US2016168212A1PendingUtilityA1
Compositions for treatment of neurodegenerative diseases
Est. expiryMar 9, 2029(~2.6 yrs left)· nominal 20-yr term from priority
A61P 25/16A61P 25/28A61P 25/00A61K 38/00C07K 7/08G01N 33/68G01N 33/6896G01N 2800/28G01N 2800/2835C07K 7/06C07K 14/47G01N 2333/47G01N 2800/2821G01N 2800/2814
43
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Claims
Abstract
Isolated peptides are provided, being less than 20 amino acids in length. The peptides comprising an amino acid sequence GVLYVGSKTREGV (SEQ ID NO: 12) AAATGLVKREE (SEQ ID NO: 13) or GVVAAAEKTKQG (SEQ ID NO: 14), mimetics and/or fragment thereof, the peptides being capable of inhibiting alpha synuclein aggregation. Pharmaceutical compositions comprising same are also provided as well as uses thereof.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . An isolated or synthetic peptide being less than 20 amino acids in length, the peptide comprising the amino acid sequence as set forth in SEQ ID NO: 1, 2, 3 or 4.
2 . The peptide of claim 1 , comprising a synthetic beta breaker amino acid.
3 . The peptide of claim 1 , wherein said amino acid sequence comprises at least one D-amino acid residue.
4 . The peptide of claim 1 , wherein said amino acid sequence consists of D-amino acid residues.
5 . The peptide of claim 1 , comprising an end cap modification.
6 . The peptide of claim 5 , wherein said end cap modification comprises at least one of N-terminus acetylation and C-terminus amidation.
7 . The peptide of claim 1 , being a decamer.
8 . The peptide of claim 1 , being a cyclic peptide.
9 . The peptide of claim 1 comprising an amino acid sequence as set forth in SEQ ID NO: 1.
10 . A pharmaceutical composition comprising as an active ingredient the peptide of claim 1 and a pharmaceutically acceptable carrier.
11 . A method of inhibiting alpha-synuclein aggregation, the method comprising contacting alpha-synuclein with the peptide of claim 1 , thereby inhibiting alpha-synuclein aggregation.
12 . The method of claim 11 , wherein inhibition of alpha synuclein aggregation comprises inhibition of alpha synuclein oligomerization, inhibition of alpha synuclein fibril formation or a combination thereof.
13 . A method of treating or preventing a medical condition associated with alpha-synuclein aggregation, the method comprising administering to a subject in need thereof a therapeutically effective amount of the peptide of claim 1 , thereby treating the medical condition associated with alpha-synuclein aggregation.
14 . The method of claim 13 , wherein said medical condition is selected from the group consisting of Parkinson's disease (PD), Alzheimer's disease (AD), diffuse Lewy body disease, mixed AD-PD, multiple system atrophy, Hallervorden-Spatz disease and Huntington's chorea.
15 . A method of detecting alpha-synuclein monomers, the method comprising:
(a) contacting a biological sample suspected of comprising said alpha-synuclein monomers with the peptide of claim 1 under conditions which allow complex formation between said monomers and said peptide; and (b) detecting presence or level of said complex, thereby detecting alpha-synuclein monomers.Join the waitlist — get patent alerts
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