IP Library › Granted Patent US 7,541,036
Granted Patent B2
US 7,541,036 · App. 10/485,980 · Granted Jun 2, 2009

Human immunodeficiency virus type 1 (HIV-1) matrix (MA or p17) polypeptide capable of inducing anti-p17 antibodies that neutralize the proinflammatory activities of the MA protein

Assignee: Medestea Internazionale S.r.l.
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Quick Facts
Patent No.
US 7,541,036
App. No.
10/485,980
Granted
Jun 2, 2009
Kind
B2
Abstract

New isolated polypeptides of the protein p17 of HIV are described, represented by the formula: NH 2 -X 1 -Gly-X 2 -X 3 -Leu-Asp-X 4 -Trp-Glu-X 5 -Ile-X 6 -Leu-Arg-COOH (SEQ ID NO:1) in which X 1 is an amino acid residue selected from Ser and Arg; X 2 is an amino acid residue selected from Gly, Glu and Ser; X 3 is an amino acid residue selected from Glu, Lys, Asp and Arg; X 4 is an amino acid residue selected from Arg, Ala, Lys, Thr, Ser, Glu, Asp and Gln; X 5 is an amino acid residue selected from Lys, Arg and Ser; and X 6 is an amino acid residue selected from Arg and Gln. These polypeptides, when administered to a subject, are able to evoke anti-p17 neutralizing antibodies and are therefore useful as vaccine or inoculum. Monoclonal and polycolonal anti-p17 antibodies which are able to neutralize the biological activity of this viral protein and to recognize its neutralization epitope in a specific manner are also described.

Claims (8)

1. An isolated polypeptide capable of evoking an anti-p17 antibody that inhibits the proinflammatory biological function of HIV p17 protein consisting of an amino acid sequence NH 2 -X 1 -Gly-X 2 -X 3 -Leu-Asp-X 4 -Trp-Glu-X 5 -Ile-X 6 -Leu-Arg-COOH (SEQ ID NO: 1), wherein X 1 is an amino acid residue selected from Ser and Arg, X 2 is an amino acid residue selected from Gly, Glu and Ser; X 3 is an amino acid residue selected from Glu, Lys, Asp and Arg; X 4 is an amino acid residue selected from Arg, Ala, Lys, Thr, Ser, Glu, Asp and Gln; X 5 is an amino acid residue selected from Lys, Arg and Ser; and X 6 is an amino acid residue selected from Arg and Gln.

2. A polypeptide according to claim 1 , in which said amino acid sequence is NH 2 -Ser-Gly-Gly-Glu-Leu-Asp-Arg-Trp-Glu-Lys-Ile-Arg-Leu-Arg-COOH (SEQ ID NO: 2).

3. A polypeptide according to claim 1 , in which a second amino acid sequence capable of increasing the solubility of the polypeptide is directly bound to the amino acid residue in the carboxyterminal position of SEQ ID NO:1 or SEQ ID NO: 2.

4. A polypeptide according to claim 3 , in which the second amino acid sequence is -Pro-Gly-Gly-Lys-Lys-Lys-Tyr-Lys-COOH (SEQ ID NO:3).

5. A polypeptide according to claim 1 , which is conjugated with a carrier.

6. A polypeptide according to claim 5 , which is conjugated with a carrier through an additional residue of cysteine (Cys) or an additional dipeptide -Nleu-Cys in the carboxyterminal position.

7. A polypeptide according to claim 1 , which is in the form of a branched peptide.

8. An immunogenic composition comprising a polypeptide according to claim 1 and a pharmaceutically acceptable vehicle.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 30, 2004
From: CARUSO, ARNALDO; FRANZONE, JOSE SEBASTIAN
To: MEDESTEA INTERNAZIONALE S.R.L.
Reel/Frame 015625/0989 →
Priority Claims (2)
IT TO2001A0795 · Aug 7, 2001 · national
IT TO2001A1042 · Nov 2, 2001 · national
Continuity (1)
Related Publication 20040249124A1 · Dec 9, 2004