Enolase 1 (Eno1) compositions and uses thereof
View Patent ↗The invention provides compositions comprising Eno1 for delivery to a muscle. Further, the invention provides a method for normalizing blood glucose in a subject with elevated blood glucose, comprising administering to the subject enolase 1 (Eno1), thereby normalizing blood glucose in the subject. The invention also provides methods of treating one or more conditions including impaired glucose tolerance, insulin resistance, pre-diabetes, and diabetes, especially type 2 diabetes in a subject, comprising administering to the subject enolase 1 (Eno1), thereby treating the condition in the subject. In certain methods of the invention, the Eno1 is delivered to muscle.
1. A pharmaceutical composition comprising enolase 1 (Eno1) or a fragment thereof and a muscle targeting peptide, wherein the Eno1 or a fragment thereof and the muscle targeting peptide are in a complex;
wherein the Eno1 or a fragment thereof has glycolytic activity and is present in a therapeutically effective amount; and
wherein the muscle targeting peptide is a smooth muscle targeting peptide, a skeletal muscle targeting peptide, or a smooth muscle and skeletal muscle targeting peptide.
2. The pharmaceutical composition of claim 1 , wherein the composition is for delivery to a muscle cell.
3. The pharmaceutical composition of claim 1 , wherein the Eno1 comprises an Eno1 polypeptide or a fragment thereof.
4. The pharmaceutical composition of claim 1 , wherein the Eno1 or fragment thereof has at least 90% of the activity of a purified endogenous human Enol polypeptide.
5. The pharmaceutical composition of claim 1 , wherein the Eno1 is human Eno1.
6. The pharmaceutical composition of claim 1 , wherein the composition further comprises a microparticle.
7. The pharmaceutical composition of claim 1 , wherein the composition further comprises a nanoparticle.
8. The pharmaceutical composition of claim 1 , wherein the composition further comprises a liposome.
9. The pharmaceutical composition of claim 1 , wherein the Eno1polypeptide is human Eno1 polypeptide.
10. The pharmaceutical composition of claim 1 , wherein the complex further comprises a linker.
11. The pharmaceutical composition of claim 10 , wherein the linker is selected from the group consisting of a covalent linker, a non-covalent linkage, and a reversible linker.
12. The pharmaceutical composition of claim 1 , wherein the complex further comprises a pharmaceutically acceptable dendrimer.
13. The pharmaceutical composition of claim 12 , wherein the pharmaceutically acceptable dendrimer is a PAMAM dendrimer.
14. The pharmaceutical composition of claim 12 , wherein the pharmaceutically acceptable dendrimer is a G5 dendrimer.
15. The pharmaceutical composition of claim 12 , wherein the pharmaceutically acceptable dendrimer is an uncharged dendrimer.
16. The pharmaceutical composition of claim 12 , wherein the pharmaceutically acceptable dendrimer is an acylated dendrimer.
17. The pharmaceutical composition of claim 12 , wherein the pharmaceutically acceptable dendrimer is a PEGylated dendrimer or an acetylated dendrimer.
18. The pharmaceutical composition of claim 1 , wherein the Eno1is released from the complex upon delivery to a muscle cell.
19. The composition of claim 13 , wherein the dendrimer and the ENO1 are present in the complex at a ratio of about 1:1 to about 10:1.
20. The composition of claim 13 , wherein the dendrimer and the ENO1 are present in the complex at a ratio of about 3:1 to about 5:1.
21. The composition of claim 13 , wherein the muscle targeting moiety and the dendrimer are present in the complex at a ratio of about 0.1:1 to about 10:1.
22. The composition of claim 13 , wherein the muscle targeting moiety and the dendrimer are present in the complex at a ratio of about 1:1 to about 3:1.
23. The composition of claim 1 , wherein the Eno1 and the muscle targeting moiety are present in the complex at a ratio of about 1:1 to about 1:30.
24. The pharmaceutical composition of claim 1 , wherein the composition is formulated for parenteral administration.
25. The pharmaceutical composition of claim 1 , wherein the composition is formulated for oral administration.
26. The pharmaceutical composition of claim 1 , wherein the composition is formulated for intramuscular administration, intravenous administration, or subcutaneous administration.