IP Library Granted Patent US 8,846,899
Granted Patent B2
US 8,846,899 · App. 13/272,090 · Granted Sep 30, 2014

Maltoside and phosphocholine derivatives, uses thereof and methods of preparing artificial lipid structures thereof

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Quick Facts
Patent No.
US 8,846,899
App. No.
13/272,090
Granted
Sep 30, 2014
Kind
B2
Abstract

Disclosed are saccharide and phosphocholine derivatives. The derivatives include azide and alkyne derivatives which form one end of a variable length carbon chain. The opposite end of the variable length carbon chain is covalently linked to the saccharide or phosphocholine. The saccharide may be, for instance, a maltoside. The alkyne and azide derivatives of the saccharides and phosphocholine may be reacted together to form amphiphilic molecules useful in cellular membrane studies and applications. By adjusting the length of the carbon chain, the biochemical and biophysical properties of the resultant 1,4-disubstituted 1,2,3-triazole compounds may be custom tailored for the intended application. Resultant molecules may form micelles, bicelle, lipid bilayers and other like structures useful in the isolation and purification of membrane bound or membrane associated proteins and biochemical components. The saccharides and phosphocholine molecules may be alternatively substituted as desired to provide additional flexibility in designing the desired end product.

Claims (93)

1. A composition comprising:

an azide linked to a saccharide via a carbon chain having the formula:

wherein:

Az=azide,

Sac=saccharide selected from the group consisting of: trehalose, glucose and maltose,

n=7-20, and

wherein the carbon chain is covalently attached to an oxygen of an anomeric carbon of the saccharide.

2. The composition according to claim 1 , wherein the saccharide is β-D-maltose.

3. The composition according to claim 2 , wherein the azide linked to a saccharide via a carbon chain is 11-azido-undecyl-β-D-maltoside or 16-azido-hexadecyl-β-D-maltoside.

4. A composition comprising:

an alkyne linked to a saccharide via a carbon chain having the formula:

wherein:

Alk=C≡C—H

Sac=saccharide selected from the group consisting of: trehalose, glucose and maltose,

n=7-20, and

wherein the carbon chain is covalently attached to an oxygen of an anomeric carbon of the saccharide.

5. The composition according to claim 4 , wherein the saccharide is β-D-maltose.

6. The composition according to claim 4 , wherein the alkyne linked to a saccharide via a carbon chain is selected from the group consisting of: 9-decynyl-β-D-maltoside, 10-undecynyl-β-D-maltoside and 12-tridecynyl-β-D-maltoside.

7. A composition comprising:

an alkyne linked to phosphocholine via a carbon chain having the formula:

wherein:

Alk=H—C≡C

PC=phosphocholine, and

7≦n≦20.

8. The composition according to claim 7 , wherein the alkyne linked to phosphocholine via a carbon chain is 9-decynyl-1-phosphocholine.

9. A composition comprising:

an azide linked to a saccharide via a first carbon chain having the formula:

wherein:

Az=azide,

Sac=saccharide selected from the group consisting of: trehalose, glucose and maltose,

7≦m≦20, and

wherein the carbon chain is covalently attached to an oxygen of an anomeric carbon of the saccharide, and

an alkyne linked to phosphocholine via a second carbon chain according to:

wherein:

Alk=H—C≡C

PC=phosphocholine, and

7≦n≦20.

10. The composition according to claim 9 , wherein the saccharide is maltose.

11. The composition according to claim 10 , wherein the azide linked to a saccharide via a carbon chain is 11-azido-undecyl-β-D-maltoside or 16-azido-hexadecyl-β-D-maltoside, and wherein the alkyne linked to phosphocholine via a carbon chain is 9-decynyl-1-phosphocholine.

12. A composition comprising:

an azide linked to phosphocholine via a carbon chain having the formula:

wherein:

Az=azide,

PC=phosphocholine, and

n=8-20.

13. The composition according to claim 12 , wherein the azide linked to phosphocholine via a carbon chain is 11-azido-undecyl-1-phosphocholine.

14. A composition comprising a 1,4-disubstituted [1,2,3]-triazole formed from the reaction of:

an alkyne linked to a saccharide via a first carbon chain having the formula:

wherein:

Alk=C≡C—H

Sac=saccharide selected from the group consisting of: trehalose, glucose and maltose,

7≦m≦20, and

wherein the carbon chain is covalently attached to an oxygen of an anomeric carbon of the saccharide, and

an azide linked to phosphocholine via a second carbon chain having the formula:

wherein:

Az=azide,

PC=phosphocholine, and

7≦n≦20.

15. The composition according to claim 14 , wherein the saccharide is maltose.

16. A method of forming a micelle or lipid bilayer, which comprises:

(A) reacting an alkyne linked to a saccharide via a first carbon chain having the formula:

wherein:

Alk=C≡C—H

Sac=saccharide selected from the group consisting of: trehalose, glucose and maltose,

7≦m≦20, and

wherein the carbon chain is covalently attached to an oxygen of an anomeric carbon of the saccharide,

with

an azide linked to phosphocholine via a second carbon chain having the formula:

wherein:

Az=azide,

PC=phosphocholine, and

7≦n≦20,

under conditions which form a 1,4-disubstitued [1,2,3]-triazole; and

incubating the 1,4-disubstitued [1,2,3]-triazole under conditions conducive to formation of a micelle or lipid bilayer,

or

(B) reacting an azide linked to a saccharide via a first carbon chain having the formula:

wherein:

Az=azide,

Sac=saccharide selected from the group consisting of: trehalose, glucose and maltose,

7≦m≦20, and

wherein the carbon chain is covalently attached to an oxygen of an anomeric carbon of the saccharide,

with

an alkyne linked to phosphocholine via a second carbon chain having the formula:

wherein:

Alk=H—C≡C

PC=phosphocholine, and

7≦n≦20

under conditions which form a 1,4-disubstitued [1,2,3]-triazole; and

incubating a sufficient quantity of the 1,4-disubstitued [1,2,3]-triazole under conditions conducive to formation of a micelle or lipid bilayer.

17. The method according to claim 16 , wherein the saccharide is a maltose.

18. The method according claim 16 , further comprising:

mixing a sufficient quantity of the 1,4-disubstituted [1,2,3]-triazole from step (A) with the 1,4-disubstituted [1,2,3]-triazole from step (B); and

incubating the mixture under conditions conducive to formation of a micelle or lipid bilayer.

Assignments (14)
SECURITY INTEREST Recorded Jun 10, 2020
From: ALPHA-TEC SYSTEMS, INC.; ANATRACE PRODUCTS, LLC; EDGE BIOSYSTEMS, INC.; MOLECULAR DIMENSIONS, INC.
To: CVC CREDIT PARTNERS, LLC
Reel/Frame 052896/0983 →
RELEASE OF SECURITY INTEREST Recorded Jun 10, 2020
From: LBC CREDIT AGENCY SERVICES, LLC, AS AGENT
To: ANATRACE PRODUCTS, LLC
Reel/Frame 052896/0295 →
RELEASE OF SECURITY INTEREST Recorded Jul 17, 2017
From: OPUS BANK
To: ANATRACE PRODUCTS, LLC; EDGE BIOSYSTEMS, INC.
Reel/Frame 043026/0351 →
RELEASE OF SECURITY INTEREST Recorded Jul 17, 2017
From: FIDUS MEZZANINE CAPITAL, L.P.
To: ANATRACE PRODUCTS, LLC; EDGE BIOSYSTEMS, INC.
Reel/Frame 043026/0361 →
SECURITY INTEREST Recorded Jul 14, 2017
From: ANATRACE PRODUCTS, LLC
To: LBC CREDIT AGENCY SERVICES, LLC, AS AGENT
Reel/Frame 043008/0364 →
SECURITY INTEREST Recorded Dec 30, 2015
From: EDGE BIOSYSTEMS, INC.; ANATRACE PRODUCTS, LLC
To: FIDUS MEZZANINE CAPITAL, L.P.
Reel/Frame 037380/0659 →
PATENT SECURITY AGREEMENT Recorded Dec 29, 2015
From: EDGE BIOSYSTEMS, INC.; ANATRACE PRODUCTS, LLC
To: OPUS BANK
Reel/Frame 037396/0638 →
RELEASE OF SECURITY INTEREST IN PATENTS Recorded Dec 29, 2015
From: FIDUS MEZZANINE CAPITAL, L.P., AS COLLATERAL AGENT
To: ANATRACE PRODUCTS, LLC
Reel/Frame 037396/0225 →
RELEASE OF SECURITY INTEREST Recorded Nov 13, 2015
From: GENERAL ELECTRIC CAPITAL CORPORATION, AS AGENT
To: AFFYMETRIX, INC.
Reel/Frame 037109/0132 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 11, 2013
From: AFFYMETRIX, INC.
To: ANATRACE PRODUCTS, LLC
Reel/Frame 031388/0920 →
RELEASE OF SECURITY INTEREST Recorded Oct 11, 2013
From: GENERAL ELECTRIC CAPITAL CORPORATION
To: AFFYMETRIX, INC.
Reel/Frame 031389/0481 →
SECURITY AGREEMENT Recorded Oct 11, 2013
From: ANATRACE PRODUCTS, LLC
To: FIDUS MEZZANINE CAPITAL, L.P., AS COLLATERAL AGENT
Reel/Frame 031397/0298 →
SECURITY AGREEMENT Recorded Jun 27, 2012
From: AFFYMETRIX, INC.
To: GENERAL ELECTRIC CAPITAL CORPORATION, AS AGENT
Reel/Frame 028465/0541 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 3, 2012
From: TRAVIS, BENJAMIN R.; MITTAL, RITESH; HUANG, LIJUN; TANG, LIANG
To: AFFYMETRIX, INC.
Reel/Frame 027470/0479 →