CHIMERIC GAS VESICLE AND PROTEIN EXPRESSION SYSTEM THEREFOR

Abstract

The present disclosure features the chimeric gas vesicle (CGV) and its expression in E. coli. The chimeric gas vesicle comprises two or more gas vesicle rib proteins. The heterologous peptides, 6-AA to 56-AA long, can be inserted into one recombinant rib protein in frame. The resulting CGV carrying the heterologous peptide can be used in many applications.

Claims

1. A chimeric gas vesicle (CGV) comprising at least two Gyp rib proteins, wherein the rib protein is selected from a group consisting of a major rib protein and a minor rib protein, and wherein the major rib protein differentiates from the minor rib protein in that the major rib protein is capable of forming a gas vesicle independently.

2. The chimeric gas vesicle as claimed in claim 1, wherein any one of the Gyp rib proteins is derived from P. megaterium.

3. The chimeric gas vesicle as claimed in claim 2, wherein the minor rib protein comprises a core sequence and a heterologous peptide inserted in frame at C-terminus or N-terminus of the core sequence.

4. The chimeric gas vesicle as claimed in claim 3, wherein the core sequence comprises a GvpA core sequence.

5. The chimeric gas vesicle as claimed in claim 3, wherein the core sequence comprises 9.sup.th to 61.sup.st amino acid of a GvpA protein derived from P. megaterium.

6. The chimeric gas vesicle as claimed in claim 3, wherein the heterologous peptide is at least 6 amino acids long.

7. The chimeric gas vesicle as claimed in claim 4, wherein the heterologous peptide is derived from a native peptide sequence selected from a group consisting of, a ligand, a hormone, a cytokine, a receptor, a paratope of antibody, a toxic protein and a fluorescent protein, or a human designed peptide sequence.

8. The chimeric gas vesicle as claimed in claim 1, wherein the CGV is expressed in and purified from E. coli.

9. The chimeric gas vesicle as claimed in claim 1, wherein the CGV is assembled with assistance of at least one assembly protein.

10. The chimeric gas vesicle as claimed in claim 9, wherein the assembly protein comprises a GvpP protein, a GvpQ protein or a combination thereof.

11. The chimeric gas vesicle as claimed in claim 1, wherein the major rib protein and the minor rib protein form at least 90% of the chimeric gas vesicle by dry weight.

12. A protein expression system for expressing the CGV as claimed in claim 1, comprising: a first polynucleotide fragment encoding one of the Gyp rib proteins; and a second polynucleotide fragment encoding the other one of the Gyp rib proteins.

13. The protein expression system as claimed in claim 12, wherein the second polynucleotide fragment comprises: a core polynucleotide fragment encoding a core sequence; and a heterologous polynucleotide fragment encoding a heterologous peptide.

14. The protein expression system as claimed in claim 13, wherein the core sequence comprises a GvpA core sequence.

15. The protein expression system as claimed in claim 13, wherein the core sequence comprises 9.sup.th to 61st amino acid of a GvpA protein derived from P. megaterium.

16. The protein expression system as claimed in claim 13, wherein the heterologous peptide is at least 6 amino acids long.

17. The protein expression system as claimed in claim 13, wherein the heterologous peptide is derived from a native peptide sequence selected from a group consisting of a ligand, a hormone, a cytokine, a receptor, a paratope of antibody, a toxic protein and a fluorescent protein, or a human designed peptide sequence.

18. The protein expression system as claimed in claim 13, further comprising an assembly polynucleotide fragment encoding an assembly protein.

19. The protein expression system as claimed in claim 13, wherein the CGV is expressed in and purified from E. coli.

20. A chimeric gas vesicle (CGV) expressed in and purified from E. colicomprising at least two Gyp rib proteins, wherein the rib protein is selected from a group consisting of a major rib protein and a minor rib protein, wherein the major rib protein differentiates from the minor rib protein in that the major rib protein is capable of forming a gas vesicle independently, and wherein one of the rib proteins having a core sequence with a heterologous peptide inserted in frame at C-terminus or N-terminus of the core sequence.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0025] FIG. 1 is a cartoon graph to illustrate native gas vesicle as previously discovered.

[0026] FIG. 2 is a cartoon graph to illustrate chimeric gas vesicle (CGV) with two or more different kinds of gas vesicle rib proteins in the present invention.

[0027] FIG. 3 is a cartoon graph to illustrate CGVs with heterologous peptides.

[0028] FIG. 4a shows alignment of gas vesicle rib proteins.

[0029] FIG. 4b shows alignment of recombinant minor rib protein with heterologous peptide.

[0030] FIGS. 5 to 6 demonstrate genetic manipulation of gyp operons for CGV.

[0031] FIG. 7 demonstrates Western Dot Blot for confirmation of CGVs carrying various heterologous.

[0032] FIG. 8a is an electron microscopic graph of negative stained gas vesicles and the scale bar is equivalent to 200 nm.

[0033] FIG. 8b is an electron microscopic graph of negative stained chimeric gas vesicles and the scale bar is equivalent to 200 nm.

[0034] FIG. 9 is a flowchart illustrating a method for producing a chimeric gas vesicle (CGV).

[0035] FIG. 10 is a flowchart illustrating a method for eliciting immune response by administrating CGV-Covid-19 to a subject in need.

DETAILED DESCRIPTION OF THE INVENTION

[0036] In the gas vesicle research field, as shown in FIG. 1, it is widely believed that only one protein, GvpA, forms the rib of the gas vesicle. In other words, in a given gas vesicle, there is only one kind of rib protein GvpA, such as from cyanobacteria, halobacteria and soil bacteria, or its homolog GvpB from P. megaterium, to be found.

[0037] In one aspect, the present invention provides a chimeric gas vesicle comprising at least two Gyp rib proteins, wherein the rib protein is selected from a group consisting of a major rib protein and a minor rib protein, and wherein the major rib protein differentiates from the minor rib protein in that the major rib protein is capable of forming a gas vesicle independently. Preferably, as shown in FIGS. 2 and 3, there is less than 95% homology between the major rib protein and the minor rib protein, and the Gyp rib protein is derived from P. megaterium.

[0038] In exemplary embodiments, the at least two Gyp rib protein can be two major rib proteins, two minor rib proteins or a combination of one major rib protein and one minor rib protein. Preferably, the minor rib protein forms a complete CGV when the major rib protein is present, and under such circumstances the CGV is more stabilized.

[0039] In various embodiments, the major rib protein and the minor rib protein constitute at least 90% of the chimeric gas vesicle by dry weight.

[0040] In one or various embodiments, the minor rib protein comprises a core sequence and a heterologous peptide inserted in frame at C-terminus or N-terminus of the core sequence, wherein the core sequence is characterized by a protein structure comprising a first alpha helix, a first beta sheet at C-terminus of the first alpha helix; a second beta sheet at C-terminus of the first beta sheet; and a second alpha helix at C-terminus of the second beta sheet.

[0041] In preferred embodiments, the core sequence is selected from a group consisting of a GvpA core sequence and a GvpB core sequence.

[0042] In various embodiments, wherein the first alpha helix comprises an amino acid sequence of SSSLAEVIDRILD or SSGLAEVLDRVLD, the first beta sheet comprises an amino acid sequence of KGIVIDAFARVSL, KGIVIDAFARVSV, KGIVIDAWVRVSL, KGVVVDVWARISL or KGVVVDVWARVSL, the second beta sheet comprises an amino acid sequence of VGIEILTIEARVVI, VGIELLAIEARIVI or VGIEILTVEARVVA, and the second alpha helix comprises an amino acid sequence of ASVDTWLRYAEXZ, ASVETYLKYAEXZ or ASVDTFLHYAEXZ. Preferably, the X residue is Ala or Glu, and the Z residue is Val or Ile.

[0043] To be specific, the core sequence is a hydrophobic region of GvpA protein or GvpB protein. As illustrated in FIG. 4a, the core sequence is a tertiary protein structure consisting of 4 secondary protein structures arranged in a sequential manner: α-helix, β-sheet, β-sheet, α-helix. The GvpA protein or the GvpB protein is derived from cyanobacteria, halobacteria or soil bacteria. Preferably, the soil bacteria is Priestia Megaterium; the halobacteria is Halobacterium salinarum; the cyanobacteria is Anabaena flos-aquae.

[0044] In preferred embodiments, the GvpA protein has an amino acid sequence of SEQ ID NO.: 1, and the GvpB protein has an amino acid sequence of SEQ ID NO.: 2.

[0045] More specifically, the core sequence comprises 9 .sup.th amino acid (Serine) to the 61.sup.st amino acid (Valine) of a GvpA protein or a GvpB protein from P. megaterium but not limited by this. In addition, all gas vesicle rib proteins carry the core sequence. Moreover, any homologs of GvpA protein or GvpB protein from cyanobacteria, halobacteria or soil bacteria, or any protein sequence homologous to the core sequence, can be genetically modified and play the role as the minor rib protein.

[0046] It should be noted that the secondary structures as mentioned above are predicted by Jpred 4, an online protein secondary structure prediction program. In FIG. 4a, regions forming a-helix are underlined and labelled as H, while regions forming β-sheet are labelled as S.

[0047] Illustrated in FIG. 4b is alignment of the minor rib protein with heterologous peptide, implying a schematic design of the minor rib protein, wherein the heterologous peptide is inserted at C-terminus of the core sequence.

[0048] In other embodiments, the heterologous peptide is at least 6 amino acid long, and the heterologous peptide is derived from a human designed peptide sequence, a ligand, a hormone, a cytokine, a receptor, a paratope of antibody, a toxic protein, or a fluorescent protein.

[0049] In preferred embodiments, the major rib protein is a GvpB protein, and the minor rib protein is a core sequence with a heterologous peptide, wherein the heterologous peptide has at least 6 amino acids and is inserted in frame at C-terminus or at N-terminus of the core sequence.

[0050] Preferably, the core sequence comprises a truncated rib protein keeping the 1st amino acid (Methionine) to the 61″ amino acid (Valine) of GvpA protein or GvpB protein from P. megaterium.

[0051] Exemplarily, the heterologous peptide of 6 to 56 amino acids or longer can be inserted at C-terminus of the core sequence, and the core sequence is a truncated form of the Gyp rib protein. The truncated Gyp rib protein and the heterologous peptide together forms the minor rib protein which carries a foreign peptide and results in a variety of applications in the biotech field. However, longer heterologous peptide leads to less stability of CGV and reduces the yield of CGV production.

[0052] In some embodiments, the heterologous peptide can be derived from two or more heterologous proteins as well. For example, 20-AA from protein A and 25-AA from protein B form a 45-AA heterologous peptide for the insertion to form the minor rib protein. Preferably, the heterologous peptides are derived from the protein sequence of pathogens, variable regions of antibodies, hormones, cytokines and ligands.

[0053] In various embodiments, the CGV is expressed in and purified from E. coli.

[0054] In one or various embodiments, the chimeric gas vesicle further comprises an assembly protein, and the assembly protein comprises a GvpP protein, a GvpQ protein or a combination thereof. The assembly protein is derived from P. megaterium. These proteins promote or accelerate or stabilize the formation of the CGV. The minor rib proteins are more evenly distributed on the CGV's surface with the presence of GvpP and GvpQ proteins. CGVs formed with the assistance of GvpP and GvpQ are more stable than CGVs without the assistance of GvpP and GvpQ.

[0055] In one particular embodiment, the GvpP protein has an amino acid sequence of SEQ ID NO.: 3, and the GvpQ protein has an amino acid sequence of SEQ ID NO.: 4.

[0056] In preferred embodiments, the CGV further comprises at least one accessory protein selected from a group consisting of a GvpR, a GvpN, a GvpF, a GvpG, a GvpL, a GvpS, a GvpK, a GvpJ, a GvpT and a GvpU.

[0057] By “chimeric gas vesicles (CGVs)” it means the gas vesicles which constitute with at least two kinds of Gyp rib proteins with different protein sequences. That is in contrast to all the gas vesicles described in previous publications which involve only one major rib protein, GvpA.

[0058] By “rib protein” it means the gas vesicle protein which forms the “rib” of GV and CGV. Once a gas vesicle forms, the rib protein can't be removed from a gas vesicle without the destruction of the gas vesicle. The gas vesicle rib protein(s) form ˜4.6-nm ‘ribs’ that stack in array and run nearly perpendicular to the long axis of the gas vesicle and constitute the majority (97%) of the gas vesicle wall. The wall is 2-nm thick and consists of a single layer of the rib protein (FIG. 1). All gas vesicle rib protein has a hydrophobic tertiary structure including 4 secondary structures: α-helix, β-sheet, β-sheet and α-helix. The protein sequence of the tertiary structure is defined as “core sequence” (FIG. 4a, 4b).

[0059] By “major rib protein” it means the GvpA protein in cyanobacteria, halobacteria, and soil bacteria, and GvpB in P. megaterium, or any Gyp proteins homologous to and functionally equivalent to the GvpA protein, which forms the rib of the gas vesicle. The gas vesicle major rib protein is a rib protein with the “core sequence”. Combining with a trace amount of Gyp accessory structure proteins (GvpF, GvpG, GvpJ, GvpK, GvpL, GvpS), it forms complete gas vesicles. It is sufficient to form gas vesicles without the involvement of other rib proteins. Once GV forms, the major rib protein cannot be removed from GV without GV destruction. The gas vesicle major rib protein constitutes 20 to 99.9% of total protein in the GV. It has been referred to as the major structure protein, the major constituent protein, the rib protein, etc.

[0060] By “minor rib protein” it means a rib protein with the “core sequence”. It forms a complete gas vesicle only when another kind of rib protein is present. Most of the time the other kind of rib protein is a gas vesicle major rib protein, but it could be another gas vesicle minor rib protein with a different protein sequence. Once CGV forms, the minor rib protein cannot be removed from CGV without CGV destruction. The gas vesicle minor rib protein constitutes 3 to 80% of total protein in the CGV.

[0061] The native rib protein is a gas vesicle rib protein, GvpA or its homolog, found in nature. The truncated rib protein is a native gas vesicle rib protein with part of its amino acid sequence removed. The recombinant rib protein is a gas vesicle rib protein, either native or truncated, inserted in frame with a heterologous peptide at C-terminus, N-terminus or in the middle.

[0062] By “core sequence” it means the hydrophobic region of GvpA and its homologs which is a tertiary structure consisting of four secondary structures: α-helix, β-sheet, β-sheet, α-helix as indicated in FIGS. 4a to 4b. The “core sequence” spans from the 9.sup.th amino acid (Serine) to the 61.sup.st amino acid (Valine) of GvpA/B from P. megaterium. All gas vesicle rib proteins carry the core sequence.

[0063] In another aspect, the present invention discloses a protein expression system for expression of the chimeric gas vesicle, wherein the protein expression system comprises a first polynucleotide fragment encoding one of the Gyp rib proteins and a second polynucleotide fragment encoding the other one of the Gyp rib proteins. The protein expression system can be a DNA-based protein expression system or an RNA-based protein expression system.

[0064] In various embodiments, the first polynucleotide fragment encoding the major rib protein; and a second polynucleotide fragment encoding the minor rib protein, wherein the second polynucleotide fragment comprises a core polynucleotide encoding a core sequence; and a heterologous polynucleotide fragment encoding a heterologous peptide.

[0065] In preferred embodiments, the core sequence is characterized by a protein tertiary structure comprising a first alpha helix; a first beta sheet at C-terminus of the first alpha helix; a second beta sheet at C-terminus of the first beta sheet; and a second alpha helix at C-terminus of the second beta sheet. Preferably, the core sequence is selected from a group consisting of a GvpA core sequence and a GvpB core sequence.

[0066] In particular, the core sequence is a hydrophobic region of GvpA protein or GvpB protein as illustrated in FIG. 4a, wherein the core sequence comprises 9th to 61st amino acid of a GvpA protein or a GvpB protein. Preferably, the core sequence is a tertiary protein structure consisting of 4 secondary protein structures arranged in a sequential manner: a-helix, β-sheet, β-sheet, a-helix, wherein the GvpA protein or the GvpB protein is derived from cyanobacteria, halobacteria or soil bacteria. Preferably, the soil bacteria is P. Megaterium; the halobacteria is H. salinarum; the cyanobacteria is A. flos-aquae.

[0067] In one preferred embodiment, the first polynucleotide fragment has a nucleotide sequence of SEQ ID NO.: 5 or SEQ ID NO.: 6.

[0068] In various embodiments, the heterologous peptide is at least 6 amino acids long, wherein the heterologous peptide is derived from a native protein sequence selected from a group consisting of a ligand, a hormone, a cytokine, a receptor, a paratope of antibody, a toxic protein and a fluorescent protein, or a human designed peptide sequence.

[0069] In some embodiments, the protein expression system further comprises an assembly polynucleotide fragment encoding an assembly protein, wherein the assembly protein comprises a GvpP protein, a GvpQ protein or a combination thereof. With presence of the assembly proteins, the minor rib proteins are more evenly distributed on the CGV's surface. While in absence of GvpP or GvpQ protein, CGVs demonstrate less stability and tend to assemble inappropriately or produce less amount than CGVs with the assistance of the assembly protein.

[0070] In certain embodiments, the assembly polynucleotide fragment is derived from P. megaterium gvpP, gvpQ or a combination thereof. Preferably, the assembly polynucleotide fragment has a nucleotide sequence of SEQ ID NO.: 7,

[0071] SEQ ID NO.: 8 or SEQ ID NO.: 9.

[0072] In some embodiments, the protein expression system further comprises an accessory polynucleotide fragment encoding at least one accessory protein, wherein the accessory protein is selected from a group consisting of a GvpR, a GvpN, a GvpF, a GvpG, a GvpL, a GvpS, a GvpK, a GvpJ, a GvpT and a GvpU. In certain embodiments, the accessory polynucleotide fragment is derived from P. megaterium gvpR, gvpN, gvpF, gvpG, gvpL, gvpS, gvpK, gvpJ, gvpT, gvpU or a combination thereof. Preferably, the accessory polynucleotide fragment has a nucleotide sequence of SEQ ID NO.: 10.

[0073] In some embodiments, the protein expression system can be induced in a host to express the Gyp rib proteins, wherein the host comprises an archaeon cell, a prokaryotic cell, or a eukaryotic cell. Preferably, the archaeon cell is H. salinarum; the prokaryotic cell is E. coli; the eukaryotic cells are a mammalian cell, a yeast cell or an insect cell. More preferably, the host is E. coli.

[0074] As illustrated in FIG. 8a, the GVs purified from E. coli transformant with P. megaterium genes: gvpB (encoding a major rib protein) and gvpRNFGLSKJTU. The GVs are generally small (40×40 nm) with some large sized GV (40×200 nm). In an exemplary embodiment, as shown in FIG. 8b, the CGVs purified from E. coli transformant with P. megaterium genes: gvpA (encoding a recombinant minor rib protein), gvpPQ (assembly proteins), gvpB (encoding a major rib protein) and gvpRNFGLSKJTU. The CGVs are large in size (40×200 nm) in the presence of the two Gyp rib proteins and the assembly proteins. In the example as described above, the minor rib protein is a 77-AA truncated GvpA protein fused with a 17-AA heterologous peptide.

[0075] In some embodiments, to minimize the influence brought by longer heterologous peptide, numbers of amino acid deletion of the Gyp rib protein shall be considered. Without interruption of CGVs assembly and formation, a maximal deletion at GvpA C-terminus is 25-AA, while the maximal deletion at

[0076] GvpB C-terminus is 27-AA. In an exemplary embodiment, maximal GvpA truncation and maximal heterologous peptide insertion were determined. As shown in TABLE 1, 25 amino acids can be removed from GvpA of P. megaterium without the destruction of CGV, and at least 56-AA heterologous peptide can be inserted into the truncated GvpA at C-terminus without the destruction of CGV. Besides, it can be inferred from TABLE 1 that less deletion of rib protein GvpA or GvpB at C-terminus is applicable when shorter heterologous peptide insertion is required.

TABLE-US-00001 TABLE 1 CGV produc- C- Heter- Preserved tion terminus ologous GvpA (μg/ml Plasmid deletion peptide C-terminus per Name (AA) (AA) AA sequence culture) pNL39 0 0 WLRYAEAVGLLTD 10 KVEEEGLPGRTEE RGAGLSF pNL114 6 0 WLRYAEAVGLLTD 10 KVEEEGLPGRTEE R pNL115 10 0 WLRYAEAVGLLTD 10 KVEEEGLPGR pNL119 13 0 WLRYAEAVGLLTD 10 KVEEEGL pNL118 16 0 WLRYAEAVGLLTD 10 KVEE pNL105 18 0 WLRYAEAVGLLTD 10 KV pNL106 19 0 WLRYAEAVGLLTD 10 K pNL107 20 0 WLRYAEAVGLLTD 10 pNL131 22 0 WLRYAEAVGLL 10 pNL132 24 0 WLRYAEAVG 10 pNL135 25 0 WLRYAEAV 10 pNL133 26 0 WLRYAEA N/A pNL136 27 0 WLRYAE N/A pNL134 28 0 WLRYA N/A pNL151 25 47 WLRYAEAV + 6 to 8 47-AA pNL148 25 48 WLRYAEAV + 6 to 8 48-AA pNL149 25 49 WLRYAEAV + 6 to 8 49-AA pNL150 25 50 WLRYAEAV + 6 to 8 50-AA pNL162 25 53 WLRYAEAV + 1 to 2 53-AA pNL163 25 56 WLRYAEAV + 1 to 2 56-AA

[0077] In some other embodiments, the protein expression system can be carried out by two or more different expression vectors for subsequent CGVs expression in a host. In one exemplary embodiment, a polynucleotide fragment encoding GvpA, GvpP and GvpQ is inserted in a first vector, and another polynucleotide fragment encoding GvpB, GvpR, GvpN, GvpF, GvpG, GvpL, GvpS, GvpK, GvpJ, GvpT and GvpU is inserted in a second vector. The first vector and the second vector are co-transformed into a host for production of the CGVs. Preferably, the vectors are derived from plasmid pST39 and plasmid pLysS for E. coli host.

[0078] By “vector” it means a nucleic acid molecule comprising gene-expressing elements and elements for genetic engineering so as to carry genes of interest into a selected host for specific biological functions such as protein expression or amplifying the copy number of genes of interest.

[0079] In other preferred embodiments, as illustrated in FIG. 5, to establish a gyp operon system comprising a single operon for protein expression of the CGVs, 3′ end of the gvpAPQ polynucleotide fragment or the gypBPQ polynucleotide fragment is covalently linked to 5′ end of the gypBRNFGLSKJTU polynucleotide fragment so that a gvpAPQBRNFGLSKJTU polynucleotide fragment or a gypBPQBRNFGLSKJTU polynucleotide fragment is formed.

[0080] As illustrated in FIG. 6, to establish the gyp operon system comprising two operons for protein expression of the CGVs when the major rib protein and the minor rib protein are expressed separately, 3′ end of the second polynucleotide fragment is covalently linked to 5′ end of the assembly polynucleotide fragment so as to form a gvpAPQ polynucleotide fragment or a gvpBPQ polynucleotide fragment, while 3′ end of the first polynucleotide fragment is covalently linked to 5′ end of the accessory polynucleotide fragment so as to form a gvpARNFGLSKJTU polynucleotide fragment or a gvpBRNFGLSKJTU polynucleotide fragment.

[0081] Practically, an operator or a promoter is required upstream the gvpAPQ polynucleotide fragment, the gvpBPQ polynucleotide fragment, the gvpBRNFGLSKJTU polynucleotide fragment, the gvpAPQBRNFGLSKJTU polynucleotide fragment and the gypBPQBRNFGLSKJTU polynucleotide fragment so that the gyp operon system can be operated for synthesis of proteins required for CGV assembly upon induction of isopropylthiogalactoside (IPTG), lactose, methyl-β-D-thiogalactoside, phenyl-β-D-galactose or ortho-nitrophenyl-β-galactoside (ONPG), but not limited by this.

[0082] In one preferred embodiment, the gvpAPQBRNFGLSKJTU polynucleotide fragment has a 7053-bp DNA sequence encoding GvpA, GvpP, GvpQ, GvpB, GvpR, GvpN, GvpF, GvpG, GvpL, GvpS, GvpK, GvpJ, GvpT and GvpU proteins and can be inserted into an appropriate expression vector for CGVs protein expression; preferably the gvpAPQBRNFGLSKJTU polynucleotide fragment has a nucleotide sequence of SEQ ID NO.: 11.

[0083] In one another aspect, the present invention as shown in FIG. 9 discloses a method for producing the chimeric gas vesicles (CGVs) with a heterologous peptide fused with a genetically engineered gas vesicle minor rib protein GvpA or GvpB, the method comprises steps of:

[0084] (Step S1) Construction of plasmid: a plasmid is constructed by inserting a DNA sequence encoding a heterologous peptide having 6 to 56 amino acids or above in-frame at the C-terminus and/or N-terminus of the genetically engineered GvpA or GvpB protein in a recombinant gyp operon derived from P. megaterium by PCR and Gibson Assembly.

[0085] (Step S2) Transformation of plasmid: the constructed plasmid is transformed into E. coli or other suitable bacteria hosts capable of expression and production of CGV.

[0086] (Step S3) Induction: the transformant is grown in a proper environment to an optimal condition for inducing protein expression. The transformant is stimulated with IPTG (Isopropyl β-d-1-thiogalactopyranoside) or other inducers for the expression of the CGV.

[0087] (Step S4) Purification and quantification of the CGV.

[0088] To verify the sequence of the recombinant operon, the method further comprises a step of:

[0089] (Step S1.1) Sequence validation: The plasmid sequence with desired insertion is confirmed by DNA sequencing after step S1.

[0090] In some embodiments, the step S1 comprises constructing a CGV expression plasmid by inserting a DNA sequence encoding the minor rib protein into a gyp operon vector by PCR and Gibson Assembly, wherein the minor rib protein has a heterologous peptide at least 6 amino acids (AAs) inserted in frame as a recombinant.

[0091] In yet one another aspect, the present invention as shown in FIG. 10 discloses a method for eliciting immune response by administrating CGV-Covid-19 to a subject in need, the method comprising steps of:

[0092] (Step A) Purification and quantification of CGV-Covid-19 vaccine in PBS.

[0093] (Step B) Administration of the CGV-Covid-19 vaccine into the subject in need.

[0094] (Step C) Detection of the immune responses on the subject.

[0095] In a certain embodiment, CGV-Covid-19 is administrated on the subject in need via intranasal administration, wherein a 17-AA heterologous peptide derived from S-protein of Covid-19 virus is inserted at C-terminus of the core sequence so that the CGV presents an epitope derived from SARS-CoV-2 (Covid-19) spike protein. Enzyme-linked immunosorbent assay (ELISA) is applied to measure elicitation of the immune responses by the CGV-Covid-19 vaccine, but the measure for detection is not limited by this. The subject in need includes human, mice, canine, porcine, chimpanzee or other mammal.

[0096] The CGVs of the invention may be used as vaccines for infectious diseases, therapeutic vaccines for cancer and other diseases. They can be therapeutic agents (such as carrying hormones, cytokines, ligands, or part of variable regions of antibodies) for cancer, metabolic diseases, and other diseases. They can also function as non-invasive contrast agents for ultrasound, MRI and other imaging technologies. In short, a wide variety of applications are possible with the CGVs used as a nanoparticle.

Example 1

[0097] Construction and Confirmation of Plasmid

[0098] Any effective E. coli plasmid/host expression system can be used, such as pBB322 derived plasmids/BL21 E. coli strain (New England Biolab), pET28 plasmid/BL21(A1) E. coli strain (Thermo Fisher) or pST39 plasmid/Rosetta E. coli strain (Millipore Sigma).

[0099] The plasmid was digested with restriction enzyme/enzymes or PCR with particular primers to generate the corresponding DNA fragment. The proper DNA primers encoding a peptide of interest were designed and ordered from any commercial primer vendors by one of ordinary skill in the art.

[0100] The DNA fragment encoding heterologous truncated GvpA protein or GvpB protein with a peptide of interest, and a DNA fragment carrying the rest of 13 gyp genes: gvpPQBRNFGLSKJTU from P. megaterium were amplified by PCR with the proper DNA primers. The fragments were subsequently ligated by Gibson Assembly (Thermo Fisher). The Gibson Assembly mixture was transformed into proper E. coli competent cells and transformants were analyzed and sequenced by one of ordinary skill in the art.

[0101] Expression and Production of CGV

[0102] The plasmids with the correct DNA sequence insertion were transformed into desired E. coli hosts. A single colony was picked and inoculated with LB media with appropriate selection antibiotics. CGV expression can be induced by IPTG or other inducers and purification is done by a modified protocol. The protocol including following steps:

[0103] a. Transformed E. coli were cultured for 20 to 22 hours and then centrifuged at 500 g for 1 to 2 hours.

[0104] b. The pellet was resuspended in PBS buffer and lysed by detergent, lysozyme and DNase.

[0105] c. The cell lysate was centrifuged at 500 g for 5 to 30 minutes so that CGV was isolated from cell debris. Of note, the CGV floated at the top of the lysate suspension.

[0106] d. The cell debris and the midnatant were removed by a needle.

[0107] e. The remaining CGV was suspended in PBS.

[0108] f. Step c to Step e were repeated for 10 times and 99% purity of CGV was obtained.

[0109] g. Final concentration of CGV was measured by a spectrophotometer at OD.sub.500(NanoDrop ND-1000, Thermo Scientific). Of note, one OD.sub.500 of CGV is equivalent to 145 μg/ml of protein.

Example 2

[0110] To verify that insertion of heterologous peptide from one foreign protein or more foreign proteins can be realized in the present invention, in example 2, one 20-AA peptide from H1N1 virus HA (hemagglutinin) protein and another 20-AA peptide from Covid-19 virus Spike protein were linked to form a 40-AA insertion peptide. Then, the minor rib genes with heterologous peptide from two foreign proteins were inserted into the 14 gene gyp operon on the same plasmid or on two individual plasmid vectors. Transformation or co-transformation of the plasmid(s) into E. coli competent cells such that CGV particles carrying two or more heterologous peptides were brought on mass production.

Example 3

[0111] To further validate protein expression of CGVs carrying various heterologous peptides, CGVs produced and isolated by procedures as described in example 1 were confirmed by Western Dot Blot.

TABLE-US-00002 TABLE 2 Heter- ologous CGV Peptide S-Protein Dot samples Sequences Sequence 1 Positive Covid-19 S-Protein control S-protein 2 pNL39 GvpA No without hetero insertion geneous of peptide hetero- sequence geneous sequence 3 pNL66 TGCVIAW T430 to NSNNLDS S443 4 pNL67 NLDSKVG N440 to GNYNYLY Y453 5 pNL68 NYLYRLF N450 to RKSNLKP P463 6 pNL69 NLKPFER N460 to DISTEIY Y473 7 pNL70 TEIYQAG T470 to STPCNGV V483 8 pNL71 CNGVEGF C480 to NCYFPLQ Q493 9 pNL72 FPLQSYG F490 to FQPTNGV V503 10 pNL73 TNGVGYQ T500 to PYRVVVL S513

[0112] CGV samples with various heterologous peptides were purified from the E. coli culture transformed with the corresponding plasmid constructs. The Western Dot Blot was done with rabbit anti-Covid-19 S protein as the primary antibody and goat anti-rabbit IgG-HRP as secondary antibody.

[0113] As shown in FIG. 7, dots representing positive CGVs were Dot 5 to 8, which suggests that antigen region of Covid-19 S-protein is between 450.sup.th to 493.sup.rd AA. In TABLE 2, detailed information of Covid-19 S protein sequences serving as inserts in recombinant gyp operons were listed down, and antigen regions of Covid-19 S protein were identified as NYLYRLFRKSNLKP (N450 to P463), NLKPFERDISTEIY (N460 to Y473), TEIYQAGSTPCNGV (T470 to V483) and CNGVEGFNCYFPLQ (C480 to Q493), respectively.

[0114] The advantages of the present invention, chimeric gas vesicles (CGVs), over traditional GV and GVNP are numerous.

[0115] For example, previous attempts of direct genetic modification of GvpA in the conventional GV are unsuccessful due to the rigidity of GvpA in the GV. To date, no more than 5-AA heterologous peptide can be inserted at the C-terminus of GvpA without the destruction of GV. The CGV disclosed in the present invention overcomes this stability limitation and makes the CGVs possible for various applications. In GV research in halobacteria, the genetically modified GvpC of GVNP attaches to GV via protein-protein interaction, and is vulnerable to thermohaline fluctuations. This makes the GvpC easy to fall off from the GVNP, thus greatly reduces the possibility of using the conventional GVs for applications. In the CGVs, the heterologous peptide can be inserted or fused covalently with the truncated/native GvpA or its homolog to form the rib protein. As a part of the rib structure, the fall-off problem of the heterologous peptide present in the conventional GVs is eliminated. For industrial or commercial productions, the making of the CGVs can be accomplished in much shorter production cycle. In some instances, it can be produced within 2 days, which is drastically shorter than the production cycle of GVNPs in halobacteria or GVs in cyanobacteria. The CGVs are more stable than the conventional GVs. The CGVs produced in E. coli with gyp operon from P. megaterium are more stable than any other GVs previously known. The CGVs of the present invention have a higher “critical collapse pressure” than the conventional GVs. For storage, the CGVs in one of the embodiments maintain their integrity at room temperature for at least one month, and at 4° C. for at least six months, without any degradation. All these features of the CGVs of the present invention increases immensely the possibilities of its applications in the future.

[0116] Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Although methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention, the preferred methods and materials are described below. All publications, patent applications, patents, and other references mentioned herein are incorporated by reference in their entirety. In case of conflict, the present specification, including definitions, will control. In addition, the materials, methods, and examples are illustrative only and not intended to be limiting.