阅读说明：本技术 利用hek293细胞制备新型冠状病毒核衣壳蛋白的方法 (Method for preparing novel coronavirus nucleocapsid protein by using HEK293 cell ) 是由 秦丽丽 王晓菲 张�林 张晓慧 于 2021-01-25 设计创作，主要内容包括：本发明提供一种利用HEK293细胞制备新型冠状病毒核衣壳蛋白的方法,包括：1)构建新冠病毒核衣壳蛋白(N蛋白)重组表达载体；2)用重组表达载体转染HEK293细胞；3)体外培养细胞,从培养上清中分离纯化N蛋白。利用HEK293表达系统可在短时间内获得大量新冠病毒N蛋白,通过一步亲和层析法可获得纯度高达98%以上的N蛋白。与大肠杆菌相比,采用HEK293表达系统制备的N蛋白在与抗体的结合活性及新冠抗体胶体金检测方面均表现出极大优势,且HEK293表达系统制备的N蛋白其蛋白空间构象接近于病毒N基因在宿主体内的蛋白表达构象,具有更高的免疫诊断和抗体制备的准确性,将其用于制作诊断试剂和疫苗前景广阔。(The invention provides a method for preparing a novel coronavirus nucleocapsid protein by using HEK293 cells, which comprises the following steps: 1) constructing a new recombinant expression vector of the coronavirus nucleocapsid protein (N protein); 2) transfecting HEK293 cells with the recombinant expression vector; 3) the cells were cultured in vitro, and the N protein was isolated and purified from the culture supernatant. A large amount of new coronavirus N protein can be obtained in a short time by using an HEK293 expression system, and the N protein with the purity of more than 98 percent can be obtained by a one-step affinity chromatography. Compared with escherichia coli, the N protein prepared by the HEK293 expression system has great advantages in the aspects of the binding activity with an antibody and the colloidal gold detection of a new crown antibody, and the protein space conformation of the N protein prepared by the HEK293 expression system is close to the protein expression conformation of a virus N gene in a host body, so that the N protein has higher immunodiagnosis and antibody preparation accuracy, and has wide prospects in preparing diagnostic reagents and vaccines.)

1. The method for preparing the novel coronavirus nucleocapsid protein by using the HEK293 cell is characterized by comprising the following steps of:

1) constructing a novel coronavirus nucleocapsid protein recombinant expression vector;

2) transfecting HEK293 cells by using the recombinant expression vector constructed in the step 1);

3) culturing cells in vitro, and separating and purifying the recombinant expression novel coronavirus nucleocapsid protein from the culture supernatant by adopting a one-step affinity chromatography.

2. The method according to claim 1, wherein the novel recombinant expression vector for the coronavirus nucleocapsid protein in step 1) is constructed by a method comprising: introducing leader peptide shown as SEQ ID NO 2 into the N end of the novel coronavirus nucleocapsid protein, introducing a label for protein purification into the C end of the novel coronavirus nucleocapsid protein, artificially synthesizing a nucleic acid construct corresponding to the recombinant protein, and constructing the nucleic acid construct on a eukaryotic expression vector.

3. The method of claim 2, wherein the tag is a6 × His tag.

4. The method according to claim 3, wherein the amino acid sequence of the recombinant protein is shown as SEQ ID NO. 4.

5. The method of claim 4, wherein the nucleic acid construct has the nucleotide sequence set forth in SEQ ID NO 5.

6. The method according to claim 2, wherein the promoter adopted by the eukaryotic expression vector is an EF-1 alpha promoter, an hCMV promoter or an SV40 late promoter;

wherein the promoter is operably linked to the nucleic acid construct.

7. The method of claim 6, wherein the eukaryotic expression vector is pcDNA3.1 (+).

8. The method of claim 1, wherein step 2) comprises: HEK293 cells were cultured to a cell density of 1.8-2.2X 10⁶One per mL, the activity rate is more than 95%; mixing the recombinant expression vector with a PEI transfection reagent and then adding the mixture into HEK293 cells;

wherein, 1 is multiplied by 10⁶Each cell corresponds to 1 ug of plasmid; the mass ratio of the recombinant expression vector to the PEI transfection reagent is 1: 3.

9. The method according to claim 1, wherein the HEK293 cell of step 3) is cultured under the following conditions: 37 ℃ and 5% CO₂130-200 rpm for 96 h;

the cell culture medium used was CD 293 TGE medium.

10. The method according to any one of claims 3 to 9, wherein the step 3) of separating and purifying the recombinant protein by using a His-tag affinity chromatography column comprises the following steps: the cell culture supernatant was collected by centrifugation at 1000g for 30min, filtered and applied to a GE HisTrap excel column equilibrated in PBS buffer in advance, followed by gradient elution sequentially with PBS buffer containing 0, 30, 100, 250 and 500mM imidazole at an elution volume of 10 CV per concentration, and the protein eluate was collected.

Technical Field

The invention relates to the technical field of biology, in particular to a method for preparing a novel coronavirus nucleocapsid protein by using HEK293 cells.

Background

The novel coronavirus (SARS-CoV-2, or COVID-19) is a new strain of coronavirus which is exploded in large scale in 2020 in the world, and is a beta coronavirus with SARS coronavirus. The common signs of human infection with the novel coronavirus include respiratory symptoms, fever, cough, shortness of breath, dyspnea and the like. In more severe cases, the infection can lead to pneumonia, severe acute respiratory syndrome, renal failure, and even death, posing a serious threat to human health.

The novel coronavirus nucleocapsid protein (N protein) is one of the most important structural proteins in the capsid of the novel coronavirus, and accounts for the largest proportion of the structural proteins of the virus. The COVID-19-N protein and the virus genome RNA are intertwined to form the virus nucleocapsid, which plays an important role in the synthesis process of the virus RNA. The N protein is relatively conserved in the new coronavirus, and an organism at an early stage can generate a high-level antibody for resisting the N protein when infected, so the N protein has the potential of establishing a method for quickly detecting a novel coronavirus serum antibody, the researches such as monoclonal antibody preparation and the like can be further carried out, and the N protein of the coronavirus on the market is mostly expressed by adopting an escherichia coli prokaryotic expression system. Prokaryotic expression has the advantages of capability of obtaining gene expression products in a short time, relatively low cost and simpler method. However, compared with a eukaryotic expression system, the escherichia coli prokaryotic expression system has many defects such as protein folding error and post-translational modification, and the N protein prepared by using the escherichia coli expression has different risks from the N protein structure and modification expressed by human cells after a new coronavirus infects a human body, so that the accuracy of immunodiagnosis and antibody preparation is reduced.

Disclosure of Invention

The invention aims to provide a method for preparing a novel coronavirus nucleocapsid protein by using HEK293 cells.

In order to achieve the object of the present invention, in a first aspect, the present invention provides a method for preparing a novel coronavirus nucleocapsid protein using HEK293 cells, comprising the steps of:

1) constructing a novel coronavirus nucleocapsid protein recombinant expression vector;

2) transfecting HEK293 cells by using the recombinant expression vector constructed in the step 1);

3) culturing cells in vitro, and separating and purifying the recombinant expression novel coronavirus nucleocapsid protein from the culture supernatant by adopting a one-step affinity chromatography.

The method for constructing the novel coronavirus nucleocapsid protein recombinant expression vector in the step 1) comprises the following steps: introducing leader peptide shown as SEQ ID NO:2 at the N end of the novel coronavirus nucleocapsid protein, introducing a tag (such as 6 XHis tag) for protein purification at the C end of the novel coronavirus nucleocapsid protein, artificially synthesizing a nucleic acid construct corresponding to the recombinant protein, and constructing the nucleic acid construct on a eukaryotic expression vector.

Furthermore, the amino acid sequence of the recombinant protein is shown as SEQ ID NO. 4.

Further, the nucleotide sequence of the nucleic acid construct is shown as SEQ ID NO. 5.

The promoter adopted by the eukaryotic expression vector can be an EF-1 alpha (human electrophoresis factor-1 alpha) promoter, an hCMV (human cytokine) promoter or an SV40 (Simian vacuating virus 40) late promoter and the like.

Wherein the promoter is operably linked to the nucleic acid construct.

The eukaryotic expression vector is pcDNA3.1 (+).

The method, step 2), comprises: HEK293 cells were cultured to a cell density of 1.8-2.2X 10⁶Per mL (preferably 2X 10)⁶one/mL), the activity rate is more than 95%; and mixing the recombinant expression vector with a PEI transfection reagent, and adding the mixture into HEK293 cells.

Preferably, 1 × 10⁶Each cell corresponds to 1 ug of plasmid; the mass ratio of the recombinant expression vector to the PEI transfection reagent is 1: 3.

HEK2 in step 3) of the aforementioned method93 the culture conditions of the cells were: 37 ℃ and 5% CO₂130-200 rpm (preferably 135 rpm) for 96 h.

The cell culture medium used may be CD 293 TGE medium.

In the foregoing method, step 3) of separating and purifying the recombinant protein with a His-tag affinity chromatography column includes: the cell culture supernatant was collected by centrifugation at 1000g for 30min, filtered and applied to a GE HisTrap excel column equilibrated in PBS buffer in advance, followed by gradient elution sequentially with PBS buffer containing 0, 30, 100, 250 and 500mM imidazole at an elution volume of 10 CV per concentration, and the protein eluate was collected. And subjected to SDS-PAGE analysis. According to SDS-PAGE results, the purity of N protein eluted under the conditions of 100mM, 250 mM and 500mM of imidazole is over 95 percent, the partial protein is mixed and dialyzed, and the molecular weight cut-off of a dialysis bag used is 30 KDa. Dialyzing overnight at 4 ℃ in a refrigerator using the following dialyzates: PBS buffer (pH7.4). And SDS-PAGE detection was performed on the dialyzed samples.

In a second aspect, the present invention provides the use of any one of the following novel coronavirus nucleocapsid proteins prepared according to the above method:

(1) for the preparation of novel coronavirus vaccines;

(2) is used for preparing a novel coronavirus antibody detection reagent.

Compared with the prior art, the invention has at least the following advantages:

the invention can obtain a large amount of new coronavirus nucleocapsid protein in a short time by using an HEK293 expression system, the purity is up to more than 98 percent, and the expression amount is up to 300 mg/L.

Compared with the nucleocapsid protein prepared by using an escherichia coli expression system, the new coronary nucleocapsid protein prepared by using the HEK293 expression system has great advantages in the aspects of the binding activity with an antibody and the colloidal gold detection of the new coronary antibody, the protein space conformation of the new coronary nucleocapsid protein prepared by using the HEK293 expression system is close to the protein expression conformation of a virus N gene in a host body, the protein space conformation of the new coronary nucleocapsid protein is more close to the structure and modification of the nucleocapsid protein expressed by human body cells after the new coronary virus infects a human body, the immunodiagnosis and the antibody preparation accuracy are higher, and the diagnostic reagent and the vaccine prepared by using the new coronary nucleocapsid protein have wide prospects.

And (III) the whole set of nucleocapsid protein expression and purification process is simple to operate, the method has high repeatability, and the method can be applied to the mass production process.

Drawings

FIG. 1 is a map of expression vector pcDNA3.1.

FIG. 2 is a schematic diagram of the construction of a recombinant plasmid according to a preferred embodiment of the present invention.

FIG. 3 is a SDS-PAGE picture of N protein purification of the novel coronavirus according to a preferred embodiment of the present invention. Wherein, lane 1: cell culture supernatant; lane 2: flowing through the liquid; lane 3: 0mM imidazole; lane 4: 30mM imidazole; lane 5: 100mM imidazole; lane 6: 2500mM imidazole; lane 7: 500mM imidazole; lane 8: and (3) protein Marker.

FIG. 4 is an SDS-PAGE pattern of the dialyzed N protein of the novel coronavirus of the preferred embodiment of the invention.

FIG. 5 is a diagram showing the activity of detecting the binding of the antibody to the N protein expressed in E.coli and the N protein expressed in HEK293 cells by ELISA in accordance with a preferred embodiment of the present invention.

FIG. 6 shows the results of detecting the sample of the novel coronavirus antibody using the E.coli-expressed N-protein colloidal gold test strip (A) and the HEK293 cell-expressed N-protein colloidal gold test strip (B) in the preferred embodiment of the present invention. In the figure, negative control represents negative serum of healthy people, and samples 1-5 represent positive serum of 5 newly diagnosed patients.

Detailed Description

The invention provides a method for efficiently expressing a novel coronavirus nucleocapsid protein by using HEK293 cells, wherein the HEK293 cells are human embryonic kidney293 cells (HEK 293); the amino acid sequence of the novel coronavirus nucleocapsid protein is shown as SEQ ID NO. 1.

The specific technical scheme is as follows:

1. constructing a new coronavirus N protein recombinant expression plasmid;

2. transfecting HEK293 cells by the N protein recombinant expression plasmid;

3. recombinant expression of the N protein in HEK293 cells;

4. the recombinantly expressed N protein was harvested from the culture supernatant.

In the invention, a leader peptide is introduced into the N end of the N protein of the new coronavirus to help the N protein expressed by recombination to be successfully secreted into a culture supernatant, and the amino acid sequence of the leader peptide is shown as SEQ ID NO. 2.

In the invention, a section of poly His label is introduced into the C end of the N protein of the new coronavirus for separating and purifying the protein, and the amino acid sequence is shown as SEQ ID NO. 3.

The amino acid sequence containing the leader sequence, the novel coronavirus N protein and the poly His tag is shown as SEQ ID NO. 4, and the corresponding nucleotide sequence is shown as SEQ ID NO. 5.

The genes encoding the above amino acid sequences can be prepared by conventional synthetic methods.

The coding gene containing the leader peptide is constructed into a mammalian cell expression vector for guiding the secretory expression of the N protein.

The promoter of the expression vector may be EF-1 alpha (human electrophoresis factor-1 alpha) promoter, hCMV (human cytokine) promoter, SV40 (Simian vacuating virus 40) late promoter, or the like.

The following examples are intended to illustrate the invention but are not intended to limit the scope of the invention. Unless otherwise indicated, the examples follow conventional experimental conditions, such as the Molecular Cloning handbook, Sambrook et al (Sambrook J & Russell DW, Molecular Cloning: a Laboratory Manual, 2001), or the conditions as recommended by the manufacturer's instructions.

EXAMPLE 1 construction of recombinant expression vectors

Construction of recombinant pHEK-N1 expression vector: a polynucleotide (SEQ ID NO: 5) with an amino acid sequence shown as SEQ ID NO:4 is synthesized by Shanghai bioengineering company Limited, and a restriction enzyme BamH I restriction site and a Kozak sequence are added at the 5' end; the 3' end is added with a stop codon TAA and a restriction site of restriction enzyme XhoI. The synthesized product is subjected to double enzyme digestion by restriction enzymes BamH I and Xho I, then agarose gel electrophoresis is carried out, and the gel is cut to recover the target fragment. The target fragment was ligated to pcDNA3.1(+) (Invitrogen, cat # V790-20) (FIG. 1) which was similarly double-digested with restriction enzymes BamHI and XhoI, respectively, to construct a recombinant eukaryotic expression vector, which was named pHEK-N1. The recombinant plasmid construction is schematically shown in FIG. 2. Transforming Escherichia coli E.coli DH5 alpha by pHEK-N1, culturing at 37 deg.C for 16h, selecting single colony for plasmid extraction, double digesting the extracted plasmid with restriction enzymes BamH I and Xho I, performing agarose gel electrophoresis identification, sequencing the positive clone by Shanghai bioengineering Co., Ltd, selecting the clone with correct sequencing for plasmid amplification and extraction, sterile filtering the extracted plasmid, and storing at-20 deg.C for use.

Example 2 transfection of HEK293 cells with recombinant expression vectors and expression of novel coronavirus nucleocapsid proteins

And (3) transfecting HEK293 cells with the constructed recombinant plasmid pHEK-N1 by using a PEI transfection reagent to perform recombinant expression of the N protein of the new coronavirus. HEK293 cells were plated at 1X 10 on the day before transfection⁶passage/mL, culture at 37 ℃. The cells were counted on the day of transfection and adjusted to a cell density of 2X 10⁶The activity rate is more than 95 percent.

Calculating the dosage of each component in the transfection complex according to the cell density, wherein the corresponding relation between the plasmid dosage and the cell number is 1 × 10⁶cells corresponds to 1 ug of plasmid, and the corresponding relation between the PEI dose and the plasmid dose is that the mass of PEI is 3 times of that of DNA.

The transfection complexes were prepared according to the calculated amounts of the components: 50 ug of 200 ug/mL recombinant plasmid was added to CD 293 TGE medium to 0.5mL (solution A), 150 ug of 1mg/mL PEI transfection reagent was added to CD 293 TGE medium to 0.5mL (solution B), and after mixing, solution B was slowly added to solution A, after mixing and standing at room temperature for 10-15 min, the transfection mixture was slowly added dropwise to 10 mL HEK293 cells. 37 ℃ and 5% CO₂After culturing at 135rpm for 96 hours, the supernatant was collected. The cell culture medium used was CD 293 TGE medium (ACROYOSystems, cat # CM-1156-11).

Example 3 isolation and purification of the novel coronavirus nucleocapsid protein

Separating and purifying the recombinant protein by using a His-tag affinity chromatography column, which specifically comprises the following steps: the cell culture supernatants were collected by centrifugation at 1000g for 30min, the supernatants were filtered and combined with GE HisTrap excel columns equilibrated in advance with PBS buffer, and then gradient eluted sequentially with PBS buffer containing 0, 30, 100, 250 and 500mM imidazole at an elution volume of 10 CV per concentration, and protein eluates were collected and analyzed by SDS-PAGE (FIG. 3). According to SDS-PAGE results, the purity of N protein eluted under the conditions of 100mM, 250 mM and 500mM of imidazole is all higher than 95%, the partial protein is mixed and dialyzed, the molecular weight cut-off of a dialysis bag used is 30KDa, and the dialysis is carried out in a refrigerator at 4 ℃ overnight, and the used dialysate is: PBS buffer (pH7.4). And SDS-PAGE detection is carried out on the dialyzed sample, and SDS-PAGE results show that a purified protein band is positioned between 45 and 66KDa, the protein band accords with the theoretical molecular weight of the protein, the purity is up to more than 98 percent, and the expression level is up to 300mg/L (figure 4).

Example 4 comparison of binding Activity of N protein expressed by HEK293 cells and N protein expressed by E.coli with antibodies

In this example, the binding activity of the N protein expressed by HEK293 of the present invention and the N protein expressed by escherichia coli to an antibody was compared by ELISA (enzyme-linked immunosorbent assay).

1. Coating: a96-well plate (Corning, cat # 42592) was coated with 0.1. mu.g/well (1. mu.g/ml, 100. mu.l/well) of an antibody against the N protein of novel coronavirus (Anyuan Biotech Co., Ltd., cat # NP 031901), and then overnight (or 16 h) at 4 ℃. The coating buffer used for antibody dilution was 15 mM Na₂CO₃，35 mM NaHCO₃，7.7 mM NaN₃，pH9.6。

2. Washing: wells were washed 4 times with 300. mu.l of washing buffer (TBS, 0.05% Tween-20, pH7.4) per well. Note: thorough removal of the wash buffer is critical. After washing, the residual solution was removed by suction and complete drying was ensured;

3. and (3) sealing: each well was blocked with 300. mu.l of blocking buffer (TBS, 0.05% Tween-20, 2% BSA, pH 7.4) for 1.5 h at 37 ℃.

4. Washing: and (5) repeating the step (2).

5. Adding a sample: mu.l of 0.195313-200 ng/ml of the N protein prepared in example 3 or the N protein expressed by E.coli (ACRObiosystems, cat # NUN-C51H 9) was added to each well and incubated at 37 ℃ for 1H. The samples were diluted beforehand with dilution buffer (TBS, 0.05% Tween-20, 0.5% BSA, pH 7.4).

6. Washing: and (5) repeating the step (2).

7. Adding a detection antibody: mu.l of anti-His-tag antibody (HRP) (GeneTex, cat # GTX 628914-01) was added to each well and incubated at 37 ℃ for 1 h. The antibody was diluted beforehand with a dilution buffer (TBS, 0.05% Tween-20, 0.5% BSA, pH 7.4) at a ratio of 1: 20000;

8. washing: and (5) repeating the step (2).

9. Adding a substrate: to each well, 200. mu.l of substrate solution was added and incubated at 37 ℃ for 20 min. And (4) avoiding light. Preparing a substrate solution: in 10 ml of substrate solution (50 mM Na)₂HPO₄·12H₂O, 25 mM Citric acid, pH 5.5) 8. mu.l of 3% H₂O₂And 100. mu.l of 10 mg/ml TMB (BBI Life sciences, cat # A600954).

10. And (3) terminating the reaction: 50. mu.l of 1M sulfuric acid was added to each well.

11. Reading OD value: OD was read at 450 nm and then OD₄₅₀-OD_BlankThe final OD value was obtained. Wherein OD_BlankThe corresponding wells were blank as measured in step 5 without sample addition but with an equal volume of dilution buffer.

The detection results are shown in FIG. 5, and it can be seen that EC combined with antibody is the N protein expressed by E.coli₅₀EC with a value of 21.11ng/ml for binding of antibody to N protein expressed by HEK293 cells of the invention₅₀The value was 1.32ng/ml, indicating that the binding activity of the N protein expressed by HEK293 to antibodies against the N protein of the novel coronavirus was higher.

Example 5 colloidal gold assay of the nucleocapsid protein of the novel coronavirus

In this example, the sensitivity and positive detection rate of the new crown antibody colloidal gold were compared between the N protein expressed by the HEK293 cell of the present invention and the N protein expressed by escherichia coli.

Preparation of colloidal gold test strip

1. The colloidal gold test strip comprises the following components: the test strip consists of a sample pad, a gold label pad, an NC membrane, a water absorption pad and a PVC plate, and is consistent with the composition of a conventional colloidal gold detection card.

2. Sample pad pretreatment: using PBS buffer system, 0.5% bovine serum albumin, 0.2% Triton X-100 and 0.1% PC-300 were added, and after soaking the sample pad, it was dried overnight for use.

3. Pretreating a gold-labeled pad: in the embodiment, a gold spraying process is adopted to pretreat a gold label pad, a PB buffer solution system is selected in an experiment, 0.5% of bovine serum albumin, 0.2% of Triton X-100 and 0.1% of PC-300 are added, 0.5% of macromolecular skeleton protein PVA-124 is added, and after the pad is soaked, the pad is dried overnight for later use.

4. The preparation method of the gold labeled pad is as follows (labeling gold of the new coronavirus nucleocapsid protein): to each 1000. mu.l of the colloidal gold solution was added 16. mu.l of 0.2M K₂CO₃Adding 20 mu g of the N protein prepared in the example 3 into the solution, sealing and uniformly mixing the solution at room temperature for reacting for 30min, adding 100 mu l of 10% BSA, and sealing the reaction for reacting for 30 min; centrifuging at 4 ℃ and 10000rpm for 20min, removing the supernatant, collecting colloidal gold particle precipitate, and redissolving with 30 mul PB buffer solution to obtain a gold-labeled solution; then, the gold-labeled solution is uniformly sprayed on the gold-labeled pad according to the spraying amount of 2 mu L/cm, and the gold-labeled pad is dried in a vacuum drying oven for 4 hours under ventilation at 37 ℃.

Wherein the concentration of the colloidal gold solution is 0.01 percent, and the particle size of the colloidal gold particles is 40 nm.

PB buffer contained 0.5% BSA, 0.5% PEG20000, 2% trehalose and 0.2% Triton X-100.

5. The quality control line corresponds to the gold standard of mouse IgG: similar to the gold-labeled condition of the new coronavirus nucleocapsid protein, the difference is that 0.2M K is added₂CO₃The volume of the solution was varied, and 10. mu.l of 0.2M K was added to 1ml of 0.01% colloidal gold solution₂CO₃Solution, other conditions were consistent.

6. Spraying gold and drying: the gold-labeled solution after redissolution was sprayed on a gold-labeled pad with a gold spraying instrument of Shanghai gold-labeled Biotech Co., Ltd at a spraying amount of 2. mu.L/cm, and then dried in a vacuum oven at 37 ℃ for 4 hours under ventilation.

7. Film scribing and coating: detecting a T-shaped coil on an NC membrane to detect an anti-human secondary antibody (Changshaben-good biological technology Co., Ltd.), coating a quality control line with a goat anti-mouse secondary antibody, diluting the secondary antibody to a coating concentration of 1mg/mL by using a PB solution, scribing the membrane at a speed of 1 muL/cm, scribing the well membrane, and drying in a vacuum drying oven at 37 ℃ for 4 hours in a ventilation manner.

8. Assembling the test strip, aligning and sticking the test strip on a PVC plate correctly according to the sequence of the water absorption pad, the NC membrane, the gold label pad and the sample pad from top to bottom, cutting the test strip into the test strip with the width of 3mm by a cutting machine, embedding the test strip into a card shell, and pressing the shell to ensure sealing.

9. The method for preparing the colloidal gold test strip by using the N protein expressed by the escherichia coli is the same as the method.

(II) detection of New coronavirus antibody sample

The sample detected in this example is a serum sample of Xinguan patient, 10 μ L of the sample to be detected is added to each test strip, 70 μ L of the sample diluent is added, the reaction is carried out for 15min, the color reaction is observed, and the result is recorded, and the result is shown in fig. 6. The comparison result of the N protein colloidal gold test strip (A) expressed by escherichia coli and the N protein colloidal gold test strip (B) expressed by the HEK293 cell of the invention can find that the colloidal gold test strip prepared by the N protein expressed by the HEK293 cell of the invention is superior to the colloidal gold test strip prepared by the N protein expressed by escherichia coli in terms of detection rate and sensitivity.

Although the invention has been described in detail hereinabove with respect to a general description and specific embodiments thereof, it will be apparent to those skilled in the art that modifications or improvements may be made thereto based on the invention. Accordingly, such modifications and improvements are intended to be within the scope of the invention as claimed.

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Gln Leu Pro Gln Gly Thr Thr Leu Pro Lys Gly Phe Tyr Ala Glu Gly

180 185 190

Ser Arg Gly Gly Ser Gln Ala Ser Ser Arg Ser Ser Ser Arg Ser Arg

195 200 205

Asn Ser Ser Arg Asn Ser Thr Pro Gly Ser Ser Arg Gly Thr Ser Pro

210 215 220

Ala Arg Met Ala Gly Asn Gly Gly Asp Ala Ala Leu Ala Leu Leu Leu

225 230 235 240

Leu Asp Arg Leu Asn Gln Leu Glu Ser Lys Met Ser Gly Lys Gly Gln

245 250 255

Gln Gln Gln Gly Gln Thr Val Thr Lys Lys Ser Ala Ala Glu Ala Ser

260 265 270

Lys Lys Pro Arg Gln Lys Arg Thr Ala Thr Lys Ala Tyr Asn Val Thr

275 280 285

Gln Ala Phe Gly Arg Arg Gly Pro Glu Gln Thr Gln Gly Asn Phe Gly

290 295 300

Asp Gln Glu Leu Ile Arg Gln Gly Thr Asp Tyr Lys His Trp Pro Gln

305 310 315 320

Ile Ala Gln Phe Ala Pro Ser Ala Ser Ala Phe Phe Gly Met Ser Arg

325 330 335

Ile Gly Met Glu Val Thr Pro Ser Gly Thr Trp Leu Thr Tyr Thr Gly

340 345 350

Ala Ile Lys Leu Asp Asp Lys Asp Pro Asn Phe Lys Asp Gln Val Ile

355 360 365

Leu Leu Asn Lys His Ile Asp Ala Tyr Lys Thr Phe Pro Pro Thr Glu

370 375 380

Pro Lys Lys Asp Lys Lys Lys Lys Ala Asp Glu Thr Gln Ala Leu Pro

385 390 395 400

Gln Arg Gln Lys Lys Gln Gln Thr Val Thr Leu Leu Pro Ala Ala Asp

405 410 415

Leu Asp Asp Phe Ser Lys Gln Leu Gln Gln Ser Met Ser Ser Ala Asp

420 425 430

Ser Thr Gln Ala Gly Ser His His His His His His

435 440

<210> 5

<211> 1332

<212> DNA

<213> Artificial Sequence (Artificial Sequence)

<400> 5

atgagcgccc tgctgatcct ggccctggtg ggcgccgccg tggtgtgggc catgagcgac 60

aatggaccac agaatcagag aaacgctcct cgaatcactt ttgggggtcc cagtgattca 120

accggctcaa accagaatgg ggaaagatca ggcgctagaa gcaagcagcg ccgcccccaa 180

ggactcccca acaataccgc cagttggttc accgctttga ctcagcacgg caaggaagat 240

ttgaaatttc ccagaggcca gggggtaccc atcaatacca attcttctcc tgacgatcaa 300

atcgggtatt atagaagagc cacacggcgc atccgagggg gggacgggaa aatgaaagac 360

ctgtctccac ggtggtattt ctattatttg ggaactggac ccgaggctgg tcttccttac 420

ggtgccaata aagacggcat tatctgggtg gccacagagg gggccttgaa tacaccgaag 480

gaccatatcg gtaccagaaa ccccgctaat aacgcggcca tcgtcctgca actgccccag 540

ggcaccacac tgcctaaggg cttttacgcc gagggctctc ggggcggctc acaggctagc 600

agtaggagta gctcacggtc aagaaacagt tccaggaact caactcccgg gagttcccgg 660

ggcacctcac cagcccggat ggccggaaac gggggcgacg ctgctctcgc gctgctgctc 720

cttgatcggc tcaatcagct ggaatcaaag atgtcaggga aaggacagca gcagcagggc 780

cagactgtca cgaagaaaag tgcagcagaa gcctccaaaa aacctagaca gaaaagaaca 840

gctacaaagg cctataatgt cactcaggcg ttcggacgac gagggcccga gcaaactcag 900

ggaaatttcg gcgaccagga gctcatcaga caaggcaccg actacaagca ttggcctcag 960

attgcccaat tcgctccttc tgcgtccgct tttttcggaa tgtcaagaat cggcatggag 1020

gttactccga gcggaacctg gctgacttac accggggcaa tcaaactgga tgacaaagac 1080

ccaaacttta aggatcaggt catcttgctg aataagcaca tcgatgcata caagaccttc 1140

ccccctacag aacccaagaa agacaaaaaa aagaaggcag atgagacaca agcactgccc 1200

cagagacaga aaaaacaaca aactgtcact ctgctcccag ccgcagatct ggacgacttc 1260

tccaagcagc tccagcagag catgtcttct gctgacagta ctcaggcggg ctcacaccac 1320

caccaccacc ac 1332