Long-acting polypeptides and methods of producing and administering same
A polypeptide and polynucleotides comprising at least two carboxy-terminal peptides (CTP) of chorionic gonadotrophin attached to a non-human peptide-of-interest are disclosed. Pharmaceutical compositions comprising the non-human polypeptides and polynucleotides of the invention and methods of using both human and non-human polypeptides and polynucleotides are also discarded.
1. A chorionic gonadotropin carboxy terminal peptide (CTP)-modified polypeptide consisting of a peptide of interest, wherein a first chorionic gonadotropin carboxy terminal peptide (CTP) is attached to the amino terminus of said peptide of interest, and a second and third chorionic gonadotropin carboxy terminal peptide are attached to the carboxy terminus of said peptide of interest, wherein said peptide of interest is an erythropoietin (EPO) peptide, and wherein the amino acid sequence of said polypeptide is set forth in SEQ ID NO: 51.
2. The polypeptide of claim 1 , wherein said peptide of interest is glycosylated.
3. The polypeptide of claim 1 , wherein said peptide of interest is non-glycosylated.
4. The polypeptide of claim 1 , wherein at least 1 of said chorionic gonadotrophin carboxy terminal peptides is glycosylated.
5. A pharmaceutical formulation comprising the polypeptide of claim 1 , wherein said formulation further comprises a buffer, and a tonicity agent.
6. The formulation of claim 5 , wherein said buffer is citrate or acetate.
7. The formulation of claim 5 , wherein said tonicity agent is sodium chloride.
8. The formulation of claim 5 , wherein said formulation is formulated for injection in a multidose container, with optionally, a preservative.
9. The formulation of claim 8 , wherein said preservative is benzalkonium chloride or thimerosal.
10. A liquid formulation, comprising the formulation of claim 5 .
11. The liquid formulation of claim 10 , wherein said formulation is at a pH between about 6 to 7.
12. A method of improving a biological half life of a peptide of interest, wherein said peptide of interested is an erythropoietin peptide (EPO), said method comprising the step of attaching a first chorionic gonadotrophin carboxy terminal peptide (CTP) to an amino terminus of said peptide of interest and a second and third chorionic gonadotrophin carboxy terminal peptide (CTP) to a carboxy terminus of said peptide of interest, wherein the amino acid sequence of said CTP-modified peptide of interest is set forth in SEQ ID NO: 51, thereby improving a biological half life of a peptide of interest.