IP Library Granted Patent US 7,511,095
Granted Patent B2
US 7,511,095 · App. 11/353,656 · Granted Mar 31, 2009

Thioester-terminated water soluble polymers and method of modifying the N-terminus of a polypeptide therewith

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Quick Facts
Patent No.
US 7,511,095
App. No.
11/353,656
Granted
Mar 31, 2009
Kind
B2
Abstract

The invention provides reagents and methods for conjugating a polymer specifically to the α-amine of a polypeptide. The invention provides monofunctional, bifunctional, and multifunctional PEGs and related polymers having a terminal thioester moiety capable of specifically conjugating to the α-amine of a polypeptide having a cytokine or histidine residue at the N-terminus. The invention provides reactive thioester-terminated PEG polymers that have suitable reactivity with an N-terminal cysteine or histidine residue of a polypeptide to produce an amide bond between the PEG molecule and the polypeptide.

Claims (36)

1. A thioester-terminated reactive polymer, comprising a water soluble and non-peptidic polymer backbone having at least one terminus bonded to the structure:

wherein:

L is the point of bonding to the polymer backbone,

Z is a linker;

m is from 0 to about 12;

Y is a heteroatom;

each X is independently selected from H and alkyl;

a is 0 or 1; and

Q is a sulfur-containing leaving group.

2. The reactive polymer of claim 1 , wherein each X is H or C1-C6 alkyl.

3. The reactive polymer of claim 2 , wherein each X is H or methyl.

4. The reactive polymer of claim 1 , wherein Y is O or S.

5. The reactive polymer of claim 1 , wherein Q has the formula —S—R 1 , wherein R 1 is selected from the group consisting of hydrogen, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocycle, and substituted heterocycle.

6. The reactive polymer of claim 5 , wherein R 1 is selected from the group consisting of phenol, nitrophenol, benzoic acid, pyridine, pyridinecarboxylic acid, and nitropyridine.

7. The reactive polymer of claim 5 , wherein R 1 is substituted or unsubstituted pyridine.

8. The reactive polymer of claim 1 , wherein a is 1 and Z is selected from the group consisting of —O—, —S—, —NHCO—, —CONH—, O 2 C—, —NHCO 2 — and —O 2 CNH—.

9. The reactive polymer of claim 1 , wherein the polymer backbone is selected from the group consisting of poly(alkylene glycol), poly(oxyethylated polyol), poly(olefinic alcohol), poly(vinylpyrrolidone), poly(α-hydroxy acid), poly(vinyl alcohol), polyphosphazene, polyoxazoline, poly(N-acryloylmorpholine), polyacrylate, polyacrylamides, polysaccharides, and copolymers, terpolymers, and mixtures thereof.

10. The reactive polymer of claim 1 , wherein said water soluble and non-peptidic polymer backbone is selected from the group consisting of poly(ethylene glycol), poly(propylene glycol), and copolymers of ethylene glycol and propylene glycol.

11. The reactive polymer of claim 1 , wherein said polymer backbone is poly(ethylene glycol) having a number average molecular weight of about 100 Da to about 100,000 Da.

12. The reactive polymer of claim 1 , wherein m is 1 to about 4.

13. The reactive polymer of claim 1 , having the structure:

wherein:

POLY is a water soluble and non-peptidic polymer backbone;

R is a capping group or a functional group; and

R 1 is selected from the group consisting of hydrogen, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocycle, and substituted heterocycle.

14. The reactive polymer of claim 13 , wherein R is selected from the group consisting of alkoxy, alkyl, benzyl, aryl, aryloxy, hydroxyl, active ester, active carbonate, acetal, aldehyde, aldehyde hydrate, alkenyl, acrylate, methacrylate, acrylamide, active sulfone, amine, hydrazide, thiol, carboxylic acid, isocyanate, isothiocyanate, maleimide, vinylsulfone, dithiopyridine, vinylpyridine, iodoacetamide, epoxide, glyoxal, dione, mesylate, tosylate, tresylate, and -(Z) a -(CXH) m —CO—S—R 1 .

15. The reactive polymer of claim 13 , wherein POLY is poly(ethylene glycol).

16. The reactive polymer of claim 1 , having the structure:

wherein:

each POLY is a water soluble and non-peptidic polymer backbone;

R′ is a central core molecule;

y is from about 3 to about 100; and

R 1 is selected from the group consisting of hydrogen, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocycle, and substituted heterocycle.

17. The reactive polymer of claim 16 , wherein POLY is poly(ethylene glycol).

18. The reactive polymer of claim 16 , wherein R′ is a residue of a molecule selected from the group consisting of polyols, polyamines, and molecules having a combination of alcohol and amine groups.

19. The reactive polymer of claim 16 , wherein R′ is a residue of a molecule selected from the group consisting of glycerol, glycerol oligomers, pentaerythritol, sorbitol, and lysine.

Assignments (5)
RELEASE OF SECURITY INTEREST Recorded Apr 17, 2020
From: TC LENDING, LLC, AS COLLATERAL AGENT
To: NEKTAR THERAPEUTICS
Reel/Frame 053180/0009 →
RELEASE OF SECURITY INTEREST RECORDED AT REEL 28571, FRAME 0141 Recorded Oct 14, 2015
From: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
To: NEKTAR THERAPEUTICS
Reel/Frame 036866/0700 →
GRANT OF SECURITY INTEREST IN UNITED STATES PATENTS Recorded Oct 6, 2015
From: NEKTAR THERAPEUTICS
To: TC LENDING, LLC, AS COLLATERAL AGENT
Reel/Frame 036796/0562 →
GRANT OF SECURITY INTEREST Recorded Jul 17, 2012
From: NEKTAR THERAPEUTICS
To: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 028571/0141 →
MERGER Recorded Aug 31, 2009
From: NEKTAR THERAPEUTICS AL, CORPORATION
To: NEKTAR THERAPEUTICS
Reel/Frame 023196/0394 →