Stabilization of biomolecules using sugar polymers

Patent metadata

Field	Value
Publication number	US-9901648-B2
Application number	US-201314374388-A
Country	US
Kind code	B2
Filing date	Jan 25, 2013
Priority date	Jan 27, 2012
Publication date	Feb 27, 2018
Grant date	Feb 27, 2018

Abstract

Compositions and methods for stabilizing biomolecules are disclosed. Specifically, the compositions include novel homopolymers or copolymers containing trehalose side chains conjugated to biomolecules. When such homopolymers or copolymers are placed in close proximity to biomolecules, such as proteins, the homopolymers or copolymers protect and/or stabilize the biomolecule. The compositions and methods may be suitable for use in various industries such as healthcare (pharmaceuticals), molecular biology, biofuels, paper, personal care, detergent, photographic, rubber, brewing, dairy and food processing industries.

First claim

We claim:

1. A monomer for use in making a homopolymer or a copolymer for stabilizing a biomolecule, the monomer having the general structure:
R 1 R 2 C═CR 3 R 4 ,

wherein R 1 -R 4 are independently selected from hydrogen or a side chain comprising at least one carbon atom, and wherein at least one of R 1 -R 4 is -L-trehalose, wherein L is a linking group that links trehalose to the monomer through at least one of the trehalose hydroxyl groups (—OH), wherein L is selected from group consisting of -aryl-(CH 2 ) n1 — ( n1 =0-6), —(COO)—(CH 2 ) n2 — ( n2 =1-6), —(CH 2 ) n4 — ( n4 =0-6), -aryl-(CH)—, —(COO)—(CH 2 ) n7 —(CH)— ( n7 =1-6) and —(CO)—, wherein both R 1 and R 2 are Hs.

2. A homopolymer or co-polymer made from one or more of the monomer of claim 1 , the homopolymer or copolymer comprising the general structure:
R 5 —[R 1 R 2 C—CR 3 R 4 ] n —R 6 ,

wherein n defines a number of repeat units sufficient to yield a molecular weight of said homopolymer or co-polymer from 4.200 g/mol to 19.000 g/mol,
wherein R 1 -R 4 are independently selected from hydrogen or a side chain comprising at least one carbon atom, and wherein at least one of R 1 -R 4 is -L-trehalose, wherein L is a linking group that links trehalose to the monomer through at least one of the trehalose hydroxyl groups (—OH),
wherein R 5 and R 6 are independently selected from the group consisting of -Alkyl, -Alkenyl, -Alkynyl, -aryl, —C(CN)(Alkyl) 2 , —S 2 C—S-Alkyl, —C(CO)(Alkyl)-(OCH 2 CH 2 ) n5 —COO—CH 2 CH 2 —CO-Alkyl ( n5 =1-10), and biomolecules, and
wherein L is selected from group consisting of -aryl-(CH 2 ) n1 — ( n1 =0-6), —(COO)—(CH 2 ) n6 — ( n2 =0-6), —(CONH)—(CH 2 ) n3 — ( n3 —0-5), —(CH 2 ) n4 — ( n4 =0-6), -aryl-(CH)—, —(COO)—(CH 2 ) n7 —(CH)— ( n7 =1-6) and —(CO)—.

3. The homopolymer or copolymer of claim 2 , wherein the biomolecule is selected from the group consisting of proteins, enzymes, antibodies, DNAs, RNAs, and siRNAs.

4. The homopolymer or copolymer of claim 2 , wherein the side chain -L-trehalose has a structure selected from the group consisting of:

5. The homopolymer or co-polymer of claim 2 , wherein any of R 1 -R 4 that is not -L-trehalose is either hydrogen or an alkyl group.

6. The homopolymer or copolymer of claim 5 , wherein the alkyl group is a methyl group.

7. The homopolymer or copolymer of claim 2 , wherein one of R 1 -R 4 is an alkyl group and two of R 1 -R 4 are hydrogens.

8. The homopolymer or copolymer of claim 7 , wherein the alkyl group is a methyl group.

9. The homopolymer or co-polymer of claim 8 , having the structure:

10. The homopolymer or copolymer of claim 2 , wherein three of R 1 -R 4 are hydrogens.

11. The homopolymer or co-polymer of claim 10 , having the structure selected from the group consisting of:

12. A method of synthesizing a homopolymer or copolymer for stabilizing a biomolecule, the method comprising the steps of:
(a) incorporating a side chain comprising a trehalose molecule into a polymerizable monomer, wherein said trehalose molecule optionally comprises protecting groups;
(b) polymerizing the resulting monomer to obtain a polymer: and
(c) optionally deprotecting said trehalose molecule in said polymer, to obtain a homopolymer or co-polymer according to claim 2 .

13. The method of claim 12 , wherein the homopolymer or copolymer is generated through chemical synthesis.

14. The method of claim 13 , wherein the polymerizable monomer is selected from the group consisting of a styrene monomer, an acrylate monomer, a methacrylate monomer, an acrylamide monomer, a methacrylamide monomer, a vinyl monomer, a norborenyl monomer, and a strained cycle alkene monomer.

15. The method of claim 12 , wherein the step of polymerizing the resulting monomer to obtain a homopolymer or copolymer is performed by any one of, but not limited to the following techniques; reversible addition-fragmentation (RAFT) polymerization, atom transfer radical polymerization (ATRP), nitroxide mediated polymerization (NMP), cyanoxyl-mediated free radical polymerization, conventional radical polymerization, or ring opening polymerization (ROMP).

16. The method of claim 13 , wherein one or more of the hydroxyl groups of the trehalose are protected by the formation of an acetal or an ether.

17. A method of stabilizing a biomolecule comprising the step of conjugating the biomolecule with a homopolymer or copolymer according to claim 2 .

18. The method of claim 17 , wherein the biomolecule is covalently conjugated to the homopolymer or copolymer backbone.

19. The method of claim 18 , wherein the biomolecule is conjugated to the homopolymer or copolymer backbone through a biomolecule reactive group attached to one or both termini of the homopolymer or copolymer backbone.

20. The method of claim 19 , wherein the biomolecule reactive group is a thiol reactive group.

21. The method of claim 17 , wherein the biomolecule is selected from the group consisting of proteins, enzymes, antibodies, DNAs, RNAs and siRNAs.

22. A composition comprising a biomolecule conjugated to a homopolymer or copolymer comprising the general structure:
—[R 1 R 2 C—CR 3 R 4 ] m —

wherein m defines a number of repeat units sufficient to yield a molecular weight of said homopolymer or co-polymer from 4,200 g/mol to 19,000 g/mol,
wherein R 1 -R 4 are independently selected from hydrogen or a side chain comprising at least one carbon atom, and wherein at least one of R 1 -R 4 is -L-trehalose, wherein L is a linking group that links trehalose to the monomer through at least one of the trehalose hydroxyl groups (—OH),
wherein the homopolymer or copolymer further comprises a biomolecule reactive chain transfer agent attached to one or both termini of the homopolymer or copolymer backbone, and
wherein L is selected from group consisting of -aryl-(CH 2 ) n1 — ( n1 =0-6), —(COO)—(CH 2 ) n6 — ( n2 =0-6), —(CONH)—(CH 2 ) n3 — ( n3 —0-5), —(CH 2 ) n4 — ( n4 =0-6), -aryl-(CH)—, —(COO)—(CH 2 ) n7 —(CH)— ( n7 =1-6) and —(CO)—.

23. The composition of claim 22 , wherein the biomolecule is selected from the group consisting of a protein, an enzyme, an antibody, a DNA, a RNA and an siRNA.

24. The homopolymer having the structure of:

wherein n defines a number of repeat units sufficient to yield a molecular weight of said homopolymer from 4,200 g/mol to 19,000 g/mol.

25. A composition comprising a biomolecule conjugated to the homopolymer of claim 24 .

Assignees

• Univ California

Inventors

• Maynard Heather D
• Mancini Rock J
• Lee Juneyoung
• Lin En Wei

Classifications

• C12Y302/01017

  Lysozyme (3.2.1.17) · CPC title

• A61K38/47

  acting on glycosyl compounds (3.2), e.g. cellulases, lactases · CPC title

• C07H3/04

  Disaccharides · CPC title

• C08F110/00

  Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond · CPC title

• A61K47/58 Primary

  obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. poly[meth]acrylate, polyacrylamide, polystyrene, polyvinylpyrrolidone, polyvinylalcohol or polystyrene sulfonic acid resin · CPC title