Methods for separating compounds
View Patent ↗Methods and systems for analyzing samples using multi-dimensional chromatography are disclosed.
1. A method for analyzing a sample containing at least one analyte, the method comprising:
a) subjecting the sample to a first chromatographic separation mode at a first pH with a first mobile phase;
b) collecting at least one fraction from the first chromatographic separation;
c) subjecting the at least one fraction to a second chromatographic separation mode at a second pH with a second mobile phase; and
d) detecting the presence or absence of the at least one analyte in the sample;
wherein the first pH and the second pH differ by at least about 3 pH units.
2. The method of claim 1 , wherein the first and second chromatographic separations are substantially orthogonal to each other.
3. The method of claim 1 , wherein the first and/or second chromatographic separation mode is high performance liquid chromatography (HPLC).
4. The method of claim 1 , wherein the first and/or second chromatographic separation mode is hydrophilic interaction chromatography (HILIC).
5. The method of claim 1 wherein an HPLC separation is a reversed-phase HPLC separation.
6. The method of claim 1 wherein the first chromatographic separation mode has a peak capacity of at least 100 peaks.
7. The method of claim 1 , wherein the at least one analyte is a peptide, polypeptide, or protein.
8. The method of claim 1 , wherein the at least one analyte is a small organic molecule.
9. The method of claim 1 , wherein the sample contains at least 1000 analytes.
10. The method of claim 1 , wherein the total peak capacity of the method is at least 1,000 peaks.
11. The method of claim 1 , in which the HPLC separation is performed using a microbore column, capillary column, or nanocolumn.
12. The method of claim 1 , wherein the at least one fraction collected in step b) is concentrated or diluted prior to subjecting the at least one fraction to the second chromatographic separation mode.
13. The method of claim 12 , wherein the at least one fraction is concentrated by evaporation.
14. The method of claim 12 , wherein the at least one fraction collected in step b) is diluted on-line prior to performing the second chromatographic separation mode.
15. The method of claim 1 , wherein the step of detecting is performed using mass spectrometry.
16. The method of claim 1 , wherein the first and second chromatographic modes are the same.
17. The method of claim 1 , wherein the first and/or second mobile phase is substantially free of non-volatile salts.
18. The method of claim 1 , wherein the first and/or second mobile phase comprises less than about 20 mM of non-volatile salts.
19. The method of claim 1 , wherein a plurality of portions are collected and subjected to the second chromatographic separation.
20. The method of claim 1 , wherein the first and second chromatographic separation modes comprise liquid chromatographic separations.
21. A method for separating a plurality of analytes in a sample, the method comprising:
a) subjecting at least a portion of the sample to a first chromatographic separation mode at a first pH;
b) collecting at least one fraction from the first chromatographic separation; and
c) subjecting the at least one fraction to a second chromatographic separation mode at a second pH, wherein the first pH and the second pH differ by at least about 3 pH units; under conditions such that at least two analytes in the sample are separated.
22. The method of claim 21 , wherein the first and second chromatographic separation modes comprise HPLC separations.
23. The method of claim 21 , wherein the first and second chromatographic separations are substantially orthogonal to each other.
24. The method of claim 21 , wherein the first and/or second chromatographic separation mode is high performance liquid chromatography (HPLC).
25. The method of claim 21 , wherein the first and/or second chromatographic separation mode is hydrophilic interaction chromatography (HILIC).
26. The method of claim 21 wherein an HPLC separation is a reversed-phase HPLC separation.
27. The method of claim 21 wherein the first chromatographic separation mode has a peak capacity of at least 100 peaks.
28. The method of claim 21 , wherein the at least one analyte is a peptide, polypeptide, or protein.
29. The method of claim 21 , wherein the at least one analyte is a small organic molecule.
30. The method of claim 21 , wherein the sample contains at least 1000 analytes.
31. The method of claim 21 , wherein the total peak capacity of the method is at least 10,000 peaks.
32. The method of claim 21 , in which the HPLC separation is performed using a microbore column, capillary column, or nanocolumn.
33. The method of claim 21 , wherein the at least one fraction collected in step b) is concentrated or diluted prior to subjecting the at least one fraction to the second chromatographic separation mode.
34. The method of claim 21 , wherein the step of detecting is performed using mass spectrometry.
35. The method of claim 21 , wherein the first and second chromatographic modes are the same.
36. The method of claim 21 , wherein the first and/or second mobile phase is substantially free of non-volatile salts.
37. The method of claim 21 , wherein the first and/or second mobile phase comprises less than about 20 mM of non-volatile salts.
38. The method of claim 21 , wherein a plurality of portions are collected and subjected to the second chromatographic separation.
39. A method for characterizing a sample containing a plurality of polypeptides in a multi-dimensional liquid chromatography system, the method comprising:
a) injecting the sample into a first dimension chromatography apparatus of said multi-dimensional liquid chromatography system;
b) chromatographically separating at least a first polypeptide component of said sample from at least a second polypeptide of said sample in a chromatography column of said first dimension chromatography apparatus using a first mobile phase;
c) eluting said separated first and second polypeptide components in an eluent from said chromatography column;
d) sampling at least one discrete volume of said eluent;
e) injecting said at least one discrete volume into a second dimension chromatography apparatus of said multi -dimensional liquid chromatography system;
f) subjecting the injected discrete volume to a chromatographic separation in a chromatography column of said second dimension chromatography apparatus using a second mobile phase, wherein the pH of said first and second mobile phases differs by about 3 pH units;
g) characterizing an eluent from said chromatography column of said second dimension chromatography apparatus using mass spectroscopy, thereby characterizing the sample containing a plurality of polypeptides.
40. The method of claim 39 , wherein the multi-dimensional liquid chromatography system comprises a two-dimensional liquid chromatography system.
41. A method for purifying a compound in a sample containing the compound and at least two impurities, the method comprising:
a) subjecting the sample to a first chromatographic separation mode at a first pH, under conditions such that the compound is separated from a first impurity;
b) collecting at least one compound-containing fraction from the first chromatographic separation;
c) subjecting the at least one compound-containing fraction to a second chromatographic separation mode at a second pH, under conditions such that the compound is separated from a second impurity, wherein the first pH and the second pH differ by at least about 3 pH units; and
d) collecting the purified compound.
42. A method for analyzing a sample containing at least one analyte, the method comprising:
a) subjecting the sample to a first chromatographic separation at a first pH with a first mobile phase;
b) collecting at least one portion from the first chromatographic separation;
c) subjecting the at least one portion to a second chromatographic separation at a second pH with a second mobile phase, wherein the first pH and the second pH differ by at least about 3 pH units; and
d) detecting the presence or absence of the at least one analyte in the sample;
wherein both the first and second mobiles phases are substantially free of non-volatile salts.