IP Library Granted Patent US 7,192,714
Granted Patent B2
US 7,192,714 · App. 09/977,155 · Granted Mar 20, 2007

LDL receptor signaling assays

Assignee: Board of Regents, The University of Texas System
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Quick Facts
Patent No.
US 7,192,714
App. No.
09/977,155
Granted
Mar 20, 2007
Kind
B2
Abstract

The invention provides methods and compositions for modeling and detecting LDL receptor transmembrane signaling by detecting proteolysis of an LDL receptor transmembrane domain. The method comprises the steps of: a) providing a sample comprising a cell membrane comprising (i) a polypeptide comprising an LDL receptor transmembrane domain fused to a C-terminal tail, and (ii) a protease which specifically cleaves the domain and thereby releases the tail from the membrane; b) incubating the sample under conditions wherein the protease cleaves the domain and thereby releases the tail from the membrane; and c) detecting a resultant released tail.

Claims (23)

1. A method for detecting proteolysis of an LDL (Low Density Lipoprotein) receptor transmembrane domain, comprising the steps of:

a) providing a sample comprising a cell membrane comprising (i) a polypeptide comprising an LDL receptor transmembrane domain fused to a C-terminal tail, and (ii) a protease which specifically cleaves the domain and thereby releases the tail from the membrane;

b) incubating the sample under conditions wherein the protease cleaves the domain and thereby releases the tail from the membrane; and

c) detecting a resultant released tail, which indicates proteolysis of the LDL receptor transmembrane domain.

2. A method according to claim 1 , wherein the sample comprises a viable cell which comprises the membrane.

3. A method according to claim 1 , wherein the sample comprises a viable cell which comprises the membrane, the tail comprises an intracellular transcription factor domain, the cell further comprises a transcriptional reporter responsive to release of the transcription factor domain from the membrane, and the detecting step comprises detecting expression of the reporter as an indication of the released tail.

4. A method according to claim 1 , wherein the sample comprises a cellular membrane extract which comprises the membrane.

5. A method according to claim 1 , wherein the sample comprises a cellular membrane extract which comprises the membrane, and the detecting step comprises selectively detecting released, soluble tails.

6. A method according to claim 1 , wherein the sample comprises a cellular membrane extract which comprises the membrane, and the detecting step comprises selectively detecting released, soluble tails by solid-phase affinity adsorption assay.

7. A method according to claim 1 , wherein the tail comprises an affinity tag.

8. A method according to claim 1 , wherein the tail comprises at least a portion of the cytoplasmic domain of the LDL receptor.

9. A method according to claim 1 , wherein the protease is native to the membrane.

10. A method according to claim 1 , wherein the protease is gamma secretase.

11. A method according to claim 1 , wherein the LDL receptor is selected from the group consisting of LRP (LDL Receptor-related Protein), LRP1b (LDL Receptor-related Protein 1b), megalin, LDLR (Low Density Lipoprotein Receptor), VLDLR (very Low Density Lipoprotein Receptor), ApoER2 (Apolipoprotein E Receptor 2), MEGF7 (Multiple Epidermal Growth Factor-like domain protein 7), LRP5 (Low density lipoprotein Receptor-related Protein 5), LRP6 (Low density lipoprotein Receptor-related Protein 5) and LR11 (Low density lipoprotein Receptor 11).

12. A method according to claim 1 , wherein the LDL receptor is LRP and the protease is native to the membrane.

13. A method according to claim 3 , wherein the LDL receptor is LRP and the protease is native to the membrane.

14. A method according to claim 5 , wherein the LDL receptor is LRP and the protease is native to the membrane.

15. A method according to claim 1 , wherein the LDL receptor is LRP1b and the protease is native to the membrane.

16. A method according to claim 3 , wherein the LDL receptor is LRP1b and the protease is native to the membrane.

17. A method according to claim 5 , wherein the LDL receptor is LRP1b and the protease is native to the membrane.

18. A method according to claim 1 , wherein the LDL receptor is megalin and the protease is native to the membrane.

19. A method according to claim 3 , wherein the LDL receptor is megalin and the protease is native to the membrane.

20. A method according to claim 5 , wherein the LDL receptor is megalin and the protease is native to the membrane.

Assignments (4)
CONFIRMATORY LICENSE Recorded Jan 16, 2020
From: UT SOUTHWESTERN MEDICAL CENTER
To: NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR
Reel/Frame 051536/0561 →
CONFIRMATORY LICENSE Recorded Jan 12, 2020
From: UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER
To: NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR
Reel/Frame 051567/0583 →
CONFIRMATORY LICENSE Recorded Oct 19, 2008
From: UNIVERSITY OF TEXAS SW MEDICAL CENTER AT DALLAS
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 021699/0934 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 12, 2001
From: HERZ, JOACHIM; MAY, PETRA
To: BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM
Reel/Frame 012269/0226 →
Continuity (1)
Related Publication 20030077672A1 · Apr 24, 2003