Multidimensional liquid chromatography/spectrometry

• US 20060157647A1
• Filed: 01/18/2005
• Published: 07/20/2006
• Est. Priority Date: 01/18/2005
• Status: Abandoned Application

• Current Assignee: Becton, Dickinson & Co, Mass Consortium Corporation
• Original Assignee: Becton, Dickinson & Co
• Inventors: Shen, Zhouxin, Siuzdak, Gary
• Application Number:
  US11/036,160
• Publication Number:
  US 20060157647A1
• Time in Patent Office: Days
• US Class Current: 250/288
• CPC Class Codes: G01N 30/463 for multidimensional chromatography

Abstract

A liquid chromatography configuration providing at least three dimensions of separation coupled with spectrometry greatly improves the ability to detect ions present in samples, including complex biological samples such as blood. Liquid chromatography columns in one embodiment are connected with an in-line trapping column the alternately communicates with the second and third liquid chromatography columns. The liquid chromatography columns are operably connected either to a mass spectrometer (MS) or a nuclear magnetic resonance (NMR) spectrometer. The improved dynamic range of detection allows a method of detecting molecular components present in complex biological samples that serve as biomarkers for a disease state, such as sepsis.

Claims

1. A liquid chromatograph spectrometer comprising:

a) a first liquid chromatography (LC) column comprising a first resin connected in tandem to a second LC column having an outlet and comprising a second resin;

b) a third LC column having an outlet and an inlet, and comprising a third resin; and

c) a spectrometer operably connected to the third column outlet;

wherein the first, second and third resins have distinct separation characteristics, and wherein the third LC column inlet is operably connected to the second LC column outlet.

2. The liquid chromatograph spectrometer of claim 1, wherein the spectrometer comprises a mass spectrometer.

3. The liquid chromatograph spectrometer of claim 2, wherein the mass spectrometer comprises an electrospray ionization mass spectrometer, a matrix-assisted laser desorption ionization time-of-flight mass spectrometer, a surface-enhanced laser desorption/ionization time-of-flight mass spectrometer, a desorption/ionization on silicon spectrometer, a secondary ion mass spectrometer, a quadrupole time-of-flight spectrometer, an atmospheric pressure chemical ionization mass spectrometer, an atmospheric pressure photoionization mass spectrometer, a quadrupole spectrometer, a fourier transform mass spectrometer, or an ion trap.

4. The liquid chromatograph spectrometer of claim 1, wherein the spectrometer comprises a NMR spectrometer.

5. The liquid chromatograph spectrometer of claim 1, wherein the operable connection between the second and third LC columns comprises a trapping column containing a trapping resin, which alternately communicates with the second LC column outlet and the third LC column inlet, wherein a fraction of molecules eluted from the second resin is capable of being contained within the trapping column when the trapping column communicates with the second LC column, and wherein the trapping resin and third resin bind the molecule on the basis of the same physical characteristic.

6. The liquid chromatograph mass spectrometer of claim 5, wherein the operable connection further comprises an automated mechanism for moving the trapping column from the second column outlet to the third column inlet.

7. The liquid chromatograph spectrometer of claim 1, wherein the liquid chromatograph spectrometer comprises four operably linked LC columns, each possessing a distinct separation characteristic.

8. The liquid chromatograph spectrometer of claim 7, wherein the liquid chromatograph spectrometer comprises five operably linked LC columns, each possessing a distinct separation characteristic.

9. The liquid chromatograph spectrometer of claim 1, wherein the third LC column is an analytical column that fractionates molecules with a resolution higher than that achieved by the first or second LC columns.

10. The liquid chromatograph spectrometer of claim 1, wherein the resins comprise a normal-phase, reversed-phase, ion exchange or size exclusion resin.

11. The liquid chromatograph spectrometer of claim 10, wherein at least one resin comprises a reversed-phase resin.

12. The liquid chromatograph spectrometer of claim 11, wherein at least one other resin comprises a strong cation exchange resin.

13. The liquid chromatograph spectrometer of claim 1, wherein at least one column comprises a filter at an outlet or inlet of the at least one column.

14. The liquid chromatograph spectrometer of claim 1, further comprising an in-line precolumn or guard column.

15. The liquid chromatograph spectrometer of claim 1, wherein the first and second resin are directly and sequentially adjoined.

16. A method of detecting a molecular component of a sample, comprising:

a) fractionating a sample with a first liquid chromatography (LC) column comprising a first resin connected in tandem to a second LC column comprising a second resin;

b) loading a fraction of molecules eluted from the second column onto a third LC column comprising a third resin that is operably connected to the second column;

c) eluting a fraction of the molecules loaded onto the third column; and

d) analyzing the fraction with a spectrometer that is operably linked to the third column,

wherein the first, second and third resins have distinct separation characteristics, and wherein the analysis provides detection of at least one molecular component of the sample.

17. The method of claim 16, wherein the spectrometer comprises a mass spectrometer.

18. The method of claim 17, wherein the mass spectrometer comprises an electrospray ionization mass spectrometer, a matrix-assisted laser desorption ionization time-of-flight mass spectrometer, a surface-enhanced laser desorption/ionization time-of-flight mass spectrometer, a desorption/ionization on silicon spectrometer, a secondary ion mass spectrometer, a quadrupole time-of-flight spectrometer, an atmospheric pressure chemical ionization mass spectrometer, an atmospheric pressure photoionization mass spectrometer, a quadrupole spectrometer, a fourier transform mass spectrometry, or an ion trap.

19. The method of claim 16, wherein the spectrometer comprises a NMR spectrometer.

20. The method of claim 16, wherein the operable connection between the second and third LC columns comprises a trapping column containing a trapping resin, which alternately communicates with an outlet of the second LC column and an inlet of the third LC column, wherein a fraction of molecules eluted from the second resin is capable of being contained within the trapping column when the trapping column communicates with the second LC column, and wherein the trapping resin and third resin bind the molecule on the basis of the same physical characteristic.

21. The method of claim 20, wherein the operable connection further comprises an automated mechanism for moving the trapping column from the second column outlet to the third column inlet.

22. The method of claim 16, wherein the liquid chromatograph spectrometer comprises four operably linked LC columns, each possessing a distinct separation characteristic.

23. The method of claim 22, wherein the liquid chromatograph spectrometer comprises five operably linked LC columns, each possessing a distinct separation characteristic.

24. The method of claim 16, wherein the third LC column comprises an analytical column that fractionates molecules with a resolution higher than that achieved by the first or second LC columns.

25. The method of claim 16, wherein the resins comprise a normal-phase, reversed-phase, ion exchange or size exclusion resin.

26. The method of claim 25, wherein at least one resin comprises a reversed-phase resin.

27. The method of claim 26, wherein at least one other resin comprises a strong cation exchange resin.

28. The method of claim 16, wherein the first and second resin are directly and sequentially adjoined.

29. The method of claim 16, wherein the sample is biological in origin or is an environmental sample.

30. The method of claim 29, wherein the sample is biological in origin.

31. The method of claim 30, wherein the sample is blood, plasma, serum, lymph, excretia, an exudate, synovial fluid, vitreous fluid, a whole cell, a cellular extract, a whole organism, tissue, or a biopsy sample.

32. The method of claim 29, wherein the sample is from an individual.

33. The method of claim 32, wherein the presence, absence or change in the level of expression of the molecular component of the sample is indicative or diagnostic of a change in the physiological condition of the individual.

34. The method of claim 33, where the change in the physiological condition of the individual comprises the appearance of systemic inflammatory response syndrome or sepsis in the individual.

35. The method of claim 16, wherein the sample is pretreated to remove at least one contaminant.

36. The method of claim 35, wherein the pretreatment comprises chemical or enzymatic modification of at least one molecular component of the sample.

37. The method of claim 35, wherein the pretreatment comprises dialysis, filtration, ultra-filtration, centrifugation, ultra-centrifugation, differential precipitation, or organic extraction.

38. The method of claim 30, further comprising immunodepleting of at least one component on the sample prior to fractionating the sample with the first liquid LC column.

39. The method of claim 38, wherein the immunodepleted component is albumin, an immunoglobulin, α

-1 antitrypsin, α

-2 macroglobulin, transferrin or haptoglobin-type 2-1.

40. The method of claim 16, wherein the molecular component of the sample is a circulating protein.

41. The method of claim 40, wherein analyzing the fraction with a spectrometer comprises using an algorithm to identify the circulating protein.