CN1480731A - Method for detecting small molecule protein and peptides by using sandwich immunization sensing method - Google Patents
Method for detecting small molecule protein and peptides by using sandwich immunization sensing method Download PDFInfo
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- CN1480731A CN1480731A CNA031276318A CN03127631A CN1480731A CN 1480731 A CN1480731 A CN 1480731A CN A031276318 A CNA031276318 A CN A031276318A CN 03127631 A CN03127631 A CN 03127631A CN 1480731 A CN1480731 A CN 1480731A
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Abstract
The invention belongs to immunity detection area, especially related to method for quantitative measuring proteins and peptides with molecular weight under 20kDa. Gold-coated slide glass or triangular prism is as detection substrate. The method includes following procedures: forming an assembling body, forming duality immune complex of first antibody - antigen, forming sandwich ternary immune complex of first antibody - antigen - second antibody as well as resonant wavelength testing. The antigens to be detected are insulin bFGF, T3 or T4 etc. the first antibody and second antibody are first and second monoclone antibodies possessing specificities and complementarity for anti each antigen to be detected. The invention monitors dynamic reaction procedure of biomoleculars, and tests change of concentration of object to be detected with high sensitivity. The combination of second anti body generates stronger optical signal, creating biologic amplified activate.
Description
Technical field
The invention belongs to field of immunodetection, relate to the method for a kind of quantitative detection of molecules amount, particularly relate to a kind of sandwich immunoassays method that is based upon on the sensing membrane in following protein of 20kDa or peptide class.
Background technology
The prior art close with the present invention is that a piece of open report in 1998 is the method that the double-monoclonal antibody sandwich method in middle layer detects a kind of sensitivity of micro-interferon with the plasmalogen.See Wink T, Anal Chem., 1; 70 (5): the article of 827-32.Liposome-mediated enhancement of the sensitivity in immunoassaysof proteins andpeptides in surface plasmon resonance spectrometry..This analytical approach is to finish by surface plasmon resonance (SPR) technology on a polystyrene thin layer that about 20nm is thick, the surface is coated with golden film.Through wrapping the antibody (first antibody) that is captured, add tested sample, add biotinylated detection antibody (second antibody), add processes such as Avidin and biotinylation plasmalogen at last again, by the content of interferon in the tested sample of change-detection of the caused resonant wavelength of monitoring final step.Wherein, plasmalogen has been brought into play the biology amplification.Respond and all in pH7.4,10mM phosphate buffer (PBS), carry out, avoid different solutions to produce different refractivities, influence testing result.
Prior art is to add the plasmalogen amplification light reaction signal that can be connected to by the affinity interaction of Avidin-biotin on the second antibody to improve detection sensitivity, therefore operate loaded down with trivial details, time-consuming, sense cycle is long, even under the situation of usage flag particles all, plasmalogen is also big than colloid gold particle labelled antibody difficulty with being connected of antibody.
Summary of the invention
Development along with surface plasmon resonance (SPR) technology, set up based on the immunoassay on the sensing membrane by using specific antibody, detect corresponding antigens, become the focus of research in recent years, it is the enzyme-linked immunosorbent assay that continues, a kind of novel analytical approach after the chemiluminescence enzyme immunoassay method, radiommunoassay.The technical problem to be solved in the present invention provides the novel sandwiching immunity detection method of a kind of detection by quantitative small protein and peptide class (molecular weight is below 20kDa), used antibody is mark or only use colloid gold label not, operation is simple, do not need further chromogenic reaction, can directly show testing result.
The present invention is with sensing membrane, can be to be coated with the microslide of golden film or prism for detecting substrate, finish through processes such as the formation of the formation of the formation of assembly, first antibody-antigen binary immune complex, the sandwich ternary immune complex of first antibody-antigen-second antibody, resonant wavelength detections.The formation of said assembly is to resist the monoclonal antibody of small molecular protein to be measured or peptide class to be fixed on the sensing membrane as first antibody (being capture antibodies) strain, constitutes the assembly with specific immune activity; After the formation of said first antibody-antigen binary immune complex was meant and adds testing sample, the first antibody and the determined antigen in the testing sample that detect on the carrier formed first antibody-antigen binary immune complex; The formation of the sandwich ternary immune complex of said first antibody-antigen-second antibody is when adding the monoclonal antibody of the small molecular protein anti-to be measured of another strain and first antibody complementation or peptide class as second antibody (promptly detecting antibody) in the sensing sample cell, to detect on-chip first antibody-antigen binary immune complex and combine formation first antibody-antigen-second antibody ternary immune complex with the second antibody specificity by antigen; Said testing sample is small protein or the peptide class that molecular weight is lower than 20kDa; It is the variation of the resonant wavelength that causes according to second antibody that said resonant wavelength detects, and with the typical curve contrast, calculates small molecular protein to be measured or peptide class content in the sample.
The use of second antibody, the sensitivity that has obviously improved immune detection.
Above-mentioned molecular weight to be measured is lower than small protein or the peptide class of 20kDa, can be insulin, basic fibroblast growth factor, trilute (T
3), tetraiodothyronine (T
4) etc.Corresponding first antibody and second antibody should be the monoclonal first antibody and the second antibody of the anti-every kind of determined antigen of specificity, and this two strains monoclonal antibody should be discerned epitopes different on the determined antigen molecule, promptly have complementarity, can be attached to simultaneously on the same antigen molecule.They are respectively the anti-insulin monoclonal antibodies, alkali resistance fiber mother cell growth factor monoclonal antibody, anti-T
3Monoclonal antibody, anti-T
4Monoclonal antibody etc.Use different monoclonal antibodies, just can detect different corresponding determined antigens, promptly different small molecular proteins or peptide class.
The second antibody of being mentioned among the present invention can be the non-marked second antibody, also can be the second antibody with the colloid gold particle mark.
The forming process of above-mentioned assembly can be that first antibody is directly linked on the golden film, also can attach on the golden film by intermediate connecting layer is intermolecular, the intermediate connecting layer molecule can be staphylococcal protein A or Avidin, and they can play the biology amplification, improves detection sensitivity.
The sample of three-layer sandwich structure of the present invention and forming process thereof can be explained visually with Fig. 1.Said three-layer sandwich structure is exactly the sandwich structure of three layers of molecule of two monoclonal antibody two point forms of antibody/antigen/antibody.Among Fig. 1,1 for detecting substrate, and 2 is golden film, and 3 is intermediate connecting layer molecule (staphylococcal protein A or Avidin), and 4 is first antibody, and 5 is the antigen of testing sample, and 6 is second antibody.In the three-layer sandwich structure, ground floor is a first antibody, and the second layer is the antigen of testing sample, and the 3rd layer is second antibody.Among Fig. 1,11 is the formation of assembly, and 12 is the formation of first antibody-antigen binary immune complex, and 13 is the formation of the sandwich ternary immune complex of first antibody-antigen-second antibody.
Compare with common method for biosensor, this law has the following advantages: when (1) three-layer sandwich immune complex forms, the 3rd layer is that the combination of second antibody has produced stronger optical signalling, brought into play the biology amplification, this be since the molecular weight (160KDa) of antibody obviously greater than antigen (being lower than 20kDa) molecular weight, caused light reaction signal strengthens at least 10 times thereupon, and therefore, the corresponding direct method of detection sensitivity improves 10-100 doubly; In like manner, the second antibody of colloid gold particle mark can be brought into play bigger biology amplification, and therefore, the corresponding direct method of detection sensitivity improves 100-1000 doubly; (2) this law is particularly useful for the small protein and the peptide class that can not detect with the direct pick-up method.
Comparing this law with the routine immunization analytic approach has: the first, monitoring property in real time, the dynamic reaction process of monitoring bio molecule obtains the intermolecular combination that has or not in real time, in conjunction with intensity and speed, the speed that dissociates, information such as binding site distribution; The second, simplification does not need any biomolecule related in the marker detection or only uses colloid gold label antibody, does not need chromogenic substrate, directly detects the variation of testing concentration; The 3rd, the combination of second antibody has produced stronger optical signalling, has brought into play the biology amplification, and is therefore highly sensitive, no background interference; The 4th, reagent cost is low.
Compare with background technology, common advantage is the dynamic reaction process of monitoring bio molecule in real time, variation that can simple and easy direct detection testing concentration; Highly sensitive, no background interference; Reagent cost is low.Method of the present invention is used mark not or with the second antibody of colloid gold particle mark, has been saved the process that adds Avidin and biotinylation plasmalogen, therefore have simple to operate, save time, advantage such as sense cycle is short; Energy quantitative detection of molecules amount is in following small protein of 20kDa and peptide class.
Description of drawings
Fig. 1 is the sample and the forming process synoptic diagram thereof of three-layer sandwich structure of the present invention.
Fig. 2 is the light reaction signal graph that the anti-TnC monoclonal second antibody that is attached on the golden film of the present invention produces.
Fig. 3 is the light reaction signal graph that alkali resistance fiber mother cell growth factor (bFGF) the monoclonal second antibody that is attached on the golden film of the present invention produces.
Fig. 4 is the anti-T that is attached on the golden film of the present invention
3The light reaction signal graph that the monoclonal second antibody produces.
Fig. 5 is the anti-T that is attached on the golden film of the present invention
4The light reaction signal graph that the monoclonal second antibody produces.
Embodiment:
The present invention is further elaborated below in conjunction with embodiment, rather than will limit the invention with this.
Embodiment 1: the sandwich immunoassay sensing method of TnC (TnC) detects
(1) has the formation of the assembly of immunologic competence
1) activation of golden film: in sample cell, add dimercapto acetate or mercaptopropionic acid earlier with ethanol preparation 6.7mmol/L; Add the N-hydroxy-succinamide (NHS) of 0.87mol/L and 1-ethyl-3-(3-dimethylamino-propyl) carbodiimide hydrochloride (EDC) solution reaction 15min of 0.52mol/L behind the reaction 15min, wash flow cell 3 times with phosphate buffer (PBS).
2) after following each step reaction is finished (resonance wave reaches stationary value), wash flow cell 3 times, remove non-specific adsorption, inject next step reaction reagent then with phosphate buffer (pH7.4 contains NaCl 8.5g/L for PBS, 10mmol/L).Except that the anti-ThC monoclonal antibody reactive of specificity 30min, all the other per step 20min can finish.Adding is with the Avidin of the 0.2g/L of PBS preparation; Reaction finish bovine serum albumin (BSA) that the back adds 5g/L with seal on the golden film remaining can with the site of protein molecular reaction.
3) the anti-TnC monoclonal of the biotinylation specificity first antibody of 20 times of dilutions of adding.
(2) formation of first antibody-antigen binary immune complex
Add sample to be measured, if it is wherein contain corresponding determined antigen, then single with the anti-TnC on golden film surface
The combination of clone's first antibody specificity, the binary complex of formation first antibody-TnC.Because it is to be measured anti-
Original molecule amount less (being lower than 20kDa), when determined antigen concentration is low, the optics that this reaction causes
It is not obvious that signal changes, usually detect less than.
(3) formation of the sandwich ternary immune complex of first antibody-antigen-second antibody
Second antibody is to be attached to another strain monoclonal antibody on the same TnC molecule simultaneously with first antibody, both are in conjunction with the different epitopes on the TnC molecule, therefore, the second antibody that adds can combine with the TnC antigen on the golden film, forms the ternary immune complex of first antibody-TnC-second antibody three-layer sandwich.
The measuring principle of sandwich immunoassay sensor is to be attached to optical signalling that the second antibody molecule on golden film surface produces by detection to realize the detection of measured object.Be attached to the thickness and the density difference of golden film surface second antibody molecule, produce the optical signalling of varying strength, the thickness and the density of second antibody molecule that is attached to golden film surface is big more, and the light reaction signal of generation is strong more.Compare with common direct sensing method, the sensitivity of sandwich method has improved 10 times, the combination that shows second antibody has produced stronger optical signalling, has brought into play the biology amplification, this be since the molecular weight (16KDa) of antibody obviously greater than TnC antigen (1.8kDa) molecular weight.
In embodiment 1, the adding of second antibody makes resonant wavelength increase the 2.8nm (see figure 2), can contain TnC in the judgement sample.By contrasting the concentration that to obtain TnC in the sample with standard reference material.Standard reference material can obtain by following process: the standard solution of known TnC content is mixed with 5 kinds of variable concentrations from low to high, with the detection method identical with sample to be measured, promptly repeat the operation of front (), (two) step, measuring the resonant wavelength that the standard solution of every kind of concentration causes changes, logarithm value with TnC concentration is a horizontal ordinate, the logarithm value that resonant wavelength increases is an ordinate, the drawing standard curve.
Embodiment 2: the specificity that TnC (TnC) sandwich immunoassay sensing method detects
For the specificity of this sandwich immunoassay testing result is described, replace TnC to carry out immune detection with BSA as sample to be checked, repeat the overall process of embodiment 1.Among the embodiment 2, anti-TnC monoclonal antibody of two used strains and BSA are non-matching antigen-antibody or irrelevant antibody, do not have optionally recognition reaction, therefore, can not the specificity combination, can not form the immune complex of three-layer sandwich, promptly can not produce corresponding optical signalling, the resonant wavelength no change illustrates and does not contain TnC in the sample to be checked, irrelevant albumen in the sample can not cause nonspecific reaction, and this sandwiching immunity detection method has high degree of specificity.
Embodiment 3: the sandwich immunoassay sensing method of basic fibroblast growth factor (bFGF) detects
As each step operation of embodiment 1, different is that first antibody, second antibody are the monoclonal antibody of anti-bFGF, and antigen to be checked can only be bFGF.The sample that will contain bFGF equally is as sample to be checked, by detecting the content that can measure bFGF in the sample.Fig. 3 is the testing result of embodiment 3, and the combination of anti-bFGF second monoclonal antibody makes resonant wavelength increase 2.9nm, can contain bFGF in the judgement sample, by contrasting the concentration that can obtain bFGF in the sample with standard reference material.
Embodiment 4:T
3The sandwich immunoassay sensing method detect
As each step operation of embodiment 1, different is that first antibody, second antibody are anti-T
3Monoclonal antibody, antigen to be checked can only be T
3To contain T equally
3Sample as sample to be checked, can measure T in the sample by detecting
3Content.Fig. 4 is the testing result of embodiment 4, anti-T
3The combination of second monoclonal antibody makes resonant wavelength increase 3.6nm, can contain T in the judgement sample
3, by obtaining T in the sample with the standard reference material contrast
3Concentration.
Embodiment 5:T
4The sandwich immunoassay sensing method detect
As each step operation of embodiment 1, different is that first antibody, second antibody are anti-T
4Monoclonal antibody, antigen to be checked can only be T
4To contain T equally
4Sample as sample to be checked, can measure T in the sample by detecting
4Content.Fig. 5 is the testing result of embodiment 5, anti-T
4The combination of second monoclonal antibody makes resonant wavelength increase 3.8nm, can contain T in the judgement sample
4, by obtaining T in the sample with the standard reference material contrast
4Concentration.
Embodiment 6: second antibody is used after with the colloid gold particle mark
All second antibody can be used after with the colloid gold particle mark among above-mentioned 5 embodiment, other conditions are constant, and at this moment the more common sensing method of sensitivity (direct method) of this sandwich immunoassay sensing detection method improves 100-1000 doubly.Here except that second antibody becomes colloid gold label antibody, additive method and operate same the various embodiments described above is no longer given an example.
Claims (3)
1, a kind of sandwich immunoassay sensing method detects the method for small protein and peptide class, detecting on the substrate, finish through assembly formation, the formation of first antibody-antigen binary immune complex, the formation of the sandwich ternary immune complex of first antibody-antigen-second antibody, resonant wavelength testing process; It is to resist the monoclonal antibody of small molecular protein to be measured or peptide class to be fixed on the sensing membrane as first antibody that said assembly forms; After the formation of said first antibody-antigen binary immune complex was meant and adds testing sample, the determined antigen that detects in on-chip first antibody and the testing sample formed first antibody-antigen binary immune complex; The formation of the sandwich ternary immune complex of said first antibody-antigen-second antibody is when pointing to the small molecular protein anti-to be measured that adds another strain and first antibody complementation in the sample cell or peptide class monoclonal antibody as second antibody, to detect on-chip first antibody-antigen binary immune complex and combine formation first antibody-antigen-second antibody ternary immune complex with the second antibody specificity by antigen; It is characterized in that said detection substrate is to be coated with microslide or the prism that golden film is made sensing membrane; Said determined antigen is small protein or the peptide class that molecular weight is lower than 20kDa; It is the variation of the resonant wavelength that causes according to second antibody that said resonant wavelength detects, and with the typical curve contrast, calculates small molecular protein to be measured or peptide class content in the sample.
2, detect the method for small protein and peptide class according to the described sandwich immunoassay sensing method of claim 1, it is characterized in that said determined antigen is insulin, basic fibroblast growth factor, trilute or tetraiodothyronine; Said second antibody is the second antibody with the colloid gold particle mark.
3, detect the method for small protein and peptide class according to claim 1 or 2 described sandwich immunoassay sensing methods, it is characterized in that, said assembly forms, and first antibody is linked on the golden film by the intermediate connecting layer molecule, and the intermediate connecting layer molecule is staphylococcal protein A or Avidin.
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Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102062778A (en) * | 2009-11-17 | 2011-05-18 | 上海荣盛生物药业有限公司 | Composition for in-vitro detection of antibody |
| CN107238713A (en) * | 2017-06-23 | 2017-10-10 | 浙江诺迦生物科技有限公司 | The detection method of trace hemp and the SPR chips used in a kind of saliva sample |
| CN107345958A (en) * | 2017-06-23 | 2017-11-14 | 浙江诺迦生物科技有限公司 | The detection method of trace methamphetamine and the SPR chips used in a kind of saliva sample |
| CN107345909A (en) * | 2017-06-23 | 2017-11-14 | 浙江诺迦生物科技有限公司 | The detection method of trace morphine and the SPR chips used in a kind of saliva sample |
| CN110501506A (en) * | 2018-07-05 | 2019-11-26 | 东莞东阳光医疗智能器件研发有限公司 | A kind of biosensor and its application |
| CN112461794A (en) * | 2020-11-13 | 2021-03-09 | 天津大学 | Long-range SPR sensor and preparation method thereof |
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2003
- 2003-07-16 CN CNB031276318A patent/CN1193232C/en not_active Expired - Fee Related
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102062778A (en) * | 2009-11-17 | 2011-05-18 | 上海荣盛生物药业有限公司 | Composition for in-vitro detection of antibody |
| CN107238713A (en) * | 2017-06-23 | 2017-10-10 | 浙江诺迦生物科技有限公司 | The detection method of trace hemp and the SPR chips used in a kind of saliva sample |
| CN107345958A (en) * | 2017-06-23 | 2017-11-14 | 浙江诺迦生物科技有限公司 | The detection method of trace methamphetamine and the SPR chips used in a kind of saliva sample |
| CN107345909A (en) * | 2017-06-23 | 2017-11-14 | 浙江诺迦生物科技有限公司 | The detection method of trace morphine and the SPR chips used in a kind of saliva sample |
| CN110501506A (en) * | 2018-07-05 | 2019-11-26 | 东莞东阳光医疗智能器件研发有限公司 | A kind of biosensor and its application |
| CN112461794A (en) * | 2020-11-13 | 2021-03-09 | 天津大学 | Long-range SPR sensor and preparation method thereof |
| CN112461794B (en) * | 2020-11-13 | 2022-09-16 | 天津大学 | Long-range SPR sensor and preparation method thereof |
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