IP Library › Granted Patent US 10,822,595
Granted Patent B2
US 10,822,595 · App. 15/869,518 · Granted Nov 3, 2020

Cell penetrating peptide, conjugate comprising same, and composition comprising conjugate

Inventor: Sang Jae Kim (Seoul, KR)
Assignee: GemVax & KAEL Co., Ltd.
C12N9/1276A23L33/18A61K8/64A61K8/66A61K47/64A61K49/0002A61K49/0043A61K49/0056A61Q19/00C07K7/08C07K14/00G01N33/582A23V2002/00A61K38/00A61K2800/10A61K2800/57C07K2319/10G01N2458/30
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Quick Facts
Patent No.
US 10,822,595
App. No.
15/869,518
Granted
Nov 3, 2020
Kind
B2
Abstract

The present invention relates to a conjugate of cell penetrating peptide and an active ingredient; and its use. Specifically, a conjugate including a cell penetrating peptide which is a peptide comprising any one amino acid sequence of SEQ ID NO: 1 to SEQ ID NO: 156, a fragment of any one sequence of SEQ ID NO: 1 to SEQ ID NO: 156, or a peptide having above 80% homology with the above-mentioned sequence; and a composition comprising the same are disclosed.

Claims (18)

1. A conjugate of a cell penetrating carrier peptide and a heterologous active ingredient, wherein the carrier peptide is 20 amino acids in length and is the amino acid sequence of SEQ ID NO: 121, or the carrier peptide is 20 amino acids in length and has at least 80% sequence identity with the amino acid sequence of SEQ ID NO: 121 and maintains cell penetrating ability.

2. The conjugate according to claim 1 , wherein the active ingredient is at least one selected from protein, nucleic acid, peptide, lipid, glycol-lipid, mineral, sugar, nanoparticle, biological products, contrast agent, drugs and chemical compounds.

3. The conjugate according to claim 2 , wherein the active ingredient is a cytokine, antibody, fragment of antibody, therapeutic enzyme, soluble receptor or ligand.

4. The conjugate according to claim 2 , wherein the contrast agent is selected from a group consisting of radiopaque contrast agent, paramagnetic contrast agent, superparamagnetic contrast agent and CT contrast agent.

5. The conjugate according to claim 2 , wherein the contrast agent is based on iron.

6. The conjugate according to claim 5 , wherein the contrast agent is a ferrocene carboxylate.

7. The conjugate according to claim 1 , wherein the carrier peptide and the active ingredient are combined via a covalent bond, selectively mediated by a linker, wherein the active ingredient and the linker are heterologous to the carrier peptide.

8. The conjugate according to claim 1 , wherein the carrier peptide and the heterologous active ingredient are combined via non-covalent bond.

9. A contrast agent comprising a conjugate of any one of claims 1 , 2 - 8 , and 3 .

10. A composition comprising the conjugate according to claim 1 .

11. The composition according to claim 10 wherein the composition is selected from the group consisting of a pharmaceutical composition, a cosmetic composition, and a health food composition.

12. A cell penetrating carrier peptide, wherein the carrier peptide is 20 amino acids in length and is the amino acid sequence of SEQ ID NO: 121, or is the carrier peptide that is 20 amino acids in length and having at least 80% sequence identity with the amino acid sequence of SEQ ID NO: 121 and maintains cell penetrating ability.

13. A polynucleotide that encodes the cell penetrating peptide according to claim 12 , wherein upon expression of the polynucleotide the carrier peptide that is 20 amino acids in length and is the amino acid sequence of SEQ ID NO: 121, or the carrier peptide is 20 amino acids in length and having at least 80% sequence identity with the amino acid sequence of SEQ ID NO: 121 and maintains cell penetrating ability is produced.

14. A vector that comprises the polynucleotide according to claim 13 .

15. A transformed cell that comprises the vector according to claim 14 .

16. A method of treating a subject having a mitochondrial-related disease or disorder comprising administering to the subject a pharmaceutical composition comprising the conjugate of claim 1 .

17. The method of claim 16 , wherein the pharmaceutical composition is administered though oral, rectal, transdermal, intravenous, intramuscular, intraperitoneal, in the bone marrow, epidural, or subcutaneous means.

18. The method of claim 16 , wherein the pharmaceutical composition comprises additives selected from the group consisting of diluents, excipients, lubricants, binders, disintegrants, buffers, dispersants, surfactants, coloring agents, aromatics or sweeteners.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 6, 2023
From: GEMVAX & KAEL CO. LTD.
To: GEMVAX & KAEL CO. LTD.; KIM, SANG JAE
Reel/Frame 065471/0754 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 16, 2018
From: KIM, SANG JAE
To: GEMVAX & KAEL CO., LTD.
Reel/Frame 045814/0697 →
Priority Claims (5)
KR 10-2012-0104144 · Sep 19, 2012 · national
KR 10-2012-0104173 · Sep 19, 2012 · national
KR 10-2012-0109207 · Sep 28, 2012 · national
KR 10-2012-0109216 · Sep 28, 2012 · national
KR 10-2013-0017169 · Feb 18, 2013 · national
Continuity (2)
Division 14429637
Related Publication 20180208912A1 · Jul 26, 2018