IP Library › Granted Patent US 8,367,360
Granted Patent B2
US 8,367,360 · App. 11/630,720 · Granted Feb 5, 2013

Method of screening for inhibitors of tau protein phosphororylation by tyrosine kinase c-Abl

Inventors: Malcolm Ward (Surrey, GB); Helen Byers (Surrey, GB); Brian Henry Anderton (London, GB); Pascal Derkinderen (London, GB); Christopher Hugh Reynolds (London, GB); Ritchie Williamson (London, GB)
Assignees: Proteome Sciences plc; King's College London
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Quick Facts
Patent No.
US 8,367,360
App. No.
11/630,720
Granted
Feb 5, 2013
Kind
B2
Abstract

The present invention provides methods of screening for candidate compounds useful in the treatment of Alzheimer's disease and related conditions by inhibiting specific phosphorylation of tau protein by tyrosine kinase c-Abl.

Claims (11)

1. An in vitro method of screening for substances which are candidate therapeutic agents for the treatment of a tauopathy selected from the group consisting of Alzheimer's disease (AD), frontotemproal dementia with Parkinsonism linked to chromosome 17 (FTDP-17), progressive supranuclear palsy (PSP), Pick's disease, corticobasal degeneration and multiple system atrophy (MSA), said substance being effective to inhibit the phosphorylation of a tau protein by a tyrosine kinase, wherein the tau protein comprises at least one phosphorylation site, the method comprising:

(a) contacting at least one said substance, the tau protein and the tyrosine kinase under conditions in which the tyrosine kinase is capable of phorphorylating said phosphorylation site(s) of the tau protein in the absence of the substance;

(b) detecting whether, and optionally the extent to which, said substance inhibits the phosphorylation of the tau protein at said at least one phosphorylation site of the tau protein by the tyrosine kinase; and,

(c) selecting the substance which inhibits phosphorylation of the tau protein at said at least one site;

wherein the tyrosine kinase is c-Abl;

and wherein the tau protein is a protein which undergoes phosphorylation by c-Abl and has at least 80% sequence identity with the amino acid sequence of SEQ ID NO: 1, or a fragment of said tau protein, said fragment comprising at least 25 amino acids and including at least one said phosphorylation site.

2. The method of claim 1 , wherein the tau protein is in the form of a paired helical filament tau.

3. The method of claim 1 , wherein the tau protein has at least 90% sequence identity with the tau protein having the amino acid sequence set out in SEQ ID NO: 1.

4. The method of claim 1 , wherein c-Abl phosphorylates the tau protein at one or more sites selected from the group consisting of Y197, Y310 and Y394 of the tau protein.

5. The method of claim 4 , wherein c-Abl phosphorylates tau protein at Y394 of tau protein.

6. The method of claim 1 , wherein the step of determining the presence, absence or extent of phosphorylation at one or more sites of the tau protein employs mass spectroscopy or a site specific recognition agent which is capable of distinguishing between phosphorylated and-non-phosphorylated sites.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 26, 2012
From: ANDERTON, BRIAN; DERKINDEREN, PASCAL; REYNOLDS, CHRISTOPHER; WILLIAMSON, RITCHIE
To: KING'S COLLEGE LONDON
Reel/Frame 029525/0711 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 26, 2012
From: WARD, MALCOLM; BYERS, HELEN
To: PROTEOME SCIENCES PLC
Reel/Frame 029525/0755 →
Continuity (2)
Provisional Application 60580901 · Jun 21, 2004
Related Publication 20080103107A1 · May 1, 2008