to 20 mg, more preferably about 0.1 to 10 mg by intravenous injection. In the case of other animals, the amount can be administered in terms of the weight per 60 kg.

[3] Quantification of the protein of the present invention, its partial peptide or its salt An antibody against the protein of the present invention (hereinafter sometimes abbreviated as the antibody of the present invention) specifically recognizes the protein of the present invention. Therefore, it can be used for quantification of the protein of the present invention in a test solution, particularly for quantification by sandwich immunoassay. That is, the present invention
(I) reacting the antibody of the present invention with a test solution and a labeled protein of the present invention competitively, and measuring the ratio of the labeled protein of the present invention bound to the antibody. And (ii) simultaneously or sequentially reacting the test solution with the antibody of the present invention insolubilized on a carrier and another antibody of the present invention labeled on a carrier. The present invention provides a method for quantifying the protein of the present invention in a test solution, which comprises measuring the activity of a labeling agent on an insolubilized carrier after the reaction. In the quantitative method (ii), it is desirable that one antibody is an antibody that recognizes the N-terminal of the protein of the present invention and the other antibody is an antibody that reacts with the C-terminal of the protein of the present invention.

The protein of the present invention can be quantified using a monoclonal antibody against the protein of the present invention (hereinafter sometimes referred to as the monoclonal antibody of the present invention), and can also be detected by tissue staining or the like. . For these purposes, the antibody molecule itself may be used, or F (ab ') ₂ , Fab', or Fab fraction of the antibody molecule may be used. The method for quantifying the protein of the present invention using the antibody of the present invention is not particularly limited. Any measurement method may be used as long as the amount is detected by chemical or physical means and the amount is calculated from a standard curve prepared using a standard solution containing a known amount of antigen. For example, nephelometry, competition method, immunometric method and sandwich method are preferably used, but in terms of sensitivity and specificity, it is particularly preferable to use the sandwich method described later. As a labeling agent used in a measurement method using a labeling substance, for example, a radioisotope, an enzyme, a fluorescent substance, a luminescent substance and the like are used. Examples of the radioisotope include [ ¹²⁵ I], [ ¹³¹ I], [ ³ H], and [ ¹⁴ H].
C] is used. As the above enzyme, a stable enzyme having a large specific activity is preferable. For example, β-galactosidase, β-glucosidase, alkaline phosphatase, peroxidase, malate dehydrogenase and the like are used. As the fluorescent substance, for example, fluorescamine, fluorescein isothiocyanate and the like are used. As the luminescent substance, for example, luminol, a luminol derivative, luciferin, lucigenin and the like are used. Further, a biotin-avidin system can be used for binding the antibody or antigen to the labeling agent.

For insolubilization of the antigen or antibody, physical adsorption may be used, or a method using a chemical bond usually used for insolubilizing and immobilizing proteins or enzymes may be used. Examples of the carrier include insoluble polysaccharides such as agarose, dextran, and cellulose; synthetic resins such as polystyrene, polyacrylamide, and silicon; and glass. In the sandwich method, the test solution is reacted with the insolubilized monoclonal antibody of the present invention (primary reaction), and further reacted with another labeled monoclonal antibody of the present invention (secondary reaction). By measuring the activity of the labeling agent, the amount of the protein of the present invention in the test solution can be determined. The primary reaction and the secondary reaction may be performed in the reverse order, may be performed simultaneously, or may be performed at staggered times. The labeling agent and the method of insolubilization can be in accordance with those described above. In addition, in the immunoassay by the sandwich method,
The antibody used for the solid phase antibody or the labeling antibody is not necessarily one kind, and a mixture of two or more kinds of antibodies may be used for the purpose of improving measurement sensitivity and the like. In the method for measuring the protein of the present invention by the sandwich method of the present invention, as the monoclonal antibody of the present invention used in the primary reaction and the secondary reaction, an antibody having a different site to which the protein of the present invention binds is preferably used. That is, the antibody used in the primary reaction and the secondary reaction is preferably, for example, when the antibody used in the secondary reaction recognizes the C-terminal of the protein of the present invention, the antibody used in the primary reaction is preferably For example, an antibody that recognizes an N-terminal other than the C-terminal is used.

The monoclonal antibody of the present invention can be used in a measurement system other than the sandwich method, for example, a competition method, an immunometric method, or a nephrometry. In the competition method, an antigen in a test solution and a labeled antigen are allowed to react competitively with an antibody, and then the unreacted labeled antigen is reacted.
(F) is separated from the labeled antigen (B) bound to the antibody (B / F separation), the amount of labeling of either B or F is measured, and the amount of antigen in the test solution is quantified. In this reaction method, a soluble antibody is used as the antibody, B / F separation is performed using polyethylene glycol, a liquid phase method using a second antibody to the antibody, or a solid phase antibody is used as the first antibody, or A solid-phase method using a soluble antibody as the first antibody and using a solid-phased antibody as the second antibody is used. In the immunometric method, an antigen in a test solution and a solid-phased antigen are subjected to a competitive reaction with a fixed amount of a labeled antibody, and then the solid phase and the liquid phase are separated. And an excess amount of the labeled antibody, and then immobilized antigen is added to bind unreacted labeled antibody to the solid phase, and then the solid phase and the liquid phase are separated.
Next, the amount of label in any phase is measured to determine the amount of antigen in the test solution. In nephelometry, the amount of insoluble precipitates generated as a result of an antigen-antibody reaction in a gel or in a solution is measured. Even when the amount of antigen in the test solution is small and only a small amount of sediment is obtained, laser nephrometry utilizing laser scattering is preferably used.

In applying these individual immunoassays to the quantification method of the present invention, there is no need to set special conditions, operations, and the like. What is necessary is just to construct the protein measurement system of the present invention by adding ordinary technical considerations of those skilled in the art to ordinary conditions and operation methods in each method. For details of these general technical means, reference can be made to reviews, books, and the like. For example, Hiroe Irie, "Radio Immunoassay" (Kodansha, published in 1974), Hiroshi Irie, "Sequence Radioimmunoassay" (Kodansha, published in 1974), Eiji Ishikawa et al., "Enzyme Immunoassay" (Medical Shoin, Showa Ed. Ishikawa et al., “Enzyme Immunoassay” (Second Edition) (Issue Shoin, 1982) Published in 1962, "Methods in ENZYMOLOGY" Vol. 70 (Immunochem
ical Techniques (Part A)), ibid.Vol. 73 (Immunochem
ical Techniques (Part B)), ibid.Vol. 74 (Immunochem
ical Techniques (Part C)), ibid.Vol. 84 (Immunochem
ical Techniques (Part D: Selected Immunoassays)),
Ibid.Vol. 92 (Immunochemical Techniques (Part E: Mono
clonal Antibodies and General Immunoassay Method
s)), ibid.Vol. 121 (Immunochemical Techniques (Part
I: Hybridoma Technology and Monoclonal Antibodie
s)) (above, published by Academic Press). As described above, the protein of the present invention can be quantified with high sensitivity by using the antibody of the present invention. Furthermore, by quantifying the concentration of the protein of the present invention using the antibody of the present invention, (1)
When a decrease in the concentration of the protein of the present invention is detected, it can be diagnosed that there is a high possibility of, for example, a muscular disease, a central nervous system disease, a heart disease and the like. (2) Conversely, for example, when an increase in the concentration of the protein of the present invention is detected, it can be diagnosed that the possibility of muscular disease, central nervous system disease, or heart disease is high. Further, the antibody of the present invention can be used for detecting the protein of the present invention present in a subject such as a body fluid or a tissue. Further, for preparation of an antibody column used for purifying the protein of the present invention, detection of the protein of the present invention in each fraction at the time of purification, analysis of the behavior of the protein of the present invention in test cells, etc. Can be used.

[4] Gene Diagnostic Agent The DNA of the present invention can be used, for example, as a probe to produce a human or warm-blooded animal (eg, rat, mouse, guinea pig, rabbit, bird, sheep, pig, cow,
DNA or mRNA abnormalities (genetic abnormalities) encoding the protein of the present invention or its partial peptide in horses, cats, dogs, monkeys, chimpanzees, etc.) can be detected.
It is useful as an agent for genetic diagnosis such as damage, mutation or decreased expression of DNA, and increase or excessive expression of the DNA or mRNA. The above-described genetic diagnosis using the DNA of the present invention can be performed, for example, by the known Northern hybridization or PCR-SSCP method (Genomics,
5, 874-879 (1989), Proceedings of the National Academy of Sciences of USA
heNational Academy of Sciences of the United State
s of America), Vol. 86, pp. 2766-2770 (1
989)). For example, when an increase in expression is detected by Northern hybridization, it can be diagnosed that the possibility of muscular disease, central nervous system disease, or heart disease is high. On the contrary, when a decrease in expression is detected or when the DNA is
Is detected, for example, it can be diagnosed that the possibility of muscular disease, central nervous system disease, or heart disease is high.

[5] Pharmaceuticals Containing Antisense Nucleotides The antisense nucleotides of the present invention, which can complementarily bind to the DNA of the present invention and suppress the expression of the DNA, have low toxicity, and Since the function of the protein of the present invention or the DNA of the present invention (eg, K ⁺ ion permeation activity) can be suppressed, for example,
It can be used as a therapeutic / prophylactic agent for central nervous system diseases, heart diseases and the like. When the antisense nucleotide is used as the therapeutic or prophylactic agent, it can be formulated and administered according to a known method. For example, when the antisense nucleotide is used, the antisense nucleotide is inserted alone or into a suitable vector such as a retrovirus vector, an adenovirus vector, an adenovirus associated virus vector or the like, and then inserted into a human or mammal ( For example, rats, rabbits, sheep, pigs, cows, cats, dogs, monkeys, etc.) can be administered orally or parenterally. The antisense nucleotide can be administered as it is or in the form of a formulation together with a physiologically acceptable carrier such as an adjuvant for promoting uptake, and administered with a gene gun or a catheter such as a hydrogel catheter. The dose of the antisense nucleotide varies depending on the target disease, the administration subject, the administration route, and the like.For example, when the antisense nucleotide of the present invention is locally administered to the liver for the purpose of treating a muscular disease, it is generally used. Adults (weight 60k
In g), about 0.1 to 100 mg of the antisense nucleotide is administered per day. Furthermore, the antisense nucleotide can also be used as a diagnostic oligonucleotide probe for examining the presence of the DNA of the present invention in tissues or cells and the state of its expression.

In the present specification and drawings, when bases, amino acids and the like are represented by abbreviations, IUPAC-IUB
It is based on the abbreviation by the Commission on Biochemical Nomenclature or the abbreviation commonly used in the relevant field, examples of which are described below. When an amino acid can have an optical isomer, the L-form is indicated unless otherwise specified. DNA: deoxyribonucleic acid cDNA: complementary deoxyribonucleic acid A: adenine T: thymine G: guanine C: cytosine RNA: ribonucleic acid mRNA: messenger ribonucleic acid dATP: deoxyadenosine triphosphate dTTP: deoxythymidine triphosphate dGTP: deoxyguanosine triphosphate Phosphate dCTP: Deoxycytidine triphosphate ATP: Adenosine triphosphate EDTA: Ethylenediaminetetraacetic acid SDS: Sodium dodecyl sulfate Gly: Glycine Ala: Alanine Val: Valine Leu: Leucine Ile: Isoleucine Ser: Serine Thr: thyronine : Methionine Glu: Glutamic acid Asp: Aspartic acid Lys: Lysine Arg: Arginine His: Histidine Phe Phenylalanine Tyr: tyrosine Trp: tryptophan Pro: proline Asn: asparagine Gln: glutamine pGlu: pyroglutamic acid

The substituents, protecting groups and reagents frequently used in the present specification are represented by the following symbols. Me: methyl group Et: ethyl group Bu: butyl group Ph: phenyl group TC: thiazolidine -4 (R) - carboxamide group Tos: p-toluenesulfonyl CHO: formyl Bzl: benzyl Cl ₂ -Bzl: 2,6-dichlorobenzyl Bom: benzyloxymethyl Z: benzyloxycarbonyl Cl-Z: 2-chlorobenzyloxycarbonyl Br-Z: 2-bromobenzyloxycarbonyl Boc: t-butoxycarbonyl DNP: dinitrophenyl Trt: trityl Bum: t-butoxymethyl Fmoc : N-9-fluorenylmethoxycarbonyl HOBt: 1-hydroxybenztriazole HOOBT: 3,4-dihydro-3-hydroxy-4-oxo- 1,2,3-benzotriazine HONB: 1-hydroxy-5-no Bornene-2,3-dicarboximide DCC: N, N'-dicyclohexylcarbodiimide

The sequence numbers in the sequence listing in the present specification indicate the following sequences. [SEQ ID NO: 1] This shows the amino acid sequence of human TCH033 protein. [SEQ ID NO: 2] This shows the base sequence of DNA encoding TCH033 protein having the amino acid sequence represented by SEQ ID NO: 1.

[0057]

The protein having the same or substantially the same amino acid sequence as the amino acid sequence represented by SEQ ID NO: 1 is useful as a diagnostic marker for muscular disease, central nervous system disease, heart disease and the like. The compound that promotes or inhibits the activity of the protein obtained by the screening method using can be used, for example, as a prophylactic / therapeutic agent for diseases such as muscular disease, central nervous system disease, and heart disease.

[0058]

[Sequence List] SEQUENCE LISTING <110> Takeda Chemical Industries, Ltd. <120> Novel Protein and its DNA <130> P2001-019 <140> <141> <160> 2 <170> PatentIn Ver. 2.1 <210> 1 <211> 801 <212> PRT <213> Human <400> 1 Met Leu Lys Gln Ser Glu Arg Arg Arg Ser Trp Ser Tyr Arg Pro Trp 1 5 10 15 Asn Thr Thr Glu Asn Glu Gly Ser Gln His Arg Arg Ser Ile Cys Ser 20 25 30 Leu Gly Ala Arg Ser Gly Ser Gln Ala Ser Ile His Gly Trp Thr Glu 35 40 45 Gly Asn Tyr Asn Tyr Tyr Ile Glu Glu Asp Glu Asp Gly Glu Glu Glu 50 55 60 Asp Gln Trp Lys Asp Asp Leu Ala Glu Glu Asp Gln Gln Ala Gly Glu 65 70 75 80 Val Thr Thr Ala Lys Pro Glu Gly Pro Ser Asp Pro Pro Ala Leu Leu 85 90 95 Ser Thr Leu Asn Val Asn Val Gly Gly His Ser Tyr Gln Leu Asp Tyr 100 105 110 Cys Glu Leu Ala Gly Phe Pro Lys Thr Arg Leu Gly Arg Leu Ala Thr 115 120 125 Ser Thr Ser Arg Ser Arg Gln Leu Ser Leu Cys Asp Asp Tyr Glu Glu 130 135 140 Gln Thr Asp Glu Tyr Phe Phe Asp Arg Asp Pro Ala Val Phe Gln Leu 145 150 155 160 Val Tyr Asn Phe Tyr Leu Ser Gly Val Le u Leu Val Leu Asp Gly Leu 165 170 175 Cys Pro Arg Arg Phe Leu Glu Glu Leu Gly Tyr Trp Gly Val Arg Leu 180 185 190 Lys Tyr Thr Pro Arg Cys Cys Arg Ile Cys Phe Glu Glu Arg Arg Asp 195 200 205 Glu Leu Ser Glu Arg Leu Lys Ile Gln His Glu Leu Arg Ala Gln Ala 210 215 220 Gln Val Glu Glu Ala Glu Glu Leu Phe Arg Asp Met Arg Phe Tyr Gly 225 230 235 240 Pro Gln Arg Arg Arg Leu Trp Asn Leu Met Glu Lys Pro Phe Ser Ser 245 250 255 Val Ala Ala Lys Ala Ile Gly Val Ala Ser Ser Thr Phe Val Leu Val 260 265 270 Ser Val Val Ala Leu Ala Leu Asn Thr Val Glu Glu Met Gln Gln His 275 280 285 Ser Gly Gln Gly Glu Gly Gly Pro Asp Leu Arg Pro Ile Leu Glu His 290 295 300 Val Glu Met Leu Cys Met Gly Phe Phe Thr Leu Glu Tyr Leu Leu Arg 305 310 315 320 Leu Ala Ser Thr Pro Asp Leu Arg Arg Phe Ala Arg Ser Ala Leu Asn 325 330 335 Leu Val Asp Leu Val Ala Ile Leu Pro Leu Tyr Leu Gln Leu Leu Leu 340 345 350 Glu Cys Phe Thr Gly Glu Gly His Gln Arg Gly Gln Thr Val Val Gly Ser 355 360 365 Val Gly Lys Val Gly Gln Val Leu Arg Val M et Arg Leu Met Arg Ile 370 375 380 Phe Arg Ile Leu Lys Leu Ala Arg His Ser Thr Gly Leu Arg Ala Phe 385 390 395 400 Gly Phe Thr Leu Arg Gln Cys Tyr Gln Gln Val Gly Cys Leu Leu Leu 405 410 415 Phe Ile Ala Met Gly Ile Phe Thr Phe Ser Ala Ala Val Tyr Ser Val 420 425 430 Glu His Asp Val Pro Ser Thr Asn Phe Thr Thr Ile Pro His Ser Trp 435 440 445 Trp Trp Ala Ala Val Ser Thr Phe Ala Leu Gly Phe Pro Ile Leu Phe 450 455 460 Pro Ser Pro Val Ser Cys Ser Ser Leu Pro Trp Leu Ser Ala Thr Arg 465 470 475 480 Leu Trp Leu Leu Ile Leu Val Phe Pro Pro Thr Pro Asn Arg Arg Ile 485 490 495 Gln Leu Thr Lys Arg Arg Trp Met Ser Lys Val Val Glu Arg Glu Leu 500 505 510 Ser Arg Ser Val Asn Ser Ser Ser His Met Ser Met Ala Val Ala Lys 515 520 525 Asn Lys Arg Glu Asn Ala Ser Pro Ile Met Gln Thr Leu His Lys Phe 530 535 540 Leu Phe Met Ala Phe Ala Gln Pro Ile Gly Gln Ser Lys Ser His Gly 545 550 555 560 Gln Ala Ala Ser Gln Arg Ala Gly Gln Val Ser Ile Ser Thr Val Gly 565 570 575 Tyr Gly Asp Met Tyr Pro Glu Thr His Leu G ly Arg Phe Phe Ala Phe 580 585 590 Leu Cys Ile Ala Phe Gly Ile Ile Leu Asn Gly Met Pro Ile Ser Ile 595 600 605 Leu Tyr Asn Lys Phe Ser Asp Tyr Tyr Ser Lys Leu Lys Ala Tyr Glu 610 615 620 620 Tyr Thr Thr Ile Arg Arg Glu Arg Gly Glu Leu His Arg Lys Thr Ile 625 630 635 640 Gln Val Gln Thr Glu Ser Pro Val Ile Glu Asp Arg Ile Leu Trp Val 645 650 655 Lys Thr Ala Phe Glu Ser Cys Cys Gln Pro Pro Ser Pro Thr Ser Glu 660 665 670 Lys Lys Val Ala Ala Gly Asn Asp Thr Val Arg Leu Gly Glu Ile Pro 675 680 685 Lys Leu Gln Ser Thr Ser Thr Pro Ala Ser Val Gln Ala Leu Asp Ala 690 695 700 Ile Val Arg Arg Asn Ser Arg Met Ser Gln Lys Ile Val Lys Ala Trp 705 710 715 720 Arg Tyr Thr Ala Lys Gln Asn Val His Thr Gln Gly Ser Ala Gly Leu 725 730 730 735 Leu Lys Ser His Thr Gln Arg Gly Leu Gly Leu Leu Pro Leu Trp Val 740 745 750 Ser Leu Thr Lys Gly Trp Asn Ile His Glu Asn Ser Trp Lys Lys Val 755 760 765 Glu Ile Ser Gln Asn Gly Ser Ala Ile His Phe Tyr Thr Lys Tyr Gly 770 775 780 Ser Ser Arg Asn Phe His Gly Thr Gly Gly LeuSer Val Leu Met His 785 790 795 800 Ile <210> 2 <211> 2403 <212> DNA <213> Human <400> 2 180 GGCGAGGAGG AGGACCAGTG GAAGGACGAC CTGGCAGAAG AGGACCAGCA GGCAGGGGAG 240 GTCACCACCG CCAAGCCCGA GGGCCCCAGC GACCCTCCGG CCCTGCTGTC CACGCTGAAT 300 GTGAACGTGG GTGGCCACAG CTACCAGCTG GACTACTGCG AGCTGGCCGG CTTCCCCAAG 360 ACGCGCCTAG GTCGCCTGGC CACCTCCACC AGCCGCAGCC GCCAGCTAAG CCTGTGCGAC 420 GACTACGAGG AGCAGACAGA CGAATACTTC TTCGACCGCG ACCCGGCCGT CTTCCAGCTG 480 GTCTACAATT TCTACCTGTC CGGGGTGCTG CTGGTGCTCG ACGGGCTGTG TCCGCGCCGC 540 TTCCTGGAGG AGCTGGGCTA CTGGGGCGTG CGGCTCAAGT ACACGCCACG CTGCTGCCGC 600 ATCTGCTTCG AGGAGCGGCG CGACGAGCTG AGCGAACGGC TCAAGATCCA GCACGAGCTG 660 CGCGCGCAGG CGCAGGTCGA GGAGGCGGAG GAACTCTTCC GCGACATGCG CTTCTACGGC 720 CCGCAGCGGC GCCGCCTCTG GAACCTCATG GAGAAGCCAT TCTCCTGCGT GGCCGCGTGC CATCGGGG TGGCCTCCAG CACCTTCGTG CTCGTCTCCG TGGTGGCGCT GGCGCTCAAC 840 ACCGTGGAGG AGATGCAGCA GCACTCGGGG CAGGGCGAGG GCGGCCCAGA CCTGCGGCCC 900 ATCCTGGAGC ACGTGGAGAT GCTGTGCATG GGCTTCTTCA CGCTCGAGTA CCTGCTGCGC 960 CTAGCCTCCA CGCCCGACCT GAGGCGCTTC GCGCGCAGCG CCCTCAACCT GGTGGACCTG 1020 GTGGCCATCC TGCCGCTCTA CCTTCAGCTG CTGCTCGAGT GCTTCACGGG CGAGGGCCAC 1080 CAACGCGGCC AGACGGTGGG CAGCGTGGGT AAGGTGGGTC AGGTGTTGCG CGTCATGCGC 1140 CTCATGCGCA TCTTCCGCAT CCTCAAGCTG GCGCGCCACT CCACCGGACT GCGTGCCTTC 1200 GGCTTCACGC TGCGCCAGTG CTACCAGCAG GTGGGCTGCC TGCTGCTCTT CATCGCCATG 1260 GGCATCTTCA CTTTCTCTGC GGCTGTCTAC TCTGTGGAGC ACGATGTGCC CAGCACCAAC 1320 TTCACTACCA TCCCCCACTC CTGGTGGTGG GCCGCGGTGA GTACCTTTGC CCTGGGCTTT 1380 CCCATCCTCT TCCCCAGCCC AGTGAGCTGC TCCTCCCTCC CCTGGTTATC AGCCACCAGG 1440 CTTTGGCTTC TGATCCTCGT CTTCCCCCCC ACCCCCAATC GCCGCATACA GCTAACAAAA 1500 CGGCGATGGA TGTCAAAAGT GGTGGAAAGA GAACTCAGCA GATCAGTAAA CTCCAGCAGC 1560 CACATGTCCA TGGCTGTGGC AAAGAACAAG AGAGAGAATG CAAGCCCCAT CATGCAAACA 1620 CTTCATAAGT TTCTTTTCAT GGCATTTGCT CAGCCCATTG GCCAGAGTAA GTCACATGGC 1680 CAAGCTGCAA GTCAAAGGGC AGGGCAGGTG AGCATCTCCA CCGTGGGCTA CGGAGACATG 1740 TACCCAGAGA CCCACCTGGG CAGGTTTTTT GCCTTCCTCT GCATTGCTTT TGGGATCATT 1800 CTCAACGGGA TGCCCATTTC CATCCTCTAC AACAAGTTTT CTGATTACTA CAGCAAGCTG 1860 AAGGCTTATG AGTATACCAC CATACGCAGG GAGAGGGGAG AGCTGCATAG GAAAACTATA 1920 CAAGTCCAGA CAGAGTCACC TGTCATCGAA GACAGGATTC TGTGGGTGAA GACAGCTTTT 1980 GAATCCTGTT GCCAGCCCCC TAGCCCAACC AGTGAAAAAA AAGTTGCAGC TGGAAATGAT 2040 ACTGTTAGGC TGGGAGAGAT CCCCAAACTC CAGAGCACTT CAACCCCAGC CAGTGTCCAG 2100 GCTCTTGACG CTATCGTGAG AAGGAATTCA AGGATGAGTC AGAAAATAGT GAAAGCATGG 2160 AGATATACTG CGAAGCAAAA CGTACACACT CAGGGGAGTG CAGGCCTACT CAAGAGTCAC 2220 ACGCAACGGG GTTTGGGGCT GCTACCCTTA TGGGTTTCTT TAACCAAGGG GTGGAACATT 2280 CATGAAAATT CCTGGAAAAA GGTGGAAATT TCTCAGAACG GCAGTGCCAT CCATTTTTAT 2340 ACCAAATATG GGTCTTCCCG GAACTTTCAT GGCACTGGTG GACTTAGTGT TTTAATGCAC 2400 ATA 2403

──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. ⁷ Identification symbol FI Theme coat ゛ (Reference) A61P 21/00 C07K 14/705 4C086 25/00 16/28 4H045 C07K 14/705 C12N 1/15 16/28 1/19 C12N 1/15 1/21 1/19 C12P 21/02 C 1/21 G01N 33/15 Z 5/10 33/50 Z C12P 21/02 A61K 48/00 G01N 33/15 C12P 21/08 33 / 50 C12N 15/00 ZNAA // A61K 48/00 A61K 37/02 C12P 21/08 C12N 5/00 A F term (reference) 2G045 AA34 AA35 BB20 DA13 DA36 FB02 4B024 AA01 AA11 BA80 CA01 DA02 DA05 DA11 DA12 EA04 GA11 GA18 GA19 HA15 4B064 AG01 AG26 AG27 CA02 CA05 CA06 CA10 CA19 CA20 CC24 DA01 DA13 4B065 AA01X AA57X AA72X AA90X AA93Y AB01 BA02 CA24 CA44 CA46 4C084 AA02 AA06 AA07 AA13 AA17 BA01 BA22 CA53 DC50 ZA022A 942 4C086 AA01 AA02 AA03 AA04 EA16 MA01 MA04 ZA02 ZA36 ZA94 4H045 AA10 AA11 AA20 AA30 BA10 CA40 DA75 DA76 EA21 EA23 EA50 FA74

Claims (16)

[Claims] 1. A protein comprising an amino acid sequence identical or substantially identical to the amino acid sequence represented by SEQ ID NO: 1, or a salt thereof. 2. A partial peptide of the protein according to claim 1, or a salt thereof. 3. A D-containing DNA encoding the protein according to claim 1 or the partial peptide according to claim 2.
NA. 4. The DNA according to claim 3, which has the base sequence represented by SEQ ID NO: 2. 5. A recombinant vector containing the DNA according to claim 4. 6. A transformant transformed with the recombinant vector according to claim 5. 7. The method according to claim 1, wherein the transformant according to claim 6 is cultured to produce and accumulate the protein according to claim 1 or the partial peptide according to claim 2, and collect the protein. 3. A method for producing a protein according to claim 2, or a partial peptide according to claim 2, or a salt thereof. 8. A pharmaceutical comprising the protein according to claim 1, the partial peptide according to claim 2, or a salt thereof. 9. A pharmaceutical comprising the DNA according to claim 3. 10. An antibody against the protein according to claim 1, the partial peptide according to claim 2, or a salt thereof. 11. The activity of the protein according to claim 1, the partial peptide according to claim 2, or a salt thereof, wherein the protein according to claim 1 or the partial peptide according to claim 2 or a salt thereof is used. A method of screening for a compound that promotes or inhibits or a salt thereof. 12. The activity of the protein according to claim 1, the partial peptide according to claim 2, or a salt thereof, comprising the protein according to claim 1 or the partial peptide according to claim 2, or a salt thereof. A kit for screening a compound to be inhibited or a salt thereof. (13) promoting or inhibiting the activity of the protein of (1), the partial peptide of (2), or a salt thereof obtained by using the screening method of (11) or the screening kit of (12); Or a salt thereof. 14. The protein according to claim 1, which is obtained by using the screening method according to claim 11 or the screening kit according to claim 12.
A medicament comprising a compound or a salt thereof that promotes or inhibits the activity of the partial peptide or a salt thereof described above. 15. A muscle disease, a central nervous system disease, a heart disease,
The medicament according to claim 8 or 9, which is a prophylactic / therapeutic agent for: 16. A muscle disease, a central nervous system disease, a heart disease,
The medicament according to claim 14, which is a prophylactic or therapeutic agent for: