US2013150288A1PendingUtilityA1
Treatment of viral infections
Est. expiryDec 17, 2023(expired)· nominal 20-yr term from priority
Inventors:Curtis Dobson
A61P 31/22A61P 31/12A61P 31/18A61P 37/04C07K 7/08C07K 14/775A61K 38/00
45
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Claims
Abstract
The present invention concerns polypeptides derived from a tandem repeat of apoE 141-149 and their uses as medicaments. The peptides may comprise the tandem repeat, and truncations thereof, for which at least one Leucine (L) is replaced by an amino acid with a side chain comprising at least 4 carbon atoms and at least one Nitrogen atom. Such peptides are useful for preventing or treating viral infections.
Claims
exact text as granted — not AI-modified1 - 22 . (canceled)
23 . An isolated and purified antiviral polypeptide comprising between 14 and 18 amino acids of the apoE 141-149 tandem repeat set forth in SEQ ID NO: 2, wherein said polypeptide comprises one or more amino acid substitutions of an amino acid with a side chain comprising at least 4 carbon atoms and at least one nitrogen atom for leucine (L).
24 . The polypeptide of claim 23 , wherein the amino acid with a side chain comprising at least 4 carbon atoms and at least one nitrogen atom is arginine (R) or lysine (K).
25 . The polypeptide of claim 23 , wherein at least two substitutions are made.
26 . The polypeptide of claim 23 , wherein at least one further leucine amino acid is replaced with Phenylalanine (F) or is deleted.
27 . The polypeptide of claim 23 , wherein an amino acid is added to the N terminal, C terminal and/or between the ninth and tenth amino acids of SEQ ID NO: 2.
28 . An isolated and purified antiviral polypeptide comprising YRKYRKRYYYRKYRKRYY (SEQ ID NO: 6).
29 . An isolated and purified antiviral polypeptide comprising LRKLRKLRKLRKLRKLRK (SEQ ID NO: 9).
30 . A composition, comprising the polypeptide of claim 23 .
31 . A method of inhibiting viral replication, comprising administering to a subject in need of such treatment a therapeutically effective amount of the polypeptide of claim 23 .
32 . The method of claim 31 , wherein the polypeptide is the polypeptide of claim 24 .
33 . The method of claim 31 , wherein the polypeptide is the polypeptide of claim 25 .
34 . The method of claim 31 , wherein the polypeptide is the polypeptide of claim 26 .
35 . The method of claim 31 , wherein the polypeptide is the polypeptide of claim 27 .
36 . The method of claim 31 , wherein the polypeptide is an isolated and purified antiviral polypeptide comprising YRKYRKRYYYRKYRKRYY (SEQ ID NO: 6).
37 . The method of claim 31 , wherein the polypeptide is an isolated and purified antiviral polypeptide comprising LRKLRKLRKLRKLRKLRK (SEQ ID NO: 9).
38 . An isolated and purified antiviral polypeptide derived from the apoE 141-149 tandem repeat set forth in SEQ ID NO: 2 selected from the group consisting of:
(SEQ ID NO: 56)
WRKCRKRCWWRKCRKRCW,
(SEQ ID NO: 57)
LRKLRKRLLWRKWRKRWW,
(SEQ ID NO: 58)
LRKLRKRLLLRKLRKRWW,
(SEQ ID NO: 59)
LRKLRKRLLWRKWRKRLL,
(SEQ ID NO: 60)
WRKWRKRLLLRKLRKRLL,
(SEQ ID NO: 61)
WRKLRKRLLLRKLRKRLL,
(SEQ ID NO: 62)
WRKWRKFFFRKWRKRWW,
(SEQ ID NO: 63)
WRKWRKRWWFRKFRKRFF,
(SEQ ID NO: 64)
RRKRRKRRRRRKRRKRRR,
and
(SEQ ID NO: 65)
KRKKRKRKKKRKKRKRKK.
39 . A method of inhibiting viral replication, comprising administering to a subject in need of such treatment a therapeutically effective amount of the polypeptide of claim 38 .Join the waitlist — get patent alerts
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