Hybrid polypeptides with enhanced pharmacokinetic properties
The present invention relates to enhancer peptide sequences originally derived from various retroviral envelope (gp41) protein sequences that enhance the pharmacokinetic properties of any core polypeptide to which they are linked. The invention is based on the discovery that hybrid polypeptides comprising the enhancer peptide sequences linked to a core polypeptide possess enhanced pharmacokinetic properties such as increased half life. The invention further relates to methods for enhancing the pharmacokinetic properties of any core polypeptide through linkage of the enhancer peptide sequences to the core polypeptide. The core polypeptides to be used in the practice of the invention can include any pharmacologically useful peptide that can be used, for example, as a therapeutic or prophylactic reagent.
What is claimed is:
1. A hybrid polypeptide comprising an enhancer peptide sequence linked to a core polypeptide, wherein the enhancer peptide comprises an amino-terminal:
WXXWXXXI, WXXWXXX, WXXWXX, WXXWX, WXXW, WXXXWXWX, XXXWXWX, XXWXWX, XWXWX, WXWX, WXXXWXW, WXXXWX WXXXW, IXXXWXXW, XXXWXXW, XXWXXW, XWXXW, XWXWXXXW, XWXWXXX, XWXWXX, XWXWX, XWXW, WXWXXXW, or XWXXXW, and wherein the core polypeptide comprises thefollowing amino acid sequence:
TALLEQAQIQQEKNEYELQKLDK; (SEQ ID NO:1286).
2. The hybrid polypeptide of claim 1, further comprising an enhancer peptide sequence linked to the carboxy-terminal end of the core polypeptide.
3. A hybrid polypeptide comprising an enhancer peptide sequence linked to a core polypeptide, wherein the enhancer peptide sequence comprises WQEWEQKI (SEQ ID NO:1129) or WASLWEWF (SEQ ID NO:1433) and the core polypeptide comprises the followingamino acid sequence:
TALLEQAQIQQEKNEYELQKLDK (SEQ ID NO:1286).
4. A method for enhancing the pharmacokinetic properties of a core polypeptide, comprising linking an enhancer peptide sequence to the core polypeptide to produce a hybrid polypeptide, wherein the enhancer peptide sequence comprises:
WXXWXXXI, WXXWXXX, WXXWXX, WXXWX, WXXW, WXXXWXWX, XXXWXWX, XXWXWX, XWXWX, WXWX, WXXXWXW, WXXXWX, WXXXW, IXXXWXXW, XXXWXXW, XXWXXW, XWXXW, XWXWXXXW, XWXWXXX, XWXWXX, XWXWX, XWXW, WXWXXXW, or XWXXXW, and wherein the core polypeptide comprisesTALLEQAQIQQEKNEYELQKLDK (SEO ID NO:1286) such that, when introduced into a living system, the hybrid polypeptide exhibits enhanced pharmacokinetic properties relative to those exhibited by the core polypeptide.
5. A polypeptide comprising the amino acid sequence:
WQEWEQKITALLEQAQIQQEKNEYELQKLDKWASLWEWF (SEQ ID NO:1310).
6. The polypeptide of claim 5, further comprising an amino terminal acetyl group and a carboxy terminal amido group.
7. A hybrid polypeptide comprising an enhancer peptide sequence linked to a core polypeptide, wherein the enhancer peptide sequence comprises a carboxy-terminal:
WXXWXXXI, WXXWXXX, WXXWXX, WXXWX, WXXW, WXXXWXWX, XXXWXWX, XXWXWX, XWXWX, WXWX, WXXXWXW, WXXXWX, WXXXW, IXXXWXXW, XXXWXXW, XXWXXW, XWXXW, XWXWXXXW, XWXWXXX, XWXWXX, XWXWX, XWXW, WXWXXXW, or XWXXXW, and wherein the core polypeptide comprises thefollowing amino acid sequence:
TALLEQAQIQQEKNEYELQKLDK (SEQ ID NO:1286).
8. The hybrid polypeptide of claim 7, further comprising an enhancer peptide sequence linked to the amino-terminal end of the core polypeptide.
9. The hybrid polypeptide of claims 1,2, 8, 3, or 7 further comprising an amino terminal acetyl group and a carboxy terminal amido group.
10. A polypeptide comprising TALLEQAQIQQEKNEYELQKLDK (SEQ ID NO:1286).
11. The polypeptide of claim 10, further comprising an amino terminal acetyl group and a carboxy terminal amido group.
12. A pharmaceutical composition comprising the polypeptide:
TALLEQAQIQQEKNEYELQKLDK (SEQ ID NO:1286), and a pharmaceutically acceptable carrier.
13. The pharmaceutical composition of claim 12, wherein the polypeptide further comprises an amino terminal acetyl group and a carboxy terminal amido group.
14. A pharmaceutical composition comprising the polypeptide:
WQEWEQKITALLEQAQIQQEKNEYELQKLDKWASLWEWF (SEQ ID NO:1310), and a pharmaceutically acceptable carrier.
15. The pharmaceutical composition of claim 14, wherein the polypeptide further comprises an amino terminal acetyl group and a carboxy terminal amido group.
Patent number:
6258782
View patent at USPTO
Filing date:
May 20, 1998
Issue date:
July 10, 2001
Inventors:
Mohmed K. Anwer (Foster City, CA)
Shawn Barney (Apex, NC)
Kelly I. Guthrie (Graham, NC)
Dennis M. Lambert (Cary, NC)
Gene Merutka (Hillsborough, NC)
Assignee:
Trimeris, Inc. (Durham, NC)
Primary Examiner:
Jeffrey E. Russel
Attorney, Agent or Firm:
Pennie & Edmonds LLP
Current U.S. Classification: 514/12 514/13 514/15 514/2 530/300 530/313 530/324 530/328 530/350
