IP Library Granted Patent US 9,458,191
Granted Patent B2
US 9,458,191 · App. 14/536,513 · Granted Oct 4, 2016

Nanolipoprotein particles and related methods and systems for protein capture, solubilization, and/or purification

Inventors: Brett A. Chromy (Danville, CA); Paul Henderson (Dublin, CA); Paul D. Hoeprich, Jr. (Pleasanton, CA)
Assignee: Lawrence Livermore National Security, LLC
C07K1/145C12N11/02C12P3/00Y10S977/799
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Quick Facts
Patent No.
US 9,458,191
App. No.
14/536,513
Granted
Oct 4, 2016
Kind
B2
Abstract

Provided herein are methods and systems for assembling, solubilizing and/or purifying a membrane associated protein in a nanolipoprotein particle, which comprise a temperature transition cycle performed in presence of a detergent, wherein during the temperature transition cycle the nanolipoprotein components are brought to a temperature above and below the gel to liquid crystalling transition temperature of the membrane forming lipid of the nanolipoprotein particle.

Claims (13)

1. A method for solubilizing a membrane associated protein from a cell membrane, the method comprising

contacting the cell membrane with a scaffold protein and a membrane forming lipid to provide an admixture, the membrane forming lipid having a membrane forming lipid gel-crystalline transition temperature; and

subjecting the admixture to at least three temperature transition cycles in presence of a detergent, for a time and under condition to allow assembly of a nanolipoprotein particle comprising a solubilized target protein, the temperature transition cycle comprising:

a temperature increase step wherein the admixture is brought to a temperature above said membrane forming lipid gel crystalline transition temperature and

a temperature decrease step wherein the admixture is brought to a temperature below said membrane forming lipid gel crystalline transition temperature.

2. The method of claim 1 , wherein the cell membrane contacted with the membrane forming lipid and the scaffold protein, is in a crude cell pellet or a membrane fraction.

3. The method of claim 1 , wherein the cell membrane is an inner membrane of gram-negative bacteria, an outer membrane of gram-negative bacteria, a single bilayer membrane of gram-positive bacteria, or a plasma membrane of a eukaryotic cell.

4. The method of claim 1 , further comprising incubating the admixture subjected to the temperature transition cycle at the membrane forming lipid gel-crystalline transition temperature for a predetermined amount of time that is functional to a desired amount of assembled nanolipoprotein particles.

5. The method of claim 1 , further comprising removing the detergent from the admixture subjected to the temperature transition cycle.

6. The method of claim 1 , wherein the membrane forming lipid is contacted with the membrane associated protein and the scaffold protein at a temperature above the membrane forming lipid gel-crystalline transition temperature.

7. The method of claim 1 , wherein subjecting the admixture to a temperature transition cycle in presence of a detergent is performed by subjecting the admixture to multiple temperature transition cycles.

8. The method of claim 1 , wherein the temperature increase step and/or the temperature decrease step are performed for a time and under conditions such that at least a fraction of the membrane forming lipid molecules in the admixture changes state.

9. The method of claim 1 , wherein the membrane associated protein contacted with the membrane forming lipid and with the scaffold protein is comprised in a cell membrane.

Assignments (2)
CONFIRMATORY LICENSE Recorded Mar 30, 2015
From: LAWRENCE LIVERMORE NATIONAL SECURITY, LLC
To: U.S. DEPARTMENT OF ENERGY
Reel/Frame 035284/0349 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 9, 2015
From: CHROMY, BRETT A.; HENDERSON, PAUL; HOEPRICH, PAUL D.
To: LAWRENCE LIVERMORE NATIONAL SECURITY, LLC
Reel/Frame 034670/0015 →
Continuity (4)
Continuation 12352548 · Jan 12, 2009
Provisional Application 61020638 · Jan 11, 2008
Provisional Application 61115446 · Nov 17, 2008
Related Publication 20150105538A1 · Apr 16, 2015