CN117624354B - Anti-human acetylated tau281 rabbit monoclonal antibody and application thereof - Google Patents
Anti-human acetylated tau281 rabbit monoclonal antibody and application thereof Download PDFInfo
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Abstract
The application relates to an anti-human acetylated tau281 rabbit monoclonal antibody and application thereof. The anti-human acetylated tau281 rabbit monoclonal antibody provided by the application comprises a light chain variable region and a heavy chain variable region, wherein the light chain variable region comprises LCDR1-3, LCDR1 comprises an amino acid sequence shown as SEQ ID NO. 3, LCDR2 comprises an amino acid sequence shown as SEQ ID NO. 4, and LCDR3 comprises an amino acid sequence shown as SEQ ID NO. 5; the heavy chain variable region comprises HCDR1-3, wherein HCDR1 comprises an amino acid sequence shown as SEQ ID NO. 6, HCDR2 comprises an amino acid sequence shown as SEQ ID NO. 7, and HCDR3 comprises an amino acid sequence shown as SEQ ID NO. 8. The rabbit monoclonal antibody can be combined with human acetylated tau281 protein with high specificity, and can be applied to double antibody sandwich ELISA for detecting human acetylated tau281 standard antigen, and the detection sensitivity is less than 78 pg/ml.
Description
Technical Field
The application relates to the technical field of immunodetection, in particular to an anti-human acetylated tau281 rabbit monoclonal antibody and application thereof.
Background
Alzheimer's disease (Alzheimer disease, AD) is a common neurodegenerative disease, which belongs to the central nervous system degenerative disease, and the clinical inter-subject is progressive decline of memory function, cognitive dysfunction, language and social function, personality changes, loss of life ability and the like, which ultimately lead to death. Typical histopathological changes are deposition of β -amyloid (aβ) leading to senile plaques, neurofibrillary tangles caused by abnormal phosphorylation of Tau protein, loss of neurons and synapses.
Tau protein is widely present in the nervous system, and is a major component constituting microtubules, and has functions of promoting microtubule assembly and maintaining microtubule stability. In the course of AD onset, microtubule structure changes, the integrity of microtubule structure is destroyed, dissociation of tubulin is promoted, and stability is destroyed. While tau protein bound to microtubules is also altered, neurofibrillary tangles, which are predominantly hyperphosphorylated tau protein, are an important pathological feature of AD, other forms of posttranslational modification of tau protein, such as acetylation, also directly or indirectly regulate the conformation and function of the protein.
In recent years, acetylated tau has been reported to be a blood biomarker for mouse and human traumatic brain injury-induced neurodegeneration. Brain injury induces neuronal tau protein acetylation, driven by non-classical signals, which in a cellular model of AD is associated with S-nitrosylation of GAPDH, which synergistically enhances p300/CBP acetyltransferase activity and inhibits Sirtuinl (Sirtl) deacetylase activity to increase the total amount of acetylation, leading to axonal initial segment degradation and pathological tau localization errors.
Therefore, the concentration of acetylated tau281 can be used as a biomarker for distinguishing AD from non-AD dementia in blood examination, and there is a great need for an anti-human acetylated tau281 rabbit monoclonal antibody and a detection method which can realize high sensitivity, high specificity and high affinity for human acetylated tau 281.
Disclosure of Invention
In order to overcome the technical problems, the application provides the anti-human acetylated tau281 rabbit monoclonal antibody with high sensitivity, strong specificity and high affinity, and the application thereof in a double-antibody sandwich ELISA immunoassay kit, and provides auxiliary diagnosis for Alzheimer's disease and senile dementia related to human acetylated tau 281.
In a first aspect, the application provides a rabbit monoclonal antibody against human acetylated tau281 comprising a light chain variable region and a heavy chain variable region.
The light chain variable region comprises LCDR1-3, wherein LCDR1 comprises an amino acid sequence shown as SEQ ID NO. 3, LCDR2 comprises an amino acid sequence shown as SEQ ID NO. 4, and LCDR3 comprises a sequence shown as SEQ ID NO. 5;
The heavy chain variable region comprises HCDR1-3, the HCDR1 comprises an amino acid sequence as shown in SEQ ID NO. 6, the HCDR2 comprises an amino acid sequence as shown in SEQ ID NO. 7, and the HCDR3 comprises a sequence as shown in SEQ ID NO. 8.
Alternatively, the light chain variable region comprises the amino acid sequence shown in SEQ ID NO. 1, VL of 110 amino acids in full length, FR of 26, 17, 36 and 10 amino acids in the 4 domains, LCDR of 8, 3 and 10 amino acids in the 3 domains, LCDR1, LCDR2 and LCDR3 of 27aa-34aa,52aa-54aa and 91aa-100aa, respectively, and the amino acid sequences are: QNVYGNNR (SEQ ID NO. 3), QAS (SEQ ID NO. 4), AGWASDYTHA (SEQ ID NO. 5).
The heavy chain variable region comprises an amino acid sequence shown as SEQ ID NO. 2, wherein the total length of VH is 112 amino acids, the amino acid numbers of 4 domains of FR are respectively 24, 17, 37 and 11, the amino acid numbers of 3 domains of HCDR are respectively 8, 7 and 8, HCDR1, HCDR2 and HCDR3 are respectively 25aa-32aa,50aa-56aa and 94aa-101aa, and the amino acid sequences thereof are respectively GFSLSNDW (SEQ ID NO. 6), ISHSGTT (SEQ ID NO. 7) and ARHIGGDD (SEQ ID NO. 8).
In a second aspect, the application also provides an isolated polynucleotide encoding the rabbit monoclonal antibody against human acetylated tau281 in the first aspect.
In a third aspect, the application also provides a recombinant expression vector comprising a polynucleotide according to the second aspect of the application.
In a fourth aspect, the application also provides a host cell comprising the recombinant expression vector of the third aspect, preferably the host cell is a prokaryotic cell or a eukaryotic cell.
In a fifth aspect, the application also provides an immunoassay product for detecting human acetylated tau281, the immunoassay product comprising a rabbit monoclonal antibody according to the first aspect of the application.
Optionally, the immunodetection product is a detection kit, a chip or a detection test paper.
In a sixth aspect, the application also provides the use of a rabbit monoclonal antibody according to the first aspect in the preparation of an immunoassay for detecting human acetylated tau281 protein.
Optionally, the immunodetection product is a detection kit, a chip or a detection test paper.
Optionally, the detection kit is a double-antibody sandwich ELISA detection kit or a chemiluminescent immunoassay kit.
Compared with the prior art, the rabbit monoclonal antibody of the anti-human acetylated tau281 can be combined with human acetylated tau281 protein in a high specificity, has high affinity, and the affinity constant Ka can reach 6.7X10 8 L/mol. The rabbit monoclonal antibody for resisting the human acetylated tau281 can also be prepared into an immunodetection kit for detecting the acetylated tau281, and particularly can be applied to a double-antibody sandwich ELISA immunodetection kit, and the detection sensitivity is less than 78pg/ml.
Drawings
FIG. 1 is an electrophoretogram of full-length amplification products of heavy and light chains of rabbit monoclonal antibody OTIR D9, M being a DNA molecular weight Marker.
FIG. 2 shows the detection of human acetylated tau281 polypeptides, non-acetylated tau281 polypeptides, human acetylated tau281 full-length proteins and non-phosphorylated full-length tau full-length protein samples by indirect sandwich ELISA, with the ordinate of the OD values detected.
FIG. 3 shows the detection of human acetylated tau281 standard antigen by double antibody sandwich ELISA, the abscissa shows the concentration (ng/ml) of human acetylated tau281 standard antigen and the ordinate shows the OD value of the detection. R 2 = 0.9904 for standard curve, linear detection range 0-10000pg/mL, and the sample concentration calculation formula is deduced: y=0.0002x+0.1459.
Detailed Description
The invention will be further illustrated with reference to specific examples. It is to be understood that these examples are illustrative of the present invention and are not intended to limit the scope of the present invention. The experimental procedures, which do not address the specific conditions in the examples below, are generally performed under conventional conditions, those described in the laboratory manual, or those suggested by the manufacturer.
Example 1 preparation of anti-human acetylated tau281 Rabbit monoclonal antibodies
1) Preparation of human acetylated tau281 immunogen
The immunogenic polypeptide is designed according to the 1-441aa sequence of tau protein (NP-005901.2) (2N 4R variant), the polypeptide sequence is 270-300aa, the polypeptide purity is above 90%, and the purity requirement for preparing monoclonal antibody is met. The polypeptides were synthesized by peptide biochemistry limited in a third party.
2) Immunization of animals
The synthesized human acetylated tau281 polypeptide is emulsified by complete Freund's adjuvant in a volume ratio of 1:1, about 2kg of New Zealand white rabbits are immunized by a subcutaneous injection method, the immunization dose is 800 mug/animal, the immunization is carried out for the second time after two weeks, the incomplete Freund's adjuvant is emulsified in a volume ratio of 1:1, and the immunization dose is 400 mug/animal. Tail blood is taken after two times of immunization, and serum titer is measured by ELISA method gradient dilution; and judging whether to collect PBMCs or continue immunization according to the result by taking OD450 at ELISA titer 128000 as a standard and selecting the rabbit with the highest antibody titer for collecting the PBMCs.
3) PBMCs separation, specific B cell separation, cloning recombination
Fixing rabbit on operation table, removing hair from heart, sterilizing skin with alcohol, selecting the most obvious heart beat, puncturing with 50ml syringe, injecting blood into syringe after needle, rapidly removing needle after obtaining required blood volume, transferring whole blood in syringe into sterile 50ml tube, mixing with equal amount of PBS, slowly adding dropwise above lymphocyte separating liquid, centrifuging at room temperature 400×g for 30 min, and separating liquid level into four layers from top to bottom: the rabbit PBMCs are obtained by carefully sucking the mononuclear cell layer and washing and removing the platelet and lymphocyte separating liquid by PBS.
Antigen-specific B cells were further sorted from rabbit PBMCs for culture, and the supernatant of the cultured B cells was screened for positive clones using antigen-coated ELISA plates. The positive cloned cells are collected, lysed, RNA is extracted and reversely transcribed into cDNA, the natural paired rabbit monoclonal antibody light chain and heavy chain full-length sequences are amplified from the cDNA corresponding to the positive clone, a rabbit monoclonal antibody expression vector is constructed by a cloning recombination method, the sequences are determined by sequencing, and the amplified full-length PCR product results are shown in figure 1.
4) Preparation and purification of monoclonal antibodies
To obtain a plurality of rabbit monoclonal antibodies recognizing human acetylated tau281 proteins, heavy chain and light chain genes of the rabbit monoclonal antibodies are loaded on an expression vector, KEK293 cells are transfected by plasmids, and the recombinant rabbit monoclonal antibodies recognizing human acetylated tau281 proteins are obtained from culture supernatants after 120-144 hours of transfection. Collecting cell suspension, centrifuging to obtain supernatant, and performing antibody purification by affinity chromatography. The concentration of the purified monoclonal antibody was measured by BCA method, and then sub-packaged and lyophilized to give the purified antibody designated rabbit monoclonal antibody OTIR D9.
Example 2 identification of anti-human acetylated tau281 rabbit monoclonal antibody OTIR D9
1) Specificity identification of Rabbit monoclonal antibodies
Indirect ELSA assay was used. Coating ELISA plates with human acetylated tau281 polypeptide, non-phosphorylated tau281 polypeptide, human acetylated tau281 full-length protein and non-phosphorylated full-length tau protein, blocking the ELISA plates with PBST containing 1% BSA at 4 ℃ overnight, adding 10 4 times of purified rabbit monoclonal antibody OTIR D9, reacting for 50min at 37 ℃, washing the PBST for 3 times, adding HRP-sheep anti-rabbit Ig secondary antibody, reacting for 50min at 37 ℃, washing the PBST for 5 times, adding TMB for developing for 10min, adding a stop solution, and measuring A450 by using an ELISA meter.
FIG. 2 shows that the non-phosphorylated tau281 polypeptide and the non-phosphorylated full-length tau protein react negatively with rabbit monoclonal antibody OTIR D9, and OD450 is less than 0.1; the human acetylated tau281 polypeptide and the human acetylated tau281 full-length protein react positively with OTIR D9 antibody, and OD450 is larger than 1, which shows that the anti-human acetylated tau281 rabbit monoclonal antibody OTIR D9 specifically recognizes the 281 th threonine (T) phosphorylation site epitope in tau protein.
2) Affinity constant determination of rabbit monoclonal antibodies
Affinity constants (Ka) were determined by non-competitive ELISA.
Coating: diluting antigen with carbonate buffer solution to concentration of 1, 0.5, 0.1 and 0.05 mug/mL, respectively coating the antigen with 96-well ELISA plates according to 100 mug/well, and incubating for 24 hours at 4 ℃;
Closing: the plates were washed 4 times with PBST, BSA solution was added at 200. Mu.L/well and incubated for 2h at 37 ℃;
Adding monoclonal antibody: plates were washed 4 times with PBST, and mab OTIR D9 was diluted at a starting doubling ratio of 100. Mu.g/mL with carbonate buffer, added 100. Mu.L per well and incubated for 2h at 37 ℃;
Adding enzyme-labeled secondary antibodies: washing the plate with PBST for 4 times, adding 100 mu L of L10000 times diluted goat anti-rabbit Ig secondary antibody at 37 ℃ into each hole, and standing for 30min;
Color development and termination: washing the plate with PBST for 4 times, adding 100 mu L of substrate color development liquid into each hole, and carrying out light-shielding reaction for 15min at 37 ℃; 50 mu L of 1.0mol/L H 2SO4 stop solution is added into each hole to stop the reaction;
And (3) detection: the absorbance at a wavelength of 450nm (A450 nm) was measured.
The affinity constant ka=6.7x 8 L/mol of anti-human acetylated tau281 rabbit monoclonal antibody OTIR D9 was calculated by plotting an S-shaped curve with the logarithm of the antibody concentration as the abscissa and the OD value as the ordinate.
3) Antibody pairing
To select the best combination of coated and detection antibodies, three purified rabbit monoclonal antibodies OTIR H6, OTIR1D9 and OTIR D9 were coated on the elisa plate, respectively, overnight at 4 ℃. The enzyme label plate is taken out the next day, PBST is washed once, 1% BSA solution is blocked for 2 hours at 37 ℃, and PBST is washed 3 times; 100 μl of human acetylated tau281 full-length protein was added to each well, at a concentration of 20ng/ml, and incubated at 37deg.C for 1 hour; after the incubation, the ELISA plate was removed, washed 3 times with PBST, and HRP-labeled murine monoclonal antibody OTI9A5 was added as a detection antibody, and incubated at 37℃for 1 hour. PBST was washed 5 times, TMB substrate was added, and color development was performed at 37℃for 10min. After removal, stop solution was added and OD450 readings were measured on an microplate reader. The optimal rabbit monoclonal antibody pair is selected according to the OD value of the sample and the background value of the negative control, and the pairing screening result is shown in Table 1.
Table 1 results of screening of antibody pairing experiments
It can be seen that the antibody OTIR D9 according to the present application was used as a coating antibody, and murine monoclonal antibody OTI9A5 was used as a detection antibody.
Example 3 analysis of Rabbit monoclonal antibody OTIR D9 variable region Gene and amino acid sequence A recombinant plasmid of OTIR D9 antibody was used as a DNA template, light chain variable region and heavy chain variable region sequencing primers were designed from the 5' end vector sequences of the light chain and heavy chain on the template, and sequencing was performed using a sequencer ABI 3730. The nucleotide sequence of the light chain and heavy chain variable region of the rabbit monoclonal antibody OTIR D9 is obtained through sequencing.
The nucleotide sequences of the light chain variable region and the heavy chain variable region are respectively subjected to sequencing result data analysis by using IMGT/V-QUEST analysis software on http:// www.imgt.org through the Internet, the amino acid sequence of the light chain variable region of the rabbit monoclonal antibody OTIR D9 is shown as SEQ ID NO.1, and the amino acid sequence of the heavy chain variable region is shown as SEQ ID NO. 2. VL is 110 amino acids in total, the number of amino acids in 4 domains of FR is 26, 17, 36 and 10 respectively, the number of amino acids in 3 domains of LCDR is 8, 3 and 10 respectively, and the regions of LCDR1, LCDR2 and LCDR3 are 27aa-34aa,52aa-54aa and 91aa-100aa respectively, and the amino acid sequences thereof are: QNVYGNNR (SEQ ID NO. 3), QAS (SEQ ID NO. 4), AGWASDYTHA (SEQ ID NO. 5); the total length of VH is 112 amino acids, the number of 4 structural domain amino acids of FR is 24, 17, 37 and 11 respectively, the number of 3 structural domain amino acids of HCDR is 8, 7 and 8 respectively, HCDR1, HCDR2 and HCDR3 are 25aa-32aa,50aa-56aa and 94aa-101aa respectively, and the amino acid sequences thereof are GFSLSNDW (SEQ ID NO. 6), ISHSGTT (SEQ ID NO. 7) and ARHIGGDD (SEQ ID NO. 8) respectively.
Example 4 anti-human acetylated tau281 rabbit monoclonal antibody OTIR D9 is used for preparing a double-antibody sandwich ELISA detection kit based on the detection technology of the ELISA double-antibody sandwich method principle, and the human acetylated tau281 detection kit is prepared for the auxiliary diagnosis of clinical diseases related to human acetylated tau 281.
1. Kit composition
1. Strips coated with OTIR D9 antibody: diluting the antibody to 1 mug/ml with PBS buffer, coating onto a microplate, incubating overnight at 4 ℃ with 100 mug/well, washing 3 times with PBST, and spin-drying; blocking with PBS containing 1% BSA, 5% sucrose and 0.05% proclin300, reacting at 37deg.C for 2 hr, discarding the blocking solution in the hole, and drying; and (3) placing the coating plate in a baking oven at 37 ℃ for 2 hours to finish coating, sealing by an aluminum foil bag, and storing at 4 ℃ for standby.
2. Reagent preparation
2.1 Preparation of enzyme conjugate the simple sodium periodate method is adopted to mark anti-human non-phosphorylated Tau protein murine monoclonal antibody OTI9A5, the working concentration is titrated to prepare 1:20 concentrated solution, the diluted solution is PBS containing 1% BSA, 5% glycerol and 0.05% Proclin 300, and the solution is filtered and sterilized.
2.2 Washing buffer was conventional PBST at pH7.4 containing 0.05% Proclin300 and was formulated as a 20-fold concentrate.
2.3 Substrate solution (color developing solution) of enzyme one-component TMB (purchased from market).
2.4 Sample dilutions contained 1% BSA, 0.05% Proclin 300 in PBS, and were sterilized by filtration.
2.5 Stop solution 10ml HCl (36-38%) was added to 110ml distilled water and the mixing was slowly performed to prepare 1N HCl.
2.6 Standard full Length human acetylated tau281 protein, diluted to 20 μg/ml with PBS containing 1% BSA, 5% sucrose, 10% glycerol, 0.05% Proclin300, filtered, sterilized and aseptically packaged.
2. Detecting the operation key points
1. In order to ensure the accuracy of the detection result, it is suggested that both the standard and the sample are provided with double-hole measurement. Standard curves are needed for each detection.
2. If the content of the substance to be detected in the sample is too high, the sample is diluted by the sample diluent to ensure that the sample accords with the detection range of the kit, and finally, the sample is multiplied by the corresponding dilution multiple during calculation.
3. Sample adding: during sample addition, a disposable clean suction head is required to be used, so that cross contamination is avoided. The sample should be added as slowly as possible to avoid foaming, and the sample is added at the bottom of the ELISA plate hole without adding the sample along the hole wall.
4. Incubation: to prevent sample evaporation or contamination, the microplate must be applied during incubation and dried during the experiment. During the incubation process, whether the temperature of the incubator is constant at 37 ℃ or not should be observed at any time, and the temperature should be adjusted in time. During the incubation, the incubator is not easily opened too many times to avoid affecting the temperature balance.
5. Washing: the washing process is very important, and insufficient washing is prone to false positives.
6. Color development: in order to ensure the accuracy of the experimental result, the stop solution should be added as soon as possible after the substrate reaction time. The color development can be observed at intervals after the substrate solution is added to control the reaction time (e.g., at intervals of 10 minutes). When the front 3-4 holes of the standard product are visible to naked eyes and have obvious gradient blue, and the color development of the rear 3-4 holes is not obvious, stopping solution can be added to stop the reaction, and the blue color immediately turns yellow. The order of addition of the stop solution should be as similar as possible to the order of addition of the substrate solution.
7. The substrate solution should be bluish or colorless and must be discarded if the color becomes severely darkened. The substrate solution is easy to be polluted and is required to be preserved properly in dark place.
3. Determination of standard human acetylated tau281 protein different dilution standard curve
The prepared double-antibody sandwich ELISA detection kit for detecting the human acetylated tau281 protein is taken out from a refrigerator at 4 ℃ and balanced to the room temperature. The standard was diluted from 20. Mu.g/ml to 10000pg/ml with PBS to prepare 9 series of concentration standard substances of 0, 78, 156, 313, 625, 1250, 2500, 5000, 10000pg/ml, 100. Mu.l of the standard substance was added to each well for incubation according to the above detection method, then the liquid was discarded, an HRP-labeled detection antibody working solution was added for incubation, the liquid in the well was discarded, a substrate solution was added to each well after spin-drying, a stop solution was added to each well after development in the absence of light, and the optical density OD value of each well was measured sequentially at 450nm with an enzyme-labeled instrument within 5 minutes after termination of the reaction to make a standard curve, and the results are shown in Table 2.
Table 2 double antibody sandwich ELISA method for detecting human acetylated tau281 standard substance
A human acetylated tau281 detection standard curve was made according to table 2, see figure 3. R 2 = 0.9904 for standard curve, linear detection range 0-10000pg/mL, and the sample concentration calculation formula is deduced: y=0.0002x+0.1459, the detection sensitivity is less than 78pg/ml.
In conclusion, the anti-human acetylated tau281 rabbit monoclonal antibody is applied to double-antibody sandwich ELISA for detecting phosphorylated tau281 standard antigen, and the detection sensitivity is less than 78pg/ml.
The present embodiment is only for explanation of the present application and is not to be construed as limiting the present application, and modifications to the present embodiment, which may not creatively contribute to the present application as required by those skilled in the art after reading the present specification, are all protected by patent laws within the scope of claims of the present application.
Claims (10)
1. The rabbit monoclonal antibody for resisting human acetylated tau281 is characterized by comprising a light chain variable region and a heavy chain variable region, wherein the light chain variable region comprises LCDR1-3, the amino acid sequence of the LCDR1 is shown as SEQ ID NO. 3, the amino acid sequence of the LCDR2 is QAS, and the amino acid sequence of the LCDR3 is shown as SEQ ID NO. 5; the heavy chain variable region comprises HCDR1-3, the amino acid sequence of the HCDR1 is shown as SEQ ID NO. 6, the amino acid sequence of the HCDR2 is shown as SEQ ID NO. 7, and the amino acid sequence of the HCDR3 is shown as SEQ ID NO. 8.
2. The rabbit monoclonal antibody of claim 1, wherein the amino acid sequence of the light chain variable region is shown in SEQ ID No. 1 and the amino acid sequence of the heavy chain variable region is shown in SEQ ID No. 2.
3. An isolated polynucleotide encoding the rabbit monoclonal antibody of any one of claims 1-2.
4. A recombinant expression vector comprising the polynucleotide of claim 3.
5. A host cell comprising the recombinant expression vector of claim 4, wherein the host cell is a prokaryotic cell or a eukaryotic cell.
6. An immunoassay product of human acetylated tau281, comprising the rabbit monoclonal antibody of claim 1 or 2.
7. The immunoassay product of claim 6, wherein the immunoassay product is a test kit, chip or test strip.
8. Use of a rabbit monoclonal antibody according to claim 1 or 2 for the preparation of an immunoassay product for detecting human acetylated tau281 protein.
9. The use according to claim 8, wherein the immunodetection product is a detection kit, a chip or a detection strip.
10. The use according to claim 9, wherein the detection kit is a double antibody sandwich ELISA detection kit or a chemiluminescent immunoassay kit.
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