IP Library Granted Patent US 9,540,620
Granted Patent B2
US 9,540,620 · App. 14/398,678 · Granted Jan 10, 2017

Methods and compositions for modulating G-alpha-Q signaling

Inventors: John Sondek (Chapel Hill, NC); Thomas Kendall Harden (Westfield, NC); Gary Lynn Waldo (Chapel Hill, NC); Matthew Owen Barrett (Carrboro, NC); Thomas Henry Charpentier (Chapel Hill, NC)
Assignee: The University of North Carolina at Chapel Hill
C12N9/16A61K38/465A61K47/48046A61K47/48246C07K14/4703C12Q1/34C12Y301/04011G01N2333/914G01N2500/02G01N2500/04G01N2500/20
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Quick Facts
Patent No.
US 9,540,620
App. No.
14/398,678
Granted
Jan 10, 2017
Kind
B2
Abstract

The present invention provides compositions and methods for modulating G-alpha-q activity and methods of screening of test substances for the ability to modulate G-alpha-q activity.

Claims (35)

1. A method of downregulating G-alpha-Q signaling in a cell, comprising introducing into the cell a peptide comprising the amino acid sequence HQDYAEALANPIKHVSL-Nle-DQR (SEQ ID NO:1).

2. The method of claim 1 , wherein the peptide further comprises from one to six additional amino acids, X 22 , X 23 , X 24 , X 25 , X 26 and X 27 , wherein

X 22 is A or any nonnatural amino acid or any amino acid listed in Table 2;

X 23 is R or any nonnatural amino acid or any amino acid listed in Table 2;

X 24 is Q or any nonnatural amino acid or any amino acid listed in Table 2;

X 25 is L or any nonnatural amino acid or any amino acid listed in Table 2;

X 26 is A or any nonnatural amino acid or any amino acid listed in Table 2; and

X 27 is A or any nonnatural amino acid or any amino acid listed in Table 2.

3. A method of treating a cancer associated with a Gαq mutation in a subject in need thereof, comprising introducing to the subject an effective amount of a peptide comprising the amino acid sequence HQDYAEALANPIKHVSL-Nle-DQR (SEQ ID NO:1).

4. The method of claim 3 , wherein the peptide further comprises from one to six additional amino acids, X 22 , X 23 , X 24 , X 25 , X 26 and X 27 , wherein

X 22 is A or any nonnatural amino acid or any amino acid listed in Table 2;

X 23 is R or any nonnatural amino acid or any amino acid listed in Table 2;

X 24 is Q or any nonnatural amino acid or any amino acid listed in Table 2;

X 25 is L or any nonnatural amino acid or any amino acid listed in Table 2;

X 26 is A or any nonnatural amino acid or any amino acid listed in Table 2; and

X 27 is A or any nonnatural amino acid or any amino acid listed in Table 2.

5. The method of claim 1 , wherein the peptide further comprises amino acids YIPX 28 D at the amino terminus, wherein X 28 is a nonnatural amino acid.

6. The method of claim 5 , wherein the peptide is YIP X 28 DHQDYA X 28 ALANPIKHVSLMDQRARALAA and wherein X 28 is a nonnatural amino acid.

7. The method of claim 1 , wherein the peptide further comprises a protein transduction domain (PTD) at the amino and/or carboxy terminus.

8. The method of claim 7 , wherein the protein transduction domain is selected from the group consisting of GRKKRRQRRPPQ (SEQ ID NO: 18), RQIKIWFQNRRMKWKK (SEQ ID NO: 19), GWTLNSAGGYLLGKINLKALAALAKKI (SEQ ID NO: 21), RRRRRRRRR (SEQ ID NO: 22), RRRRRRR (SEQ ID NO: 23), KETWWETWWTWWSQPKKKRKV (SEQ ID NO: 24), YGRKKRRQRRR (SEQ ID NO: 25), YARAAARQARA (SEQ ID NO: 26), KETWWETWWTEWS (SEQ ID NO: 27), GWTLNSAGYLLGKINLKALAALAKKIL (SEQ ID NO: 28), Cre recombinase, DAATATRGRSAASRPTERPRAPARSASRPRRPVE (SEQ ID NO: 29), KMTRAQRRAAARRNRRWTAR (SEQ ID NO: 30) and any combination thereof.

9. The method of claim 1 , wherein an alphahelical transmembrane domain is added to the peptide with one or more PEG linkers.

10. The method of claim 1 , wherein a lipid is added to the peptide with one or more PEG linkers.

11. The method of claim 10 , wherein the lipid is selected from the group consisting of palmitic acid, myristic acid and farnesylic acid.

12. The method of claim 11 , wherein the peptide is Palm-PEG-PEG-HQDYAEALANPIKHVSL-Nle-DQRARQLAA.

13. The method of claim 1 , wherein the cell is in a subject.

14. The method of claim 13 , wherein the subject is a human.

15. The method of claim 3 , wherein the cancer is uveal melanoma.

16. A method of identifying a test substance having the ability to inhibit G-alpha-q activity, comprising:

a) contacting a peptide comprising the amino acid sequence HQDYAEALANPIKHVSL-Nle-DQRARQLAA (SEQ ID NO: 4) and further comprising a TAMRA label with G-alpha-q and GDP and aluminum fluoride and determining a baseline fluorescence polarization value; and;

b) contacting the peptide of (a) with G-alpha-q and GDP, aluminum fluoride and the test substance and determining a fluorescence polarization value,

wherein a fluorescence polarization value of (b) that is lower than the fluorescence polarization value of (a) identifies the test substance as having the ability to inhibit G-alpha-q activity.

17. A method of identifying a test substance having the ability to increase G-alpha-q activity, comprising:

a) contacting a peptide comprising the amino acid sequence HQDYAEALANPIKHVSL-Nle-DQRARQLAA (SEQ ID NO:4) and further comprising a TAMRA label with G-alpha-q and GDP and aluminum fluoride and determining a baseline fluorescence polarization value; and

b) contacting the peptide of (a) with G-alpha-q, GDP, aluminum fluoride and the test substance and determining a fluorescence polarization value,

wherein a fluorescence polarization value of (b) that is greater than the fluorescence polarization value of (a) identifies the test substance as having the ability to increase G-alpha-q activity.

Assignments (2)
CONFIRMATORY LICENSE Recorded Jun 6, 2017
From: UNIV OF NORTH CAROLINA CHAPEL HILL
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 042692/0863 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 12, 2014
From: SONDEK, JOHN; HARDEN, THOMAS KENDALL; WALDO, GARY LYNN; BARRETT, MATTHEW OWEN; CHARPENTIER, THOMAS HENRY
To: THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL
Reel/Frame 034495/0841 →
Continuity (3)
Provisional Application 61643670 · May 7, 2012
Provisional Application 61642368 · May 3, 2012
Related Publication 20150218538A1 · Aug 6, 2015