Recombinant protein body-inducing polypeptides
Polypeptide sequences for inducing recombinant protein bodies are described. The sequences comprise a polyproline II (PPII) structure and/or a proline-rich sequence between two cysteine residues on either end. Recombinant protein bodies are useful for protein production because they allow for simple and efficient purification of high quantities of recombinant protein. In addition, other methods of using recombinant protein bodies, for example, in vaccination and food products, are also described.
1. A recombinant protein body-inducing polypeptide sequence (PBIS) comprising a polyproline II (PPII) structure that is at least 36 amino acids in length and has an N-terminus and a C-terminus wherein
(i) the PPII structure is located between at least two cysteines at the N-terminus and at least two cysteines at the C-terminus;
(ii) no more than 10% of the amino acids in the PPII structure are lysine or arginine;
(iii) the PPII structure does not contain the sequence (PPPVHL) 6 showing the sequence set forth in SEQ ID NO:115; and
(iv) the PPII structure is selected from the group consisting of a non-amphipathic PPII structure, an amphipathic and negatively charged PPII structure, and an amphipathic and non-charged PPII structure, wherein the non-amphipathic PPII structure, is selected from the group consisting of a sequence comprising at least 6 repeats of the sequence set forth in SEQ ID NO: 121, a sequence comprising at least 6 repeats of the sequence set forth in SEQ ID NO: 122, a sequence comprising at least 6 repeats of the sequence set forth in SEQ ID NO: 123, a sequence comprising at least 6 repeats of the sequence set forth in SEQ ID NO: 120 wherein the X residues are proline, and a sequence comprising at least 6 repeats of the sequence set forth in SEQ ID NO: 129; wherein the amphipathic and negatively charged PPII structure is selected from the group consisting of a sequence comprising at least 6 repeats of the sequence set forth in SEQ ID NO: 124 and a sequence comprising at least 6 repeats of the sequence set forth in SEQ ID NO: 125; and wherein the non-charged PPII structure is selected from the group consisting of a sequence comprising at least 6 repeats of the sequence set forth in SEQ ID NO: 126, a sequence comprising at least 6 repeats of the sequence set forth in SEQ ID NO: 127, and a sequence comprising at least 6 repeats of the sequence set forth in SEQ ID NO: 128.
2. The recombinant PBIS of claim 1 wherein at least 40% of the amino acids in the PPII structure are proline.
3. The recombinant PBIS of claim 1 wherein no more than 98% of the amino acids in the PPII structure are proline.
4. The recombinant PBIS of claim 1 , wherein no more than 5% of the amino acids in the PPII structure are lysine or arginine.
5. The recombinant PBIS of claim 1 , wherein no more than 15% of the amino acids in the PPII structure are histidine.
6. The recombinant PBIS of claim 1 , wherein the PBIS further comprises a cysteine and a proline-rich sequence between the PPII structure and the two C-terminal cysteines or between the PPII structure and the two N-terminal cysteines.
7. A recombinant protein body-inducing polypeptide sequence (PBIS) comprising a proline-rich sequence that is at least 36 amino acids in length and has an N-terminus and a C-terminus, wherein;
(i) the proline-rich sequence is located between at least two cysteines at the N-terminus and at least two cysteines at the C-terminus;
(ii) no more than 10% of the amino acids in the proline-rich sequence are lysine or arginine;
(iii) the proline-rich sequence does not contain the sequence (PPPVHL) 6 showing the sequence set forth in SEQ ID NO:115,
(iv) the proline-rich sequence comprises at least 40% of proline residues and wherein the proline-rich sequence is selected from the group consisting of a non-amphipathic proline-rich sequence, an amphipathic and negatively charged proline-rich sequence, and an amphipathic and non-charged proline-rich sequence, wherein the non-amphipathic proline-rich sequence is selected from the group consisting of a sequence comprising at least 6 repeats of the sequence set forth in SEQ ID NO: 121, a sequence comprising at least 6 repeats of the sequence set forth in SEQ ID NO: 122, a sequence comprising at least 6 repeats of the sequence set forth in SEQ ID NO: 123, a sequence comprising at least 6 repeats of the sequence set forth in SEQ ID NO: 120 wherein the X residues are proline, and a sequence comprising at least 6 repeats of the sequence set forth in SEQ ID NO: 129; wherein the amphipathic and negatively charged proline-rich sequence is selected from the group consisting of a sequence comprising at least 6 repeats of the sequence set forth in SEQ ID NO: 124 and a sequence comprising at least 6 repeats of the sequence set forth in SEQ ID NO: 125; and wherein the non-charged proline-rich sequence is selected from the group consisting of a sequence comprising at least 6 repeats of the sequence set forth in SEQ ID NO: 126, a sequence comprising at least 6 repeats of the sequence set forth in SEQ ID NO: 127, and a sequence comprising at least 6 repeats of the sequence set forth in SEQ ID NO: 128.
8. The recombinant PBIS of claim 7 , wherein the PBIS further comprises a cysteine and PPII structure between the proline-rich sequence and the two C-terminal cysteines or between the proline-rich sequence and the two N-terminal cysteines.
9. The recombinant PBIS of claim 7 , wherein the PBIS further comprises a cysteine and a second proline-rich sequence between the proline-rich sequence and the two C-terminal cysteines or between the proline-rich sequence and the two N-terminal cysteines.
10. The recombinant PBIS of claim 1 , wherein the non amphipathic PPII structure is selected from the group consisting of RX3(A) showing the sequence set forth in SEQ ID NO:89; RX3(L) showing the sequence set forth in SEQ ID NO:86; RX3(A3) showing the sequence set forth in SEQ ID NO:71; PP showing the sequence set forth in SEQ ID NO: 132; PA showing the sequence set forth in SEQ ID NO: 133; PA2 showing the sequence set forth in SEQ ID NO: 172; PP2 showing the sequence set forth in SEQ ID NO: 74 and PP3 showing the sequence set forth in SEQ ID NO: 171; wherein the amphipathic and negatively charged PPII structure is selected from the group consisting of RX3(D) showing the sequence set forth in SEQ ID NO:56 and RX3 (E) showing the sequence set forth in SEQ ID NO: 83 and the amphipathic and non-charged PPII structure is selected from the group consisting of RX3(T) showing the sequence set forth in SEQ ID NO:62; RX3(N) showing the sequence set forth in SEQ ID NO: 65 and RX3(Q) showing the sequence set forth in SEQ ID NO: 68.
11. The recombinant PBIS of claim 1 , wherein the recombinant PBIS is capable of forming a recombinant protein body like assembly (RPBLA) when expressed in a eukaryotic cell.
12. The recombinant PBIS of claim 1 , further comprising a sequence that directs the PBIS to the endoplasmic reticulum (ER).
13. A fusion protein comprising the recombinant PBIS of claim 1 and a heterologous protein.
14. The fusion protein of claim 13 , further comprising a cleavage site between the recombinant PBIS and the heterologous protein.
15. A nucleic acid molecule comprising a sequence that encodes the recombinant PBIS of claim 1 .
16. A vector comprising the nucleic acid of claim 15 .
17. A host cell comprising the recombinant PBIS of claim 1 .
18. A host cell comprising the nucleic acid of claim 15 .
19. A recombinant protein body like assembly (RPBLA) comprising the recombinant PBIS of claim 1 .
20. A recombinant PBIS or fusion protein isolated from the RPBLA of claim 19 .
21. A method for producing an RPBLA comprising culturing the cell of claim 17 under suitable conditions for RPBLA formation.
22. A method for purifying an RPBLA comprising (i) culturing the cell of claim 17 under suitable conditions for RPBLA formation; and (ii) purifying the recombinant protein body.
23. A method for producing an RPBLA comprising (i) transforming a plant host system with the nucleic acid of claim 15 ; (ii) generating plants from said transformed plant host system; and (iii) growing said plants under conditions suitable for RPBLA formation.
24. A method for producing an RPBLA comprising (i) transforming a plant host system with the nucleic acid of claim 15 ; (ii) generating plants from said transformed plant host system; (iii) growing said plants under conditions suitable for RPBLA formation; and (iv) purifying the RPBLA.
25. A method of purifying a fusion protein comprising (i) providing RPBLAs that comprise a membrane-enclosed fusion protein, wherein the fusion protein is the fusion protein of claim 13 ; (ii) contacting the RPBLAs with an aqueous buffer containing a membrane-disassembling amount of a surfactant; (iii) maintaining the contact for a time period sufficient to disassemble the membrane and at a temperature that does not denature the fusion protein to separate the membrane from the fusion protein; and (iv) collecting the separated fusion protein.
26. A method of purifying a protein comprising (i) providing RPBLAs that comprise a membrane-enclosed fusion protein, wherein the fusion protein is the fusion protein of claim 14 ; (ii) contacting the RPBLAs with an aqueous buffer containing a membrane-disassembling amount of a surfactant; (iii) maintaining the contact for a time period sufficient to disassemble the membrane and at a temperature that does not denature the fusion protein to separate the membrane from the fusion protein; (iv) collecting the separated fusion protein; and (v) cleaving the cleavage site between the recombinant PBIS and the heterologous protein.
27. A vaccine comprising an immunogenically effective amount of the RPBLA of claim 19 .