JPH07260787A - Peroxidase immunological staining method and stabilization of aromatic primary amine compound solution - Google Patents

Abstract

PURPOSE:To simply and rapidly measure a specific component with high sensitivity and high resolving power by allowing a benzenesulfinic acid derivative to be present in a soln. of an aromatic primary amine compd. expressed by a specific formula. CONSTITUTION:A usable aromatic primary amine compd. is pref. expressed by formula I (wherein A or B is a hydrogen atom or an alkyl group and A and B may form a heterocyclic ring along with a nitrogen atom and D, E, G and J are a hydrogen atom, a halogen atom, a hydroxy group, an amino group, an alkoxy group, an acylamino group, an arylsulfonamide group, an alkylsufonamide group or an alkyl group). As a benzenesulfinic acid derivative used in the stabilization of a soln. of the compd. expressed by the formula I, a compd. expressed by formula II (wherein R is a hydrogen atom, a lower alkyl group, a lower alkoxy group or a halogen atom, M is a hydrogen atom, alkali metal or ammonium and n is a positive integer of 1-3) is mentioned.

Description

Detailed Description of the Invention

[0001]

TECHNICAL FIELD The present invention relates to a peroxidase immunostaining method, and more particularly to a method for stabilizing an aromatic primary amine compound solution used in a dye forming reaction.

[0002]

2. Description of the Related Art Various analytical methods for detecting a specific component such as a biological component have been developed. As the most accurate method among these methods, the specific component and the specific component Substances capable of binding (hereinafter referred to as specific binding substances), for example, antigens and antibodies, certain sugar chains and lectins, biotin and avidin, protein A and IgG, hormones and receptors,
A method using a specific binding reaction between an enzyme and a substrate is known.

In general, a specific component is measured by using a specific binding substance having a label (hereinafter referred to as a label) and detecting a signal of the label which is changed according to the specific component. .

In particular, a specific component supported directly or indirectly on a support is reacted with a label to immobilize the label as a complex of both, and a signal from the label substantially corresponding to the specific component is generated. The method of detection is appropriately used.

For example, an electrophoretic protein biological component (specific component) is transferred from a gel onto a nitrocellulose membrane and transferred,
A method of detecting a signal by reacting with a label such as an antibody label, a method of detecting a signal by reacting a label with a specific component such as a lipid spread on a TLC plate, D on a membrane
A method of reacting NA with a labeled complementary DNA to the DNA to detect a signal, an immunohistochemical staining method, or the like.

By these methods, not only the quantitative determination of the specific component and the reactivity of the specific component with the specific binding substance, but also a great amount of information on the property and the existing state of the specific component or the specific binding substance can be obtained. For example, after electrophoresis, a signal is detected on a complex in which a specific component of a living body such as a protein or a nucleic acid transferred or carried on a membrane or a lipid component developed on TLC and a label for the specific component are bound. In the method, information such as the molecular weight, isoelectric point or polarity of the specific component can be obtained from the position and mobility of the signal of the specific component.

Further, in the immunohistochemical staining method, information such as the location and state of the target specific component on the tissue can be obtained.

[0008]

The above-mentioned measurement of a specific component, which substantially detects a signal according to the amount of the specific component on the composite binder directly or indirectly supported on the support, is a target. It is essential that the label be detected with high sensitivity because the specific component is in a very small amount, and that the method for detecting the label has a high resolution in order to obtain more information about the specific component.

Radiolabels, fluorescent substances, luminescent substances, enzymes and the like are used as labels for specific binding substances.
Radioisotopes have problems such as decay of radioactivity, disposal, exposure, or huge cost for installation, and when detecting a signal on a label carried on a support, the photosensitivity of a photographic light-sensitive material, It has a drawback that it requires a long time and complicated operations such as development. Fluorescent substances or luminescent substances require special equipment and facilities.

On the other hand, when an enzyme is used, the operation is relatively simple and the produced dye can be easily visualized and quantified. Conventionally, peroxidase, alkaline phosphatase, β-galactosidase and the like have been used as labeling enzymes. Peroxidase is mainly used as a labeling enzyme in a method for producing and depositing a dye by an enzymatic reaction on a complex conjugate supported on a support, and in that case, depending on active oxygen quantitatively generated from hydrogen peroxide. Then, a method is known in which a dye is generated and quantified.
As a dye-forming reaction, a method of coupling a phenol compound or an active methylene compound with an aromatic primary amine compound is well known. However, when the coupling reaction is performed, a solution of an aromatic primary amine compound has been conventionally unstable, and thus was prepared just before use.

Therefore, an object of the present invention is to provide a simple, high-sensitivity, high-resolution and rapid method for measuring a specific component, which is an aromatic primary amine used in a peroxidase immunostaining method. It is to provide a long-term stabilization method for a compound solution.

[0012]

The above object of the present invention is to provide a primary aromatic compound which forms a dye by coupling with a phenol compound or an active methylene compound used as a chromogen in a peroxidase immunostaining method. This is accomplished by a peroxidase immunostaining method, which comprises allowing a benzenesulfinic acid derivative to be present in a solution of an amine compound, and a method of stabilizing the solution.

Next, the present invention will be described in detail.

The aromatic primary amine compound which can be used in the present invention includes o- or p-aminophenol compounds and o- or p-phenylenediamine compounds and salts thereof.

A p-phenylenediamine compound is preferable, and it is represented by the following general formula (1).

[0016]

[Chemical 1]

In the formula, A and B represent a hydrogen atom or an alkyl group, A and B may form a heterocycle together with a nitrogen atom, and D, E, G and J are a hydrogen atom, a halogen atom and a hydroxy group. , Amino group, alkoxy group, acylamido group,
It represents an aryl sulfonamide group, an alkyl sulfonamide group or an alkyl group.

As the alkyl group represented by A and B,
Those having 1 to 6 carbon atoms are preferable, and those having 1 to 4 carbon atoms are particularly preferable. Examples thereof include a methyl group, an ethyl group and a butyl group. These alkyl groups may have a substituent, and examples of the substituent include an ureido group,
Examples thereof include tetrahydrofuryl group, carboxyl group, methanesulfonamide group, sulfo group, methoxy group, ethoxy group, methoxyethoxy group, methoxyethoxyethoxy group, and methoxytetraethoxy group.

D, G and J are preferably a hydrogen atom, an alkoxy group, an alkylsulfonamide group or an arylsulfonamide group, more preferably a hydrogen atom. E is preferably a hydrogen atom, an alkyl group or an acylamide group, more preferably an alkyl group having 1 to 3 carbon atoms, particularly a methyl group. Further, as salts of the compound represented by the general formula (1), p-toluenesulfonic acid, sulfonic acid, sulfinic acid, sulfuric acid ester, sulfamic acid,
Thiosulfate S-ester, carboxylic acid, phosphoric acid ester, amidophosphoric acid, phosphoric acid, phosphorous acid ester, organic boron compound, salts of organic acid or inorganic acid such as hydrochloric acid and sulfuric acid, and particularly p-toluenesulfonic acid salt , Hydrochloride and sulfate are preferred.

Typical examples of the aromatic primary amine compound according to the present invention are shown below, but the present invention is not limited thereto.

Exemplified Compound (1-1) N, N-diethyl-3-methyl-4-aminoaniline (1-2) N, N-diethyl-4-aminoaniline (1-3) N-carbamidomethyl-N -Methyl-4-aminoaniline (1-4) N-carbamidomethyl-N-tetrahydrofurfuryl
-3-Methyl-4-aminoaniline (1-5) N-ethyl-N-carboxymethyl-3-methyl-4-aminoaniline (1-6) N-carbamidomethyl-N-ethyl-3-methyl-4 -Aminoaniline (1-7) N-ethyl-N-tetrahydrofurfuryl-3-methyl-
4-aminophenol (1-8) 3-acetylamino-4-aminodimethylaniline (1-9) N-ethyl-N-β-methanesulfonamide ethyl-4-
Aminoaniline (1-10) N-ethyl-N-β-methanesulfonamide ethyl-3
-Methyl-4-aminoaniline (1-11) N-methyl-N-β-sulfoethyl-p-phenylenediamine (1-12) N-ethyl-N-hydroxyethyl-3-methyl-4-aminoaniline (1 -13) N-ethyl-N- [2- (2-methoxyethoxy) ethyl] -3-methyl-4-aminoaniline (1-14) N-ethyl-N- {2- [2- (2-methoxy (Ethoxy) ethoxy] ethyl} -3-methyl-4-aminoaniline (1-15) N-ethyl-N- [2- {2- [2- [2- (2-methoxyethoxyethoxy) ethoxy] ethoxy] ethoxy] ethoxy }ethyl〕
-3-Methyl-4-aminoaniline (1-16) N, N-diethyl-3-methanesulfonamidoethyl-
4-aminoaniline.

The salt of the compound represented by the general formula (1) is generally water-soluble and can be easily dissolved in water or a buffer solution.

Examples of the benzenesulfinic acid derivative used for stabilizing the solution of the compound represented by the general formula (1) in the present invention include compounds represented by the following general formula (2).

[0024]

[Chemical 2]

In the formula, R represents a hydrogen atom, a lower alkyl group, a lower alkoxy group or a halogen atom, M represents a hydrogen atom, an alkali metal or ammonium, and n is 1 to 1
Represents a positive integer of 3. Below, the specific compound represented by General formula (2) which concerns on this invention is shown.

(2-1) Benzenesulfinic acid (2-2) Sodium benzenesulfinate (2-3) Potassium benzenesulfinate (2-4) Ammonium benzenesulfinate (2-5) p-Methyl-benzenesulfinic acid (2-6) Sodium p-methyl-benzenesulfinate (2-7) Potassium p-methyl-benzenesulfinate (2-8) Ammonium p-methyl-benzenesulfinate (2-9) m-Methyl-benzenesulfinate Sodium acid salt (2-10) o-Methyl-sodium benzenesulfinate (2-11) Sodium p-ethyl-benzenesulfinate (2-12) Potassium o-ethyl-benzenesulfinate (2-13) 2,4- Dimethyl-benzenesulfinate sodium (2-14) p-chloro-benzenesulfinate potassium (2-15) o-bromo-benzenesulfinate ammonium (2-16) p-methoxy-benzenesulfate Sodium phosphate (2-17) o-ethoxy - as preferred concentration of the compound represented by the benzene sulfinic acid potassium formula (2) is
0.2 to 1000 mg / ml, particularly preferred concentration is 1 to 200 mg
/ Ml.

The phenol compound or active methylene compound that can be used in the present invention is a compound that forms a dye by coupling with an oxidized product of an aromatic primary amine compound, and reduces the solubility of the produced dye in water. Therefore, it is a group of compounds in which appropriate substituents are substituted.

Such phenol compounds or active methylene compounds are well known as a cyan coupler, a yellow coupler, and a magenta coupler in silver halide color photography. It also includes the case where one of the hydrogen atom at the active site of the phenol compound or one of the two hydrogen atoms of active methylene is replaced by a group capable of leaving by the coupling reaction with the oxidation product of the aromatic primary amine compound. Be done. These compounds are described in TH Theory of TH by TH James.
The Photographic Process "(The Theory of th
e Photographic Process) (3rd edition) Chapter 17 and (4th edition)
It is described in Chapter 12.

Examples of cyan couplers include phenol derivatives and 1-naphthol derivatives, examples of which are described in JP-A-63-6462. As the magenta coupler, 5-pyrazolone derivative, pyrazolo [2,3-a] benzimidazole derivative, pyrazolo- (3,2-c) -5-triazole derivative, cyanoacetyl-substituted heterocyclic compound (cyanoacetyl, chroman, Thiophene, quinoline derivative, etc.) and indazolone derivatives are preferred examples, and examples of the yellow coupler include acylacetonitrile derivatives, acylacetamide derivatives, and 1,3 diketone derivatives. For these examples, see JP-A-63-71654.
It is described in.

In the present invention, the specific component may be directly supported on the support by physical adsorption, chemical bonding or the like.
It may be supported indirectly via one or more specific binding substances. Alternatively, the specific component may be directly or indirectly supported on a support and then the label may be reacted to form the complex conjugate, or the complex conjugate may be formed and then the complex bond may be formed. The body may be supported directly or indirectly on a support. Further, the label forms a complex conjugate with the specific component and is carried on the support, but the specific component may be directly bound to the label, or may be bound via one or more other specific binding substances. May be.

In the present invention, the labeled substance may be one in which the specific binding substance is overlapped and labeled with peroxidase and anti-peroxidase antibody.

Hydrogen peroxide, an aromatic primary amine compound and a phenol compound or an active methylene compound are used as substrates for the enzymatic reaction of peroxidase in the complex conjugate. The aromatic primary amine compound is oxidized by the action of peroxidase and hydrogen peroxide, and is then coupled with a phenol compound or an active methylene compound to form and deposit a dye. Analytical Biochemistry 119 , 142 using conventional hydrogen peroxide and 4-chloro-1-naphthol as substrates
Compared with the method described in −147 (1982), the method of the present invention shortened the color development time, the spot was clear, and the sensitivity was increased 10 times or more. As a result, the amount of peroxidase-labeled product can be reduced, which is advantageous in terms of cost.

In the present invention, the specific component of interest is
It is a substance or a group of substances that gives a specific binding substance that specifically binds to the specific component.

For example, proteins, nucleic acids, hormones, lipids,
Examples include complex carbohydrates, glycolipids, polysaccharides, enzymes, vitamins, antigens, antibodies and the like.

The specific binding substance which can be used in the present invention is
It is a substance that can specifically bind to a specific component or another specific binding substance, and can be appropriately selected according to the specific component. For example, proteins, nucleic acids, hormones, lipids, glycoconjugates, glycolipids, polysaccharides, enzymes, vitamins, antigens, antibodies, lectins, protein A, avidin, biotin, receptors,
Examples include coenzymes, enzyme substrates, toxins, complements and complexes thereof. Examples of the support that can be used in the present invention include membranes such as cellulose acetate and nitrocellulose, gel-like supports such as polyacrylamide, silica gel carriers such as TLC plates, plate-like and bead-like plastics,
Examples thereof include glass, metal and fiber. In the histochemical staining, the tissue itself can also be used as a support.

In order to generate and deposit the dye on the complex conjugate of the specific component and the peroxidase-labeled substance carried on the support, the support may be dipped in a color-developing substrate reagent solution.
The color-developing substrate test solution is prepared by dissolving hydrogen peroxide, an aromatic primary amine compound and an active methylene compound in a buffer solution having an appropriate pH. Active methylene compounds are used in small amounts of hydrophilic organic solvents such as methanol, ethanol, DM.
It may be dissolved in F etc. and added. The molar ratio of the aromatic primary amine compound to the active methylene compound is appropriately from 1: 100 to 100: 1, preferably from 1:10 to 10: 1.

After the dye is sufficiently formed and deposited on the support by the enzymatic reaction, the unreacted substances are washed away to stop the reaction.

Information about the dye formed can be read visually or using methods known in the art, such as a spectrophotometer.

[0039]

EXAMPLES The present invention will be specifically described below with reference to examples, but the scope of the present invention is not limited by the examples.

Example 1 (1) Preparation of stock solution of aromatic primary amine compound N-ethyl-N-β-methanesulfonamidoethyl-3-methyl-
250 mg of 4-aminoaniline 3/2 sulfuric acid monohydrate (1-10) and Table 1
The amount of benzenesulfinic acid (2-1) shown in was dissolved in 10 ml of pure water. As a comparative object, one in which benzenesulfinic acid was not dissolved was prepared in the same manner.

This solution was stored at 37 ° C., and its change with time was evaluated visually and on performance.

(2) Evaluation of Performance a) Preparation of Coloring Solution 30 mg of 4-chloro-1-naphthol was dissolved in 10 ml of methanol, and 50 ml of 50 mM Tris-HCl buffer (pH 7.4,
Containing 200 mM NaCl; hereinafter referred to as TBS) is added. Further, 400 μl of the solution prepared in (1) was added, and 400 μl of 3% hydrogen peroxide was further added to prepare a color developing solution.

B) Evaluation of color-developing ability A PVDF membrane (manufactured by Millipore) immersed in methanol for 10 minutes and then immersed in pure water for 1 hour or more was phosphate-buffered saline (pH 7.
4; Goat IgG serially diluted with PBS) was dot-blotted using a blotting device (Bio-Rad). This PVDF membrane was blocked with "1% bovine serum albumin (hereinafter referred to as BSA) -PBS solution" at 4 ° C overnight, and then "peroxidase-labeled rabbit anti-goat IgG antibody (manufactured by Kappel) 1" % BS
It was reacted with "A-PBS solution" diluted 1500 times) at 4 ° C for 2 hours. "0.05% Tween-20 (polyoxyethylene sorbitan monolaurate; manufactured by Wako Pure Chemical Industries, Ltd.)-PB
It was washed 5 times with "S solution" and immersed in a coloring solution to develop a color. After 10 minutes, it was taken out, washed with water and dried, and the detection limit was visually confirmed.

(3) Results The results of performance evaluation are shown in Table 1.

[0045]

[Table 1]

From Table 1, it can be seen that the reagent solution of the present invention has good storability and excellent detection ability.

Example 2 N-ethyl-N-β-methanesulfonamidoethyl-3-methyl-4-aminoaniline 3/2 sulfuric acid 1 in (1) of Example 1
N, N-diethyl-4-aminoaniline (1-2) instead of water salt
Similar results were obtained when using the hydrochloride salt.

In the case of using sodium p-methyl-benzenesulfinate (2-6) instead of benzenesulfinic acid in (1) or using potassium p-chloro-benzenesulfinate (2-14) Similar results were obtained when or potassium o-ethoxy-benzenesulfinate (2-17) was used.

[0049]

EFFECT OF THE INVENTION A method for easily measuring a specific component with high sensitivity, high resolution and speed can be easily obtained, and a method for long-term stabilization of an aromatic primary amine compound solution used in peroxidase immunostaining method can be obtained. Was obtained.

Claims (2)

[Claims] 1. In a peroxidase immunostaining method,
A peroxidase immunostaining method, characterized in that a benzenesulfinic acid derivative is present in a solution of an aromatic primary amine compound which forms a dye by coupling with a phenol compound or an active methylene compound used as a chromogen. 2. In the peroxidase immunostaining method,
A method for stabilizing a benzenesulfinic acid derivative, which comprises allowing a benzenesulfinic acid derivative to exist in a solution of an aromatic primary amine compound that forms a dye by coupling with a phenol compound or an active methylene compound used as a chromogen. .