Expression of fusion polypeptides transported out of the cytoplasm without leader sequences

A nucleic acid encoding a fusion polypeptide, said fusion polypeptide comprising:

• a) a fusion partner comprising a polypeptide selected from the group consisting of mature DsbC, a mutant polypeptide variant of mature DsbC lacking a double cysteine active site loop domain and a mutant polypeptide variant of mature DsbA lacking a double cysteine active site loop domain, said fusion partner lacking a signal sequence;
• b) a linker peptide comprising a ubiquitin molecule;
• and
• c) a polypeptide of interest, wherein said polypeptide of interest is positioned distal to the carboxy terminus of said fusion partner, and further wherein said linker peptide is positioned between said fusion partner and said polypeptide of interest.

A host cell comprising:

• a) an expression vector capable of expressing in said host cell a fusion polypeptide, said fusion polypeptide comprising,
• i) a fusion partner comprising a polypeptide selected from the group consisting of mature DsbC, a mutant polypeptide variant of mature E. coli DsbC lacking a double cysteine active site loop domain and a mutant polypeptide variant of mature DsbA lacking a double cysteine active site loop domain, said fusion partner lacking a signal sequence and comprising a carboxy terminus,
• ii) a linker peptide comprising a cleavage site, and
• iii) a polypeptide of interest, wherein said polypeptide of interest is positioned distal to the carboxy terminus of said fusion partner, and further wherein said linker peptide is positioned between said fusion partner and said polypeptide of interest;
• and
• b) a nucleic acid capable of expressing in said host cell a proteolytic enzyme which specifically recognizes said cleavage site.

A fusion polypeptide comprising:

• a) a fusion partner comprising a polypeptide selected from the group consisting of DsbC, mature DsbC, a mutant polypeptide variant of DsbC lacking a double cysteine active site loop domain and a mutant polypeptide variant of mature DsbA lacking a double cysteine active site loop domain, said fusion partner lacking a signal sequence and comprising a carboxy terminus;
• b) a linker peptide comprising a ubiquitin molecule;
• and
• c) a polypeptide of interest, wherein said polypeptide of interest is positioned distal to the carboxy terminus of said fusion partner, and further wherein said linker peptide is positioned between said fusion partner and said polypeptide of interest.

A method of producing a substantially purified fusion polypeptide encoded by a nucleic acid, wherein said fusion polypeptide comprises, a fusion partner capable of directing extracytoplasmic transport, comprising at least one fragment of a mature polypeptide, wherein the mature polypeptide is selected from the group consisting of DsbC, a mutant DsbC lacking a double cysteine active site loop domain, and a mutant DsbA lacking a double cysteine active site loop domain, said fusion partner lacking a signal sequence and comprising a carboxy terminus, and a polypeptide of interest, wherein said polypeptide of interest is positioned distal to the carboxy terminus of said fusion partner;

• said method comprising the steps of:
• a) introducing said nucleic acid encoding said fusion polypeptide into a host cell, thereby producing a transformed host cell;
• b) culturing said transformed host cell under conditions appropriate for expressing said fusion polypeptide;
• and
• c) purifying said fusion polypeptide, thereby obtaining a substantially purified fusion polypeptide.

A method of producing a substantially purified polypeptide of interest, said method comprising the steps of:

• a) introducing into a host cell a nucleic acid encoding a fusion polypeptide, said fusion polypeptide comprising:
• i) a fusion partner capable of directing extracytoplasmic transport, comprising at least one fragment of a mature polypeptide, wherein the mature polypeptide is selected from the group consisting of DsbC, a mutant DsbC lacking a double cysteine active site loop domain, and a mutant DsbA lacking a double Cysteine active site loop domain, said fusion partner lacking a signal sequence and comprising a carboxy terminus,
• ii) a polypeptide of interest, wherein said polypeptide of interest is positioned distal to the carboxy terminus of said fusion partner, and
• iii) a linker peptide encoding a cleavage site, wherein said linker peptide is positioned between said fusion partner and said polypeptide of interest;
• thereby producing a transformed host cell;
• b) culturing said transformed host cell under conditions appropriate for expressing said fusion polypeptide, thereby expressing said fusion polypeptide;
• c) cleaving said fusion polypeptide with a proteolytic enzyme or cleavage agent which recognizes said proteolytic cleavage site, thereby producing said polypeptide of interest;
• and
• d) purifying said polypeptide of interest, thereby obtaining a substantially purified polypeptide of interest.

A method of producing a substantially purified polypeptide of interest, said method comprising the steps of:

• a) introducing into a host cell a nucleic acid encoding a fusion polypeptide, said fusion polypeptide comprising,
• i) a fusion partner capable of directing extracytoplasmic transport, comprising at least one fragment of a mature polypeptide, wherein the mature polypeptide is selected from the group consisting of DsbC, a mutant DsbC lacking a double cysteine active site loop domain, and a mutant DsbA lacking a double cysteine active site loop domain, said fusion partner lacking a signal sequence and comprising a carboxy terminus,
• ii) a polypeptide of interest, wherein said polypeptide of interest is positioned distal to the carboxy terminus of said fusion partner, and
• iii) a linker peptide encoding a cleavage site, wherein said linker peptide is positioned between said fusion partner and said polypeptide of interest;
• thereby producing a transformed host cell;
• b) culturing said transformed host cell under conditions appropriate for expressing said fusion polypeptide, thereby expressing said fusion polypeptide;
• c) purifying said fusion polypeptide, thereby producing a substantially purified fusion polypeptide;
• d) cleaving said substantially purified fusion polypeptide with a proteolytic enzyme or cleavage agent which recognizes said proteolytic cleavage site, thereby producing said polypeptide of interest;
• and
• e) purifying said polypeptide of interest, thereby obtaining a substantially purified polypeptide of interest.

A method of producing a substantially purified polypeptide of interest comprising the steps of:

• a) introducing into a host cell a nucleic acid encoding a fusion polypeptide, said fusion polypeptide comprising,
• i) a fusion partner capable of directing extracytoplasmic transport, comprising at least one fragment of a mature polypeptide, wherein the mature polypeptide is selected from the group consisting of DsbC, a mutant DsbC lacking a double cysteine active site loop domain, and a mutant DsbA lacking a double cysteine active site loop domain, said fusion partner lacking a signal sequence and comprising a carboxy terminus,
• ii) a polypeptide of interest, wherein said polypeptide of interest is positioned distal to the carboxy terminus of said fusion partner, and
• iii) a linker peptide encoding a cleavage site, wherein said linker peptide is positioned between said fusion partner and said polypeptide of interest;
• and further wherein said host cell comprises a nucleic acid capable of expressing in said host cell a proteolytic enzyme which specifically recognizes said cleavage site, thereby producing a transformed host cell;
• b) culturing said transformed host cell under conditions appropriate for expressing said fusion polypeptide and said proteolytic enzyme, thereby expressing said fusion polypeptide, causing the in vivo cleavage of said fusion polypeptide, and producing said polypeptide of interest;
• and
• c) purifying said polypeptide of interest, thereby obtaining a substantially purified polypeptide of interest.