Method and kit for detecting and quantifying β-1,6-branched β-1,3-glucan or β-1,3-glucan

Abstract

According to the present invention: in a first step, when β-1,6-branched β-1,3-glucan is contained in a test specimen, an active reporter protein is formed with one or the other of split reporter proteins by binding the β-1,6-branched β-1,3-glucan to a first fusion protein and a second fusion protein, and when β-1,3-glucan is contained in a test specimen, an active reporter protein is formed with one or the other of split reporter proteins by binding the β-1,3-glucan to the first fusion protein and a third fusion protein; and in a second step, the active reporter protein formed in the first step is detected and quantified.

Description

[Technical field]

[0001] The present invention relates to a method and a kit for detecting and quantifying β-1,6-branched β-1,3-glucan or β-1,3-glucan. [Background technology]

[0002] β-glucans are found in large quantities in the cell walls and cells of yeasts, algae, mushrooms, molds, lactic acid bacteria, bacteria, lichens, and other microorganisms, and can also be secreted as soluble molecules outside the cells. β-glucans have a strong immune enhancing effect and are being applied to foods, cosmetics, and feed, and soluble β-glucans derived from basidiomycetes in particular have been used as medicines in Japan.

[0003] Among the polysaccharides produced by basidiomycetes such as mushrooms and yeasts, β-1,6-branched β-1,3-glucans, which have β-1,3-glucosidic bonds in the main chain and β-1,6-glucosidic bonds in the side chains, are known to exhibit particularly distinctive physiological activities.

[0004] Analytical methods such as NMR (nuclear magnetic resonance), HPLC (high performance liquid chromatography), and GC (gas chromatography) are suitable for analyzing and evaluating the structures of these β-glucans, but they require advanced purification methods that include complex steps. Furthermore, these analytical methods require purification of soluble β-glucans, making them unsuitable for analyzing crudely purified samples.

[0005] Therefore, several methods for quantifying β-1,3- / β-1,6-glucan contained in a crudely purified sample have been developed. Most of these methods combine carbohydrate decomposition enzymes such as α-glucanase, β-1,3-glucanase, and β-1,6-glucanase with acid hydrolysis methods such as the sulfuric acid method, and by quantifying the amount of glucose produced, it is possible to estimate the amount of β-1,3- / β-1,6-glucan contained in a test sample, regardless of whether it is insoluble or soluble (for example, Patent Document 1).

[0006] In addition, quantitative methods for β-1,3-glucan and β-1,6-glucan have also been developed.

[0007] Known methods for quantifying β-1,3-glucan include the Limulus method and enzymatic methods using horseshoe crab body fluids, and ELISA-based quantitative methods that combine horseshoe crab-derived β-glucan binding protein, antibodies, the mammalian β-glucan receptor Dectin-1, insect β-glucan recognition protein (BGRP), and sphingoglycolipids (e.g., Patent Documents 2, 3, and 4; Non-Patent Documents 1, 2, 3, and 4).

[0008] Known methods for quantifying β-1,6-glucan include enzyme methods and ELISA-based quantitative methods that combine antibodies, lectins, and β-1,6-glucanase mutants that have specific binding activity for β-1,6-glucan (e.g., Non-Patent Document 5).

[0009] Furthermore, by combining these β-1,3-glucan binding proteins and β-1,6-glucan binding proteins and constructing a quantitative method based on sandwich ELISA, it is also possible to quantify β-1,6-branched β-1,3-glucan. [Prior art documents] [Patent documents]

[0010] [Patent Document 1] Patent No. 5467251 [Patent Document 2] International Publication WO92 / 16651 [Patent Document 3] US Patent US9885726B2 [Patent Document 4] International Publication WO2010 / 107068 [Patent Document 5] International Publication WO2018 / 212095 [Non-patent literature]

[0011] [Non-Patent Document 1] Appl Environ Microbiol. 2001 Dec; 67(12): 5420-5424. [Non-Patent Document 2] Int J Mol Sci. 2019 Jul 16;20(14):3498. [Non-Patent Document 3] J Immunol Methods. 2006 Jul 31;314(1-2):164-9. [Non-Patent Document 4] J Immunol Methods. 2011 Feb 28;365(1-2):158-65. [Non-Patent Document 5] J Biol Chem. 2020 Apr 17; 295(16): 5362-5376. Summary of the Invention [Problem to be solved by the invention]

[0012] However, the method of Patent Document 1 is an enzyme-based quantitative method, and does not detect β-glucan branching (β-1,3-glucan having side chains formed by β-1,6-glucoside bonds in one molecule). In addition, although ELISA-based quantitative methods can quantify soluble β-glucan, they require multiple washing steps and therefore cannot quantify insoluble β-glucan.

[0013] The present invention has been made in consideration of the above-mentioned circumstances, and has as its objective the provision of a method and kit that can efficiently detect and quantify β-1,6-branched β-1,3-glucan or β-1,3-glucan without the need for washing steps, regardless of the purified purity of β-glucan or its properties such as solubility or insolubility. [Means for solving the problem]

[0014] In order to solve the above problems, the method for detecting and quantifying β-1,6-branched β-1,3-glucan or β-1,3-glucan of the present invention comprises the steps of: The process is as follows: a first step of contacting a test sample with a reagent; and A second step of detecting and quantifying the product of the first step; Including, The reagent comprises: a first fusion protein having a split reporter protein; any of a second fusion protein and a third fusion protein having a split reporter protein; Including, The split reporter protein can form an active reporter protein by pairing two separated parts, the first fusion protein comprises a β-1,3-glucan binding protein and one of the split reporter proteins; the second fusion protein comprises a β-1,6-glucan binding protein and the other of the split reporter proteins; the third fusion protein comprises a β-1,3-glucan binding protein and the other of the split reporter proteins; In the first step, when the test sample contains β-1,6-branched β-1,3-glucan, the β-1,6-branched β-1,3-glucan binds to the first fusion protein and the second fusion protein, whereby one and the other of the split reporter proteins form the active reporter protein, When β-1,3-glucan is contained in the test sample, the β-1,3-glucan binds to the first fusion protein and the third fusion protein, whereby the active reporter protein is formed by one and the other of the split reporter proteins, In the second step, the active reporter protein formed in the first step is detected and quantified. It is characterized by the following.

[0015] The kit for detecting and quantifying β-1,6-branched β-1,3-glucan or β-1,3-glucan of the present invention comprises a first fusion protein having a split reporter protein; any of a second fusion protein and a third fusion protein having a split reporter protein; A reagent comprising: The split reporter protein can form an active reporter protein by pairing two separated parts, the first fusion protein comprises a β-1,3-glucan binding protein and one of the split reporter proteins; the second fusion protein comprises a β-1,6-glucan binding protein and the other of the split reporter proteins; the third fusion protein comprises a β-1,3-glucan binding protein and the other of the split reporter proteins; the first fusion protein and the second fusion protein bind to each other, thereby forming the active reporter protein from one and the other of the split reporter proteins; The binding of β-1,3-glucan to the first fusion protein and the third fusion protein enables the formation of the active reporter protein by one and the other of the split reporter proteins. It is characterized by the following. Effect of the Invention

[0016] According to the present invention's method for detecting and quantifying β-1,6-branched β-1,3-glucan or β-1,3-glucan and its detection and quantification kit, β-1,6-branched β-1,3-glucan or β-1,3-glucan can be detected and quantified efficiently without the need for a washing step, regardless of the purified purity of the β-glucan or its properties such as solubility or insolubility. [Brief description of the drawings]

[0017] [Figure 1] The split reporter protein fusion supBGRP (first and third fusion proteins) and the split reporter protein fusion β-1,6-glucanase mutant (second fusion protein) were subjected to polyacrylamide electrophoresis and stained with CBB. [Diagram 2] This figure shows the results of mixing split reporter protein fusion supBGRP (first and third fusion proteins) and split reporter protein fusion β-1,6-glucanase mutant (second fusion protein) with particulate β-glucan and enzyme substrate, and observing the bioluminescence emitted by the activated split reporter protein (enzyme). [Diagram 3] FIG. 1 shows the results of investigating the effects of different concentrations and incubation times on the activation level of a split reporter protein (enzyme). [Figure 4] This figure shows the results of mixing various β-glucans, split reporter protein fusion supBGRP (first and third fusion proteins), and split reporter protein fusion β-1,6-glucanase mutant (second fusion protein) with an enzyme substrate, and quantifying the bioluminescence emitted by the activated split reporter protein (enzyme). [Diagram 5]This figure shows the results of mixing live yeast-type Candida alibicans cells with different cell numbers with a split reporter protein fusion supBGRP (first and third fusion proteins) and a split reporter protein fusion β-1,6-glucanase mutant (second fusion protein) and an enzyme substrate, and quantifying the bioluminescence emitted by the activated split reporter protein (enzyme). [Figure 6] Images showing the microscopic morphology of cultured C. albicans. Scale bar indicates 50 μm. [Figure 7] This figure shows the results of mixing C. albicans cultured for different periods of time with a split reporter protein fusion supBGRP (first and third fusion proteins) and a split reporter protein fusion β-1,6-glucanase mutant (second fusion protein) with an enzyme substrate, and quantifying the bioluminescence emitted by the activated split reporter protein (enzyme). [Figure 8] FIG. 1 shows the results of real-time monitoring of side chain structural changes that occur during treatment of Zymosan A, a particulate β-glucan, with various β-glucan-degrading enzymes, using a protein-fragment complementation assay. [Figure 9] FIG. 1 shows the results of comparing the reactivity of a measurement method using a split reporter protein with that of a conventional ELISA method, using CSBG, a soluble β-glucan, and D-Zymosan, an insoluble β-glucan. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0018] Hereinafter, one embodiment of the method for detecting and quantifying β-1,6-branched β-1,3-glucan or β-1,3-glucan of the present invention will be described.

[0019] The method for detecting and quantifying β-1,6-branched β-1,3-glucan or β-1,3-glucan of the present invention (hereinafter sometimes simply referred to as a "detection and quantification method" or a "protein-fragment complementation assay") comprises the following steps: a first step of contacting a test sample with a reagent; and A second step of detecting and quantifying the product of the first step; Includes.

[0020] (1st step) In the first step, the test sample is contacted with a reagent.

[0021] The test sample may contain purified or crudely purified β-1,6-branched β-1,3-glucan or β-1,3-glucan, and the nature of the β-1,3-glucan may be either soluble or insoluble.

[0022] Furthermore, the substances contained in the test sample are not particularly limited, and examples include cell walls and extracts of basidiomycetes such as mushrooms, bacteria, yeast, seaweed, plants, etc., β-glucan secreted outside the bacterial cell, and β-glucan present in environments such as indoors, soil, rivers, seawater, the atmosphere, and outer space.

[0023] The reagents are a first fusion protein having a split reporter protein; either a second fusion protein having a split reporter protein or a third fusion protein having a split reporter protein.

[0024] That is, the reagent comprises a combination of a first fusion protein and a second fusion protein and / or a first fusion protein and a third fusion protein.

[0025] As used herein, a split reporter protein refers to a reporter protein that is divided into two parts, and the two separated parts pair (bring close together or bind to each other) to form an active reporter protein.

[0026] Specifically, when the split reporter proteins are present separately from each other, they do not function as reporter proteins, but when one of the split reporter proteins and the other one are brought into close proximity or bound to each other, they begin to function as reporter proteins.

[0027] The structure of the split reporter protein is not particularly limited as long as one of the split reporter proteins can be distinguished when it is close to or bound to the other.

[0028] For example, the split reporter protein may be configured such that when one and the other of the split reporter proteins are brought into close proximity, structural complementation is promoted to form an active reporter protein.

[0029] The split reporter protein may be configured so that bioluminescence resonance energy transfer (BRET) or fluorescence resonance energy transfer (FRET) occurs when one and the other of the split reporter proteins are brought into close proximity. In this case, an active reporter protein refers to a split reporter protein in which one and the other of the split reporter proteins are brought into close proximity and in a state in which BRET or FRET occurs. When the reporter protein is one that generates BRET or FRET, a fluorescent substance may be bound to one or the other of the split reporter proteins.

[0030] Furthermore, the split reporter protein may be configured such that when one and the other of the split reporter protein are brought into close proximity, an active reporter protein is formed by protein splicing. This can be achieved by fusing a protein splicing domain to each of the one and the other of the split reporter protein. Examples of the protein splicing domain include a combination of DnaEn and DnaEc, which are protein splicing domains derived from the DnaE gene of Synechocystis sp.

[0031] More specific examples of reporter proteins include enzymes, fluorescent proteins, etc. Examples of enzymes include luciferase, alkaline phosphatase, horseradish peroxidase, invertase, β-galactosidase, β-glucuronidase, and modified versions of these enzymes. Examples of fluorescent proteins include green fluorescent protein (GFP), modified versions of GFP, etc.

[0032] The first fusion protein comprises a β-1,3-glucan binding protein and one of the split reporter proteins.

[0033] The second fusion protein comprises the β-1,6-glucan binding protein and the other of the split reporter protein.

[0034] The third fusion protein comprises the β-1,3-glucan binding protein and the other of the split reporter protein.

[0035] The β-1,3-glucan-binding protein may be any known protein, such as an antibody, Dectin-1, lectin, horseshoe crab factor G protein, insect β-glucan recognition protein (BGRP), supBGRP (described in the Examples below) and derivatives thereof, and it is preferable that the protein be one that is easy to express as a soluble recombinant protein.

[0036] The β-1,6-glucan-binding protein may be any known protein, and examples thereof include antibodies, lectins, β-1,6-glucanase mutants that do not have the activity of cleaving β-1,6-glucan and have specific binding activity for β-1,6-glucan, and derivatives thereof, and it is preferable that the soluble recombinant protein can be easily expressed.

[0037] The detection and quantification method of the present invention can be carried out by directly supplying a reagent containing the first fusion protein and the second fusion protein, or a reagent containing the first fusion protein and the third fusion protein, into a test tube containing a test sample, or can be carried out using cells expressing these fusion proteins. In this case, the expression of the first fusion protein and the second fusion protein, or the first fusion protein and the third fusion protein, may be transient or constant. That is, a cell line stably expressing the first to third fusion proteins can be used.

[0038] Specifically, the first to third fusion proteins can be exemplified by those produced in Escherichia coli, yeast, plants, animal cells, and cell-free expression systems, and in particular, those produced in large quantities in Escherichia coli are easy to use and preferred. A crudely purified solution such as a cell lysate expressing the first to third fusion proteins may be used, but it is preferable to use a fusion protein that is fused with a general low molecular weight peptide tag and highly purified by column purification or the like. In this case, examples of the fusion protein include GST tag, Protein A tag, antibody Fc region, polyhistidine tag, V5 tag, Myc tag, SBP tag, Halo tag, Strep tag, etc. In addition, examples of the cells here include animal cells, insect cells, plant cells, etc., and established cell lines are easy to use and preferred.

[0039] The first fusion protein may have one of the split reporter proteins fused to the N-terminus of the β-1,3-glucan binding protein, or one of the split reporter proteins fused to the C-terminus of the β-1,3-glucan binding protein. The second fusion protein may have the other of the split reporter proteins fused to the N-terminus of the β-1,6-glucan binding protein, or the other of the split reporter proteins fused to the C-terminus of the β-1,6-glucan binding protein. Furthermore, the third fusion protein may have the other of the split reporter proteins fused to the N-terminus of the β-1,3-glucan binding protein, or the other of the split reporter proteins fused to the C-terminus of the β-1,3-glucan binding protein. In this case, when fusing the β-1,3-glucan binding protein or the β-1,6-glucan binding protein to the split reporter protein in the first fusion protein, the second fusion protein, and the third fusion protein, it is preferable to insert a linker peptide of an appropriate length to avoid steric hindrance.

[0040] Here, the linker peptide is composed of a peptide of about 1 to 20 residues, and its amino acid sequence can be exemplified by the same as the amino acid sequence of a general linker used in the preparation of a fusion protein. Specifically, the linker peptide may be a GS linker composed of a repeating sequence containing Gly-Ser, a DDAKK linker composed of a repeating sequence of Asp-Asp-Ala-Lys-Lys (SEQ ID NO: 1), an EAAAK linker composed of a repeating sequence of Glu-Ala-Ala-Ala-Lys (SEQ ID NO: 2), etc. In addition, in the first fusion protein, the second fusion protein, and the third fusion protein, the region to which one or the other of the split reporter protein is fused is not limited to either the N-terminal side or the C-terminal side, and it is preferable to determine the region to be fused according to the characteristics of various β-1,3-glucan binding proteins and β-1,6-glucan binding proteins. In addition, the fusion protein may be fused to both the N-terminal side and the C-terminal side.

[0041] Then, in the first step, if the test sample contains β-1,6-branched β-1,3-glucan, the β-1,6-branched β-1,3-glucan binds to the first fusion protein and the second fusion protein, causing one of the split reporter proteins to come into close proximity or bind to the other, thereby forming an active reporter protein.

[0042] In addition, when the test sample contains β-1,3-glucan (including those having side chains (branched)), the β-1,3-glucan binds to the first fusion protein and the third fusion protein, causing one side of the split reporter protein to come into close proximity or bind to the other side, forming an active reporter protein.

[0043] (2nd process) In the second step, the active reporter protein formed in the first step is detected and quantified. If the activity of the reporter protein is higher than that in the absence of β-1,6-branched β-1,3-glucan or β-1,3-glucan, it indicates that β-1,6-branched β-1,3-glucan or β-1,3-glucan is present in the test sample. This allows the β-1,6-branched β-1,3-glucan or β-1,3-glucan contained in the test sample to be easily detected and quantified. The method of detection and quantification is not particularly limited, and a known method can be appropriately adopted depending on the form of the reporter protein, etc.

[0044] As described below in the Examples, the difference between the activity of the non-activated reporter protein (background) observed in the absence of β-glucan having the target structure and the activity of the reporter protein reconstituted in the presence of β-glucan is approximately 100-fold, demonstrating high sensitivity.

[0045] In addition, the detection and quantification method of the present invention does not require complicated washing operations, etc., and can screen the structure of β-glucan contained in a test sample with high throughput. Therefore, by applying the detection and quantification method of the present invention, it is possible to analyze a wide range of β-glucans that are derived from various biological species and extraction and purification methods and show various forms such as soluble and insoluble (gel-like, particulate, etc.) under the same conditions, and to screen for more useful β-1,6-branched β-1,3-glucans or β-1,3-glucans. In addition, the detection and quantification method of the present invention does not require a washing process for the test sample, etc., and can efficiently detect and quantify β-1,6-branched β-1,3-glucans or β-1,3-glucans.

[0046] Furthermore, for example, by comparing the activity of the activated reporter protein resulting from the binding of β-1,6-branched β-1,3-glucan to the first fusion protein and the second fusion protein with the activity of the activated reporter protein resulting from the binding of β-1,3-glucan to the first fusion protein and the third fusion protein for the same test sample, it is also possible to quantitate β-1,3-glucan that does not have β-1,6-branching.

[0047] Next, an embodiment of the detection and quantification kit for β-1,6-branched β-1,3-glucan or β-1,3-glucan of the present invention will be described. In the detection and quantification kit of the present invention, the description of the contents common to the above-mentioned detection and quantification method will be omitted.

[0048] The detection / quantification kit of the present invention is a kit for detecting / quantifying β-1,6-branched β-1,3-glucan or β-1,3-glucan, a first fusion protein having a split reporter protein; any of a second fusion protein and a third fusion protein having a split reporter protein; The device is provided with a reagent including:

[0049] The split reporter proteins can form an active reporter protein by pairing (bringing close to each other or binding) with each other.

[0050] The first fusion protein comprises a β-1,3-glucan binding protein and one of the split reporter proteins.

[0051] The second fusion protein comprises the β-1,6-glucan binding protein and the other of the split reporter protein.

[0052] The third fusion protein comprises the β-1,3-glucan binding protein and the other of the split reporter protein.

[0053] By binding of the β-1,6-branched β-1,3-glucan to the first fusion protein and the second fusion protein, an active reporter protein can be formed by one and the other of the split reporter proteins.

[0054] The binding of β-1,3-glucan to the first fusion protein and the third fusion protein enables the formation of an active reporter protein by one and the other of the split reporter protein.

[0055] The detection and quantification kit of the present invention can include, in addition to the above-mentioned reagents, various materials, devices, and the like for detecting and quantifying β-1,6-branched β-1,3-glucan or β-1,3-glucan.

[0056] The method and kit for detecting and quantifying β-1,6-branched β-1,3-glucan or β-1,3-glucan of the present invention are not limited to the above embodiments. EXAMPLES

[0057] The present invention will be described below with reference to examples, but the detection and quantification method and detection and quantification kit for β-1,6-branched β-1,3-glucan or β-1,3-glucan of the present invention are not limited in any way to the following examples.

[0058] Example 1: Preparation of fusion protein The expression vectors for the first fusion protein, the second fusion protein, and the third fusion protein were constructed based on the pColdI vector (Takara Bio). These were transformed into E. coli Shuffle (New England Biolabs) or BL21 (DE3), and then expressed in large quantities as x6 histidine tag (His-Tag) fusion proteins in ampicillin-added LB medium. After purification using TALON Metal Affinity Resin (Takara Bio), the presence of the purified protein was confirmed by SDS-PAGE (Figure 1).

[0059] The β-1,3-glucan binding protein used was supBGRP, which was created based on insect-derived BGRP. The amino acid sequence of supBGRP is an artificial β-1,3-glucan binding protein created by introducing amino acid mutations of about 36 residues (23 residues for silkworm) based on the amino acid sequence of conventionally known β-glucan binding proteins (BGRPs) derived from various insects such as silkworms and the inventors' findings to date.

[0060] The amino acid and DNA sequences of supBGRP are shown below. (SEQ ID NO:3) Met Asn His Lys Val His His His His His Ile Glu Gly Arg His Met Glu Leu Gly Thr Tyr Glu Val Pro Asp Ala Lys Leu Glu Ala Ile Tyr Pro Lys Gly Leu Arg Val Ser Ile Pro Asp Asp Gly Phe Ser Leu Phe Ala Phe His Gly Lys Leu Asn Glu Glu Met Glu Gly Leu Glu Ala Gly Thr Trp Ser Arg Asp Ile Thr Lys Ala Lys Asn Gly Arg Trp Thr Phe Arg Asp Arg Asn Ala Glu Leu Lys Ile Gly Asp Lys Ile Tyr Phe Trp Thr Tyr Val Ile Lys Asp Gly Leu Gly Tyr Arg Gln Asp Asn Gly Glu Trp Thr Val Thr Gly Tyr Val Asp Glu Asp Gly Asn Pro Val Asp Thr Asp Gly Pro Thr Thr Thr Thr Pro Thr Gly Ser Glu Phe Lys Leu Val Asp Leu Gln Ser Arg (SEQ ID NO: 4) atg aat cac aaa gtg cat cat cat cat cat cat atc gaa ggt agg cat atg gag ctc ggt acc tat gaa gtg cct gat gcg aaa ctc gaa gcc att tac ccc aaa ggg tta cgc gtt agc att ccg gat gat ggc ttt tcg ctg ttt gcc ttc cat ggg aaa ctg aac gag gag atg gaa ggt ctg gaa gct gga act tgg agt cgg gac atc acg aaa gcg aag aac ggt cgt tgg acc ttt cgt gac cgc aat gca gag ctg aaa att ggc gac aag atc tac ttc tgg acc tac gtc atc aaa gat ggc ttg ggt tat cgc cag gat aac gga gaa tgg acc gta acg ggc tat gtg gac gaa gat ggc aat ccg gtt gat acc gat ggt ccg act acg aca cca acc gga tcc gaa ttc aag ctt gtc gac ctg cag tct aga tag

[0061] A mutant (Neg1-E321Q) of β-1,6-glucanase derived from Aspergillus aculeatus was used as a β-1,6-glucan binding protein (Patent Document 5).

[0062] In addition, luciferase (NanoLuc, Promega) derived from deep-sea shrimp (Oplophorus gracilirostris) was used as a reporter protein. The split reporter protein (NanoLuc) used here consists of two subunits, a large fragment called LgBiT and a small fragment called SmBiT, and the active luciferase is reconstituted by forming a complex between these two subunits. Therefore, the combination of LgBiT and SmBiT constitutes a combination of one and the other of the split reporter proteins.

[0063] In this example, the first fusion protein was prepared by fusing LgBiT to the N-terminus of supBGRP with a 4×DDAKK sequence as a linker peptide (supBGRP-LgBiT). The second fusion protein was prepared by fusing SmBiT to the N-terminus of Neg1-E321Q with a GGSGGGSGG sequence (SEQ ID NO: 5) as a linker peptide (Neg1-E321Q-SmBiT). Furthermore, the third fusion protein was prepared by fusing SmBiT to the N-terminus of supBGRP with a 4×DDAKK sequence as a linker peptide (supBGRP-SmBiT).

[0064] To confirm that the fusion protein functions in the presence of β-glucan and that the activated reporter protein is reconstituted, Zymosan A, a crudely purified particulate β-glucan derived from baker's yeast, was mixed with supBGRP-LgBiT and Neg1-E321Q-SmBiT, and the presence or absence of bioluminescence was observed by adding NanoLuc substrate (NanoGlo, Promega).

[0065] The results are shown in Figure 2.

[0066] Bioluminescence was observed only in the presence of supBGRP-LgBiT, Neg1-E321Q-SmBiT, Zymosan A and NanoLuc substrate.

[0067] These results demonstrated that the protein-fragment complementation assay can be used for simple structural analysis of β-glucan.

[0068] Example 2: Optimization of protein-fragment complementation assay To develop and optimize a protein-fragment complementation assay that does not require a washing step, we investigated the reactivity of the glucan probe by varying its concentration and reaction time.

[0069] A mixed solution (5 μL) of supBGRP-LgBiT and Neg1-E321Q-SmBiT at different concentrations (50, 100, 200, 400 nM) was incubated with 10 μL of Zymosan A (0-1000 ng / mL) in a 96-well plate for 30 minutes, and luciferase activity was evaluated by adding 15 μL of NanoLuc substrate. As a result, as shown in Figure 3A, it was confirmed that luciferase activity increased in proportion to the concentration of each probe. Appropriate reaction curves were obtained in the presence of at least 200 nM of each probe.

[0070] Next, a 200 nM mixture (5 μL) of supBGRP-LgBiT and Neg1-E321Q-SmBiT was placed in a 96-well plate and incubated with 0-1000 ng / mL Zymosan A (10 μL) for 10, 30, and 60 minutes, and then 15 μL of NanoLuc substrate was added to measure luciferase activity. As a result, it was confirmed that a 10-minute incubation was sufficient to obtain a reaction curve, but that luciferase activity increased with further incubation (Figure 3B).

[0071] <Example 3> Measurement of various β-glucans using fusion proteins Five microliters of a mixture of the first fusion protein (supBGRP-LgBiT) and the second fusion protein (Neg1-E321Q-SmBiT) (200 nM each) or a mixture of the first fusion protein (supBGRP-LgBiT) and the third fusion protein (supBGRP-SmBiT) (200 nM each) was mixed with 10 μL of various polysaccharide samples (0 to 50 μg / mL) in a 96-well plate (white, flat bottom) and shaken on a plate shaker.

[0072] The polysaccharide samples used are shown in Table 1.

[0073] [Table 1]

[0074] After 30 min, 15 μL of NanoLuc substrate was added, and the bioluminescence level was measured using a luminometer (Promega). The results are shown in Figure 4.

[0075] The combination of the first fusion protein (supBGRP-LgBiT) and the second fusion protein (Neg1-E321Q-SmBiT) (supBGRP-LgBiT / Neg1-E321Q-SmBiT) emitted luminescence in samples containing β-1,6-branched β-1,3-glucan, and the combination of the first fusion protein (supBGRP-LgBiT) and the third fusion protein (supBGRP-SmBiT) (supBGRP-LgBiT / supBGRP-SmBiT) emitted luminescence in samples containing β-1,3-glucan.

[0076] Specific examples of samples containing β-1,6-branched β-1,3-glucan include Zymosan A, Pustulan, Scleroglucan, and heat-killed C. albicans (HKCA), and the mixture of the first and second fusion proteins (supBGRP-LgBiT / Neg1-E321Q-SmBiT) showed reactivity with these samples. It was shown that not only purified high-purity β-glucan but also unpurified HKCA can be detected by the same procedure.

[0077] On the other hand, specific examples of samples containing β-1,3-glucan include Zymosan A, Curdlan, Pustulan, Scleroglucan, Paramylon, Pachyman, Laminarin, and HKCA, and a mixture of the first and third fusion proteins (supBGRP-LgBiT / supBGRP-SmBiT) showed reactivity with these samples. In contrast, none of the mixtures showed any reactivity with chitin, dextran, xylan, or mannan, which do not have a β-glucan structure.

[0078] These results demonstrate that the method of the present invention enables efficient structural analysis of β-glucan in multiple samples.

[0079] Example 3: Structural analysis of natural fungal cell walls In Example 2, it was demonstrated that the presence of β-1,3-glucan or long-chain β-1,6-branched-β-1,3-glucan on the surface of HKCA could be determined (Figure 4H). However, HKCA does not necessarily mimic the native cell wall composition of C. albicans because the mannan layer covering the surface of β-glucan is often removed by heat treatment. Therefore, we investigated whether the protein-fragment complementation assay can be applied to analyze the native cell wall structure of living fungi. First, different numbers of yeast-type C. albicans (0, 10 4 , 10 5 , 106 10 cells / well) were washed in a 96-well V-bottom plate and suspended in 10 μL of PBS. This was mixed with 5 μL of a mixture of the first and third fusion proteins (supBGRP-LgBiT / supBGRP-SmBiT) or a mixture of the first and second fusion proteins (supBGRP-LgBiT / Neg1-E321Q-SmBiT). After 30 minutes, 15 μL of NanoLuc substrate was added to measure the activation level of the reporter protein reconstituted on the live cell surface. As a result, the activation level of the reporter protein reconstituted on the live cell surface was measured by 10 μL of both the combinations of supBGRP-LgBiT / supBGRP-SmBiT and supBGRP-LgBiT / Neg1-E321Q-SmBiT was 100%. 5 Bioluminescence increased significantly in response to yeast-type C. albicans cells / well or more (Figures 5A and 5B).

[0080] Next, we investigated the possibility of directly analyzing the cell wall glucan structure of mycelial C. albicans, which is generally difficult to analyze, using this method. To induce mycelial formation, yeast-type C. albicans (10 5 The cells were added to the wells (100 cells / well) and incubated at 37°C for different times (0, 2, 4, and 7 hours). To confirm the formation of mycelium, C. albicans was cultured in parallel under the same conditions in a transparent 96-well flat-bottom plate. The microscopic morphology of C. albicans at each incubation time is shown in Figure 6.

[0081] The washed mycelia were suspended in 10 μL of PBS and mixed with 5 μL of the mixture of the first and third fusion proteins (supBGRP-LgBiT / supBGRP-SmBiT) or the mixture of the first and second fusion proteins (supBGRP-LgBiT / Neg1-E321Q-SmBiT). After 30 min, NanoLuc substrate (15 μL) was added and the bioluminescence level was measured. The luciferase activity, which indicates the amount of surface β-1,3-glucan or long-chain β-1,6-branched-β-1,3-glucan, increased significantly in a mycelial growth-dependent manner (Figure 7A, B). These results indicate that this measurement method is useful for analyzing the glucan structure of intact living fungal cell walls.

[0082] Example 4: Application of protein-fragment complementation assay to real-time monitoring of structural changes in β-glucan For example, the structure of cell wall glucan changes dynamically during fungal growth due to the action of various enzymes. Therefore, we treated Zymosan A, a particulate β-glucan, with endo-β-1,6-glucanase (Neg1) or endo-β-1,3-glucanase (Zymolyase) to examine whether the time-dependent changes in the structure of β-1,6-linked β-glucan side chains or β-1,3-glucan chains can be evaluated by this method. 5 μL of the mixture of the first and third fusion proteins (supBGRP-LgBiT / supBGRP-SmBiT) or the mixture of the first and second fusion proteins (supBGRP-LgBiT / Neg1-E321Q-SmBiT) was added to 10 μL of Zymosan A (10 μg / mL) and incubated for 60 min. PBS, endo-β-1,6-glucanase (final concentration 0.5 μg / mL), or NanoLuc substrate containing endo-β-1,3-glucanase (final concentration 0.5 μg / mL) were added, and the reconstituted NanoLuc activity was measured 15 times every 2 min (30 min). As shown in Figure 8A, in the combination of the first and third fusion proteins (supBGRP-LgBiT / supBGRP-SmBiT), the luminescence intensity of the untreated control sample gradually decreased over time (natural decay). On the other hand, the luminescence intensity of Zymosan A treated with endo-β-1,3-glucanase decreased rapidly, and the bioluminescence level (RLU measurement) after 30 minutes was approximately one-third that of the untreated group. Degradation of the β-1,6-linked side chains of Zymosan A did not affect the glucan-binding ability of supBGRP. In contrast, the activity of NanoLuc reconstituted from the combination of the first and second fusion proteins (supBGRP-LgBiT / Neg1-E321Q-SmBiT) was dramatically decreased by treatment with endo-β-1,6-glucanase or endo-β-1,3-glucanase (Figure 8B). The bioluminescence level (RLU measurement) after 30 min was approximately 1 / 6 in the endo-β-1,3-glucanase-treated group and approximately 1 / 14 in the endo-β-1,6-glucanase-treated group compared to the untreated group. These results confirmed that the protein-fragment complementation assay is not only suitable for structural analysis of β-glucans, but also allows the structural changes of long-chain β-1,6-branched-β-1,3-glucans to be monitored in real time.

[0083] <Example 5> Comparison of reactivity between measurement method using fusion protein and conventional ELISA Soluble and insoluble β-glucans were measured by conventional ELISA and by a method using fusion proteins, and their reactivities were compared. As soluble β-glucan, an aqueous solution of CSBG purified from Candida cell walls was used, and as insoluble β-glucan, a suspension of Depleted-Zymosan (D-Zymosan, InvivoGen), which was prepared by washing Zymosan with a hot alkaline solution, was used (Table 1).

[0084] 5 μL of the mixture of the first fusion protein (supBGRP-LgBiT) and the second fusion protein (Neg1-E321Q-SmBiT) (each 200 nM) and 10 μL of each soluble and insoluble sample (0 to 1,000 ng / mL) were mixed in a 96-well plate (white, flat bottom) and shaken on a plate shaker. After 30 minutes, 15 μL of NanoLuc substrate was added and the bioluminescence level was measured using a luminometer (Promega).

[0085] As shown in FIG. 9A, a concentration-dependent increase in reactivity was observed when β-glucan was added, regardless of whether it was soluble or insoluble.

[0086] On the other hand, the first fusion protein (supBGRP-LgBiT) was immobilized (2 μg / mL) on a 96-well plate (white, flat bottom) and blocked with a PBS solution containing bovine serum albumin. After washing the plate, soluble and insoluble samples (0 to 1,000 ng / mL) were added. After 60 minutes, the plate was washed, and biotin-labeled β-1,6-glucan binding protein (Neg1-E321Q-Biotin, 2 μg / mL) was added and left for 60 minutes. After washing, streptavidin-labeled horseradish peroxidase was added and left for 20 minutes. After washing the plate thoroughly, a commercially available luminescent substrate for peroxidase was added, and the luminescence level was measured using a luminometer (Promega).

[0087] As shown in Figure 9B, in the conventional ELISA method, a concentration-dependent increase in reactivity was observed with CSBG, a soluble β-glucan, but no reactivity was observed with D-Zymosan, an insoluble β-glucan.

[0088] These results confirmed that the method of the present invention enables accurate measurement of the amounts of soluble and insoluble β-glucan under the same conditions.

Claims

1. A method for detecting and quantifying β-1,6-branched β-1,3-glucan or β-1,3-glucan, comprising the steps of: a first step of contacting a test sample with a reagent; and A second step of detecting and quantifying the product of the first step; Including, The reagent comprises: (A) a first fusion protein having a split reporter protein and a second fusion protein having a split reporter protein; and (B) a first fusion protein having a split reporter protein and a third fusion protein having a split reporter protein; Including, the split reporter protein is capable of forming an active reporter protein by pairing two separated parts; the first fusion protein comprises a β-1,3-glucan binding protein and one of the split reporter proteins; the second fusion protein comprises a β-1,6-glucan binding protein and the other of the split reporter proteins, and the β-1,6-glucan binding protein is a β-1,6-glucanase mutant that does not have β-1,6-glucan cleavage activity and has specific binding activity to β-1,6-glucan; the third fusion protein comprises a β-1,3-glucan binding protein and the other of the split reporter proteins; the β-1,3-glucan binding protein in the first fusion protein and the third fusion protein is supBGRP represented by SEQ ID NO: 3 or a derivative thereof; In the first step, when the test sample contains β-1,6-branched β-1,3-glucan, the β-1,6-branched β-1,3-glucan binds to the first fusion protein and the second fusion protein, whereby the active reporter protein is formed by one and the other of the split reporter proteins, When β-1,3-glucan is contained in the test sample, the β-1,3-glucan binds to the first fusion protein and the third fusion protein, whereby the active reporter protein is formed by one and the other of the split reporter proteins, In the second step, the active reporter protein formed in the first step is detected and quantified. A method comprising:

2. the first fusion protein is a fusion protein in which one of the split reporter proteins is fused to the N-terminus or C-terminus of a β-1,3-glucan binding protein, the second fusion protein is a fusion protein in which the other of the split reporter proteins is fused to the N-terminus or C-terminus of a β-1,6-glucan binding protein, The third fusion protein is a fusion protein in which the other of the split reporter proteins is fused to the N-terminus or C-terminus of the β-1,3-glucan binding protein.

2. The method of claim 1.

3. 3. The method of claim 1 or 2, wherein the test sample is insoluble.

4. A kit for detecting and quantifying β-1,6-branched β-1,3-glucan or β-1,3-glucan, comprising: (A) a first fusion protein having a split reporter protein and a second fusion protein having a split reporter protein; and (B) a first fusion protein having a split reporter protein and a third fusion protein having a split reporter protein; A reagent comprising: the split reporter protein is capable of forming an active reporter protein by pairing two separated parts; the first fusion protein comprises a β-1,3-glucan binding protein and one of the split reporter proteins; the second fusion protein comprises a β-1,6-glucan binding protein and the other of the split reporter proteins, and the β-1,6-glucan binding protein is a β-1,6-glucanase mutant that does not have β-1,6-glucan cleavage activity and has specific binding activity to β-1,6-glucan; the third fusion protein comprises a β-1,3-glucan binding protein and the other of the split reporter proteins; the β-1,3-glucan binding protein in the first fusion protein and the third fusion protein is supBGRP represented by SEQ ID NO: 3 or a derivative thereof; the first fusion protein and the second fusion protein bind to each other, thereby forming the active reporter protein from one and the other of the split reporter proteins; The first fusion protein and the third fusion protein bind to β-1,3-glucan, thereby forming the active reporter protein from one and the other of the split reporter proteins. A kit characterized by:

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