JP5339278B2 - Detection and analysis system for protein array using monolith gel - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a method and apparatus for analysis of the interaction of the protein and another protein and/or compound other than protein on a substrate. <P>SOLUTION: A system for detecting/analyzing the protein and/or another compound other than protein on a protein array contains the protein array wherein proteins are densely arranged and fixed on the substrate and a spectrophotometer and constituted so that the protein array is irradiated with light using the spectrophotometer, the light transmitted through the protein array is measured and the reduction ratio of the quantity of the transmitted light by the protein and/or another compound other than protein interacting with the immobilized protein on the protein array is measured to detect/analyze the protein and/or another compound other than protein on the protein array. In this system, the substrate for immobilized protein is a monolithic gel. <P>COPYRIGHT: (C)2010,JPO&amp;INPIT

Description

The present invention, the interaction of the protein at high density alignment immobilized protein and the protein with other proteins and / or compounds other than proteins on protein arrays on monolith gel, ultraviolet proteins, visible or infrared The present invention relates to a system for detecting and analyzing absorption in the light region by measuring using a spectrophotometer.

  A system for detecting a protein or a compound other than a protein on a protein array by measuring absorption in the ultraviolet, visible, or infrared light region using a spectrophotometer and analyzing their interaction is provided by the present inventor. Some of these have already been invented (see Patent Document 1). In the present invention, illumination light emitted from a light irradiation means in a spectrophotometer is passed through a protein array, photographed by a light detection means such as a CCD, and the image data is analyzed. For example, when a protein array is observed with ultraviolet light near 280 nm with this system, since the protein has a property of absorbing ultraviolet light near 280 nm, a region (spot) where the protein is immobilized is observed darkly. Therefore, the absorbance of the protein is obtained by calculating -log (I / Io) from the light intensity (I) of the region where the protein is immobilized and the light intensity (Io) of the region where the protein is not immobilized. Can be estimated. For example, when investigating the interaction between proteins A and B, an array in which protein A is immobilized on a hydrogel substrate is prepared, a solution of protein B is added to the array, and the array image is analyzed. It is possible to analyze the action (Japanese Patent Application No. 2007-336879).

  However, when a hydrogel is used as a substrate for a protein array, even if a protein or compound whose interaction is to be investigated is input, it takes a long time to enter the hydrogel, so the measurement takes time and is reproduced. It was difficult to obtain reliable and reliable analysis results. On the other hand, in an array in which proteins are immobilized on the surface of a glass substrate or the like, since the density of the immobilized proteins is low, it is difficult to obtain a signal with sufficient intensity by detection by light absorption. In the past, when calculating the absorbance of a spot, it was necessary for humans to determine the spot area and specify the area to compare the light intensity. It was difficult to do.

International Publication No. WO2006 / 059727 Pamphlet

  In order to solve the above-mentioned problems of conventional protein arrays and detection / analysis systems using protein arrays, the present invention fixes proteins on an array substrate with high-density fixation, ultraviolet light, visible light. The protein on the substrate is detected by irradiating the immobilized protein with light or infrared light and measuring the light that is not absorbed by the protein, and the protein on the substrate and other proteins and / or compounds other than proteins It is an object to provide a method and apparatus for analyzing the interaction with the protein, and a protein array suitable for the system. In particular, a monolith gel substrate is used as the array substrate, and the ultraviolet light that has not been absorbed by the protein is measured by irradiating the substrate on which the protein is immobilized with ultraviolet light, and the protein on the substrate is detected. It is an object of the present invention to provide a method and apparatus for analyzing an interaction between a protein and another protein or a non-protein compound, particularly a low molecular compound capable of interacting with the protein, and a protein array suitable for the system.

  In view of the problems of the prior art, the present inventor does not require protein labeling with a fluorescent dye or the like, and uses a protein array using a device that can be obtained at low cost, and the protein and protein and / or other substances. In order to develop a system for detecting and analyzing the interaction between the two, we have conducted intensive studies.

In the conventional method, proteins are immobilized on the array substrate from the femtomole order to the picomoles order (p moles order) in order to cope with the detection of minute quantities. We paid attention to labeling with pigments and using a system that requires special equipment such as SPR. The present inventor has previously completed a method of immobilizing proteins on an array substrate by controlling the orientation thereof at high density (Japanese Patent No. 2578661, Japanese Patent No. 2990271, Japanese Patent No. 3047029, Japanese Patent Laid-Open No. 2003). According to this method, the protein can be immobilized on the substrate in the order of nmole / cm ² which is one order to two orders higher than the conventional method. The present inventor uses the protein array in which the protein is immobilized at a high density in advance, so that it is widely used and can be obtained at a relatively low price without labeling with a fluorescent dye or using an expensive instrument. The inventors have completed an invention for measuring a protein on an array by measuring the optical activity of the protein using a photometer (WO 2006/059727 pamphlet). In the present invention, the protein is immobilized on the substrate in a high density and in a large amount. Therefore, irradiation is performed by irradiating the immobilized protein with light having a wavelength that is absorbed by the protein or a substance that interacts with the immobilized protein. The absorbed light is absorbed by a protein on the array or a substance that interacts with the protein. By measuring the intensity of light transmitted without being absorbed, absorption by immobilized proteins or substances that interact with proteins can be measured, and the substances that interact with proteins or proteins on the array substrate can be optically measured. It has been found that direct activity can be measured by using the activity of the target. In particular, protein absorbs ultraviolet light, but by using an ultraviolet light transmissive substrate such as quartz glass, ultraviolet light that has not been absorbed by protein is measured as transmitted light passing through the array substrate on which the protein is immobilized. I was able to. Here, in order to measure light transmission at each protein spot immobilized on the array at a time, it is desirable to use a two-dimensional photodetector such as a CCD, but two-dimensional light detection capable of detecting ultraviolet light. The vessel was extremely expensive and the system could not be constructed easily. Therefore, the present inventors use a CCD that can be obtained at low cost by converting the ultraviolet light transmitted through the substrate on which the protein is immobilized into visible light using an ultraviolet-visible light conversion device such as fluorescent glass. I was able to do that.

  The present inventor further developed a substrate that can immobilize proteins at a high density as a substrate for a protein array, and that allows the input protein or compound to easily approach and interact with the protein immobilized on the array. Therefore, we examined the possibility of using various materials. As a result, even if the light transmission at first glance is markedly reduced due to non-negligible scattering, the light passes though it is weak, and the passed light can be observed as a signal, and the solution has high permeability. The present inventors have found that monolith gels can be used as a material for an array substrate that satisfies various requirements such as high density, protein immobilization, low nonspecific adsorption to proteins, and so on. As a result of these intensive studies, interaction with the immobilized protein occurred while the protein solution or compound solution was being sent to the protein array, and the state was observed in real time. The inventors have found that it is possible to easily determine the time change of the light signal of the spot, and that it is possible to analyze the interaction between proteins or between a protein and a compound, and the present invention has been completed.

That is, the aspects of the present invention are as follows.
[1] By including a protein array and a spectrophotometer in which proteins are aligned and fixed at high density on a substrate, by irradiating the protein array with light using the spectrophotometer and measuring the amount of light that has passed through the protein array A system that detects and analyzes proteins on the protein array and / or other compounds other than proteins by measuring the rate of decrease in the amount of light passing by the compounds on the array and / or other compounds that interact with the immobilized protein. A system for detecting and analyzing proteins and / or other compounds other than proteins on a protein array, wherein the substrate on which the protein is immobilized is a monolith gel.

[2] A protein array in which proteins are aligned and fixed at a high density on a substrate, light irradiation means, and light detection means. Light that irradiates the protein array with light irradiation means and passes through the protein array with light detection means By measuring the rate of decrease in the amount of light transmitted by other compounds other than proteins interacting with proteins on the array and / or immobilized proteins, and measuring proteins on the protein array and / or other compounds other than proteins. a system for detecting and analyzing the substrate to fix the protein is Monolith gel, to detect and analyze other compounds other than proteins and / or proteins on a protein array system.

[3] A system for detecting and analyzing proteins and / or other compounds other than proteins on the protein array according to [1] or [2], wherein the monolith gel is monolithic silica gel.
[4] A system for detecting and analyzing a compound other than a protein that interacts with a protein on the protein array according to [2] or [3] and / or an immobilized protein, further comprising a data processing means.

[5] The protein is immobilized at a density of 0.01 μg / mm ² or more per spot of the protein array and interacts with the protein on the protein array and / or the immobilized protein according to any one of [1] to [4] A system that detects and analyzes other compounds besides proteins
[6] The protein interacts with the protein and / or the immobilized protein on the protein array of any one of [1] to [4] in which the light signal at one spot of the protein array is fixed at a density of 0.001 or more A system that detects and analyzes compounds other than proteins.

[7] A protein that is aligned and immobilized at high density has the formula NH ₂ —R ₁ —CO—NH—R ₂ —CO—NH—Y [wherein R ₁ and R ₂ represent any amino acid sequence; Represents a monolith gel substrate], and a system for detecting / analyzing a compound on the protein array of any one of [1] to [6] and / or other compounds other than the protein that interacts with the immobilized protein.

[8] The protein on the protein array according to any one of [1] to [7], wherein the monolith gel containing a primary amine and the C-terminal carboxy group of the amino acid sequence of the protein are covalently bonded and the protein is aligned and immobilized; Or a system that detects and analyzes compounds other than proteins that interact with immobilized proteins.
[9] The compound on the protein array according to any one of [1] to [8], wherein the light detection means is a CCD, CMOS, or photodiode array, and / or a compound other than the protein that interacts with the immobilized protein. Detection and analysis system.

[10] Contact the protein immobilized on the protein array with the sample, and measure the rate of decrease in the amount of light passing by the compound on the protein array and / or other compounds that interact with the immobilized protein before and after contact. By detecting the protein in the specimen that interacts with the immobilized protein and / or other compounds other than the protein that interacts with the immobilized protein, on the protein array according to any one of [1] to [9] A system that detects and analyzes other compounds than proteins and / or proteins that interact with immobilized proteins.

[11] A protein immobilized on the protein array is brought into contact with another protein and / or another compound other than a protein that interacts with the immobilized protein, and the protein on the protein array and / or the immobilized protein before and after the contact. The interaction between the immobilized protein and the protein or another compound other than the protein is analyzed by measuring the rate of decrease in the amount of light passing through by the compound other than the protein that interacts with [1] to [9]. A system for detecting and analyzing a protein on any protein array and / or a compound other than a protein that interacts with an immobilized protein.

[12] The protein is immobilized on the monolith gel substrate in the flow channel in the flow channel cell or microchip in which the flow channel is formed inside, and the immobilized protein and the sample are passed through the flow channel. A protein on the protein array of any one of [1] to [9] and / or an immobilized protein for analyzing an interaction with other compounds other than a protein that interacts with the protein in the protein and / or the immobilized protein A system that detects and analyzes compounds other than interacting proteins.

[13] Proteins on the array and / or immobilization by irradiating light using a spectrophotometer onto a protein array in which proteins are aligned and immobilized at high density on a monolith gel substrate and measuring the light that has passed through the protein array A method of detecting and analyzing a compound other than a protein that interacts with a protein on a protein array and / or an immobilized protein by measuring a decrease rate of the amount of light passing through by a compound other than the protein that interacts with the protein.

[14] The protein on the protein array according to [13], wherein the protein is immobilized at a density of 0.01 μg / mm ² or more per spot of the protein array, and / or other compounds other than proteins that interact with the immobilized protein How to detect and analyze
[15] The protein on the protein array according to [13], wherein the protein is immobilized at a density such that the light signal at one spot of the protein array is 0.001 or more, and / or other compounds other than the protein that interacts with the immobilized protein. How to detect and analyze.

[16] The protein aligned and immobilized at a high density has the formula NH ₂ —R ₁ —CO—NH—R ₂ —CO—NH—Y [wherein R ₁ and R ₂ represent any amino acid sequence; Represents a monolith gel substrate], and a method for detecting and analyzing a compound on the protein array of any one of [13] to [15] and / or other compounds other than the protein that interacts with the immobilized protein.
[17] The protein on the protein array of any one of [13] to [16], wherein the monolith gel containing primary amine and the C-terminal carboxy group of the amino acid sequence of the protein are covalently bonded and the protein is aligned and immobilized; Alternatively, a method for detecting and analyzing a compound other than a protein that interacts with an immobilized protein.

[18] The compound on the protein array according to any one of [13] to [17], wherein the light detection means is a CCD, CMOS, or photodiode array, and / or a compound other than the protein that interacts with the immobilized protein. How to detect and analyze.
[19] Contact the protein immobilized on the protein array with the sample, and measure the rate of decrease in the amount of light passing through the protein on the protein array and / or other compounds that interact with the immobilized protein before and after contact. On the protein array according to any one of [13] to [18], wherein the protein in the specimen that interacts with the immobilized protein and / or other compounds other than the protein that interacts with the immobilized protein are detected. A method for detecting and analyzing a compound other than a protein that interacts with a protein and / or an immobilized protein.

[20] A protein immobilized on the protein array is brought into contact with another protein or another compound other than a protein that interacts with the immobilized protein, and interacts with the protein on the protein array and / or the immobilized protein before and after the contact. The protein according to any one of [13] to [18], wherein the interaction between the protein and the protein or another compound other than the protein is analyzed by measuring the reduction rate of the amount of light passing by the compound other than the acting protein. A method for detecting and analyzing compounds other than proteins that interact with proteins on the array and / or immobilized proteins.

[21] The protein is immobilized on the monolith gel substrate in the flow channel in the flow channel cell or microchip in which the flow channel is formed inside, and the immobilized protein and the sample are passed through the flow channel. The protein on the protein array and / or the immobilized protein of any one of [13] to [18], which analyzes the interaction with other compounds other than the protein that interacts with the protein therein and / or the immobilized protein A method for detecting and analyzing compounds other than interacting proteins.

[22] Proteins represented by the formula NH ₂ —R ₁ —CO—NH—R ₂ —CO—NH—Y [wherein R ₁ and R ₂ represent arbitrary amino acid sequences] are aligned and immobilized at high density. A protein array, wherein the substrate represented by Y is a monolith gel.
[23] The protein array according to [22], wherein the monolith gel is monolithic silica gel.
[24] The protein array according to [22] or [23], wherein the protein is immobilized at a density of 0.01 μg / mm ² or more per spot of the protein array.
[25] The protein array according to [22] or [23], wherein the protein is fixed at a density such that a light signal at one spot of the protein array is 0.001 or more.
[26] The protein array according to any one of [22] to [25], wherein the protein is aligned and immobilized by covalently bonding a C-terminal carboxy group of a protein amino acid sequence to a monolith gel containing a primary amine.

  Since the protein array used in the present invention is immobilized at a high density by controlling the orientation of proteins on a monolith gel substrate, even when the amount of light passing through is significantly reduced due to scattering, it is irradiated with intense light and passes through the substrate. By measuring the measured light, the rate of decrease in the amount of light passing through the protein can be determined, and the amount of protein on the protein array can be measured from the rate of decrease in the amount of light passing through. Therefore, unlike the conventional method, it is not necessary to use a compound labeled with a fluorescent dye or the like for detection, and the amount of protein on the substrate can be directly measured by measuring the optical activity of the protein. Furthermore, since the present invention measures ultraviolet light, visible light, and infrared light, the amount of protein on the protein array can be easily measured using a widely used spectrophotometer. In particular, proteins on a protein array can be accurately measured using ultraviolet light absorption, which is widely used as a protein quantification means. Furthermore, by using a two-dimensional light detection means such as a CCD as the light detection means, it is possible to quickly measure the protein at each spot on the protein array at a time. Also, by using an ultraviolet-visible conversion device such as a fluorescent glass that can pass ultraviolet light and a fluorescent glass that can convert ultraviolet light into visible light, a CCD for digital cameras that can be easily obtained at low cost can be used. The system construction cost can be reduced.

  In addition, an interaction such as binding between a protein and another protein or a compound other than the protein can be analyzed by measuring a change in the absorbance of the protein on the array or an absorbance of the compound other than the protein.

  Furthermore, the monolith gel has a three-dimensional gel structure, so that it is possible to immobilize a sufficient amount of protein with an areal density, and the amount of light that can be transmitted by non-negligible scattering is significantly reduced. Since the amount of light passing through can be detected even in a difficult situation, it is possible to directly detect the protein in the gel by the decreasing rate of the amount of light passing through. In addition, since the monolith gel has high solution permeability, it is possible to flow a solution such as a protein to be added through the monolith gel, and the protein or compound in the solution can easily approach and interact with the immobilized protein. It is. This makes it possible to obtain highly reproducible and reliable analysis results in a short time. In particular, when a flow system is used, an analysis result can be obtained in real time.

  The protein array detection and analysis system of the present invention uses a substrate on which protein is immobilized at a high density, irradiates the protein on the substrate with light (ultraviolet light, visible light, or infrared light), and detects the protein on the substrate. Proteins are detected and analyzed by directly measuring absorption. In the system of the present invention, a substrate that is capable of passing light although ultraviolet light is weak is used as the substrate, and the protein is detected and analyzed using the decrease rate of the amount of light passing through absorption of the ultraviolet light of the protein. . Here, "detection / analysis" refers to protein-ligand interaction based on the qualitative and quantitative determination of protein, measurement of protein interaction with protein or compounds other than protein, and the rate of decrease in the amount of light passing through the absorbance of immobilized protein. Measurement, structural change monitoring of the protein itself, qualitative and quantitative determination of compounds other than proteins that interact with immobilized proteins.

  In the present invention, the protein includes peptides and polypeptides. In addition, the “protein on the array” when detecting proteins on the array is not only the immobilized protein bound on the array via the NH group, but also other proteins bound by the interaction with the immobilized protein. Including. “Detecting and analyzing proteins on the array” means not only detection and analysis of immobilized proteins on the array and other proteins that interacted with the immobilized proteins, but also proteins immobilized on the array. Changes in the structure of the protein by measuring changes in the rate of decrease in the amount of light passing through when it interacts with a compound other than a protein, such as a low molecular weight compound, and the light absorption changes due to a change in the structure of the protein due to the interaction. This also includes detecting and analyzing the above. Furthermore, “detection and analysis of other compounds that interact with proteins on the array” refers to the detection and analysis of other compounds other than proteins that interact with the proteins immobilized on the array. It means to measure a compound having absorption in the light by utilizing light of that wavelength.

  The configuration of the detection and analysis system for protein arrays of the present invention is shown in FIG. The system includes a system control unit including a light irradiation unit (optical system) 2, a light detection unit 5 such as a CCD digital camera, and a measurement unit and a data processing unit 7 including a video data processing unit 6 such as a video capture board if necessary. , Composed of a substrate 3 on which proteins are immobilized at a high density. The measurement unit may include an ultraviolet-visible light conversion device 4. Further, a lens or slit 8 may be included on the optical path from the optical system 2 to the substrate 3. Further, the data processing means can control the operation of the system control unit by the communication means 9 such as RS232C. In this system, the part including light irradiation means and light detection means that generates light, splits it, irradiates the protein array, and measures the light passing therethrough is the spectrophotometer 1, and the present invention It is also a system that uses a spectrophotometer to detect proteins on a substrate on which proteins are immobilized at high density. Here, the spectrophotometer is an apparatus for measuring infrared, visible, and ultraviolet spectrums. In the present invention, preferably, the ultraviolet spectrum is measured. Therefore, in the present invention, a widely used ultraviolet-visible spectrophotometer can be used.

  In the present invention, a flow system for measuring the interaction between a protein immobilized on a substrate and another protein or another compound other than a protein in a liquid can also be constructed. The outline of the flow system is shown in FIG. 3A and Shown in FIG. 3B. The substrate on which the protein is immobilized (array substrate) is sandwiched by a glass substrate (cover) to be covered with an appropriate spacer, the inlet of the solution is placed on one spacer (inlet), and the spacer on the opposite side, A flow system can be easily produced by creating an outlet portion (discharge port) for the solution and allowing the solution to flow from the outside. The flow system is mounted at the position of the protein-immobilized substrate 3 of the apparatus shown in FIG. The flow system can also be constructed by immobilizing proteins on the glass in the flow channel using a flow channel cell or a microchip having a micron-order high-precision flow channel formed on a glass substrate. In the case of using a microchip, a flow path substrate and a cover plate in which a flow path is formed are prepared, proteins are immobilized on the portion of the cover plate that contacts the flow path, and then the flow path substrate and the cover plate are joined together to attach the microchip. What is necessary is just to produce. Moreover, commercially available products such as the Fluence microchannel tool kit of Epigem can also be used.

  In the present invention, it is necessary to reduce the influence of stray light due to scattering as much as possible in order to irradiate light to an array that causes non-negligible scattering and measure the light absorption by the protein on the array as a reduction rate of the amount of light passing through. It is necessary to immobilize at a high density so that the number of protein molecules per unit area is increased on the array. For this purpose, it is desirable that the array substrate has a three-dimensional gel structure and proteins can be immobilized in the interior. At the same time, the array substrate must be able to pass light, particularly light near 280 nm, that can be detected by the detector. Furthermore, in the present invention, since the solution of protein and / or compound to be examined for interaction with the protein array is sent through the inside of the array substrate, the array substrate needs to be highly permeable to the liquid. In order to satisfy all of these conditions, in the present invention, a groove is formed in quartz glass and a monolith gel is formed therein. For example, a groove having a depth of 0.1 mm is formed in quartz glass, and a monolith gel formed in the groove is used as an array substrate (FIG. 2).

  The monolith gel refers to a gel made of a monolith material (monolith type polymer). The monolith material is composed of a single continuous structure and has pores that are continuous channels through the structure. The monolith gel can be produced by a solation step for producing an aqueous solution sol, a gelation step for heating the obtained sol to form a gel, and a firing step for firing the obtained gel. Examples of the monolith gel that can be used in the present invention include monolithic silica gel containing silicon. The monolith gel can be produced, for example, by a sol-gel method. The sol-gel method starts with a solution of various metal alkoxides such as silicon, boron, titanium, and aluminum, and other organic and inorganic compounds of metal, and the solution is converted into a metal compound by hydrolysis and polymerization of the compound in the solution. Alternatively, a sol in which hydroxide fine particles are dissolved is further gelled by further reaction, and the resulting porous gel is heated to produce an amorphous, glass or polycrystalline body. In the case of monolithic silica gel containing silicon, acetic acid, polyethylene glycol, and tetramethoxysilane may be mixed and the mixed solution may be baked, for example, at 40 ° C. for 24 hours. Monolith gel production methods are described in, for example, Japanese Patent Publication No. 08-029952 and Japanese Patent Application Laid-Open No. 07-041374. However, since proteins cannot be immobilized in this state, an epoxy silane is introduced into the monolith gel and an amino group-containing polymer such as poly-L-lysine is further bonded to prepare an array substrate. That's fine. Bonding of epoxy silane can be performed by immersing the monolith gel in an epoxy silane solution. In addition, amino groups may be introduced by adding an amino group-containing polymer to the surface of the monolith gel and allowing it to penetrate into the interior. By these operations, an epoxy group can be introduced into the monolith gel, and an amino group can be further covalently bonded to the epoxy group. A protein for immobilization is spotted on it, an immobilization reaction is performed, and the carboxy terminus of the protein is bonded with an amide, whereby the protein can be immobilized on the substrate. The protein immobilization reaction can be performed according to the methods described in, for example, Japanese Patent No. 2578661, Japanese Patent No. 2990271, Japanese Patent No. 3047029, and the like.

  The monolith gel has high solution permeability, and in the flow system, the monolith gel itself flows out, and the compound solution can flow through the monolith gel at high speed. For this reason, the interaction can be measured in real time by using the flow system.

Immobilization at high density means immobilization so that the number of protein molecules immobilized per unit area of the substrate increases. The amount of immobilization is not limited, but it is 0.5 nmole or more, preferably 1 nmole or more, more preferably 5 nmole or more, or 0.01 μg per one type of protein immobilized on the substrate, that is, per spot of 1 cm ² area. / mm ² or more, 0.05 [mu] g / mm ² or more, 0.1 [mu] g / mm ² or more, 0.25 [mu] g / mm ² or more at which either 0.5 [mu] g / mm ² or more, preferably 1 [mu] g / mm ² or more. If the amount of fixation per spot is less than this, it is difficult to measure the reduction rate of the amount of passing light using a spectrophotometer.

In order to immobilize the protein on the substrate at a high density, it is desirable to immobilize the protein by controlling the orientation on the substrate. Immobilization of a protein whose orientation is controlled means that the protein is immobilized on a substrate at one end of the peptide chain of the protein, for example, at the carboxy terminus or amino terminus of the peptide chain. Examples of the method for immobilizing proteins by controlling the orientation include the methods described in Japanese Patent No. 2578661, Japanese Patent No. 2990271, Japanese Patent No. 3047029, and Japanese Patent Laid-Open No. 2003-344396. For example, after preparing an altered protein by introducing an amino acid sequence consisting of several amino acid residues having a cysteine residue at the carboxy terminus of the protein represented by the formula NH ₂ -R ₁ -COOH, This can be bound to the immobilized substrate via a mercapto group at the carboxy terminal cysteine residue. In this case, NH ₂ —R ₁ —CO—NH—R ₂ —CO—NH—Y (R ₁ and R ₂ represent an arbitrary amino acid sequence, and Y represents a fixed substrate having a primary amine as a functional group. ) Can be obtained.

Protein immobilization can be performed, for example, as follows.
A protein having a sulfhydryl group represented by the formula (1) NH ₂ -R ₁ -CONH-R ₂ -CO-NH-CH (CH ₂ -SH) -CO-NH-R ₃ -COOH is represented by the formula (2) NH ₂ By aligning on an immobilized substrate represented by -Y under neutral to weakly alkaline conditions (pH 7 to 10), protein R ₁ becomes NH ₂ -R ₁ -CONH-R ₂ -CO-NH-CH ( CH ₂ -SH) -CO-NH-R ₃ -COOH (-)-(+)-NH ₂ -Y formula ((-)-(+) represents an adsorbed bond by ionic bond ) To obtain a protein array adsorbed on the substrate. Further, by treating the adsorbed proteins represented by the formula with a cyano reagent, covalent binding proteins R ₁ represented by the formula _{NH 2 -R 1 -CO-NH-} R 2 -CO-NH-Y Thus, a protein array aligned and immobilized on the substrate can be obtained. In the above formula, R ₁ and R ₂ are arbitrary amino acid sequences, R ₃ is strongly negatively charged near neutrality, and the formula (1) NH ₂ -R ₁ -CO-NH-R ₂ -CO-NH- CH (CH ₂ —SH) —CO—NH—R ₃ —COOH represents a chain of any amino acid residue that can make the isoelectric point acidic. R ₂ becomes a linker peptide between the protein to be immobilized and the substrate represented by the formula NH ₂ —R ₁ —COOH. R ₂ is arbitrary, and the type and number of amino acids are not limited. For example, Gly-Gly-Gly-Gly can be used. R ₃ is preferably a sequence containing a large amount of aspartic acid or glutamic acid, such as Asp-Asp-Asp-Asp-Asp-Asp. The isoelectric point of a protein depends on the type and number of amino acids constituting it. For example, when many basic amino acids such as lysine and arginine are contained, aspartic acid and glutamic acid exceeding the total number of basic amino acids are required. Calculation of the isoelectric point of a protein can be easily estimated by those skilled in the art. Preferably, a sequence containing a large amount of aspartic acid and glutamic acid may be designed so that the isoelectric point of the substance represented by the above formula (1) has a value between 4 and 5. A preferred example of such a sequence is alanyl-polyaspartic acid. Because the amino acid next to cyanocysteine is changed to alanine, an amide bond formation reaction via a cyanocysteine residue is likely to occur, and the carboxyl group of aspartic acid is the most acidic among the amino acid side chains. It is. As the solution for performing the adsorption reaction, any solution can be used as long as it is a solvent that guarantees the above-described electrostatic interaction, can dissolve the protein represented by the formula (1), and can adjust the pH. In addition to various buffers such as phosphate buffer and borate buffer, alcohols such as methanol and ethanol, dimethylformamide, dimethylsulfoxide, and the like can be used. A high reaction efficiency can be obtained at room temperature, but the reaction temperature can be used without any problem as long as the solvent used does not freeze or boil and the temperature is such that the protein represented by the above formula (1) does not aggregate as a result of denaturation. . The cyanation reaction can be performed using a cyanation reagent. The cyanating reagent is usually 2-nitro-5-thiocyanobennzoic acid (NTCB) (Y. Degani, A. Ptchornik, Biochemistry, 13, 1-11 (1974)). ) Or 1-cyano-4-dimethylaminopyridinium tetrafluoroborate (CDAP) or the like is convenient. Commercially available NTCB and CDAP can be used as they are. Cyanation using NTCB can be carried out efficiently between pH 7 and 9, and the reaction efficiency is increased by increasing the absorbance of free thionitrobenzoic acid at 412 nm (molecular extinction coefficient = 13,600 M ^-1 cm ^-1 ). You can investigate. The cyanation of the SH group can also be carried out according to the method described in the literature (see J. Wood & Catsipoolas, J. Biol. Chem. 233, 2887 (1963)). Cyanation with a cyanating reagent is performed on a fixed substrate with the formula (1) NH ₂ -R ₁ -CO-NH-R ₂ -CO-NH-CH (CH ₂ -SH) -CO-NH-R ₃ -COOH It may be performed after adsorbing and immobilizing the protein represented by (3) or simultaneously with the adsorption immobilization. In the latter case, the protein represented by the above formula (1) and the cyanating reagent may be simultaneously applied on the immobilization substrate. The cyanation treatment can be performed by adding a cyanating agent to the surface of the substrate on which the protein is adsorbed. Moreover, it can also cyanate by means, such as immersing the board | substrate which protein adsorb | sucked in the cyanating agent. Further, after the protein is adsorbed by the above-mentioned aligning means, the cyanating reagent may be applied to the portion on the substrate where the protein is adsorbed using the same aligning means. For example, if protein is adsorbed and aligned on a substrate with a fixed dot pattern using a pin and then spotted with a pin so that a cyanating reagent solution is superimposed on the protein instead of the protein, a cyanation reaction occurs. Protein is immobilized. In addition, a protein represented by the formula (1) NH ₂ -R ₁ -CONH-R ₂ -CO-NH-CH (CH ₂ -SH) -CO-NH-R ₃ -COOH on the immobilization substrate, and a cyanation reagent May be applied simultaneously. For example, the cyanation reaction can be performed using a commercially available cyanation reagent such as 2-nitro-5-thiocyanobennzoic acid (NTCB). Specifically, after the protein for immobilization is spotted on an array substrate and adsorbed by ionic bonding, the entire substrate is immersed in 5 mM NTCB for 4 hours to allow the cyanation reaction to proceed. The subsequent immobilization reaction can be carried out by placing the entire substrate in a weakly alkaline environment. For example, it can be carried out by immersing in a 10 mM borate buffer adjusted to pH = 9.5 for 24 hours. Thereafter, the remaining amino group can be blocked by treating the entire substrate with an acid anhydride such as acetic anhydride.

  A spotter (array machine) can be used for immobilizing the protein of the present invention. A spotter operates a pin tip or a substrate for spotting a protein sample with a high-performance motor under the control of a computer in the X, Y, and Z directions, and the protein from the container containing the protein sample such as a microtiter plate to the substrate surface. It is a device that carries a sample. A commercially available thing can be used as a spotter. Examples of commercially available spotters include SPBIO2000 from Hitachi Software Engineering, GMS417Arrayer from Takara Shuzo, Gene Tip Stamping from Nippon Laser Electronics, and a piezo-type biochip spotting system from PerkinElmer.

Furthermore, a protein array can be produced by utilizing inkjet printing technology for immobilizing the protein of the present invention. During step of immobilizing protein of the present invention, represented by formula _{(1) NH 2 -R 1 -CO} -NH-R 2 -CO-NH-CH (CH 2 -SH) -CO-NH-R 3 -COOH The protein is adsorbed and immobilized on an appropriate substrate into which an amino group represented by NH ₂ -Y is introduced by inkjet printing technology, and then the sulfhydryl group of the cysteine residue of the protein is cyanated and converted to a cyanocysteine residue, A protein array having an immobilized protein of the formula NH ₂ —R ₁ —CO—NH—R ₂ —CO—NH—Y can be made.

  Ink jet printers used for printing use an element that deforms when a voltage is applied (piezo element) due to differences in the ink ejection method, and the deformation reduces the ink storage space in the head. There are two types: a piezo type and a thermal ink jet type that generates bubbles by heating a heater in the nozzle and pushes ink out of the bubbles. Any type of printer is used for fixing in the present invention. be able to. However, in consideration of the denaturation of protein due to heat, a piezo printer is preferable. As the ink jet printer, a commercially available printer can be used, and examples thereof include a commercially available EPSON PM series and Canon PIXUS series ink jet printers.

  What is necessary is just to fill the protein solution shown by said Formula (1) into the ink cartridge of a printer, and to install in a printer. The printing pattern of the printer can be set freely by using appropriate software such as drawing software. Even if a line pattern that is fixed in a linear shape is used, it is fixed as an arbitrary number of dots (spots) on a certain area. A dot pattern may be used. At this time, the amount of the protein solution discharged at one time can be freely set. For example, when a line pattern is adopted, it may be fixed in a line shape having a width of several tens of μm to several mm. If the discharge amount and the discharge speed are appropriately set, a line pattern having an arbitrary width can be fixed within this range. In addition, when adopting a dot pattern, it is possible to immobilize proteins as circular dots with a diameter of several μm to several mm by ejecting one drop of protein solution per dot. By adjusting the patterning, dots can be formed in a rectangular shape with a side of several μm to several mm. Also at this time, the discharge amount and discharge speed of the protein solution may be appropriately set according to a desired dot pattern. The amount of protein immobilized on one dot or line is as described above, and the concentration of the protein solution used for immobilization is preferably about 1 mM to 1 M. The amount of protein solution to be immobilized is However, the concentration is not limited, and the concentration of the protein solution and the amount of the protein solution to be immobilized can be appropriately changed according to the amount of protein to be immobilized.

  The number of types or spots of proteins immobilized on one substrate is at least 1, preferably 5 or more, more preferably 10 or more, still more preferably 50 or more, and particularly preferably 100 or more.

  As described above, when a protein is immobilized on a substrate, an amino group is introduced onto the substrate, and the amino group is bound to the carboxy terminus of the protein peptide. In order to introduce an amino group on a substrate, for example, it is necessary to bind a matrix made of a polymer of a primary amine having an amino group on the substrate. Examples of the primary amine polymer include polyamine, allylamine, and polylysine. These primary amine polymers may be mixed with a suitable carrier, cast on a substrate, and a film formed on the substrate. As the carrier, for example, hydrogel or monolith gel can be used. “Hydrogel” refers to a gel containing at least a crosslinked or network structure composed of a polymer and water supported or held in the structure (dispersed liquid). Examples of water-soluble or hydrophilic polymer compounds to be provided with hydrogel include methylcellulose, dextran, polyethylene oxide, polypropylene oxide, polyvinyl alcohol, poly N-vinyl pyrrolidone, poly N-vinyl acetamide, polyvinyl pyridine, polyacrylamide, polymethacrylamide , Poly N-methylacrylamide, polyhydroxymethyl acrylate, polyacrylic acid, polymethacrylic acid, polyvinyl sulfonic acid, polystyrene sulfonic acid and their salts, poly N, N-dimethylaminoethyl methacrylate, poly N, N-diethylaminoethyl methacrylate , Poly N, N-dimethylaminopropylacrylamide and salts thereof. Amino-cellulofine (sold by Seikagaku), AF-aminotoyopearl (sold by TOSOH), EAH-Sepharose 4B and lysine-Sepharose 4B (sold by Amersham Pharmacia), Affigel 102 (sold by Bio-Rad) ), Porous 20NH (sold by Boehringer Mannheim) or a commercially available carrier having a primary amino group may be used. At this time, for bonding the primary amine polymer and a carrier such as polyacrylamide, it is necessary to polymerize the carrier. For example, ultraviolet irradiation treatment is effective.

  For example, a silane coupling agent may be used for bonding between the matrix and the substrate such as glass. The silane coupling agent is a substance that can form a covalent bond with both the glass surface and the matrix such as polyacrylamide, and is an inorganic substance. And organic substances can be combined. A silane coupling agent is generally a compound having a structure of R-Si-X3, and X is an alkoxy group such as a methoxy group (-OCH3), which is hydrolyzed to a silanol group (Si-OH). Become. This silanol group reacts with the silanol group present on the substrate surface, such as hydrogen bonding and dehydration condensation, to form a stable siloxane bond (Si-O-Si) to form a hydrophobic R- film on the substrate surface. Form. On the other hand, R- is an organic functional group (for example, H2C = C (CH3) C (= O) O- (CH2) 3- etc.) that can bind to the matrix. As the silane coupling agent, commercially available ones such as Bind-silane (3-Methacryloxypropyltrimethoxysilane) manufactured by Amersham can be used.

  By using the protein array produced as described above, the interaction between the protein immobilized on the substrate and other proteins or compounds can be analyzed. At that time, a quartz glass is put on the substrate, the array substrate is sealed, and a flow system is assembled so that a solution such as a protein to be examined inside the array substrate can be flowed (FIGS. 3A and 3B). Holes are opened at both ends of the sealing quartz glass, and it is possible to connect a tube to allow the solution to flow from one side and the solution to flow from the other side. A pump is used to flow the solution. However, since the solution permeability of the monolith gel substrate is high, the inside of the substrate can be easily fed with a commercially available low-pressure pump. As the pump, for example, Pump P-1 of GE Healthcare or LC20AD of Shimadzu Corporation can be used. In addition, this flow system can be installed inside the spectrophotometer, and it is designed to irradiate the array with light and capture an image while the liquid is being sent, and to measure the absorption by the protein on the array. Has been. The irradiation light can be any of ultraviolet light, visible light, and infrared light. However, when protein is used for measurement, ultraviolet light having a wavelength of about 280 nm is desirable. When a compound other than protein is used for measurement, light having an absorption wavelength peculiar to the compound may be used. As the solution to be sent, protein solution, compound solution, buffer solution, etc. can be used. While these various solutions are being sent, one side of the array is irradiated with light and passed to the opposite side. It is possible to capture the amount of incoming light as image data and observe how the amount of light in the spot region changes over time.

  The protein immobilized on the substrate is irradiated with light, and the rate of decrease in the amount of light passing through the absorption of light by the protein is measured. At this time, preferably, the protein immobilized on the ultraviolet transmissive substrate is irradiated with ultraviolet light, and the reduction rate of the amount of ultraviolet light passing through the protein is measured. A spectroscope may be used as the light irradiation means. As the spectrometer, any of a spectrometer using an optical filter, a dispersion spectrometer, and a Fourier transform spectrometer can be used. When ultraviolet light is used as irradiation light, a dispersive spectrometer is desirable. As the light to be used, any of ultraviolet light, visible light, and infrared light can be used. When ultraviolet light is used, the wavelength is 200 to 310 nm. When measuring protein, ultraviolet light having a wavelength around 280 nm that is absorbed by the protein is desirable. When measuring a compound other than a protein, light having a characteristic absorption wavelength of the compound may be used. For example, using a commercially available spectrophotometer, the measurement can be performed by mounting a substrate on which the protein of the present invention is immobilized in a cell chamber in which a spectrophotometer cell is mounted. The surface on which the protein is immobilized may be directed to the light irradiation means side or the opposite light detection means side. Further, a lens or a slit may be provided on the optical path for irradiating the substrate with light from the light irradiating means to adjust the width of the optical path, etc., so that light is irradiated to a necessary portion of the substrate.

  In addition, when using a two-dimensional photodetector such as a CCD, the light passing through each spot can be measured at once by irradiating the entire immobilized protein spotted on the substrate. In the case of using the original photodetector, it is only necessary to move the light irradiation means so that only a specific spot on the substrate is irradiated with light and to irradiate all spots with light. In this case, the photodetector is moved simultaneously with the movement of the light irradiation portion.

  When light is irradiated onto the substrate on which the protein is immobilized, the light is absorbed by the immobilized protein, the protein bound to the immobilized protein, and / or the compound other than the protein bound to the immobilized protein. In the present invention, light scattering in the substrate is also reflected, and the amount of light that has passed through the substrate is measured. A light detection means is used to measure the amount of light that has passed. The light detection means is means for outputting the light intensity as an electric signal, and any of an internal photoelectric effect type photodetector and an external photoelectric effect type photodetector can be used. The internal photoelectric effect detector is a detector that uses charge separation in a semiconductor by light, and a photoconductive detector that detects a change in electrical conductivity caused by carriers caused by charge separation and light that detects a potential difference. There is an electromotive force type detector. Examples of the photoconductive detector include a charge coupled device (CCD), a photodiode (PD), a photodiode array (PDA), and a CMOS. External photoelectric effect photodetectors include a phototube and a photomultiplier that detect electrons directly or after they are emitted from a photocathode by vacuuming incident photons into a vacuum.

  Any of these light detection means can be used in the apparatus of the present invention, but a PDA or CCD that is a multichannel detector is desirable, and a CCD that is a two-dimensional multichannel detector is more desirable. It is also possible to use IPDA or ICCD in which PDA and CCD are provided with an electron multiplying function using a microchannel plate. In the present invention, IPDA and ICCD are included in PDA and CCD, respectively.

When measuring the decrease rate of the amount of light passing through using ultraviolet light as irradiation light, the CCD needs to be compatible with ultraviolet light. As the CCD for ultraviolet light, for example, IMPACTRON ^™ CCD elements such as TC253SPD-30 / TC253SPD-B0 and TC285SPD-30 / TC285SPD-B0 manufactured by Texas Instruments, and CCD elements manufactured by HORIBA Joban Yvon can be used. A commercially available CCD camera using these elements may also be used. For example, there are IMPACTROM ^™ CCD digital cameras such as MC681SPD and MC285SPD-LOBO manufactured by Texas Instruments. However, there is a problem that a CCD for ultraviolet light is very expensive. When using a CCD that does not support ultraviolet light used in commercially available CCD digital cameras, an ultraviolet-visible light conversion device that is a nonlinear optical material may be used. An ultraviolet-visible light conversion device is a device that converts ultraviolet light into visible light. For example, wavelength conversion glass such as fluorescent glass, fluorescent material such as fluorescent pigment, and sensitizer such as silver salt sensitizer and non-silver salt sensitizer. Is mentioned. Of these, fluorescent glass is desirable, and fluorescent glass contains rare earth ions that become fluorescently active ions, and is converted to visible light of 400 nm or more by irradiation with ultraviolet light of 200 to 400 nm. As fluorescent glass, for example, there are Lumilas-G9, Lumilas-R7, Lumilas-B, etc. manufactured by Sumita Optical Glass Co., Ltd. , Emits blue fluorescence of 410 nm. The fluorescent glass may be placed between the substrate on which the protein is immobilized and the light detection means in the apparatus of the present invention. Alternatively, the fluorescent pigment or sensitizer may be applied to a glass plate, and the glass plate may be placed between the protein-immobilized substrate and the light detection means, or on the opposite side of the protein-immobilized substrate. It may be applied. In the latter case, the surface on which the protein is immobilized is irradiated with ultraviolet light.

  As described above, the ultraviolet light is irradiated to the substrate on which the protein is immobilized, and the reduction rate of the passing light amount derived from the absorption of the immobilized protein or the decreasing rate of the passing light amount of the visible light converted from the ultraviolet light is detected by light detection means. Detect with.

  A signal is output as image data or video data from the light detection means, the signal is processed by the analysis means, and the absorbance of the protein on the substrate is measured. The type of image data is not limited. For example, image data can be obtained as a BMP image and processed. When processing image data or video data, the light intensity of each spot on the substrate is determined. For example, the processing data can be displayed in different colors according to the difference in absorption at each spot, or can be displayed in three-dimensional coordinates for displaying the absorbance in height corresponding to the two-dimensional coordinates on the substrate.

  Video data is obtained by imaging a substrate on which a protein is immobilized with a video camera having a CCD. By obtaining video data, protein absorption on the substrate can be analyzed in real time. In order to process video data in real time, a video capture board and commercially available software can be used. For example, Direct X (manufactured by Windows) may be used.

At this time, the amount of light that has passed through the portion where the protein is not immobilized is measured by measuring the intensity of the light that has passed from the portion where the protein is not immobilized on the substrate and the intensity of the light that has been transmitted from the portion where the protein is immobilized. And the logarithm of the ratio of the amount of light that has passed through the site where the protein is immobilized, that is, the reduction rate of the amount of light passing through, is used as the light signal. The data obtained by the light detection means is organized as pixels, and for any part where the protein is not immobilized, data on the light intensity for multiple pixels is obtained and averaged (I ₀ ), and the protein is immobilized For each portion (spot or dot), data on the light intensity is obtained and averaged for a plurality of pixels, and the light transmittance of each spot can be obtained (I). The light signal can be obtained by -log (I / I ₀ ) in the amount of light passing through the substrate where scattering cannot be ignored. At this time, the immobilization density or the immobilization density of the immobilized protein to be measured is obtained by obtaining the relationship between the immobilization density and the absorbance of a standard protein whose protein amount in one spot is known in advance. be able to. For example, when the light signal of a standard protein of density D is As and the light signal of a test protein of unknown density is At, the density of the test protein can be obtained by the formula D × (At / As). At this time, a standard protein with a known density may be immobilized on the substrate as a control spot.

  The ultraviolet light irradiated from the light irradiation means onto the substrate on which the protein is immobilized may be ultraviolet light immobilized at a certain wavelength, or may have a wavelength width of 1 nm to several tens of nm.

  The immobilized protein and another protein that interacts with the protein or a compound other than a protein such as a low molecular weight compound can be contact-reacted to measure a light signal at a spot on the substrate. For example, the interaction between the immobilized protein and a ligand protein that binds to the protein can be detected and analyzed. In addition, the interaction between the immobilized protein and a ligand other than the protein can be detected and analyzed. For example, after immobilizing an antibody or antigen at a constant density and reacting with the antigen or antibody that specifically binds to the antibody or antigen, the light signal is measured from the rate of decrease in the amount of light passing through the absorption of the protein on the substrate. Thus, the amount of antibody or antigen bound to the immobilized antigen or antibody can be measured. In this case, if the light signal on the protein array is measured before and after contacting the immobilized protein with another protein or non-protein compound, the measured value before the contact greatly reflects the absorbance of the immobilized protein. Subsequent measurements reflect complexes where the immobilized protein interacts with other proteins or non-protein compounds. Therefore, by taking the difference in light signals before and after contact, the amount of other proteins or compounds other than proteins that interact with the immobilized protein can be determined. After obtaining the optical signal of the protein immobilized on the substrate in advance, interacting with other proteins, measuring the optical signal again, and determining the change in the optical signal before and after the interaction, the immobilized protein The amount of interaction and other proteins that interacted can be measured. In addition, by constructing a flow system using a flow chip or a microchip with a liquid flow path as a substrate, changes in the optical signal on the protein array during contact can be measured in real time before and after contact, and interaction Can be monitored over time.

  The present invention further detects proteins on protein arrays and / or other compounds other than proteins that interact with immobilized proteins, including protein arrays and spectrophotometers in which proteins are aligned and immobilized at high density on a substrate. A system for analysis other than proteins that interact with proteins on the array and / or immobilized proteins by irradiating the protein array with a spectrophotometer and measuring the light that has passed through the protein array Other compounds other than proteins that interact with proteins and proteins using a system that measures the reduction rate of the amount of light passing by other compounds and detects and analyzes proteins and / or other compounds on the protein array Protein is immobilized when detecting and analyzing By comparison, operation of the transmission light intensity of the minute part of the transmitted light intensity and the protein is not immobilized, includes a method of estimating the amount of protein and / or other compounds other than proteins on the array. In this method, the substrate on which the protein is immobilized is not limited to a monolithic gel substrate, and a decrease in the amount of light passing due to scattering of glass (quartz glass, pyrex glass, etc.), plastic, synthetic quartz glass, fused silica glass, etc. is ignored. Even if it is possible or cannot be ignored, it can be applied to any substrate that can detect the light that has passed through. For example, when detecting and analyzing proteins and other compounds other than proteins that interact with proteins using the system described in WO 2006/059727 pamphlet, proteins on the array of the present invention and / or other than proteins Methods for estimating the amount of other compounds can be applied. As a system for detecting and analyzing other compounds other than proteins that interact with proteins on the protein array and / or immobilized proteins, including protein arrays and spectrophotometers in which proteins are aligned and immobilized at high density on a substrate For example, the system shown in FIG. 1 can be used. FIG. 11 shows details when the substrate on which the protein of 3 in FIG. 1 is immobilized is a flow cell. That is, the interaction is measured by sending a protein to be measured for interaction or a compound other than protein in a solution and measuring the concentration of the spot before and after that. However, the method of the present invention is not limited to the case where the substrate is a flow type. The substrate is once removed from the measurement system of FIG. 1 and subjected to the same treatment in an appropriate container, and then returned to the measurement system diagram 1 for measurement. It is also possible to compare before and after, and in the latter case, the same principle can be applied with a simple change. In FIG. 11, light (preferably 280 nm with protein absorption) enters from the left of the figure, passes through glass 12 made of a material that transmits ultraviolet light 280 nm (for example, quartz), and is fixed to the array substrate 10. Absorbed by the absorbed protein 11 and goes out to the right side of the figure. At that time, the amount of light reaching the opposite side is remarkably reduced due to scattering derived from the substrate, but can pass through at a certain rate. The direction of the light is not limited, and may be from the right to the left in the figure. Although there is no particular limitation between 11 and 12, it is most preferable that the carrier is a carrier that can pass through the solution, can transmit ultraviolet rays, and can firmly fix the protein thereto. Examples thereof include acrylamide gel and liquid chromatography. There are various fillers or monolithic carriers used in the graph. Reference numeral 15 denotes this carrier.

  FIG. 12 is a front view (FIG. 12A) and a cross-sectional view (FIG. 12B) showing an example of protein spots on the substrate of FIG. 2. As shown in the front view of FIG. 12A, the protein is fixed to the carrier 15 in a total of 96 proteins in 8 rows × 12 rows. In this case, the spot is driven from the left side of the carrier, and the carrier 15 is fixed to the substrate 10 that does not allow the solution to pass therethrough. From the left, the glass base 12 serves as a lid to prevent the solution from leaking out.

In the system shown in FIG. 1, the light that has passed through the substrate 3 is then converted into electrical image data by an ultraviolet / visible photoelectric conversion device 4 (specifically, a CCD (charge coupled device) sensor or the like). FIG. 13 shows the operation of the system in the case where the flow cell shown in FIG. 2 is used and protein or another compound other than protein is sent in a solution. FIG. 13 shows the time change of the optical signal derived from the decrease rate of the amount of light passing through the solution of a specific spot when the components of the solution are changed. Initially, when a solution containing no protein and other compounds other than protein is flowed, the light passing therethrough is strong (this is set as I ₀ ). However, when a solution containing protein or another compound other than protein is flowed, the light passing therethrough is gradually weakened (FIG. 14). This is because the protein in the solution or another compound other than the protein is adsorbed to the protein fixed to the spot, and the concentration of the spot is further increased. When put every passage to come light after passing a protein or other compound solution other than a protein sufficient time and I _1, the amount of other compounds other than adsorbed proteins or proteins derived from the scattering by the substrate This is considered to be proportional to -log ₁₀ (I ₁ / I ₀ ) in a range where so-called stray light is negligible. Thereafter, when a solution that dissociates adsorption is flowed, proteins or other compounds other than proteins again dissociate from the spot, and the intensity of light passing through the spot increases. If calibration is performed by flowing a protein having a known concentration in advance or another compound other than the protein, the absolute amount of the protein concentration can be measured. Thus, the affinity with the protein immobilized on the protein spot in the solution or other compounds other than the protein can be understood.

  FIG. 15 shows a conceptual diagram of the method of the present invention. FIG. 15A shows the distribution of transmitted light intensity around a protein immobilization part (corresponding to one point 11 in FIG. 11 and 11 in FIG. 12) and its periphery. FIG. 15B is a conceptual diagram in which the concentration of the adsorbed protein or other compounds other than protein is plotted on the vertical axis in order to explain FIG. 15A.

Before the protein or other compound solution other than protein flows (state of I ₀ in FIG. 13), the protein is only immobilized, which is shown in 16 of FIG. 15B. The intensity of the light passing at this time is slightly dark at the protein immobilization portion (portion 11 in FIGS. 2 and 3) and bright at the periphery. As shown in FIG. 15A, the center is I _{0X and the} periphery is I ₀₀ . Next, consider the state after flowing a protein or another compound solution other than protein (state I ₁ in FIG. 13). In this state, it is considered that some of the proteins in the solution are adsorbed non-specifically evenly in all regions to some extent. This is shown at 17 (three places) in FIG. 15B. In the portion where the protein is immobilized, binding due to the affinity between the immobilized protein and the protein in the solution or other compounds other than the protein (18) is added, and as a result, more proteins or other proteins other than the surroundings are added. The compound adsorbs (FIG. 15B). On the other hand, as shown in FIG. 15A, the intensity of the light passing therethrough is slightly dark due to non-specific adsorption in the peripheral part (the intensity is set to I _0X ), but non-specific adsorption in the protein-immobilized portion. And the specific adsorption due to the affinity, the absorbance further increases, and the intensity of the light passing therethrough is further reduced (this intensity is referred to as I _1X ).

  FIG. 16 shows a method for determining the concentration of a protein adsorbed by affinity from each intensity measured as described above (that is, excluding the contribution of nonspecific adsorption) or other compounds other than protein. The left column is the protein immobilization site (spot site), and the right column is the peripheral site. The calculation compares the light intensity before and after running the protein or other compound other than protein in each column (ie, at the spot site and the surrounding site, respectively), and absorbance = concentration of other compounds other than protein or protein Finally, subtract the concentration of the peripheral site (this is the nonspecific adsorption component) from the concentration of the protein immobilization site (spot site), and adsorb it according to the target affinity (that is, remove the contribution of nonspecific adsorption) I) Concentrations of proteins or other compounds other than proteins are required.

  FIG. 17 shows an example in which a protein spot in which proteins on a substrate are aligned and fixed is observed with a CCD sensor. As shown in FIG. 17, the CCD sensor is composed of a number of pixels (pixels), and the CCD pixels receive light, and the intensity of light at each pixel can be detected. As shown in FIG. 17, the protein spot and the pixel (measurement point) overlap, and there are a large number of pixels on one protein spot, and there are also pixels in parts other than the protein spot. FIG. 18 is a diagram showing the relationship between protein spots and pixels more precisely. In FIG. 18, a portion surrounded by an inner circle of the central double circle indicates a protein spot portion, and a portion between the outer circle and the inner circle indicates a peripheral portion of the protein spot. Small squares, circles, and triangles indicate pixels one by one, squares indicate pixels on the protein spot site, circles indicate pixels in the peripheral region of the protein spot, and triangles indicate other pixels. As shown in FIG. 18, the protein spot portion and the peripheral portion of the protein spot can be indicated by concentric circles. In the present invention, the relationship between the area of the protein spot and the peripheral portion of the protein spot may be determined in advance. For example, the radius of the protein spot peripheral part of the area of the protein peripheral part is 1.1 to 2 times, preferably 1.1 to 1.5 times the protein spot radius. The ratio of the number of pixels included in the protein spot and the number of pixels included in the peripheral part of the protein spot is the same as the ratio of the area of the protein spot and the area of the peripheral part of the protein spot. The number of pixels included in is 1.2 to 4 times, preferably 1.2 to 1.75 times the number of pixels included in the protein spot. Further, the relationship between the area of the protein spot and the peripheral portion of the protein spot can be determined for each measurement by the method described in Example 10 described later.

  The present invention will be specifically described by the following examples, but the present invention is not limited to these examples.

  In this example, a ligand protein array in which an antibody ligand protein having affinity for an antibody was immobilized was prepared, and an antibody solution was added to observe the binding of the antibody, and then an acidic buffer was added. The state of antibody dissociation was observed. The spot was automatically recognized from the obtained image, the light signal derived from the decrease rate of the amount of passing light was calculated, and the interaction between the antibody ligand protein and the antibody was analyzed.

Example 1 Production of Monolith Substrate A depression of 0.1 mm depth is produced on the surface of quartz glass, a silica monolith gel is formed in the depression, an epoxy group is introduced, and an amino group-containing polymer is further introduced therein. Thus, a monolith substrate for protein immobilization was produced (FIG. 2). Details of the manufacturing process are described below.

  By polishing the surface of quartz glass with sand, a hexagonal depression (width 20 mm x length 35 mm) with a depth of 0.1 mm was produced. A sol-state silica was poured into the depression, and the cover was covered and allowed to stand overnight at 40 ° C. to gel the silica, and then fired at about 600 ° C. to produce a silica monolith gel substrate. Next, the monolith substrate was immersed in an epoxy silane (3-glycidyloxypropyltrimethoxysilane) solution diluted to 20% with toluene, and allowed to stand at 80 ° C. overnight to introduce epoxy groups into the monolith substrate. Next, 20 mg of poly-L-lysine (molecular weight 4,000 to 15,000, purchased from Sigma), an amino group-containing polymer, is dissolved in 1 ml of pure water, and 50 μl of 1M borate buffer (pH 8.5) is added thereto to adjust the pH. Prepare a polymer solution adjusted to 8.5, add this solution to the surface of the monolith substrate, and gently stir for 16 hours to immerse the poly-L-lysine in the monolith substrate and covalently bond to the epoxy group The amino group was introduced into the monolith substrate. Then, the entire quartz glass is immersed in a 0.5M monoethanolamine solution containing 0.5M sodium chloride (adjusted with hydrochloric acid to pH = 8.3) and gently stirred for 12 hours to block residual epoxy groups and unreacted polymer. -L-lysine was removed. Subsequently, monoethanolamine and unreacted poly-L-lysine were removed by washing several times with 20 ml of pure water. Thereafter, the monolith substrate was dried (FIG. 2).

Example 2 Immobilization of Ligand Protein on Monolith Substrate Ligand protein having antibody binding properties was immobilized on the monolith substrate prepared in Example 1. In the following examples, proteins are spotted and immobilized on 96 grid points of 12 rows × 8 columns.

  The ligand protein for each spot is dissolved in 10 mM phosphate buffer (pH = 7.0) so that the maximum protein concentration to be used is 2 mg / ml, and DTT is added to a final concentration of 1 mM for 4 hours. The reduction reaction was performed at 37 ° C. above to reduce the cysteine residue of the ligand protein. Diluting the protein solution treated in this way into protein solutions of various concentrations, using this, using a dedicated spotter (spot device; purchased from Musashi Engineering), 0.1 μl of ligand protein solution of various concentrations Each spot was spotted on 96 grid points of 12 rows × 8 columns on a monolith substrate at intervals of 1.4 mm. Immediately after the spot, the sample was soaked into the protein solution monolith substrate without diffusing. Put the whole protein-spotted substrate in a petri dish, add 20 ml of 5 mM 2-nitro-5-thiocyanobenzoic acid (NTCB) solution, and gently agitate it at room temperature for about 4 hours. The cyanation reaction was performed. Thereafter, the whole substrate was transferred to another petri dish, 10 mM borate buffer (pH 9.5) was added, and the mixture was gently stirred at room temperature for about 24 hours to perform an immobilization reaction. After completion of the immobilization reaction, the reaction mixture was further transferred to another petri dish, immersed in a 10 mM phosphate buffer (pH 7.0) containing 1 M KCl, and gently stirred for 4 hours or more to remove unreacted proteins and side reaction products. Thereafter, an amino group blocking reaction was carried out by placing in a petri dish filled with 20 ml of 0.5 M borate buffer (pH 8.5) and adding 200 μl of acetic anhydride 6 times about every 10 minutes. After the blocking reaction, the immobilization reaction was completed by washing with 10 mM phosphate buffer (pH 7.0). The ligand protein array thus prepared could be stored for a long period of time by immersing it in 10 mM phosphate buffer (pH 7.0) and storing at 4 ° C.

Example 3 Assembly of Flow Cell A flow cell using a monolith substrate was assembled. The configuration is shown in FIG. 3A. FIG. 3B shows a photograph of the flow cell.

  On the monolith substrate shown in Fig. 2, both of them are pressure-bonded using a quartz glass plate with two holes for passing the solution, and then tightened using a clamp as shown in the photograph in Fig. 3B. A line was installed to enable liquid delivery. This is set in the detection analyzer, and by observing the signal derived from the immobilized ligand protein and using the antibody protein that binds to the ligand during feeding, the signal derived from the antibody bound to the ligand protein can be observed. I was able to serve.

Example 4 Detection of Signal Derived from Protein on Substrate The monolithic substrate is opaque at first glance due to effects such as scattering derived from the substrate, and the amount of light passing through the substrate while being scattered in the middle is measured. I was wondering if it could be measured. Therefore, we examined the behavior of the amount of light that passes through the opposite side, that is, the so-called passing light, when irradiated with intense parallel light. Note that the light passing therethrough includes light due to multiple scattering derived from a substrate such as a gel, and becomes so-called stray light.

  As shown in Example, an array substrate on which a ligand protein is immobilized is constructed as shown in Example 3, and a flow cell is constructed based on the description of the pamphlet of International Publication No. WO2006 / 059727 that has been developed previously. Set in a spectrophotometer consisting of the components, send 10 mM phosphate buffer (pH = 7) to the flow cell, irradiate the array substrate with 280 nm light, and use the detector on the opposite side of the irradiation side The amount of light that can be detected on the opposite side (the amount of light passing through) was measured. The amount of light that can be detected was clearly different between the spot where the ligand protein was spotted and the rest.

The light signal derived from the protein is expressed as Ip where the light intensity of the protein-immobilized part is Ip and the light intensity of the non-immobilized part is Io.
S = -log (Ip / Io)
As sought. The expression representing this signal has the same format as the degree of light absorption when the transmitted light is used as a reference, so-called absorbance.

  When this signal was plotted against the amount of protein used for immobilization, the relationship of FIG. 4 was obtained. That is, the signal amount increased in proportion to the amount of immobilized protein. Therefore, it was shown that the amount of protein present in the monolith substrate can be measured using this signal as an index.

  In the figure, ligand protein 1 uses an AIST-2 ligand, and 2 to 4 use a single amino acid variant thereof. It is shown that the optical signal used in this way is significantly impaired in linear relationship at a certain value due to stray light derived from multiple scattering derived from the substrate, but the optical signal is maintained within a range not exceeding 0.1. It was. Therefore, it was shown that the amount of light passing through the substrate can be measured while being opaque due to effects such as scattering derived from the substrate at first glance.

Example 5 Detection of Signal Derived from Protein Bound to Ligand Protein on Substrate By sending a human polyclonal antibody solution as a protein that binds to the immobilized ligand to the flow cell used in Example 3, which signal was detected We observed how it changed.

  The signal was stabilized by feeding 0.2 mg / ml antibody solution to the flow cell at a speed of about 0.6 ml per minute for 30 minutes. When the signal at that time was plotted against the amount of immobilized ligand protein, the result of FIG. 5 was obtained. The amount of antibody binding is expected to increase depending on the amount of ligand protein, but reflecting this, the amount of signal observed also increased (FIG. 5A). When the increased amount of light signal derived from antibody binding was plotted against the amount of ligand protein, a saturation relationship was obtained depending on the amount. This suggests the upper limit of the linear relationship in this detection method, and shows that the upper limit is about 0.1 as the signal amount in the substrate used. On the other hand, as long as the signal below that is used, it is suggested that the amount of antibody protein binding to the ligand and protein can be measured.

Example 6 Observation of Binding between Ligand Protein and Antibody on Substrate By sending a human polyclonal antibody solution as a protein that binds to an immobilized ligand to the flow cell used in Example 3, the signal was criminalized. We observed how it changed.

  First, in order to put the antibody into the array (binding process), a 0.2 mg / ml antibody solution was fed at a speed of about 0.6 ml per minute for 24 minutes. During this period, images of the array were captured at intervals of 15 seconds, but the spots (regions where the ligand was immobilized) gradually became darker (FIG. 6). This is because the antibody bound to the ligand protein immobilized on the array. Next, in order to wash the array (washing process), 10 mM phosphate buffer (pH = 7) was fed at the same speed for 25 minutes. There was little change in the signal during this process. Next, in order to elute the antibody (elution process), an elution buffer (0.1 M acetate buffer: pH = 5) was fed at the same speed for 25 minutes. In this process, it was found that the antibody quickly dissociated from the ligand because the spot became bright immediately after the start of liquid feeding (FIG. 6). Finally, in order to regenerate the array (regeneration process), 0.1 M glycine buffer (pH = 2.5) was fed at the same speed for 25 minutes. By this process, the spot became brighter and almost returned to the original brightness, indicating that the antibody was completely dissociated from the ligand and the array was regenerated (FIG. 6). It was confirmed that the same observation was possible again after reproduction, that is, reuse was possible.

  Such an analysis process was performed for all spots in all images, and how the absorbance changed while feeding various solutions was determined (FIG. 7). In the adsorption process, the absorbance rapidly increased after the start of liquid feeding, but after a while, the rate of increase slowed down and hardly changed after 24 minutes. This indicates that the input antibody was adsorbed to the ligand until it was almost saturated. In the next washing process, the absorbance hardly changed, indicating that the antibody remained adsorbed to the ligand (FIG. 7). In the elution process, since the absorbance decreased rapidly when the liquid feeding was started, it was found that the antibody quickly dissociated from the ligand (FIG. 7). In the regeneration process, the absorbance almost returned to the value at the start.

Example 7 Production of Array Immobilizing Various Ligand Proteins In this example, a ligand protein array in which 8 different ligands were immobilized was produced as follows. Eight types of ligand proteins for immobilization include various modifications of protein A (Staphylococcus aureus) antibody binding domain A, and modifications of protein G (Streptococci) antibody binding domain. In which the amino acid sequence was linked to each carboxy terminus was used. In the same manner as shown in Example 2, genes encoding these amino acid sequences were expressed in E. coli and purified, and spotted on a monolith substrate for immobilization. However, in the spot, 12 each of the ligand proteins were spotted so that each of the 8 types of ligands crossed 96 grid points of 12 rows × 8 columns in an oblique direction (FIG. 8). By averaging the data obtained for the ligands arranged in this way, location-dependent effects were eliminated as much as possible. Operations such as immobilization reaction after spotting and amino group blocking reaction were all carried out in the same manner as shown in Example 2.

Example 8 Observation of antibody binding / dissociation in various ligand protein-immobilized arrays Regarding the ligand array 2 prepared in Example 3 in order to detect differences in properties (affinity to antibodies) for various types of ligands According to the method shown in Example 4, antibody binding / dissociation was observed (FIG. 7). In the binding process and the washing process, the absorbance changed in almost the same manner for all types of ligands. However, in the elution process, there was a large difference in the speed of decrease in absorbance depending on the type of ligand. This indicates that under the environment of pH = 5, the speed at which the antibody dissociates from various ligands is different, that is, there is a great difference in antibody affinity depending on the type of ligand.

Example 9 Observation of Dye Solution Movement in Monolith Substrate In order to check whether the solution can easily diffuse inside the monolith, a dye molecule solution (1% brilliant blue aqueous solution) is used to determine which dye molecules move through the monolith gel substrate. It was observed as follows how it moved.

  The monolith substrate for immobilization was set in the holder in accordance with the method shown in Example 4, and a peristatic pump was connected so that the inside of the substrate could be fed at a speed of about 0.6 ml per minute. First, after flowing pure water, 0.05 ml of 1% brilliant blue aqueous solution was fed, and pure water was poured again. The situation at this time was filmed with a single-lens reflex camera (Olympus, C-7070), and it was confirmed how the dye solution moved in the substrate. It was shown that when the dye solution was fed, the dye was flowing almost evenly throughout the substrate, and when pure water was fed, it quickly flowed out of the gel substrate (dye diffusion). The state is shown in FIG. 8 at intervals of 2 seconds). This result shows that the solution is moving uniformly within the monolith substrate.

Example 10
The data processing method of this invention is shown. The apparatus shown in FIG. 1 was used. In this embodiment, data processing from a specific image until the affinity is calculated will be mainly described.

  An example of a screen viewed with the CCD sensor 5 in FIG. 1 is shown in FIG. Reference numeral 11 denotes an immobilized protein spot, and reference numeral 19 denotes a CCD sensor measurement point (pixel). (In actuality, the number of pixels is a very large number such as 1024 horizontal, 512 vertical, etc., but in this figure, a smaller number of pixels is schematically shown). For the sake of explanation, one of these spots 20 is taken up and the periphery is enlarged in FIG.

FIG. 18 shows a spot, measurement points (pixels) around it, and a region for calculating the intensity of light passing through the present invention. 20 is a spot, and 21 is a radius of the spot on the image. Reference numeral 23 (square) denotes a measurement point (pixel) in the spot. The pixels are indicated by squares, circles, and triangles to distinguish the positions. Reference numeral 22 denotes a radius to the area around the spot. The result of calculating the average of the intensity of light passing through each of the 23 measurement points is shown in Iox (before flowing the protein solution) or I ₁ x (after flowing the protein solution) in FIG. 15A. A measurement point (pixel) inside 22 and outside 21 is a peripheral part of the site (spot) where the protein is immobilized, which is indicated by 24. The result of calculating the average of the transmitted light intensity at each of the 24 measurement points is Io ₀ (before flowing the protein solution) or I ₁₀ (after flowing the protein solution) in FIG. 15A, and is shown in FIG. By calculation, the amount of protein finally adsorbed by affinity can be determined.

  Here, there are roughly two methods for determining the spot area range 21 and the spot peripheral area range 22 in FIG.

First Method The first method is a method for distinguishing between a portion (spot) where proteins are aligned and immobilized and a portion where proteins are not immobilized, based on image information of the intensity of light passing through them. It is characterized in that the part of is automatically determined.

  FIGS. 19A and 19B (FIG. 19B is a continuation of FIG. 19A) show the setting of the range of the spot part and the peripheral part by the first method. In FIG. 19, (i) is an image after measurement, the circle is a spot, and the intensity of light passing through this portion is weak. A dotted line indicates a part of a specific row of CCD measurement points (pixels). This is smoothed by (ii). As a smoothing method, a moving average or a digital filter can be considered. Next, the average of the intensity of the light passing through (iii) is calculated. Next, the average value (iii) is compared with the signal (ii) before averaging by (iv). This is shown in (iv). The straight line is the average value, and the inverted trapezoid is the signal. Since the intensity of light passing through the spot portion is small, the signal is weak, and the trapezoidal depression is the spot portion. Therefore, a measurement point (pixel) at which a signal smaller than the average value appears is a spot portion (v). This pixel corresponds to a square in the lower diagram of FIG.

  For pixels other than this (ie, the portion equal to or larger than the average value (vi)), the distance between each pixel and the spot part (v) is calculated, and this is less than the predetermined distance (preset or entered by the user) In this case, this pixel is regarded as the periphery (peripheral region) (viii) of the spot. Specifically, for example, when the position of the pixel is (p, q) and the distance is d, the area surrounded by (pd, qd) and (p + d, q + d) It is determined whether or not there is a pixel. In the former case, the pixel is set as “peripheral region”, and in the latter case, “other than that” (ix). In the lower part of FIG. 20, the “peripheral part” pixels when d = 1 are indicated by circles.

  The spot part and the spot peripheral part set as described above are nothing but 23 (spot part) and 24 (peripheral part) in FIG. 18, and thereafter, the range of the spot part and the peripheral part is set by taking the above-described method. be able to.

Second method The second method is a method in which the user distinguishes between the site where each protein is aligned and immobilized (spot site) and the site where the protein is not immobilized. A distinction is made by inputting the number of rows, the number of spot columns, etc., and applying the pattern formed thereby to an actual image by moving, enlarging, reducing, rotating, etc. on the screen.

  FIG. 21 shows the setting of the range of the spot part and the peripheral part by the second method. In this software, as shown in (b), the user inputs the spot diameter, the spot interval, the number of spot rows, the number of spot columns, etc. in advance. Thereby, a grid-like pattern is created, and this is enlarged / reduced / rotated (c), and is first applied to the measurement result image (a) to set a spot area (d). The peripheral area (22 in FIG. 18) is set by the user moving the radius of the concentric circle of the spot while viewing the actual spot signal (e).

  The spot and the spot periphery set as described above correspond to 23 (spot part) and 24 (peripheral part) in FIG. 18, and thereafter, the range of the spot part and the peripheral part can be set by taking the above-described method. .

It is a figure which shows the system of this invention. It is a figure which shows the monolith substrate for protein fixation. FIG. 2B shows a photograph of the protein array. It is a figure which shows the protein array set to the flow system for liquid feeding. It is the photograph of the flow system for liquid feeding which set the protein array. It is a figure which shows the increase in the signal intensity depending on the protein amount fix | immobilized on the board | substrate. It is a figure which shows the result of the human polyclonal antibody binding measurement using an array board | substrate. It is a figure which shows the observation result by the optical signal derived from the reduction | decrease rate of the passage light quantity of an antibody coupling | bonding and elution. It is a figure which shows the time change of the average value of the optical signal derived from the decreasing rate of the spot passage light quantity in the process of antibody binding / elution. It is a figure which shows the array which fix | immobilized various ligand proteins. It is a figure which shows the observation result of the coupling | bonding and elution of the antibody with respect to various ligands. It is a figure which shows the time change of the optical signal derived from the decreasing rate of the passage light amount of the various ligands of FIG. 9A. It is a figure which shows the result of having observed the pigment solution movement in a monolith substrate. It is a figure which shows the outline | summary of the flow system containing a protein fixed board | substrate. It is a figure which shows the example of the spot of the protein on a board | substrate. It is a figure which shows the change of the signal of the specific spot at the time of changing a solution with the flow system of FIG. It is a figure which shows the example of a signal of the specific spot when there exists nonspecific adsorption | suction. It is a figure which shows the concept of the method of estimating the quantity of other compounds other than protein and / or protein on an array. FIG. 15A shows the distribution of transmitted light intensity around the protein immobilization portion and its periphery, and FIG. 15B is a conceptual diagram in which the adsorbed protein concentration is taken along the vertical axis to explain FIG. 15A. It is a figure which shows the measuring method of protein concentration. It is a figure which shows the state observed with the protein spot CCD sensor on a board | substrate. It is a figure which shows the measurement point inside and outside the spot of the protein spot periphery on a board | substrate. It is a figure which shows the 1st method of discriminating a protein spot and the peripheral site | part of a protein spot. It is a figure which shows the 1st method of discriminating a protein spot and the peripheral part of a protein spot (continuation of FIG. 19A). It is a figure which shows the 2nd method of discriminating a protein spot and the peripheral part of a protein spot.

Explanation of symbols

1 Spectrophotometer 2 Optical system (light irradiation means)
3 Protein-immobilized light-transmitting substrate 4 UV-visible light conversion device 5 CCD camera (light detection means)
6 video capture board 7 data processing means 8 lens or slit 9 communication means 10 array substrate 11 immobilized protein 12 cover 13 solution inlet 14 solution outlet 15 carrier 16 immobilized protein concentration 17 of protein in solution Specific adsorbed concentration 18 Concentrated adsorbed with specific affinity with fixed protein among proteins in solution 19 1 pixel of CCD detector 20 Spot site 21 Spot site radius 22 Spot periphery radius 23 Spot site Measurement point 24 Measurement point 25 around the spot Measurement point 25 other than the spot periphery

Claims (24)

A flow channel cell having a flow channel formed therein, and a flow channel cell in which the protein is aligned and fixed at a high density on a monolith gel substrate formed on a quartz glass surface, and a spectrophotometer By irradiating the monolith gel substrate on which the protein in the flow channel cell is immobilized using a spectrophotometer, and measuring the amount of light passing through the monolith gel substrate with less influence of stray light due to scattering Measure the rate of decrease in the amount of light passing by other compounds other than the protein that interacts with the protein on the monolith gel substrate and / or the immobilized protein, and other than the protein that interacts with the protein on the monolith gel substrate and / or the immobilized protein. A system for detecting and analyzing chemical compounds. A flow channel cell having a flow channel formed therein, in which the protein is aligned and fixed at a high density on a monolith gel substrate formed on a quartz glass surface , light irradiation means, light Including a detecting means, irradiating light to the monolith gel substrate on which the protein in the flow channel cell is immobilized by the light irradiating means, and reducing the influence of stray light due to scattering of the passing light passing through the monolith gel substrate by the light detecting means. By measuring the rate of decrease in the amount of light passing through by a compound other than the protein that interacts with the protein on the monolith gel substrate and / or the immobilized protein, it interacts with the protein on the monolith gel substrate and / or the immobilized protein. A system that detects and analyzes compounds other than proteins. 3. The system for detecting and analyzing proteins and / or other compounds other than proteins on a monolith gel substrate according to claim 1 or 2, wherein the monolith gel is monolithic silica gel. Further comprising a data processing means, for detecting and analyzing the other compounds other than proteins interacting with protein and / or immobilized proteins Monorisugeru substrate according to claim 2 or 3 systems. Protein interacts with protein and / or immobilized proteins Monorisugeru substrate according to 1 any one spot per 0.01 [mu] g / mm ² or more claims is immobilized at a density of 1 to 4 Monorisugeru substrate A system that detects and analyzes compounds other than proteins. The protein that interacts with the protein on the monolith gel substrate and / or the immobilized protein according to any one of claims 1 to 4, wherein the protein is immobilized at a density such that an optical signal at one spot of the monolith gel substrate is 0.001 or more. System for detecting and analyzing other compounds. Proteins aligned and immobilized at high density are of the formula NH ₂ -R ₁ -CO-NH-R ₂ -CO-NH-Y [wherein R ₁ and R ₂ represent any amino acid sequence, Y is a monolith gel substrate The system which detects and analyzes other compounds other than the protein which interacts with the protein on the monolith gel substrate of any one of Claims 1-6, and / or the immobilized protein. The protein on the monolith gel substrate according to any one of claims 1 to 7, wherein the protein is aligned and immobilized by covalently bonding the C-terminal carboxy group of the amino acid sequence of the protein to the monolith gel containing the primary amine. A system that detects and analyzes compounds other than proteins that interact with immobilized proteins. The compound on the monolith gel substrate according to any one of claims 1 to 8, wherein the light detection means is a CCD, CMOS, or photodiode array, and / or detects other compounds other than the protein that interacts with the immobilized protein.・ A system to analyze. By contacting the sample immobilized with the protein immobilized on the monolith gel substrate and measuring the reduction rate of the amount of light passing by the compound on the monolith gel substrate and / or other compounds other than the protein that interacts with the immobilized protein before and after contact. The protein on the monolith gel substrate according to any one of claims 1 to 9, wherein a protein in the specimen that interacts with the immobilized protein and / or a compound other than the protein that interacts with the immobilized protein is detected. And / or a system for detecting and analyzing compounds other than proteins that interact with immobilized proteins. The protein immobilized on the monolith gel substrate is brought into contact with other proteins and / or other compounds that interact with the immobilized protein, and interacts with the protein and / or immobilized protein on the monolith gel substrate before and after the contact. The interaction between the immobilized protein and the protein and / or another compound other than the protein is analyzed by measuring the reduction rate of the amount of light passing through by the other compound other than the protein to be analyzed. The system which detects and analyzes other compounds other than the protein which interacts with the protein on the monolith gel board | substrate of claim | item, and / or the immobilized protein. In the flow path within a flow channel cell inside passage is formed, it split into Monorisugeru board of the flow channel cell in which the protein is aligned immobilized at a high density Monorisugeru substrate formed on a quartz glass surface irradiated with light using a photometer, other than proteins interacting with protein and / or immobilized proteins Monorisugeru substrate by measuring with less stray light effects of by scattering transmission light having passed the Monorisugeru substrate A method for detecting and analyzing a compound other than a protein that interacts with a protein on a monolith gel substrate and / or an immobilized protein by measuring a decrease rate of the amount of light passing by the compound of 1. The protein on the monolith gel substrate according to claim 12 , wherein the protein is immobilized at a density of not less than 0.01 μg / mm ² per spot of the monolith gel substrate , and / or other compounds other than the protein that interacts with the immobilized protein are detected.・ A method of analysis. The protein on the monolith gel substrate according to claim 12 , wherein the protein is immobilized at a density such that the light signal at one spot on the monolith gel substrate is 0.001 or more. How to analyze. Proteins aligned and immobilized at high density are of the formula NH ₂ -R ₁ -CO-NH-R ₂ -CO-NH-Y [wherein R ₁ and R ₂ represent any amino acid sequence, Y is a monolith gel substrate represented by a representative, claims 12-14 or the method of detecting and analyzing other compounds other than proteins interacting with protein and / or immobilized proteins Monorisugeru substrate according to one of. The protein on the monolith gel substrate according to any one of claims 12 to 15 , wherein the protein is aligned and immobilized by covalently bonding the C-terminal carboxy group of the amino acid sequence of the protein to a monolith gel containing a primary amine. A method for detecting and analyzing compounds other than proteins that interact with immobilized proteins. The compound on the monolith gel substrate according to any one of claims 12 to 16 , wherein the light detection means is a CCD, CMOS, or photodiode array, and / or other compounds other than the protein that interacts with the immobilized protein are detected.・ A method of analysis. By contacting the sample immobilized with the protein immobilized on the monolith gel substrate and measuring the reduction rate of the amount of light passing by the compound on the monolith gel substrate and / or other compounds other than the protein that interacts with the immobilized protein before and after contact. The protein on the monolith gel substrate according to any one of claims 12 to 17 , wherein a protein in the specimen that interacts with the immobilized protein and / or a compound other than the protein that interacts with the immobilized protein is detected. And / or a method for detecting and analyzing a compound other than a protein that interacts with an immobilized protein. The protein immobilized on the monolith gel substrate is brought into contact with other proteins and / or other compounds that interact with the immobilized protein, and interacts with the protein and / or immobilized protein on the monolith gel substrate before and after the contact. by measuring the decrease rate of the passing by other compounds other than proteins quantity, analyzes the interaction with other compounds other than immobilized protein and a protein and / or protein, any one of claims 12 to 17 1 A method for detecting and analyzing a compound other than a protein that interacts with the protein and / or the immobilized protein on the monolith gel substrate according to the item. A flow channel cell having a flow path formed therein, in which the formula NH ₂ -R ₁ -CO-NH-R ₂ -CO-NH-Y [where R ₁ and R ₂ are optional a flow channel cell proteins are aligned immobilized at high density represented by representing the amino acid sequence], Ri substrate Monorisugeru der represented by Y, the flow channel cells Monorisugeru substrate is formed on the quartz glass surface . 21. A flow channel cell according to claim 20 , wherein the monolith gel is monolith silica gel. The flow channel cell according to claim 20 or 21 , wherein the protein is immobilized at a density of 0.01 µg / mm ² or more per spot of the monolith gel substrate . The flow channel cell according to claim 20 or 21 , wherein the protein is fixed at a density such that an optical signal at one spot of the monolith gel substrate is 0.001 or more. The flow channel cell according to any one of claims 20 to 23 , wherein the protein is aligned and immobilized by covalently bonding a monolith gel containing a primary amine and a C-terminal carboxy group of the protein amino acid sequence.

Images