Purification methods

• US 20050266428A1
• Filed: 12/29/2004
• Published: 12/01/2005
• Est. Priority Date: 07/03/2002
• Status: Abandoned Application

• Current Assignee: Monash University
• Original Assignee: Monash University
• Inventors: Perlmutter, Patrick, Aguilar, Marie-Isabel, Lee, Tzong-Hsien
• Application Number:
  US11/032,698
• Publication Number:
  US 20050266428A1
• Time in Patent Office: Days
• US Class Current: 435/6
• CPC Class Codes: B01D 15/327 with hydrophobic interaction
• CPC Class Codes: B01D 15/3804 Affinity chromatography
• CPC Class Codes: B01J 20/286 Phases chemically bonded to a substrate, e.g. to silica or to polymers
• CPC Class Codes: B01J 20/3219 involving a particular spacer or linking group, e.g. for attaching an active group
• CPC Class Codes: B01J 20/3242 Layers with a functional group, e.g. an affinity material, a ligand, a reactant or a complexing group
• CPC Class Codes: B01J 2220/54 Sorbents specially adapted for analytical or investigative chromatography
• CPC Class Codes: C07K 1/16 by chromatography

Abstract

The present invention relates to methods of processing of chemical samples containing compounds or molecular complexes using a binding material comprising a method of separating a compound or molecular complex on the basis of the ability of the compound or molecular complex to associate with a binding material, from compounds or molecular complexes having different association characteristics, said method comprising: (a) bringing a sample containing said compound or molecular complex into contact with a binding material, the binding material comprising: (i) a support, (ii) at least one terminal moiety selected from the group consisting of lecithins, lysolecithins, cephalins, sphingomyelin, cardiolipin, glycolipids, gangliosides, cerebrosides and phospholipids, and

• • • (iii) at least one linker of the formula (I) wherein R₁ and R₂ may be the same or different and are independently selected from the group consisting of: H, OH, C₁-C₆ alkyl, C₂-C₆ alkenyl, halogen, C₁-C₆ alkoxy, C₂-C₆ alkenyloxy and aryloxy, or R₁ or R₂ when taken together with an R₁ or R₂ on an adjacent linker forms a group of formula —O—, wherein said group —O— connects the silicon atom of the linker to the silicon atom of the adjacent linker, R₃ and R₄ may be the same or different and are independently selected from the group consisting of H, C₁-C₆ alkyl, C₂-C₆ alkenyl and halogen, R₅ is H or C₁-C₆ alkyl, R₆ is H, C₁-C₆ alkyl, C₂-C₆ alkenyl, aryl and heteroaryl, X is O or S, n is an integer from 0 to 10, the terminal moiety being bound to the support via at least one linker, (b) treating the product of step (a) to separate the components of the sample on the basis of their ability to associate with the binding material.

Claims

1. A method of separating a compound or molecular complex on the basis of the ability of the compound or molecular complex to associate with a binding material, from compounds or molecular complexes having different association characteristics, said method comprising:

(a) bringing a sample containing said compound or molecular complex into contact with a binding material, the binding material comprising;

(i) a support,

(ii) at least one terminal moiety selected from the group consisting of lecithins, lysolecithins, cephalins, sphingomyelin, cardiolipin, glycolipids, gangliosides, cerebrosides and phospholipids, and

(iii) at least one linker of the formula

wherein R₁ and R₂ may be the same or different and are independently selected from the group consisting of;

H, OH, C₁-C₆ alkyl, C₂-C₆ alkenyl, halogen, C₁-C₆ alkoxy, C₂-C₆ alkenyloxy and aryloxy, or R₁ or R₂ when taken together with an R₁ or R₂ on an adjacent linker forms a group of formula —

O—

, wherein said group —

O—

connects the silicon atom of the linker to the silicon atom of the adjacent linker,

R₃ and R₄ may be the same or different and are independently selected from the group consisting of H, C₁-C₆ alkyl, C₂-C₆ alkenyl and halogen,

R₅ is H or C₁-C₆ alkyl,

R₆ is H, C₁-C₆ alkyl, C₂-C₆ alkenyl, aryl and heteroaryl,

X is O or S,

n is an integer from 0 to 10,

the terminal moiety being bound to the support via at least one linker,

(b) treating the product of step (a) to separate the components of the sample on the basis of their ability to associate with the binding material.

2. A method according to claim 1, wherein the linker is of the formula:

3. A method according to claim 1, wherein each of said terminal moieties is independently selected from the group consisting of phosphatidylcholine, phosphatidylethanolamine, N-methyl phosphatidylethanolamine, N,N-dimethylphosphatidylethanolamine, phosphatidic acid, phosphatidylserine, phosphatidylinositol and phosphatidylglycerol or derivatives thereof.

4. A method according to claim 1, wherein said binding material is a chromatographic material loaded within a chromatographic column and said contacting involving loading said sample containing the compound or molecular complex onto said column.

5. A method according to claim 1, wherein said sample contains proteins, peptides, or complexes thereof.

6. A method according to claim 5, wherein the proteins are membrane proteins.

8. A method according to claim 7 where the linker is of the formula:

19. A method according to claim 18 where the linker is of the formula:

7. A method of detection of a compound or molecular complex in a sample containing said compound or molecular complex, said method comprising:

(a) bringing a sample containing said compound or molecular complex into contact with a binding material, the binding material comprising;

(i) a support;

(ii) at least one terminal moiety consisting of lecithins, lysolecithins, cephalins, sphingomyelin, cardiolipin, glycolipids, gangliosides, cerebrosides and phospholipids; and

(iii) at least one linker of the formula

wherein R₁, R₂ may be the same or different and are independently selected from the group consisting of;

H, OH, C₁-C₆ alkyl, C₂-C₆ alkenyl, halogen, C₁-C₆ alkoxy, C₂-C₆ alkenyloxy and aryloxy, or R₁ or R₂ when taken together with an R₁ or R₂ on an adjacent linker forms a group of formula —

O—

, wherein said group —

O—

connects the silicon atom of the linker to the silicon atom of the adjacent linker,

R₃ and R₄ may be the same or different and are independently selected from the group consisting of H, C₁-C₆ alkyl, C₂-C₆ alkenyl and halogen,

R₅ is H or C₁-C₆ alkyl

R₆ is H, C₁-C₆ alkyl, C₂-C₆ alkenyl, aryl, and heteroaryl,

X is O or S,

n is an integer from 0 to 10;

the terminal moiety being attached to the support by at least one linker.

9. A method according to claim 7, wherein each of said terminal moieties is independently selected from the group consisting of phosphatidylcholine, phosphatidylethanolamine, N-methyl phosphatidylethanolamine, N,N-dimethylphosphatidylethanolamine, phosphatidic acid, phosphatidylserine, phosphatidylinositol and phosphatidylglycerol or derivatives thereof.

10. A method according to claim 7, wherein each of the terminal moieties is independently selected from the group consisting of phosphatidic acid, phosphatidylglycerol and phosphatidylcholine.

11. A method according to claim 7, wherein said support is the solid support of an array.

12. A method according to claim 7, wherein said sample contains proteins, peptides, or complexes thereof.

13. A method according to claim 12, wherein the proteins are membrane proteins.

14. A method of detection according to claim 7, wherein said method further comprises treating the contacted binding material to determine the presence of the compound or molecular complex.

15. The method according to claim 14, wherein said treating comprises treatment with a tagged compound which selectively binds to said compound or molecular complex.

16. A method according to claim 15, wherein said method further comprises testing said binding material for the presence of said tagged compound, the presence of said tagged compound being indicative of the presence of said compound or molecular complex.

17. A method according to claim 16, wherein said tag is a radioactive tag, a fluorescent tag or a chemiluminescent tag.

18. A method of increasing the purity of a compound or molecular complex from an impure sample containing said compound or molecular complex, the method comprising:

(a) bringing said sample into contact with a binding material, the binding material comprising;

(i) a support;

(ii) at least one terminal moiety selected from the group consisting of lecithins, lysolecithins, cephalins, sphingomyelin, cardiolipin, glycolipids, gangliosides, cerebrosides and phospholipids; and

(iii) at least one linker of the formula

wherein R₁, R₂ may be the same or different and are independently selected from the group consisting of;

—

H, C₁-C₆ alkyl, C₂-C₆ alkenyl, halogen, C₁-C₆ alkoxy, C₂-C₆ alkenoxy and aryloxy, or at least one of R₁ or R₂ when taken together with R₁ or R₂ on an adjacent linker forms a group —

O—

, wherein said group —

O—

connects the silicon atom of the linker to the silicon atom of the adjacent linker,

R₃ and R₄ may be the same or different and are independently selected from the group consisting of H, C₁-C₆ alkyl, C₂-C₆ alkenyl and halogen,

R₅ is H or C₁-C₆ alkyl

R₆ is H, C₁-C₆ alkyl, C₂-C₆ alkenyl, aryl, and heteroaryl,

X is O or S,

n is an integer from 0 to 10;

said terminal moiety being attached to said support by at least one linker;

(b) treating the product of step (a) to separate the compound or molecular complex from at least a portion of the other components in the ample;

(c) recovering at least a portion of the compound or molecular complex.

20. A method according to claim 18, wherein each of said terminal moieties is independently selected from the group consisting of phosphatidylcholine, phosphatidylethanolamine, N-methyl phosphatidylethanolamine, N,N-dimethylphosphatidylethanolamine, phosphatidic acid, phosphatidylserine, phosphatidylinositol and phosphatidylglycerol or derivatives thereof.

21. A method according to claim 20, wherein each of the terminal moieties is independently selected from the group consisting of phosphatidic acid, phosphatidylglycerol and phosphatidylcholine.

22. A method according to claim 18, wherein said sample contains proteins, peptides, or complexes thereof.

23. A method according to claim 22, wherein the proteins are membrane proteins.

24. A method according to claim 18, wherein said binding material is a chromatographic material loaded within a chromatographic column and said step (b) comprises elution of the column with a mobile phase followed by collection of eluted fractions.

25. A method according to claim 24, wherein said elution involves the use of a solvent gradient.

26. A method according to claim 24, wherein said mobile phase is selected from the group consisting of water, hydrocarbons, esters, alkyl esters, nitrites, alcohols, acids, aqueous solutions of acids and mixtures thereof.

27. A method according to claim 24, wherein said mobile phase is selected from the group consisting of water, ethyl acetate, acetonitrile, ethanol, methanol, and aqueous solutions of trifluoro acetic acid.

28. A method according to claim 24, wherein said recovery comprises combination of eluted fractions containing the same component followed by the removal of the mobile phase to produce the purified compound or molecular complex.

29. A method according to claim 18, wherein said step (b) comprises washing the contacted binding material to remove unbound material.

30. A method according to claim 29, wherein said step (c) comprises treating contacted binding material to remove the bound material.

31. A method of claim 18 wherein, after subjection to the method, the recovered compound or molecular complex has a purity of at least 80%.

32. A method according to claim 31 wherein, after subjection to the method, the recovered compound or molecular complex has a purity of at least 90%.

33. A method according to claim 18, wherein the compound or molecular complex is recovered in substantially pure form.

41. A method according to claim 18, wherein said sample contains proteins, peptides, or complexes thereof.

42. A method according to claim 41, wherein the proteins are membrane proteins.

34. A method of analysis of a sample containing a plurality of compounds or molecular complexes, the method comprising:

(a) bringing the sample into contact with a binding material, the binding material comprising;

(i) a support;

(ii) at least one terminal moiety selected from the group consisting of lecithins, lysolecithins, cephalins, sphingomyelin, cardiolipin, glycolipids, gangliosides, cerebrosides and phospholipids; and

(iii) at least one linker of the formula

wherein R₁, R₂ may be the same or different and are independently selected from the group consisting of —

H, C₁-C₆ alkyl, C₂-C₆ alkenyl, halogen, C₁-C₆ alkoxy, C₂-C₆ alkenoxy and aryloxy, or at least one of R₁ or R₂ when taken together with R₁ or R₂ on an adjacent linker forms a group —

O—

, wherein said group —

O—

connects the silicon atom of the linker to the silicon atom of the adjacent linker,

R₃ and R₄ may be the same or different and are independently selected from the group consisting of H, C₁-C₆ alkyl, C₂-C₆ alkenyl and halogen,

R₅ is H or C₁-C₆ alkyl

R₆ is H, C₁-C₆ alkyl, C₂-C₆ alkenyl, aryl, and heteroaryl,

X is O or S,

n is an integer from 0 to 10;

said terminal moiety being attached to said support by at least one linker;

(b) separating the components of the sample;

(c) analysing the separated components.

35. A method according to claim 34, wherein said binding material is a chromatographic support material loaded within a chromatographic column and said step (b) comprises elution of the column with a mobile phase.

36. A method according to claim 35, wherein said elution involves the use of a solvent gradient.

37. A method according to claim 35, wherein said mobile phase is selected from the group consisting of water, hydrocarbons, esters, alkyl esters, nitrites, alcohols, acids, aqueous solutions of acids and mixtures thereof.

38. A method according to claim 35, wherein said mobile phase is selected from the group consisting of water, ethyl acetate, acetonitrile, ethanol, methanol, and aqueous solutions of trifluoro acetic acid.

39. A method according to claim 34, wherein fractions of the eluent are collected and then analysed in step (c).

40. A method according to claim 39, wherein said analysis is conducted using a spectrophotometric technique or by mass spectrometry.

43. A method according to claim 34, wherein said step (b) comprises washing the contacted binding material to remove unbound material.

44. A method according to claim 43, wherein said step (c) comprises treating the contacted binding material to remove the bound material and subjecting the material thus obtained to analysis.

45. A method according to claim 44, wherein said removed bound material is subjected to analysis using a spectrophotometric technique or by mass spectrometry.