Glucagon derivative and a composition comprising a long acting conjugate of the same
The present invention relates to a glucagon derivative, a long-acting conjugate of the glucagon derivative, and a use thereof.
1. An isolated peptide comprising the amino acid sequence of the following General Formula 2:
(General Formula 2, SEQ ID NO: 46)
Y-Aib-QGTF-X7-SD-X10-S-X12-Y-L-X15-X16-X17-R-A-
X20-X21-F-V-X24-W-L-M-N-T-X30
wherein,
X7 is threonine, valine, or cysteine;
X10 is tyrosine or cysteine;
X12 is lysine or cysteine;
X15 is aspartic acid or cysteine;
X16 is glutamic acid or serine;
X17 is lysine or arginine;
X20 is glutamine or lysine;
X21 is aspartic acid or glutamic acid;
X24 is valine or glutamine; and
X30 is cysteine or is absent,
with the proviso that a peptide of the amino acid sequence of SEQ ID NO: 12 is excluded.
2. The peptide of claim 1 , wherein, the amino acid pair of X16 and X20 is respectively glutamic acid and lysine, which is capable of forming a ring.
3. The peptide of claim 1 , wherein the C-terminus of the peptide is amidated.
4. The peptide of claim 1 , wherein the peptide is a glucagon derivative capable of activating a glucagon receptor.
5. The peptide of claim 1 , wherein the peptide comprises the amino acid sequence selected from the group consisting of SEQ ID NOS: 13, 15, 19, 33, and 36 to 44.
6. An isolated conjugate, wherein the isolated peptide of claim 1 and a biocompatible material capable of increasing in vivo half-life are linked.
7. The isolated conjugate of claim 6 , wherein the biocompatible material is selected from the group consisting of polyethylene glycol, fatty acid, cholesterol, albumin and a fragment thereof, an albumin-binding material, a polymer of repeating units of a particular amino acid sequence, an antibody, an antibody fragment, an FcRn-binding material, in vivo connective tissue or a derivative thereof, a nucleotide, fibronectin, transferrin, and a polysaccharide.
8. The isolated conjugate of claim 6 , wherein the peptide is linked to a biocompatible material by a linker selected from the group consisting of polyethylene glycol, polypropylene glycol, an ethylene glycol-propylene glycol copolymer, polyoxyethylated polyol, polyvinyl alcohol, a polysaccharide, polyvinyl ethyl ether, polylactic acid (PLA), polylactic-glycolic acid (PLGA), lipid polymer, chitin, hyaluronic acid, fatty acid, a nucleotide, and a combination thereof.
9. The isolated conjugate of claim 6 ,
wherein the biocompatible material is an FcRn-binding material, and
the isolated peptide is linked to a biocompatible material by a peptide linker or a non-peptide linker selected from the group consisting of polyethylene glycol, polypropylene glycol, an ethylene glycol-propylene glycol copolymer, polyoxyethylated polyol, polyvinyl alcohol, a polysaccharide, polyvinyl ethyl ether, a polylactic acid (PLA), polylactic-glycolic acid (PLGA), lipid polymer, chitin, hyaluronic acid, and a combination thereof.
10. The isolated conjugate of claim 9 , wherein the FcRn-binding material is a polypeptide comprising an immunoglobulin Fc region.
11. A composition comprising (i) the isolated peptide of claim 1 or (ii) an isolated conjugate in which the isolated peptide of claim 1 is linked to a biocompatible material capable of increasing in vivo half-life.
12. The composition of claim 11 , which is a pharmaceutical composition comprising a pharmaceutically acceptable carrier.
13. A method for treating metabolic syndrome, comprising administering
(i) the isolated peptide of claim 1 or
(ii) an isolated conjugate in which the isolated peptide of claim 1 is linked to a biocompatible material capable of increasing in vivo half-life,
to a subject in need thereof,
wherein the metabolic syndrome is selected from the group consisting of hypercholesterolemia, obesity and nonalcoholic steatohepatitis.
14. The method of claim 13 , wherein (i) the peptide or (ii) the conjugate comprises the amino acid sequence selected from the group consisting of SEQ ID NOS: 13, 15, 19, 33, and 36 to 44.
15. A pharmaceutical composition comprising
(i-a) the isolated peptide of claim 1 or (i-b) an isolated conjugate in which the isolated peptide of claim 1 is linked to a biocompatible material capable of increasing in vivo half-life; and
(ii) at least one compound or material having a therapeutic activity for metabolic syndrome.
16. The pharmaceutical composition of claim 15 , wherein the isolated peptide comprises the amino acid sequence selected from the group consisting of SEQ ID NOS: 13, 15, 19, 33, and 36 to 44.
17. The pharmaceutical composition of claim 15 , wherein (ii) the compound or material having a therapeutic activity for metabolic syndrome is selected from the group consisting of an insulinotropic peptide, a glucagon-like peptide-1 (GLP-1) receptor agonist, a leptin receptor agonist, a dipeptidyl peptidase-IV (DPP-IV) inhibitor, a Y5 receptor antagonist, a melanin-concentrating hormone (MCH) receptor antagonist, a Y2/4 receptor agonist, a melanocortin 3/4 (MC 3/4) receptor agonist, a gastric/pancreatic lipase inhibitor, an agonist of 5-hydroxytryptamine receptor 2C (5HT2C), a β3A receptor agonist, an amylin receptor agonist, a ghrelin antagonist, a ghrelin receptor antagonist, a peroxisome proliferator-activated receptor alpha (PPARα) agonist, a peroxisome proliferator-activated receptor delta (PPARδ) agonist, a Farnesoid X receptor (FXR) agonist, an acetyl-CoA carboxylase inhibitor, a peptide YY, cholecystokinin (CCK), xenin, glicentin, obestatin, secretin, nesfatin, insulin, and a glucose-dependent insulinotropic peptide (GIP).
18. The pharmaceutical composition of claim 17 , wherein the insulinotropic peptide is selected from the group consisting of GLP-1, exendin-3, exendin-4, an agonist thereof, a derivative thereof, a fragment thereof, a variant thereof, and a combination thereof.
19. The pharmaceutical composition of claim 18 , wherein the insulinotropic peptide is an insulinotropic peptide derivative, in which the N-terminal histidine residue is substituted with one selected from the group consisting of desamino-histidyl, N-dimethyl-histidyl, β-hydroxy imidazopropionyl, 4-imidazoacetyl, and β-carboxy imidazopropionyl.
20. The pharmaceutical composition of claim 18 , wherein the insulinotropic peptide is selected from the group consisting of a native exendin-4; an exendin-4 derivative in which the N-terminal amine group of exendin-4 is deleted; an exendin-4 derivative in which the N-terminal amine group of exendin-4 is substituted with a hydroxyl group; an exendin-4 derivative in which the N-terminal amine group of exendin-4 is modified with a dimethyl group; an exendin-4 derivative in which the α-carbon of the 1 st amino acid of exendin-4, histidine, is deleted; an exendin-4 derivative in which the 12 th amino acid of exendin-4, lysine, is substituted with serine, and an exendin-4 derivative in which the 12 th amino acid of exendin-4, lysine, is substituted with arginine.
21. The method of claim 13 , further comprising administering a compound or material having a therapeutic activity for metabolic syndrome, said administering being either before or after the administration of (i) the isolated peptide or (ii) the conjugate.
22. A method for treating hypoglycemia, comprising administering
(i) the isolated peptide of claim 1 or
(ii) an isolated conjugate in which the isolated peptide of claim 1 is linked to a biocompatible material capable of increasing in vivo half-life,
to a subject in need thereof.
23. The method of claim 22 , further comprising administering a compound or material having a therapeutic activity for hypoglycemia, said administering being either before or after the administration of the isolated peptide or conjugate.
24. The method of claim 22 , wherein (i) the peptide or (ii) the conjugate comprises the amino acid sequence selected from the group consisting of SEQ ID NOS: 13, 15, 19, 33, and 36 to 44.
25. The composition of claim 11 , which is administered in combination with at least one compound or material having a therapeutic activity for metabolic syndrome or hypoglycemia.
26. A method for treating metabolic syndrome comprising administering in any sequential order
(i) a peptide comprising the isolated peptide of claim 1 or an isolated conjugate in which the isolated peptide of claim 1 is linked to a biocompatible material capable of increasing in vivo half-life; and
(ii) at least one compound or material having a therapeutic activity for metabolic syndrome,
wherein the metabolic syndrome is selected from the group consisting of hypercholesterolemia, obesity and nonalcoholic steatohepatitis.
27. The method of claim 26 , wherein (i) the peptide or conjugate comprises the amino acid sequence selected from the group consisting of SEQ ID NOS: 13, 15, 19, 33, and 36 to 44.