IP Library Granted Patent US 8,012,471
Granted Patent B2
US 8,012,471 · App. 11/712,452 · Granted Sep 6, 2011

Screening and treatment methods using IGS5 enzymes of the metalloprotease family

Assignee: Abbott Healthcare Products B.V.
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Quick Facts
Patent No.
US 8,012,471
App. No.
11/712,452
Granted
Sep 6, 2011
Kind
B2
Abstract

Polypeptides which are related to the neprilysin enzyme family and have zinc metalloprotease activities and are referred to as IGS5, polynucleotides encoding such polypeptides, vectors containing such polynucleotides, host cells containing such vectors, processes for producing such polypeptides and/or polynucleotides, screening methods for identifying compounds which stimulate or inhibit IGS5 polypeptides and/or polynucleotides, and the use of such polypeptides and/or polynucleotides in therapy of various dysfunctions, disorders or diseases, particularly cardiovascular diseases, metabolic diseases such as diabetes mellitus type II, and neurodegenerative disorders, such as Parkinson's Disease.

Claims (9)

1. A method for the treatment of a neurodegenerative disease in a mammalian subject, the method comprising the step of administering to said subject an effective amount of a compound inhibiting or decreasing activity of an neprilysin II (IGS5) polypeptide wherein said IGS5 polypeptide has a zinc metallopeptidase activity and comprises a human amino acid sequence having at least 95% sequence identity to SEQ ID NO:2, SEQ ID NO:4 or SEQ ID NO:6 and wherein said compound is selected from the group consisting of:

(i) Phosphoramidon;

(ii) (3S,2′R)-3-{1-[2′-(ethoxycarbonyl)-4′-phenylbutyl]-cyclopentane-1-carbonylamino}-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepine-1-acetic acid; and

(iii) a compound inhibiting expression of IGS5 selected from antisense sequences, oligonucleotides which form triple helices or ribozymes.

2. A method according to claim 1 , wherein the neurodegenerative disease is selected from the group consisting of Parkinson's disease, multiple sclerosis, Alzheimer disease, Huntington's disease, stroke, and cerebral ischemia.

3. A method according to claim 1 , wherein said compound is a selective inhibitor of said IGS5 polypeptide.

4. A method according to claim 1 , wherein said compound does not inhibit the activity of a neprisysin (NEP) polypeptide and/or endothelin converting enzyme-1 (ECE-1) polypeptide.

5. A method according to claim 1 , wherein said IGS5 polypeptide comprises an amino acid sequence having at least 99% sequence identity to SEQ ID NO:4 or SEQ ID NO:6.

6. The method according to claim 1 , wherein said neurodegenerative disease is associated with pituitary adenylate cyclase-activating polypeptide (PACAP) (1-27) levels decreased below normal baseline levels of PACAP(1-27).

Assignments (2)
CHANGE OF NAME Recorded May 26, 2011
From: SOLVAY PHARMACEUTICALS B.V.
To: ABBOTT HEALTHCARE PRODUCTS B.V.
Reel/Frame 026357/0071 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 4, 2007
From: DELEERSNIJDER, WILLY; KARIMI-NEJAD, YASMIN; WESKE, MICHAEL; ZIEGLER, DIETER
To: SOLVAY PHARMACEUTICALS B.V.
Reel/Frame 019376/0610 →
Priority Claims (4)
EP 99203862 · Nov 19, 1999 · regional
NL 1013616 · Nov 19, 1999 · national
EP 00201937 · May 31, 2000 · regional
NL 1015356 · May 31, 2000 · national
Continuity (5)
Continuation In Part 11433388 · May 15, 2006
Division 10870003 · Jun 18, 2004
Division 10147928 · May 20, 2002
Continuation PCTEP0011532 · Nov 17, 2000
Related Publication 20070224180A1 · Sep 27, 2007