Purification of proteins

Patent metadata

Field	Value
Publication number	US-10793593-B2
Application number	US-201313732613-A
Country	US
Kind code	B2
Filing date	Jan 2, 2013
Priority date	Dec 21, 2006
Publication date	Oct 6, 2020
Grant date	Oct 6, 2020

Abstract

The present invention relates to a selectively soluble polymer capable of binding to one or more constituents in a mixture containing various biological materials and the methods of using such a polymer to purify a biomolecule from such a mixture. The polymer is soluble in the mixture under a certain set of process conditions such as pH or temperature and is rendered insoluble and precipitates out of solution upon a change in the process conditions. While in its solubilized state, the polymer is capable of binding to a selected entity within the stream such as impurities (DNA, RNA, host cell protein, endotoxins, etc.) in a cell broth and remains capable of binding to that entity even after the polymer is precipitated out of solution. The precipitate can then be filtered out from the remainder of the stream and the desired biomolecule is recovered and further processed.

First claim

What is claimed:

1. A method of purifying a biomolecule of interest from a mixture containing the biomolecule of interest and one or more negatively charged impurities, wherein the biomolecule of interest is produced in a microbial cell and is positively charged, the method comprising:
a) providing the mixture containing a biomolecule of interest and one or more impurities, wherein the biomolecule is expressed in a microbial cell;
b) adding to said mixture a polymer solubilized in a carrier liquid, wherein the polymer is poly(4-vinyl pyridine-co-vinyl pyridinium sulphopropyl betaine or poly(4-vinyl pyridine-co-vinyl pyridinium ethylene glycol;
c) adjusting the pH of the mixture to a pH of 5.2, to precipitate the polymer and form a supernatant, wherein the precipitated polymer binds the one or more impurities; and
d) subjecting said supernatant containing the biomolecule of interest to chromatography.

2. The method of claim 1 , wherein the microbial cell is an E. coli cell.

3. The method of claim 1 , wherein the microbial cell is a yeast cell.

4. The method of claim 1 wherein the one or more impurities is selected from the group consisting of DNA, RNA, virus, host cell proteins, endotoxins, cells, cell fragments, protein aggregates and combinations thereof.

5. The method of claim 1 , wherein said chromatography is selected from the group consisting of ion exchange chromatography, hydrophobic interaction chromatography and affinity chromatography.

6. A method of purifying a biomolecule of interest from a mixture containing the biomolecule of interest and one or more negatively charged impurities, wherein the biomolecule of interest is produced in a microbial cell and is positively charged, the method comprising:
a) providing the mixture containing a biomolecule of interest and one or more impurities, wherein the biomolecule is expressed in a microbial cell;
b) adding to said mixture a cationic polyelectrolyte polymer wherein the polymer is poly(4-vinyl pyridine-co-vinyl pyridinium sulphopropyl betaine or poly(4-vinyl pyridine-co-vinyl pyridinium ethylene glycol at conditions under which said polymer is soluble in said mixture;
c) adjusting the pH of the mixture to a pH of 5.2 to precipitate the polymer and form a supernatant, wherein the precipitated polymer binds the one or more impurities; and
d) subjecting said supernatant containing the biomolecule of interest to chromatography.

Assignees

• Emd Millipore Corp

Inventors

• Moya Wilson

Classifications

• C07K16/00

  Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies · CPC title

• C07K1/32 Primary

  as complexes · CPC title

• C07K1/36

  by a combination of two or more processes of different types · CPC title

• A61K2800/5426

  cationic · CPC title

• C07K1/30

  by precipitation · CPC title