SARS-COV-2 RECOMBINANT N PROTEIN, AND PREPARATION METHOD AND PURIFICATION METHOD THEREFOR

Abstract

Provided are a recombinant N protein of SARS-CoV-2 and methods for preparing the same and for purifying the same. The recombinant N protein of SARS-CoV-2 has an N protein sequence, wherein each of both ends of the N protein sequence are linked to an oligolysine fragment. An expression method for the recombinant N protein includes: a. providing a sample including the recombinant N protein; and b. performing cation exchange chromatography resin purification treatment at least once, and collecting breakthrough substance. The method may effectively improve the expression purity of the recombinant N protein.

Claims

1. A recombinant N protein of SARS-CoV-2 having an N protein sequence as set forth in SEQ ID NO: 1, wherein each of both ends of the N protein sequence are respectively linked to an oligolysine fragment.

2. The recombinant N protein according to claim 1, wherein the oligolysine fragment at the both ends of the N protein sequence independently comprises 4 to 6 lysines.

3. A nucleic acid capable of expressing the recombinant N protein of claim 1.

4. A vector comprising the nucleic acid of claim 3.

5. A host cell incorporating the nucleic acid of claim 3 in genome thereof.

6. A method for preparing an N protein of SARS-CoV-2 comprising: culturing the host cell of claim 5 under a suitable condition, and collecting a lysate of the host cell and/or culture solution.

7. A method for purifying an N protein of SARS-CoV-2 comprising: step a) providing a sample comprising the recombinant N protein of claim 1; and step b) performing cation exchange chromatography resin purification treatment at least once, and collecting breakthrough substance.

8. The method according to claim 7, wherein the method further comprises, after step b), performing at least one anion exchange chromatography resin purification treatment on the obtained product at least once, and collecting breakthrough substance.

9. A composition obtained by purification by the method of claim 7.

10. A reagent or kit for detecting an antibody against N protein of SARS-CoV-2, comprising the recombinant N protein of claim 1.

11. The recombinant N protein according to claim 1, wherein the N protein sequence is linked to the oligolysine fragment via a linker peptide.

12. The recombinant N protein according to claim 11, wherein the linker peptide is a flexible linker peptide.

13. The recombinant N protein according to claim 11, wherein the linker peptide has an amino acid sequence having one or more amino acids selected from the group consisting of Gly, Ser, Pro, Ala, and Glu.

14. The recombinant N protein according to claim 11, wherein the sequence of the linker peptide is GSGS.

15. The nucleic acid according to claim 3, wherein the nucleic acid has a sequence as set forth in SEQ ID NO:2.

16. The method according to claim 7, wherein the cation exchange chromatography resin is SP Sepharose FF.

17. The method according to claim 7, wherein the breakthrough substance in step b) is a target protein fraction with a purity of 90%, and step b) further comprises subjecting the breakthrough substance to dialysis treatment at least once.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0016] To describe the technical solutions of the embodiments of the present disclosure or the prior art more clearly, the following briefly introduces the accompanying drawings required for describing the embodiments or the prior art. Apparently, the accompanying drawings in the following description show some embodiments of the present disclosure, and persons of ordinary skill in the art may also derive other drawings from these accompanying drawings without creative efforts.

[0017] FIG. 1 shows an electrophoresis diagram of purified N protein (from 2 μg to 10 μg) at different loading amounts in one embodiment of the present disclosure.

DETAILED DESCRIPTION OF THE EMBODIMENTS

[0018] Reference will now be provided in detail to the embodiments of the present disclosure, one or more examples of which are described below. Each example is provided by way of illustration rather than limitation to the present disclosure. In fact, it will be apparent to those skilled in the art that various modifications and variations can be made to the present disclosure without departing from the scope or spirit of the present disclosure. For example, features illustrated or described as part of one embodiment can be used in another embodiment to produce a further embodiment.

[0019] Such modifications and changes falling within the scope of the appended claims and the scope of equivalency of the claims are therefore intended to be embraced in the present disclosure. Other objects, features and aspects of the present disclosure are disclosed in or are apparent from the following detailed description. It should be understood by those of ordinary skill in the art that the present discussion is a description of exemplary embodiments only, and is not intended to limit the broader aspects of the present disclosure.

[0020] The present disclosure relates to a recombinant N protein of SARS-CoV-2 having an N protein sequence as set forth in SEQ ID NO: 1, wherein each of both ends of the N protein sequence are linked to an oligolysine fragment.

[0021] In some embodiments, the oligolysine fragments at the both ends of the N protein sequence independently comprise 4 to 6 lysines, and preferably 5 lysines.

[0022] In some embodiments, the N protein sequence is linked to the oligolysine fragment via a linker peptide.

[0023] In some embodiments, the linker peptide is a flexible linker peptide.

[0024] In some embodiments, the linker peptide has an amino acid sequence having one or more amino acids selected from the group consisting of Gly, Ser, Pro, Ala and Glu, preferably Gly and Ser.

[0025] In some embodiments, the linker peptide has 1 to 30 amino acids, and may have 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29 or 30 amino acids, preferably 3 to 5 amino acids, and more preferably 4 amino acids.

[0026] In some embodiments, the sequence of the linker peptide is GSGS.

[0027] The present disclosure also provides a nucleic acid capable of expressing the recombinant N protein as described above.

[0028] In some embodiments, the nucleic acid has a sequence as set forth in SEQ ID NO:2.

[0029] The present disclosure also provides a vector comprising the nucleic acid as described above.

[0030] The term “vector” refers to a nucleic acid carrier into which polynucleotides may be inserted. When a vector enables the expression of a protein encoded by a polynucleotide inserted therein, the vector is called an expression vector. The vector may be introduced into a host cell through transformation, transduction or transfection, so that the genetic material element it carries is expressed in the host cell. Vectors are well known to those skilled in the art, including but not limited to: plasmids; phagemids; cosmids; artificial chromosomes, such as yeast artificial chromosomes (YACs), bacterial artificial chromosomes (BACs) or P1 derived artificial chromosomes (PACs); bacteriophages, such as λ bacteriophage or M13 bacteriophage and animal viruses, etc. The animal viruses that may be used as vectors include, but are not limited to: retroviruses (including lentiviruses), adenoviruses, adeno-associated viruses, herpes viruses (such as herpes simplex virus), poxviruses, baculoviruses, papillomaviruses, and papovaviruses (such as SV40). In some embodiments, the vector described in the present disclosure comprises regulatory elements, such as enhancers, promoters, internal ribosome entry sites (IRES), and other expression control elements (such as transcription termination signals, or polyadenylation signal and poly (U) sequence, etc.) commonly used in genetic engineering. In a specific embodiment, the vector is pET-28a(+).

[0031] The present disclosure also provides a host cell incorporating the nucleic acid as described above in genome thereof

[0032] The term “host cell” refers to cells into which a vector can be introduced, including, but not limited to, prokaryotic cells, such as Escherichia coli (E.coli) or Bacterium subtilis, etc.; insect cells, such as S2 drosophila cells or Sf9, etc; or animal cells, such as fibroblasts, CHO cells, COS cells, NSO cells, HeLa cells, BHK cells, HEK 293 cells or human cells, etc. The host cell is preferably a prokaryotic cell, more preferably E. coli.

[0033] The present disclosure also relates to a method for preparing an N protein of SARS-CoV-2 including:

[0034] culturing the host cell as described above under a suitable condition, and collecting a lysate of the host cell and/or culture solution.

[0035] According to another aspect of the present disclosure, the present disclosure also relates to a method for purifying the N protein of SARS-CoV-2 including:

[0036] step a) providing a sample comprising the recombinant N protein as described above; and

[0037] step b) performing cation exchange chromatography resin purification treatment at least once, and collecting breakthrough substance.

[0038] In the present disclosure, the term “treatment” may describe a process in which a sample flows through or passes through a chromatography column, resin, membrane, filter, or other mechanisms, and shall include the continuous flow through each mechanism and the flow paused or stopped in each mechanism.

[0039] In one embodiment of the disclosure, a sample containing the recombinant N protein is provided. Any sample containing the recombinant N protein may be used in the present disclosure. A sample comprising the recombinant N protein may include, for example, cell culture (especially cell culture supernatant). As an example, the recombinant N protein may be expressed in E. coli.

[0040] Any cation exchange chromatography systems available to those skilled in the art that satisfy the purification conditions of recombinant N protein of SARS-CoV-2 may be used in this embodiment, for example, the matrix used for cation exchange chromatography may contain sulfonic groups, quaternary amine groups, and may also contain imidazolyl, pyridyl, quinolinyl, piperidinyl and other groups, the preferred group is sulfopropyl (SP); the preferred cation exchange chromatography resin is SP Sepharose FF; the cation exchange chromatography resin may have a pore size selected from 500 A to 100 A and a particle size selected from 15 μm, 30 μm, 60 μm, 80 μm, etc.

[0041] The salt of the mobile phase in the cation exchange chromatography separation may be hydrogen phosphate (especially Na.sub.2HPO.sub.4) and NaCl, etc.

[0042] In some embodiments, the cation exchange column is first equilibrated with a buffer of about 30 mM to 70 mM Na.sub.2HPO.sub.4, pH 7.1-7.7 and unbound protein is washed away.

[0043] In some embodiments, the target protein is first eluted with a linear gradient of about 30 mM to 70 mM Na.sub.2HPO.sub.4,0 mM to 600 mM NaCl, pH 7.1 to 7.7.

[0044] In some embodiments, NaCl in the equilibration and loading buffer used for the hydrophobic chromatographic separation is at a concentration of 500 mM to 2000 mM, for example, 500 mM, 600 mM, 700 mM, 800 mM, 900 mM, 1000 mM, 1100 mM, 1200 mM, 1300 mM, 1400 mM, 1500 mM, 1600 mM, 1700 mM, 1800 mM, 1900 mM, 2000 mM, or within a range between any two values.

[0045] Commonly used buffers for mobile phase in hydrophobic chromatography separation are PB/PBS, Tris-HC1, HEPES, acetate buffer, etc. In some embodiments, PB/PBS in the equilibration and loading buffer used for the hydrophobic chromatographic separation is at a concentration of≥20 mM, e.g., 30 mM, 40 mM, 50 mM, and the buffer is at a pH of 7.0˜9.0.

[0046] PB: Phosphate Buffer; PBS:Phosphate Buffered Saline.

[0047] In some embodiments, the breakthrough substance in step b) is a target protein fraction with a purity of 90%, and step b) further includes subjecting the breakthrough substance to dialysis treatment at least once.

[0048] In some embodiments, the method further includes, after step b), performing anion exchange chromatography resin purification treatment on the obtained product at least once, and collecting breakthrough substance.

[0049] In some embodiments, the present disclosure includes one or more steps of clarification (which is also called collecting sediment/supernatant), and the method for clarification may be carried out by one or more steps of processes such as centrifugation, microfiltration, ultrafiltration or depth filtration; the clarification may be performed, for example, after anyone of the above-mentioned steps has been completed, for example, before and after the collection of the breakthrough substance.

[0050] The present disclosure further provides a composition obtained by purification by the method as described above.

[0051] The purity of the recombinant N protein in the composition is about 80% to 97%, preferably not less than 95%.

[0052] According to yet another aspect of the present disclosure, the present disclosure also relates to a reagent or kit for detecting an antibody against N protein of SARS-CoV-2, comprising the recombinant N protein as described above or the composition as described above.

[0053] The antibody against N protein of SARS-CoV-2 is preferably derived from humans, and may also be derived from other potential hosts containing SARS-CoV-2, such as bats, pangolins, paguma larvatas, or other mammals.

[0054] The type of the antibody may be selected from IgM, IgE, IgA, IgD, or IgG.

[0055] The embodiments of the present disclosure will be described in detail below in combination with examples.

Example

[0056] This example provides methods for preparing and for purifying a recombinant N protein of SARS-CoV-2.

[0057] The following substances were selected: a nucleocapsid protein (N protein) having the following amino acid sequence:

TABLE-US-00001 (SEQ ID NO: 1) MSDNGPQNQRNAPRITFGGPSDSTGSNQNGERSGARSKQRRPQGLPNNTA SWFTALTQHGKEDLKFPRGQGVPINTNSSPDDQIGYYRRATRRIRGGDGK MKDLSPRWYFYYLGTGPEAGLPYGANKDGIIWVATEGALNTPKDHIGTRN PANNAAIVLQLPQGTTLPKGFYAEGSRGGSQASSRSSSRSRNSSRNSTPG SSRGTSPARMAGNGGDAALALLLLDRLNQLESKMSGKGQQQQGQTVTKKS AAEASKKPRQKRTATKAYNVTQAFGRRGPEQTQGNFGDQELIRQGTDYKH WPQIAQFAPSASAFFGMSRIGMEVTPSGTWLTYTAAIKLDDKDPNFKDQV ILLNKHIDAYKTFPPTEPKKDKKKKADETQALPQRQKKQQTVTLLPAADL DDFSKQLQQSMSSADSTQA;
and an oligolysine sequence having an amino acid sequence of RRRRR, and an linker peptide having an amino acid sequence of GSGS. An oligolysine sequence, an N protein and an oligolysine sequence were linked via the linker peptide, fusing into the recombinant N protein, which is encoded by the following DNA sequence:

TABLE-US-00002 (SEQ ID NO: 2) ATGCGTCGCAGACGTCGAGGATCTGGCTCGATGAGTGATAACGGCCCGCA GAATCAGCGCAATGCCCCGCGCATTACCTTTGGTGGCCCGAGTGATAGTA CCGGTAGTAATCAGAATGGTGAACGCAGCGGCGCCCGCAGTAAACAGCGT CGTCCGCAGGGTCTGCCGAATAATACCGCAAGCTGGTTTACCGCCCTGAC CCAGCATGGCAAAGAAGATCTGAAATTTCCGCGCGGTCAGGGTGTTCCGA TTAATACCAATAGCAGTCCGGATGATCAGATTGGTTATTATCGTCGTGCC ACCCGTCGTATTCGCGGCGGCGATGGTAAAATGAAAGATCTGAGTCCGCG TTGGTATTTTTATTATCTGGGCACCGGTCCGGAAGCAGGCCTGCCTTATG GTGCCAATAAGGATGGCATTATTTGGGTGGCAACCGAAGGCGCCCTGAAT ACCCCGAAAGATCATATTGGTACCCGTAATCCGGCCAATAATGCAGCAAT TGTGCTGCAGCTGCCGCAGGGCACCACCCTGCCTAAAGGCTTTTATGCAG AAGGTAGTCGCGGTGGCAGCCAGGCAAGCAGCCGTAGTAGTAGCCGCAGT CGTAATAGCAGTCGCAATAGCACCCCGGGTAGCAGTCGTGGTACCAGCCC GGCACGCATGGCAGGCAATGGTGGTGACGCCGCACTGGCACTGCTGCTGC TGGATCGTCTGAATCAGCTGGAAAGCAAAATGAGTGGCAAAGGTCAGCAG CAGCAGGGCCAGACCGTGACCAAAAAATCTGCCGCAGAAGCCAGCAAAAA ACCGCGTCAGAAACGTACCGCCACCAAAGCCTATAATGTGACCCAGGCAT TTGGCCGTCGCGGCCCGGAACAGACCCAGGGTAATTTTGGTGACCAGGAA CTGATTCGCCAGGGCACCGATTATAAACATTGGCCGCAGATTGCACAGTT TGCACCGAGTGCCAGTGCCTTTTTCGGCATGAGCCGCATTGGCATGGAAG TTACCCCGAGTGGTACCTGGCTGACCTATACCGGTGCCATTAAGCTGGAT GATAAAGATCCGAATTTTAAAGATCAGGTTATTCTGCTGAACAAACATAT TGATGCCTATAAAACCTTCCCGCCGACCGAACCGAAAAAAGATAAAAAGA AAAAGGCAGATGAGACCCAGGCACTGCCGCAGCGCCAGAAAAAACAGCAG ACCGTGACACTGCTGCCGGCAGCAGATCTGGATGATTTTAGTAAACAGCT GCAGCAGAGCATGAGTAGCGCCGATAGTACCCAGGCCGGATCTGGCTCGC GTCGCAGACGTCGATAA.

[0058] The DNA encoding the recombinant N protein was obtained by gene synthesis (General Biosystems (Anhui) Co., Ltd.). The DNA encoding the recombinant N protein had a NcoI site upstream and a HindIII site downstream. The DNA was digested with the corresponding restriction endonucleases and ligated into an expression vector pET-28a(+) digested with NcoI and HindIII to obtain a recombinant plasmid pET-28a(+)-N.

[0059] The recombinant plasmid was transformed into E. coli expression strain BL21(DE3), and a single clone was picked, inoculated into 100 mL of LB medium containing 50 μg/mL kanamycin, and cultured overnight at 200 rpm at 37° C. The next day, 1% volume of the overnight culture was pipetted into 1 L of fresh LB medium containing 50 μg/mL kanamycin, and cultured at 200 rpm at 37° C. until OD.sub.600 reached about 0.6, then induced with IPTG (isopropyl thiogalactoside) at a final concentration of 1 mM for 20 h at 18° C. for expression. The bacteria cells were collected by centrifugation at 12,000 g for 3 min at 4° C., and the bacteria cells in one liter of bacterial solution were suspended with 40 mL buffer (Buffer A, 50 mM Na.sub.2HPO.sub.4, pH 7.4) pre-cooled on ice. After adding a small amount of RNase, the mixture was crushed by a high-pressure homogenizer, centrifuged at 12,000 g for 30 min at 4° C. The supernatant was filtered through a 0.22 μm filter membrane and passed through a cation exchange column.

[0060] The cation exchange column was equilibrated with 10 column volumes of buffer A, then the supernatant was added, and unbound protein was washed away with at least 10 column volumes of buffer A. A buffer (Buffer B, 50 mM Na.sub.2HPO.sub.4/500 mM NaCl, pH 7.4) was prepared, and the target protein was eluted with 20 column volumes of a linear gradient of the buffer containing 0 mM to 500 mM NaCl. The target protein fractions with a purity of 90% were selected and pooled, and fully dialyzed in a buffer (Buffer C, 10 mM Tris 7.5) at 4° C. In order to further remove impurities, the dialyzed N protein was loaded onto an anion exchange column pre-equilibrated with Buffer C, and the breakthrough fluid was collected and fully dialyzed in a PBS buffer. The N protein was concentrated by ultrafiltration before stored at −20° C. for later use.

[0061] The purity of the target protein obtained through the above purification steps may reach 95% or more. SDS-PAGE shows no undesired bands can be seen in lanes loaded with various loading amounts (from 2 μg to 10 82 g). The results are shown in FIG. 1.

[0062] The respective technical features of the above-mentioned embodiments can be combined arbitrarily. For the sake of brevity, not all the possible combinations of each of the technical features in the above embodiments are described. However, all of the combinations of these technical features should be considered as within the scope of this disclosure, as long as such combinations do not contradict with each other.

[0063] The above-mentioned embodiments are merely illustrative of several embodiments of the present disclosure, which are described specifically and in detail, but should not to be construed as limiting the scope of the present disclosure. It should be noted that, for those ordinary skilled in the art, several variations and improvements may be made without departing from the concept of the present disclosure, and all of which are within the protection scope of the present disclosure. Therefore, the protection scope of the present disclosure shall be defined by the appended claims.