Patent Application
20140272945
The present invention relates to a method for manufacturing a multi-functional bio-material conjugate, and a multi-functional bio-material conjugate manufactured by means of the same, and more specifically, to a method for manufacturing a multi-functional bio-material conjugate used as a biosensor for detecting microorganisms, and the like, and a multi-functional bio-material conjugate manufactured by means of the same.
Nano- and micro-sized particles to which bio-materials are bound have been applied to biosensing, bioimaging, isolation, and the like, in various fields such as food, health care, diagnosis, and life science. For example, an antibody-magnetic nanoparticle conjugate and an antibody-gold nanoparticle have been used for detecting a target material by a bond between an antigen and an antibody in an immune sensor (Yu-Hui Bai. et al., Anal. 135:1672-1679, 2010).
One of factors having a significant effect on formation of an antigen-antibody reaction conjugate is an antibody immobilization method, and therefore, various immobilization technologies have been developed, and there are various methods for binding protein. For example, there are a method using chemical and physical adsorption, a method for binding protein to a gold nanoparticle using cystein which is an amino acid specifically bound to gold, a method for producing a monomolecular film on a gold nanoparticle and then covalently binding protein to the gold nanoparticle using a functional group of the monomolecular film, and a method for adsorbing avidin protein on a surface of the gold nanoparticle and binding protein to which biotin is bound (ZHANG zhiFeng et al., Sci china ser B-Chem. 50(1):127-134, 2007), and the like.
However, currently developed immobilization technology according to the related art has problems in that conditions of immobilization reaction such as pH are varied depending on properties of protein, and in a case of a nanoparticle, dispersion is not achieved but nanoparticles are flocculated.
Korean Patent No. 0962286 discloses a magnetic core gold nanoparticle for detecting food-borne pathogens, a manufacturing method thereof, and a detecting method of food-borne pathogens using the nanoparticle, which is characterized by including: preparing a magnetic body core containing magnetic materials; modifying a surface of the magnetic body core with an amine functional group; and forming a gold particle layer on a surface of the magnetic body core surface-modified with the amine functional group.
However, the above-mentioned patent has problems in that reproducibility or efficiency of a chemical reaction generated at the time of modifying the surface of the magnetic body core with the amine functional group may be deteriorated and flocculation phenomenon in a solution may occur. In addition, significantly long reaction time is required for forming a gold particle layer, and food-borne pathogens enable to be detected only by a separate equipment, SPR, which is inconvenient.
Accordingly, the present inventors found that in a case of coating a first nanoparticle having magnetic or fluorescent characteristics with protein, manufacturing a conjugate by adsorbing a second nanoparticle having metallic characteristics onto the first nanoparticle, and adsorbing a bio-material onto the conjugate, precipitation of the nanoparticles may be prevented and the bio-material may be easily immobilized without performing an inconvenient modification process, and desired materials are capable of multi-functionally detected and isolated using properties of the protein coating the first nanoparticle and properties of the bio-material adsorbed onto the second nanoparticle, thereby completing the present invention.
An object of the present invention is to provide a bio-material conjugate capable of multi-functionally detecting or isolating desired materials, and a method for manufacturing the same.
Another object of the present invention is to provide a method for detecting microorganisms by a simplified method in a field.
According to an exemplary embodiment of the present invention, there is provided a method for manufacturing a multi-functional bio-material conjugate, the method including: (a) coating a first nanoparticle having magnetic or fluorescent characteristics with protein; (b) manufacturing a conjugate by adsorbing a second nanoparticle having metallic characteristics onto the first nanoparticle coated with protein; and (c) manufacturing the multi-functional bio-material conjugate by adsorbing a bio-material onto the conjugate.
According to another exemplary embodiment of the present invention, there is provided a multi-functional bio-material conjugate including: a first nanoparticle having magnetic or fluorescent characteristics and coated with protein, and a second nanoparticle having metallic characteristics and adsorbed onto the protein, wherein a bio-material is adsorbed onto the second nanoparticle.
According to another exemplary embodiment of the present invention, there is provided a biosensor including the multi-functional bio-material conjugate as described above.
According to another exemplary embodiment of the present invention, there is provided a method for rapidly detecting a microorganism using a multi-functional bio-material conjugate, the method including: (a) mixing the multi-functional bio-material conjugate with a sample containing a detection-target microorganism to prepare a reaction solution, the multi-functional bio-material conjugate including a first nanoparticle having magnetic or fluorescent characteristics and coated with protein, and a second nanoparticle having metallic characteristics and adsorbed onto the protein, wherein an antibody specifically bound to the detection-target microorganism is adsorbed onto the second nanoparticle; (b) sequentially passing the reaction solution through a film for flocculating microorganism and a filtration membrane for capturing microorganism to permeate a multi-functional bio-material conjugate which is not reacted with the microorganism, thereby selectively isolating a multi-functional bio-material conjugate-microorganism composite; and (c) measuring whether or not the multi-functional bio-material conjugate-microorganism composite captured in the filtration membrane for capturing microorganism is present or a concentration of the multi-functional bio-material conjugate-microorganism composite.
The present invention confirmed that in a case where a conjugate is manufactured by coating protein with a first nanoparticle having magnetic or fluorescent characteristics and adsorbing a second nanoparticle having metallic characteristics onto the first nanoparticle and then a bio-material is adsorbed onto the conjugate, a multi-functional bio-material conjugate in which the bio-material is not flocculated and easily immobilized, and detection and analysis performance are capable of being improved by utilizing properties of protein and bio-material coating the first nanoparticle may be manufactured.
In the present invention, after the first nanoparticle having magnetic or fluorescent characteristics is coated with protein, the second nanoparticle having metallic characteristics is adsorbed onto the first nanoparticle coated with protein to thereby manufacture the conjugate, and then the bio-material is adsorbed onto the conjugate, thereby manufacturing a multi-functional bio-material conjugate.
That is, it was confirmed in an embodiment of the present invention that as a result of manufacturing BSA protein-coated magnetic nanoparticle (MNP)-gold nanoparticle (AuNP)-antibody and BSA protein-coated fluorescent latex beads (LB)-silver nanoparticle (AgNP) or gold nanoparticle (AuNP)-antibody, an immobilization efficiency of the antibodies was excellent, and using the antibodies, Staphylococcus aureus was capable of being detected with excellent sensitivity.
Therefore, according to an exemplary embodiment of the present invention, there is provided a method for manufacturing a multi-functional bio-material conjugate, the method including: (a) coating a first nanoparticle having magnetic or fluorescent characteristics with protein; (b) manufacturing a conjugate by adsorbing a second nanoparticle having metallic characteristics onto the first nanoparticle coated with protein; and (c) manufacturing the multi-functional bio-material conjugate by adsorbing a bio-material onto the conjugate.
In addition, according to another exemplary embodiment of the present invention, there is provided a multi-functional bio-material conjugate including: a first nanoparticle having magnetic or fluorescent characteristics and coated with protein, and a second nanoparticle having metallic characteristics and adsorbed onto the protein, wherein a bio-material is adsorbed onto the second nanoparticle.
The first nanoparticle may have magnetic or fluorescent characteristics and, for example, may include latex, magnetic, silica, a quantum dot, a metal nanoparticle, and the like.
The second nanoparticle may have metallic characteristics and, for example, may include gold, silver, copper, platinum, and the like. It is preferred that the second nanoparticle favorably adsorbs protein.
Here, the term: “nanoparticle” refers to an ultra-fine particle having a size of about 1 nm to 100 nm. Nanoparticles having significantly small size have different characteristics from those of general flocculation materials. The nanoparticle has a remarkably increased specific surface area as compared to the existing materials. Due to the increased specific surface area, the nanoparticle has a different surface effect as compared to the existing materials, that is, as a size of the particle becomes decreased, the number of molecules positioned on the surface thereof are increased. In a case where the particle has a diameter of 5 nm, 50% of molecules consisting of the particle are positioned on a surface of the particle and in a case where the particle has a diameter of 2 nm, 90% of molecules are positioned on the surface thereof. Since a ratio of the molecules positioned on the surface thereof is relatively high, the nanoparticles have high ratio of a surface energy to a binding energy as compared the existing materials. The ratio of the surface energy to the binding energy becomes increased from 5% to about 30% as the size of the particle becomes decreased from 20 nm to 1 nm. Atoms consisting of the particles are placed at an energy steady state reaching balance between attraction and repulsion by an interaction between the atoms and atoms adjacent thereto. However, since the atoms positioned on the surface have only attraction by inner atoms, the atoms are placed at high energy state. Due to the surface effect, the nanoparticles have characteristics such as surface activity, decrease in a melting point, low-temperature sinterablity, and the like, shown in the catalyst or on the surface of the catalyst.
It is preferred that the first nanoparticle has a size larger than that of the second nanoparticle.
For example, the first nanoparticle has a size of 20 to 500 nm, and the second nanoparticle has a size of 5 to 100 nm.
In a case of using the first nanoparticle having a size larger than that of the second nanoparticle, a small nanoparticle enables to be easily adsorbed.
Protein coating the first nanoparticle is to easily immobilize a bio-material to be immobilized by using an adsorption characteristic without a modification process, and as the protein, BSA, peroxidase, alkaline phosphatase, glucose oxidase, choline oxidase, streptavidin, skim milk, serum, peptide, and the like, may be used.
That is, in a case of coating the first nanoparticle with protein as described above, the multi-functional bio-material conjugate is capable of being manufactured by the adsorption method using the second nanoparticle favorably adsorbing protein.
The bio-material may be selected from a group consisting of an antibody, an enzyme, DNA, an aptamer, a peptide nucleic acid (PNA), and a ligand.
According to another exemplary embodiment of the present invention, there is provided a biosensor including the multi-functional bio-material conjugate.
It could be confirmed in another embodiment of the present invention that a multi-functional bio-material conjugate is manufactured using an antibody specifically bound to microorganism as a bio-material, and the microorganism is capable of being detected at a high speed at the time of reacting the conjugate with the microorganism.
Therefore, according to another exemplary embodiment of the present invention, there is provided a method for rapidly detecting a microorganism using the multi-functional bio-material conjugate, the method including: (a) mixing the multi-functional bio-material conjugate with a sample containing a detection-target microorganism to prepare a reaction solution, the multi-functional bio-material conjugate including a first nanoparticle having magnetic or fluorescent characteristics and coated with protein, and a second nanoparticle having metallic characteristics and adsorbed onto the protein, wherein an antibody specifically bound to the detection-target microorganism is adsorbed onto the second nanoparticle; (b) sequentially passing the reaction solution through a film for flocculating microorganism and a filtration membrane for capturing microorganism to permeate a multi-functional bio-material conjugate which is not reacted with the microorganism, thereby selectively isolating a multi-functional bio-material conjugate-microorganism composite; and (c) measuring whether or not the multi-functional bio-material conjugate-microorganism composite captured in the filtration membrane for capturing microorganism is present or a concentration of the multi-functional bio-material conjugate-microorganism composite.
The film for flocculating microorganism, the filtration membrane for capturing membrane, the isolation method, and the measuring method, used in the method for rapidly detecting the microorganism may be used by referring to description of Korean Patent Laid-Open Publication No. 10-2011-0058711 previously filed by the present inventors.
For example, the film for flocculating microorganism may be selected from a group consisting of polydimethylsiloxane (PDMS), polymer and aluminum tape having adhesion, rubber and latex, and a paste for screen printing. Preferably, the film for flocculating microorganism may be a film manufactured by applying the paste for screen printing such as a silver paste or a carbon paste to the filtration membrane for capturing the microorganism, provided with holes having each predetermined size, using a screen printing method. Therefore, the film for flocculating microorganism and the filtration membrane for capturing the microorganism may be configured in an integrated type, and the screen printing method may be any well-known methods in the art.
As an example of the screen printing method, there is a method for fixing a screen mesh made of nylon, polyester or stainless steel, and the like, to frame made of wood, aluminum, and the like, forming a sheet membrane thereon by a handwork scheme or a photochemical scheme to close parts rather than required images, and filling a paste for screen printing thereinto, thereby passing the paste through the mesh not having the sheet membrane when applying pressure an inner portion of the screen by a spatula to move the paste, so that the paste passed through the mesh is printed onto a material to be printed, positioned under the sheet.
The filtration membrane for capturing microorganism has a pore size of 100 nm to 10 μm. The nanoparticle to which the antibody non-bound to microorganism is immobilized passes through the filtration membrane for capturing microorganism, and the microorganism non-bound to the nanoparticle having immobilized microorganism is not indicated as a signal even though the microorganism is captured in the filtration membrane for capturing microorganism. Therefore, only the microorganism bound to the nanoparticle having immobilized antibody shows unique color, fluorescence, and the like, of the nanoparticle having immobilized antibody on the filtration membrane for capturing microorganism.
In an exemplary embodiment of the present invention, the filtration membrane for capturing microorganism having a pore size of 1.2 μm is used, but the pore size thereof is not limited thereto, which is obvious to those skilled in the art. Preferably, the filtration membrane for capturing microorganism may have a pore size selected from 100 nm to 10 μm so as to capture the microorganism reacted with the nanoparticle having immobilized antibody.
The filtration membrane for capturing microorganism may be made of a material selected from a group consisting of nitrocellulose, polycarbonate, nylon, polyester, cellulose acetate, polysulfone and polyethanesulfone.
The step (b) of selectively isolating of the multi-functional bio-material conjugate may be performed by using vacuum, centrifugation, or absorption method.
In other words, when the nanoparticle-antibody-microorganism complex is filtered by the filtration membrane for capturing microorganism after passing through the film for flocculating microorganism, the conjugate may be selectively isolated by applying vacuum, performing centrifugation, or absorbing the conjugate in the filtration membrane.
The measuring step (c) may be performed using a CCD camera or absorbance.
Hereinafter, the present invention will be described in detail with reference to the following Examples. However, the following examples are only for exemplifying the present invention, and it will be obvious to those skilled in the art that the scope of the present invention is not construed to be limited to these examples.
A bovine serum albumin (BSA) solution (pH 7.4, dissolved into 10 mM phosphate buffer) was added to a magnetic nanoparticle (MNP) solution so as to have a final volume of 1 ml and mixed with together, and 10 mM N-hydroxysuccinnimide (NHS, Biacore Inc.) and 2 mM EDC(Biacore Inc.) were added to the mixture, and left for 30 minutes. 0.1 ml of 100 mM glycin solution (pH 7.4, dissolved into 10 mM phosphate buffer) was added to the mixture, and left for 30 minutes, and divided into each 200 μlm, followed by centrifugation at 4° C. and 6,000 rpm for 20 minutes to remove a supernatant therefrom. Then, 0.2 ml of a borate buffer (10 mM, pH 8.5) was added thereto and mixed with together, followed by centrifugation at 6000 rpm for 20 minutes to remove a supernatant therefrom. After the above-described process was repeated once again, 0.4 ml of 100 nm magnetic nanoparticle-BSA was added to 0.1% BSA (pH 8.8, dissolved into 10 mM sodium bicarbonate buffer) solution, thereby finally manufacturing BSA protein-coated magnetic nanoparticle.
As the magnetic nanoparticle solution, 100 μl of 100 nm magnetic nanoparticle solution (CMX, 25 mg/ml, Chemicell) having a matrix made of carboxymethyl-dextran, 60 μl of 100 nm magnetic nanoparticle solution (PAS, 50 mg/ml, Chemicell) having a matrix made of polyacrylic acid, 180 μg of 90 nm magnetic nanoparticle (Fe3O4, provided by Prof. Sangmin Jeon from Pohang University Science and Technology: POSTECH) and 430 μg of 90 nm magnetic nanoparticle (Fe3O4—SiO2, provided by Prof. Sangmin Jeon from Pohang University Science and Technology: POSTECH) were used.
1 ml of 10 nm gold nanoparticle solution (BB International, borate buffer 10 mM, pH 8.5) concentrated by 5 times was added to the BSA protein-coated magnetic nanoparticle obtained by performing the centrifugation to remove the supernatant therefrom, thereby being subjected to adsorption for 30 minutes.
10 μg of anti-Staphylococcus aureus monoclonal antibody (anti-S. aureus mAb, Abcam) was added to each of 100 nm CMX and PAS magnetic nanoparticle solutions, having the adsorbed gold nanoparticle, and 10 μg of anti-C-reactive protein monoclonal antibody (anti-CRP mAb, Abcam) was added to 80 nm magnetic nanoparticle (Fe3O4) and 90 nm magnetic nanoparticle (Fe3O4—SiO2) solution.
After 30 minutes, 0.1 ml of 10% bovine serum albumin (BSA) solution (pH 8.8, dissolved into 10 mM sodium bicarbonate buffer) was added thereto, and left for 30 minutes. The solution was divided into each 200 μl, followed by centrifugation at 4° C. and 5,500 rpm for 20 minutes to remove a supernatant therefrom, and 0.2 ml of 0.1% BSA solution was added thereto, followed by centrifugation at 5,000 rpm for 20 minutes to remove a supernatant therefrom. The above-described process was repeated once again, and finally, 0.4 ml of 0.1% BSA (pH 8.8, dissolved into 10 mM sodium bicarbonate buffer) solution was added to 100 nm magnetic nanoparticle (CMX, PAS)-gold nanoparticle-anti-Staphylococcus aureus monoclonal antibody, and 0.1 ml thereof was added to 80 nm and 90 nm magnetic nanoparticle (Fe3O4, Fe3O4—SiO2)-gold nanoparticle-anti-C-reactive protein monoclonal antibody and mixed with together, followed by filtration with 0.45 μm syringe filter, and the filtrate was stored in fridge.
50 μl of latex bead surface-modified with a carboxylic acid was subjected to centrifugation at 4° C. and 5,000 rpm for 3 minutes to remove a supernatant therefrom. Coating the latex bead with BSA was performed as the same as Example 1-1 above. As the latex bead solution, 2 μm fluorescent latex bead (Sigma Co.) and 0.9 μm latex bead (undyed, Sigma Co.) were used.
1 ml of each of 20 nm silver nanoparticle solution (BB International, 10 mM borate buffer, pH 8.5) and 10 nm gold nanoparticle solution (BB International, 10 mM borate buffer, pH 8.5), each concentrated by 5 times, was added to 2 μm fluorescent latex bead coated with BSA, thereby being subjected to adsorption for 30 minutes, and 10 μg of anti-C-reactive protein polyclonal antibody (anti-CRP pAb, Abcam) was added thereto, and left for 30 minutes. 10 μg of each of anti-H1 monoclonal antibody (anti-H1 mAb, LS-BIO) and anti-H5 monoclonal antibody (anti-H5 mAb, Abcam) was added to only the fluorescent latex bead coated with the silver nanoparticle, and left for 30 minutes.
The fluorescent latex bead solution having the silver or gold nanoparticle adsorbed thereonto by the BSA protein was prepared by the same method as Example 1-1 above, and during the preparation, centrifugation was performed at 5000 rpm for 10 minutes, and syringe filtration was not performed, 0.4 ml of 0.1% BSA (pH 8.8, dissolved into 10 mM sodium bicarbonate buffer) solution was added to the mixture, and the reactant was stored in fridge.
0.1 ml of borate buffer (0.1 M, pH 8.5) and 10 μg anti-aldehyde activated HRP (Thermo) were added to 1 ml of 20 nm gold nanoparticle solution (BB International). After 30 minutes, the reactant was subjected to centrifugation at 4° C. and 12,000 rpm for 15 minutes to remove a supernatant therefrom. Centrifugation was performed again, and 1 ml of 15 nm gold nanoparticle solution (BB International) was added to the reactant, 0.1 ml of buffer (0.1M, pH 8.5) and then 10 μg of Troponin I monoclonal antibody (Abcam, detection antibody) were added thereto. After 1 hour, 0.2 ml of 0.1% BSA (pH 7.4, dissolved into 10 mM phosphate buffer) solution was added thereto and mixed with together (5×), and the obtained gold nanoparticle (AuNP)-antibody was stored in fridge.
0.1 ml of borate buffer (0.1 M, pH 8.5) and 10 μg anti-C-reactive protein monoclonal antibody (anti-CRP mAb which is capture Ab, Abcam) were added to 1 ml of 20 nm gold nanoparticle solution (BB International).
After 30 minutes, 0.1 ml of 10% bovine serum albumin (BSA) solution (pH 8.8, dissolved into 10 mM sodium carbonate buffer) was added thereto, and left for 30 minutes. The solution was subjected to centrifugation at 4° C. and 10,000 rpm for 20 minutes to remove a supernatant therefrom. 0.2 ml of 0.1% BSA (pH 8.8, dissolved into 10 mM sodium carbonate buffer) solution was added to the reactant and mixed with together, followed by centrifugation at 10,000 rpm for 15 minutes to remove a supernatant therefrom. The above-described process was repeated once again, and finally, 0.2 ml of 0.1% BSA (pH 8.8, dissolved into 10 mM sodium carbonate buffer) solution was added thereto and mixed with together, and the obtained gold nanoparticle (AuNP)-antibody was stored in fridge.
1 ml of borate buffer (0.1 M, pH 8.5) and 10 μg of anti-C-reactive protein monoclonal antibody (anti-CRP mAb which is capture Ab, Abcam) were added to 1 ml of 20 nm silver nanoparticle solution (BB International) and left for 30 minutes.
The silver nanoparticle solution having immobilized antibody was prepared by the same method as Example 2-1, and the silver nanoparticle (AgNP)-antibody was stored in fridge.
A PDMS solution (Sylgard 184A, Dow Corning, USA) and a curing agent (Sylgard 184B, Dow Corning, USA) were mixed at a ratio of 10:1 and poured on a flat patri dish having a diameter of 150 mm. In addition, air bubbles in the mixture were removed by a vacuum pump, and the reactant was cured at 60° C. for 24 hours. Then, the cured PDMS film was cooled at room temperature, and made 6 holes using a perforator having a diameter of 15 mm. As a result, it was confirmed that the PDMS film having holes was manufactured.
After 10 mM Phosphate buffer (PB, pH 7.4) was added to a magnetic nanoparticle solution surface-modified with carboxylic acid so as to have a final volume of 1 ml and mixed with together, 10 mM N-hydroxysuccinnimide (NHS, Biacore Inc.), 2 mM EDC (Biocore Inc.), and 10 μg of antibody were added thereto and left for about 2 hours.
As the magnetic nanoparticle solution, 100 μl of 100 nm magnetic nanoparticle solution (CMX, 25 mg/ml, Chemicell) having a matrix made of carboxymethyl-dextran, 60 μl of 100 nm magnetic nanoparticle solution (PAS, 50 mg/ml, Chemicell) having a matrix made of polyacrylic acid were used, and as an antibody, anti-Staphylococcus aureus monoclonal antibody (anti-S. aureus mAb, Abcam) was added. Anti-H1 monoclonal antibody (anti-H1 mAb, LS-BIO) and anti-H5 monoclonal antibody (anti-H5 mAb, Abcam) were added to only 100 nm magnetic nanoparticle solution having a matrix made of carboxymethyl-dextran.
The magnetic nanoparticle solution having immobilized antibody was prepared by the same method as Example 1-1.
50 μl of 0.9 μm latex bead (Sigma Co.) surface-modified with a carboxylic acid was subjected to centrifugation at 4° C. and 5,000 rpm for 3 minutes to remove a supernatant therefrom. After 10 mM Phosphate buffer (PB, pH 7.4) was added to the latex bead so as to have a final volume of 1 ml and mixed with together, 10 mM N-hydroxysuccinnimide (NHS, Biacore Inc.), 2 mM EDC(Biocore Inc.), and 10 μg of anti-human CD3 Ab, BD were added thereto and left for 2 hours.
The latex bead solution having immobilized anti-human CD3 antibody was prepared by the same method as Example 1-2 above.
Using BSA Protein-Coated Magnetic Nanoparticle (MNP, matrix: CMX)-Gold Nanoparticle (AuNP)-Antibody
40 μl of each solution containing 10 μg/ml of MNP(CMX)-BSA, BSA protein-coated MNP(CMX)-AuNP-anti-S. aureus mAb prepared by Example 1-1 above and containing MNP(CMX)-anti-S. aureus mAb conjugate prepared by Comparative Example 1, 10 μl (105 cfu) of solution prepared by suspending Staphylococcus aureus(S. aureus) in PBS and 100 μl of PBS solution were mixed together, and gently shaken for 30 minutes. After 30 minutes, 100 μl of PBS solution was added thereto, then using magnetic at room temperature, magnetic nanoparticles were separated from the solution for about 3 minutes, and S. aureus complex reacted with the supernatant and each magnetic nanoparticle conjugate was collected.
100 μl of the collected S. aureus mixture containing the supernatant and magnetic nanoparticle conjugate was smeared on agar medium (trypticase soy broth (BD 211825) 3%, agar powder 2%) in a petri dish and incubated at 37° C. for 16 to 24 hours. After the incubation, an effect of the antibody immobilization method using the magnetic nanoparticle and the gold nanoparticle was confirmed by measuring viable cell count formed on the medium.
As shown in
A state in which the antibody of the manufactured magnetic nanoparticle conjugate was immobilized by the gold nanoparticle was confirmed by using the immobilization method according to the present invention. 10 μl of solution prepared by suspending S. aureus in PBS (100-5×106 cfu), 40 μl of BSA protein-coated MNP(CMX)-AuNP-anti-S. aureus mAb(Abcam) conjugate solution prepared by Example 1-1, and 50 μl of PBS solution were mixed together, and gently shaken for 30 minutes.
100 μl of PBS solution was added to the solution, then using magnetic, the magnetic nanoparticle was separated from the solution for about 3 minutes to remove a supernatant, and S. aureus reacted with BSA protein-coated MNP(CMX)-AuNP-anti-S. aureus mAb conjugate was collected.
As a filtration membrane for capturing microorganism, a nitrocelluolose (NC) film (Millipore) having a pore size of 1.2 μm obtained by applying 1% BSA solution (dissolved into PBS) thereto and performing a drying process was used. The NC film was placed onto a filter mounted in 100 μl of erlenmeyer flask having branches and the PDMS film manufactured by Example 3 above was covered onto the NC film. The mixture solution of S. aureus reacted with the collected BSA protein-coated MNP(CMX)-AuNP-anti-S. aureus mAb conjugate was allowed to pass through pores of the PDMS film by applying vacuum through branches of the flask, thereby confirming a concentration of S. aureus.
As a result, it was confirmed from
10 mM citrate buffer (pH 3.0) containing 5 mM hydroxyl amine and 25 mM hydrogen tetrachloroaurate(III) was dropped onto the filtration membrane for capturing microorganism filtering the complex of S. aureus reacted with BSA protein-coated MNP(CMX)-AuNP-anti-S. aureus mAb conjugate of Experimental Example 1-2, and reacted at room temperature for about 15 minutes.
As a result, as shown in
A concentration of S. aureus was confirmed according to the same procedure as Experimental Example 1-2 above, using the BSA protein-coated MNP(PAS)-AuNP-anti-S. aureus mAb conjugate having a matrix made of polyacrylic acid conjugate by Example 1-1 above.
As a result, as shown in
A mixture for amplifying silver nanoparticle was prepared by mixing A (silver salt) solution and B (hydroquinone initiator) solution at a ratio of 1:1, and the mixture was dropped onto the filtration membrane for capturing microorganism of Experimental Example 2-1, and reacted at room temperature for about 10 minutes. As a result, as shown in
In order to confirm whether or not the multi-functional bio-material conjugate according to the present invention enables to selectively detect microorganism, an experiment was performed using BSA protein-coated MNP(PAS)-AuNP-anti-S. aureus mAb, and by the same procedure as Experimental Example 2-1 above except for changing a kind of the microorganism. 4 different kinds of microorganisms, that is, Salmonella typimurium, Listeria monocytogenes, Staphylococcus aureus, Escherichia coli, were reacted with the MNP(PAS)-AuNP-anti-S. aureus mAb and then analyzed.
As a result, it could be confirmed from
A conjugate manufactured by directly immobilizing anti-S. aureus mAb to MNP(PAS), that is, MNP(PAS)-anti-S. aureus mAb conjugate, and the BSA protein-coated magnetic nanoparticle (MNP, PAS)-gold nanoparticle (AuNP)-anti-S. aureus mAb conjugate were measured for each concentration by the same procedure as Experimental Example 2-1 above and compared by the naked eye.
As shown in
CRP Measurement Using BSA Protein-Coated Fluorescent Latex Bead (Fluorescent Yellow-Green, LB)-Silver Nanoparticle (AgNP) or Gold Nanoparticle (AuNP)-Antibody
1 μl of BSA protein-coated fluorescent latex bead (fluorescent yellow-green, 2 μm LB)-silver nanoparticle, 20 nm AgNP)-anti C-reactive protein polyclonal antibody (anti-CRP pAb) conjugate and BSA protein-coated fluorescent latex bead (fluorescent yellow-green, 2 μm LB)-gold nanoparticle (20 nm AuNP)-anti C-reactive protein polyclonal antibody (anti-CRP pAb) conjugate, each 0, 1 μg/ml and 10 μg/ml of CRP antigens, and 10 μl of each of the gold nanoparticle (20 nm AuNP)-anti C-reactive protein monoclonal antibody (anti-CRP mAb) conjugate manufactured by Example 2-1 above or the silver nanoparticle (20 nm AgNP)-anti C-reactive protein monoclonal antibody conjugate manufactured by Example 2-2 above were added, then phosphate buffered saline (PBS, pH 7.4) was added thereto so as to have a final volume of 200 μl, and reacted for 30 minutes.
The reaction solution was sequentially passed through the film for flocculation (PDMS) and 0.8 μm MMM (asymmetric super-micron membrane) filtration membrane by the same method as Experimental Example 1-2 above, and captured to the membrane, and comparison in view of fluorescent signal was conducted.
It could be confirmed from
CRP Measurement Using Flow-Through-Hole (FTH) Membrane
Adsorption pads cut into a square shape and a double-sided tape having three holes therein were prepared, 0.8 μm MMM (asymmetric super-micron membrane) filtration membrane was placed onto the adsorption pad, the double-sided tape having holes was attached thereonto, 1 μl of BSA protein coated fluorescent LB(2 μm)-AgNP-anti-CRP pAb conjugate was loaded in each hole. After 10 μl of each of 0, 1 μg/ml and 10 μg/ml CRP antigens and 5 μl of AuNP-anti-CRP mAb were sequentially loaded, and a concentration of CRP was measured.
As shown in
0.3 μl of anti-mouse IgG Ab (control, 1 mg/ml) and anti-CRP pAb (1 mg/ml) as 2nd Ab were spotted on each of 180 sec nitrocelluolose (NC) film, and dried at room temperature for about 20 minutes. 10 μl of each 80 nm and 90 nm BSA protein coated magnetic nanoparticle (Fe3O4, Fe3O4—SiO2)-gold nanoparticle-anti C-reactive protein monoclonal antibody conjugates manufactured by Example 1-1 above, 0, 10 ng/ml, 100 ng/ml and 1 μg/ml CRP antigens, each 1% of polyvinylpyrrolidone (PVP) and (surfactant 10G) were added, then CRP free serum (high purified) was added thereto so as to have a final volume of 100 μl, and a strip was slightly soaked into the mixture so that an end thereof contacted the mixture.
When an immune reaction was generated while the mixture moved along the strip, the immobilization state of the magnetic nanoparticle-gold nanoparticle-antibody conjugate was confirmed by observing whether or not signal was indicated. After the reaction was completed, the nitrocelluolose (NC) was washed by phosphate buffered saline (PBS, pH 7.4).
As shown in
100, 101, 102, 103, 104, and 105 pfu of H1N1 virus were added to 1 μl of each BSA protein coated fluorescent latex bead (fluorescent Red, 2 μm LB)-silver nanoparticle (20 nm AgNP)-anti H1 virus monoclonal antibody (anti-H1 mAb) conjugate manufactured by Example 1-2 so as to have a final volume of 100 μl with PBS, followed by reaction for 20 minutes, and 1 μl of magnetic nanoparticle (MNP, CMX)-anti H1 virus monoclonal antibody (anti-H1 mAb) conjugate was added thereto, followed by reaction for 20 minutes.
100 μl of PBS solution was added to the reaction solution, then using magnetic at room temperature, the magnetic nanoparticle was separated from the solution for about 3 minutes to remove a supernatant, and 100 μl of PBS was added thereto, then using magnetic at room temperature, the magnetic nanoparticle was separated from the solution for about 3 minutes to remove a supernatant, 100 μl of PBS was added thereto, thereby collecting BSA protein-coated fluorescent LB(2 μm)-AgNP-anti-H1 mAb conjugate-H1N1 virus-MNP(CMX)-H1 mAb complex. After the above-described process was repeated once again, the solution was allowed to pass through 0.8 μm MMM (asymmetric super-micron membrane) filtration membrane by the same method as Experimental Example 1-2, then collected in the membrane, and fluorescent signal was confirmed.
In
As shown in
In order to whether or not the multi-functional bio-material conjugate according to the present invention enables to selectively detect the virus, 1 μl of magnetic nanoparticle (MNP, CMX)-anti-H1 monoclonal antibody (anti-H1 mAb) conjugate manufactured by Comparative Example 1 and 103 pfu of each H1N1, H3N2 and H5N2 virus were added, then PBS was added thereto so as to have a final volume of 100 μl, and reacted for 20 minutes. The magnetic nanoparticle was separated from the reaction solution using magnetic at room temperature for about 3 minutes to remove a supernatant from the reaction solution, then 100 μl of PBS was added thereto and suspended.
1 μl of BSA protein coated fluorescent latex bead (fluorescent Red, 2 μm LB)-silver nanoparticle (20 nm AgNP)-anti H1 virus monoclonal antibody (anti-H1 mAb) conjugate manufactured by Example 1-2 was added to each solution, and reacted for 20 minutes. The magnetic nanoparticle was separated from the reaction solution using magnetic at room temperature for about 3 minutes to remove a supernatant from the reaction solution, then 100 μl of PBS was added to collect each MNP(CMX)-H1 mAb conjugate-virus-BSA protein coated fluorescent LB(2 μm)-AgNP-anti-H1 mAb complex. After the above-described process was repeated once again, the solution was allowed to pass through 0.8 μm CA(Cellulose Acetate membrane) filtration membrane by the same method as Experimental Example 4-1, then collected in the membrane, and fluorescent signal was confirmed.
As a result, as shown in
The magnetic nanoparticle (MNP, CMX)-anti H5 monoclonal antibody (anti-H5 mAb) conjugate manufactured by Comparative Example 1 and the BSA protein coated fluorescent latex bead (fluorescent Red, 2 μm LB)-silver nanoparticle (20 nm AgNP)-anti H5 virus monoclonal antibody (anti-H5 mAb) manufactured by Example 1-2 were reacted with the different sub-type virus, that is, H1N1, H3N2 and H5N2, by Experimental Example 4-2, and then analyzed.
As a result, as shown in
Each of the undyed latex bead, 0.9 μm (LB)-anti human CD3 antibody (anti-human CD3 Ab) conjugate manufactured by Comparative Example 2 and the BSA protein coated undyed latex bead, 0.9 μm (LB)-gold nanoparticle, 20 nm (AuNP)-anti human CD3 antibody (anti-human CD3Ab) manufactured by Example 1-2 was mixed with blood, and left for 20 minutes. 2% FBS-PBS having the same volume was added to the reaction solution and mixed well, then placed onto density medium(Ficoll), followed by centrifugation at room temperature under conditions of 2,000 rpm and break off. After centrifugation, cell positioned in the boundary of density medium plasma of Ficoll was collected, and whether or not T cell (CD3) is formed and selective isolation rate (removal) of T cell (CD3) were confirmed by FACS, thereby confirming an effect of the method for immobilizing the antibody to the latex bead using the gold nanoparticle. As shown in
Anti Mouse IgG antibody (Control line) and Troponin I antibody (Test line) were applied onto a nitrocellulose membrane using Dispensor (Zeta) by 8 mm at a concentration of 0.1 mg/ml. The applied nitrocellulose membrane was cut into an interval of 3.8 mm to manufacture strip sensors (the coated amount of the antibody for each sensor=38 ng/strip). In order to measure Troponin I for each concentration, the HRP coated gold nanoparticle-gold nanoparticle antibody conjugate manufactured by Example 1-3 was added to a human serum (Sigma Co.) solution containing 1×, 2% polyvinylpyrrolidone(PVP) (Sigma Co.) and 2% Surfactate 10G(Fitzgerald) and mixed with Troponine I at a concentration of 0 to 1000 ng/ml and each mixture was put into 96 well plate, and then the manufactured strip sensor was put thereinto, followed by reaction for 10 minutes. After the reaction was completed, the strip was put into 96 well plate containing PBS buffer again and washed for 20 minutes. After the washing was completed, sample pad of the strip was removed, and then the strip was treated with 20 μl of 0.1 M Tris-HCl(pH 8.8) buffer into which 2 mM luminol (Sigma Co.), 0.5 mM p-coumaricacid(Sigma Co.), and 2 mM hydrogen peroxide were dissolved. Then, chemiluminescent signal was measured for 120 seconds using Chemi-Doc(Bio-Rad), and results thereof were shown in
Although specific embodiments of the present invention are described in detail, it will be apparent to those skilled in the art that the specific description is merely desirable exemplary embodiment and should not be construed as limiting the scope of the present invention. Therefore, the substantial scope of the present invention is defined by the accompanying claims and equivalent thereof.
According to the present invention, the method for manufacturing the multi-functional bio-material conjugate may prevent precipitation of nanoparticles, easily immobilize a bio-material, and manufacture a bio-material conjugate having multiple functions, by using two kinds of particles. In addition, the multi-functional bio-material conjugate manufactured by the present method may be used to detect microorganisms at up to a concentration of 101 cfu.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2011-0105463 | Oct 2011 | KR | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/KR2012/008301 | 10/12/2012 | WO | 00 | 4/11/2014 |
