BIOLOGICAL MEMBRANE PHOSPHOINOSITIDE SEPARATION METHOD

Abstract

Provided is a method for separating PIPs by which isomers of PIPs can be separated without deacylating the PIPs. The method includes at least a separation step of injecting a sample containing a plurality of PIPs into an analysis flow path of a supercritical fluid chromatograph having a separation column filled with a separation medium containing β-cyclodextrin and separating the plurality of PIPs by supercritical fluid chromatography.

Claims

1. A method for separating biological membrane phosphoinositides, the method comprising a separation step of separating a plurality of biological membrane phosphoinositides using supercritical fluid chromatography by injecting a sample containing the plurality of biological membrane phosphoinositides into an analysis flow path of a supercritical fluid chromatograph having a separation column filled with a separation medium containing β-cyclodextrin.

2. The method according to claim 1, wherein a plurality of isomers of biological membrane phosphoinositides are included in the plurality of biological membrane phosphoinositides.

3. The method according to claim 2, wherein the plurality of isomers are any of PI(3)P, PI(4)P, PI(5)P, PI(3,4)P.sub.2, PI(3,5)P.sub.2, PI(4,5)P.sub.2, and PI(3,4,5)P.sub.3.

4. The method according to claim 1, comprising: a derivatization step of derivatizing a phosphate group of the plurality of biological membrane phosphoinositides by trimethylsilyldiazomethane before the separation step; and a detection step of detecting each of the plurality of biological membrane phosphoinositides, which are separated by the separation column, using a mass spectrometer after the separation step.

5. The method according to claim 1, wherein a formic acid methanol aqueous solution is used as a modifier in the separation step.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0017] FIG. 1 shows structural formulae showing the structures of phosphatidylinositol and PIPs.

[0018] FIG. 2 is a flow path configuration diagram showing the configuration of a supercritical fluid chromatograph.

[0019] FIG. 3 is a flowchart showing an example of a method for separating PIPs.

[0020] FIG. 4 is a diagram for illustrating the interaction between a separation medium containing β-cyclodextrin and PIPs.

[0021] FIG. 5 is an example of a chromatogram based on a mass spectrometer signal obtained by the method for separating PIPs shown in FIG. 3.

EMBODIMENT OF THE INVENTION

[0022] Hereinafter, an example of the method for separating PIPs according to the present invention will be described with reference to the drawings.

[0023] The method for separating PIPs in this example is performed using a supercritical fluid chromatograph (hereinafter, referred to as SFC). As shown in FIG. 2, the SFC used in this example includes solvent delivery pumps 4 and 6 for feeding of carbon dioxide and a modifier in an analysis flow path 2, a sample injection part 8 for injection of a sample into the analysis flow path 2 in which the fluid mixture of the carbon dioxide and the modifier flows, a separation column 10 for separation of the sample injected through the sample injection part 8, a back pressure regulator (BPR) 12 that controls the pressure in the analysis flow path 2 to a predetermined pressure so that at least the carbon dioxide flowing through the separation column 10 is in a supercritical state, a pump 15 that feeds a makeup solvent for sensitive detection, and a mass spectrometer (MS) 14 provided in the post-side of the BPR 12.

[0024] Although not shown, the separation column 10 is installed in a column oven and is constantly controlled to a set temperature. The separation column 10 is filled with a separation medium in which cyclodextrin capable of including an organic substance is bound to a silica stationary phase. For example, ULTRON AF-HILIC-CD manufactured by Shinwa Chemical Industries Ltd. can be used.

[0025] In order to enable separation and analysis of a sample containing a plurality of PIPs by the SFC, the phosphate group of the PIPs in the sample is derivatized to make each of the PIPs detectable by the MS 14.

[0026] The derivatization treatment can be performed, for example, by the following procedures (1) to (5).

[0027] (1) To a sample solution containing PIPs, 2 M trimethylsilyldiazomethane hexane solution is added.

[0028] (2) The sample solution to which the 2 M trimethylsilyldiazomethane hexane solution is added is left at room temperature for a certain period of time (for example, 10 minutes) to perform a derivatization reaction.

[0029] (3) To the sample solution, glacial acetic acid is added under a nitrogen atmosphere to stop the derivatization reaction.

[0030] (4) A predetermined washing solution (for example, a mixture of chloroform:methanol:water=8:4:3) is added and mixed to the sample solution, and then the resulting solution is centrifuged to recover the lower layer. Washing may be repeated in the same manner a plurality of times. Finally, a solution of methanol:water=9:1 is added to the sample solution.

[0031] (5) The sample solution is dried and solidified under a nitrogen atmosphere. Then, a predetermined amount of methanol is added to the sample, and the sample is dissolved by ultrasonic waves. In addition, a predetermined amount of water is added to the sample.

[0032] Derivatization of PIPs as described above is disclosed in the paper “Quantification of PtdInsP3 molecular species in cells and tissues by mass spectrometry, Jonathan Clark, Karen E Anderson, Veronique Juvin, Trevor S Smith, Fredrik Karpe, Michael J O Wakelam, Len R Stephens & Phillip T Hawkins”.

[0033] As a modifier for supercritical fluid chromatography, a mixture of 0.1% formic acid methanol and water (for example, formic acid methanol:water=97.5:2.5) can be used. Furthermore, methanol containing formic acid or ammonium formate (for example, 0.1% formic acid methanol) can be used as the modifier.

[0034] That is, in the method for separating PIPs in this example, as shown in the flowchart of FIG. 3, the above-described derivatization treatment is performed (step S1), then the sample is injected into the analysis flow path 2 of the SFC through the sample injection part 8 (step S2), and the isomers of the PIPs are separated by the separation column 10 filled with the separation medium in which cyclodextrin is bound to the silica stationary phase (step S3). Furthermore, each of the PIPs separated by the separation column 10 is introduced into the MS 14 one by one and detected (step S4).

[0035] FIG. 5 is a chromatogram obtained by analyzing a sample containing seven PIPs of PI(3)P, PI(4)P, PI(5)P, PI(3,4)P.sub.2, PI(3,5)P.sub.2, PI(4,5)P.sub.2, and PI(3,4,5)P.sub.3 using the method in the above-described example. The horizontal axis shows the time and the vertical axis shows the signal intensity. In this analysis, ULTRON AF-HILIC-CD (inner diameter: 4.6 mm, length: 250 mm) manufactured by Shinwa Chemical Industries Ltd. was used as the separation column 10, and the set temperature of the separation column 10 was 4° C. As the modifier, a mixture of 0.1% formic acid methanol and water (for example, formic acid methanol:water=97.5:2.5) was used, and the modifier concentration in the mobile phase was changed by time so as to be 5% in a time zone of 0 to 7 minutes, 30% in a time zone of 7.01 to 10 minutes, and 5% in a time zone of 10.01 to 16 minutes. The flow rate of the mobile phase was 3 mL/min, the flow rate of the makeup solvent was 0.1 mL/min, and the set pressure of the BPR 12 was 10 MPa.

[0036] From the chromatogram of FIG. 5, it can be seen that three isomers of PI(3)P, PI(4)P, and PI(5)P and three isomers of PI(3,4)P.sub.2, PI(3,5)P.sub.2, and PI(4,5)P.sub.2 are separated. The three PIPs of PI(3)P, PI(4)P, and PI(5)P and the three PIPs of PI(3,4)P.sub.2, PI(3,5)P.sub.2, and PI(4,5)P.sub.2 are each three isomers. Although the three isomers have the same mass, each isomer can be individually detected and quantified by the MS 14 because the isomers are separated by the SFC.

[0037] As described above, it can be seen that the combination of an SFC having a separation column filled with a separation medium in which cyclodextrin is bound to a silica stationary phase and an MS enables individual quantification of seven PIPs.

DESCRIPTION OF REFERENCE SIGNS

[0038] 2: Analysis flow path [0039] 4, 6, 15: Solvent delivery pump [0040] 8: Sample injection part [0041] 10: Separation column [0042] 12: Back pressure regulator (BPR) [0043] 14: Mass spectrometer (MS)