The present invention relates to a spectrum calculation processing device that performs calculation processing of a plurality of spectrums, an ion trap mass spectrometry system including the spectrum calculation processing device, a spectrum calculation processing method, an ion trap mass spectrometry method using the spectrum calculation processing method and a non-transitory computer readable medium storing a spectrum calculation processing program.
Ion trap mass spectrometers that use ion traps capturing ions by electric fields have been known. For example, WO 2008/129850 A1 describes a Matrix Assisted Laser Desorption/Ionization Digital Ion Trap Mass Spectrometer (MALDI-DIT-MS). In the ion trap mass spectrometer, ions are produced by irradiating a sample with laser light. The produced ions are introduced and captured in an ion trap, and then the ions having mass-to-charge ratios (m/z) in a range to be analyzed are discharged from the ion trap and detected by an ion detector. A mass spectrum is obtained based on a detection signal output from the ion detector.
The mass spectrum obtained by such an ion trap mass spectrometer is influenced by the space charges in the ion trap. In the mass spectrometry described in JP 2013-7637 A, a mass axis of a mass spectrum is corrected based on an amount of ions accumulated in an ion trap at the time of discharge of the ions.
However, the space charges in the ion trap influences not only the mass axis of the mass spectrum but also the width of each peak and so on. For example, when an MALDI ion source is used, the amount of ions that are produced each time a sample is irradiated with laser light varies largely depending on a crystalline state of a sample. A plurality of mass spectrums obtained by irradiating a sample with laser light multiple times, are integrated in order to improve the S/N (signal/noise) ratio of the mass spectrum. In this case, when the widths of corresponding peaks in the plurality of mass spectrums vary, a good mass spectrum is not obtained after integration.
An object of the present invention is to provide a spectrum calculation processing device, a spectrum calculation processing method, an ion trap mass spectrometry system, an ion trap mass spectrometry method and a non-transitory computer readable medium storing a spectrum calculation processing program that enable a good mass spectrum to be obtained easily based on a plurality of mass spectrums obtained by ion trap mass spectrometry.
(1) A spectrum calculation processing device according to one aspect of the present invention includes a spectrum acquirer that acquires a plurality of mass spectrums obtained by ion trap mass spectrometry with respect to a same sample, a specific physical quantity calculator that calculates a physical quantity reflecting an amount of ions as a specific physical quantity with respect to each of the plurality of mass spectrums acquired by the spectrum acquirer, a spectrum sorter that sorts the plurality of mass spectrums in order of the specific physical quantity calculated with respect to each mass spectrum, a first display controller that allows a display to display the plurality of sorted mass spectrums, a spectrum selector that selects a plurality of mass spectrums having specific physical quantities in a designated range from the plurality of displayed mass spectrums, a spectrum integrator that integrates the plurality of selected mass spectrums, and a second display controller that allows the display to display an integrated mass spectrum obtained by the spectrum integrator.
With the spectrum calculation processing device, the plurality of mass spectrums are sorted in order of the specific physical quantity reflecting the amount of ions, and displayed in the sorting order. Thus, the user can identify the specific physical quantity range in which a good mass spectrum is obtained by viewing the plurality of mass spectrums displayed in order of the specific physical quantity. The plurality of mass spectrums having the specific physical quantities in the range designated by the user are selected, and the plurality of selected mass spectrums are integrated. Thus, a good mass spectrum is obtained by integration. In this case, it is not necessary to correct the plurality of mass spectrums. Further, it is not necessary to adjust an analysis condition in order to reduce influence by the space charges in the ion trap. Therefore, a good mass spectrum can be obtained easily based on the plurality of mass spectrums obtained by the ion trap mass spectrometry.
(2) The spectrum calculation processing device may further include a storage that stores the mass spectrum obtained by the spectrum integrator, and the specific physical quantity range that is used for selection of the plurality of mass spectrums by the spectrum selector.
In this case, the good integrated mass spectrum and the specific physical quantity range for obtaining the good mass spectrum are stored. Thus, at the time of analysis of another sample of the same type, the plurality of mass spectrums to be used for integration can be selected based on the stored range of the specific physical quantity. Therefore, in the analysis that is carried out a plurality of times, the reference for selection of the plurality of mass spectrums used for integration can be constant. Further, an analysis method including the range of the specific physical quantity as one of analysis conditions can be created easily.
(3) The specific physical quantity may include an integral charge quantity in a specific mass-to-charge ratio range with respect to each mass spectrum. In this case, the integral charge quantity in the specific mass-to-charge ratio range with respect to the mass spectrum reflects the amount of ions in the ion trap. Therefore, it is possible to obtain a good mass spectrum by integration, by selecting a plurality of mass spectrums having integral charge quantities in an appropriate range.
(4) The spectrum calculation processing device may further include a mass-to-charge ratio range setter that sets the specific mass-to-charge ratio range. In this case, a good mass spectrum can be obtained in a desired range of the mass-to-charge ratio after the integration.
(5) A spectrum calculation processing method according to another aspect of the present invention includes acquiring a plurality of mass spectrums obtained by ion trap mass spectrometry with respect to a same sample, calculating a physical quantity that reflects an amount of ions as a specific physical quantity with respect to each of the plurality of acquired mass spectrums, sorting the plurality of mass spectrums in order of the specific physical quantity calculated with respect to each mass spectrum, allowing a display to display the plurality of sorted mass spectrums, selecting a plurality of mass spectrums having specific physical quantities in a designated range from the plurality of displayed mass spectrums, integrating the plurality of selected mass spectrums, and allowing the display to display an integrated mass spectrum.
(6) A non-transitory computer readable medium according to yet another aspect of the present invention, stores a spectrum calculation processing program, wherein the spectrum calculation processing program causes a computer to execute a process of acquiring a plurality of mass spectrums obtained by ion trap mass spectrometry with respect to a same sample, a process of calculating a physical quantity that reflects an amount of ions as a specific physical quantity with respect to each of the plurality of acquired mass spectrums, a process of sorting the plurality of mass spectrums in order of the specific physical quantity calculated with respect to each mass spectrum, a process of allowing a display to display the plurality of sorted mass spectrums, a process of selecting a plurality of mass spectrums having specific physical quantities in a designated range from the plurality of displayed mass spectrums, a process of integrating the plurality of selected mass spectrums, and a process of allowing the display to display an integrated mass spectrum.
(7) An ion trap mass spectrometry system according to yet another aspect of the present invention includes an ion trap spectrometer, and the above-mentioned spectrum calculation processing device that performs calculation processing with respect to a plurality of mass spectrums obtained by the ion trap mass spectrometer.
(8) An ion trap mass spectrometry method according to yet another aspect of the present invention includes obtaining a plurality of mass spectrums by ion trap mass spectrometry with respect to a same sample, and performing the above-mentioned spectrum calculation processing method with respect to the plurality of obtained mass spectrums.
Other features, elements, characteristics, and advantages of the present invention will become more apparent from the following description of preferred embodiments of the present invention with reference to the attached drawings.
A spectrum calculation processing device, an ion trap mass spectrometry system including the spectrum calculation processing device, a spectrum calculation processing method, an ion trap mass spectrometry method using the spectrum calculation processing method and a non-transitory computer readable medium storing a spectrum calculation processing program according to embodiments of the present invention will be described below in detail with reference to drawings.
The ion trap mass spectrometer 10 includes an ion source 1, an ion trap 2, a laser driver 3, an ion trap power supply 4, an ion detector 5, an output unit 6, a controller 7, an operation unit 8 and a display 9. In the present embodiment, the ion source 1 is a MALDI ion source. The controller 7 controls the laser driver 3 and the ion trap power supply 4.
The ion source 1 includes a sample plate 11, a laser irradiator 13 and an extraction electrode 14. A sample 12 mixed with a matrix is prepared on the sample plate 11. The laser driver 3 drives the laser irradiator 13. Thus, the laser irradiator 13 irradiates the sample 12 on the sample plate 11 with pulse-form laser light. As a result, various components included in the sample 12 are ionized. The produced ions are extracted by an electric field, which is formed between the sample plate 11 and the extraction electrode 14, for extracting ions.
In the present embodiment, the ion trap 2 is a three-dimensional quadrupole ion trap. The ion trap 2 includes a ring electrode 21 and a pair of end-cap electrodes 22, 24. The pair of end-cap electrodes 22, 24 is provided to be opposite to each other with the ring electrode 21 provided therebetween. An ion introduction port 23 is provided at substantially the center of the end-cap electrode 22. An ion discharge port 25 is provided at substantially the center of the end-cap electrode 24. The ions extracted from the ion source 1 are introduced into the ion trap 2 through the ion introduction port 23.
The ion trap power supply 4 applies a square-wave voltage to the ring electrode 21 as a capturing voltage. Thus, a capturing electric field that captures ions in the ion trap 2 while oscillating the ions is formed. With the square-wave voltage applied to the ring electrode 21, a high-frequency signal having a predetermined frequency is applied to the end-cap electrodes 22, 24 by the ion trap power supply 4. Thus, the ions having a specific mass are resonantly excited (excitation). The resonantly excited ions are discharged from the ion discharge port 25.
The controller 7 changes the frequency of the capturing voltage to be applied to the ring electrode 21 and the frequency of an auxiliary voltage to be applied to the end-cap electrodes 22, 24. Thus, the mass-to-charge ratio of the ions to be discharged from the ion discharge port 25 sequentially changes.
The ions discharged from the ion discharge port 25 are introduced into the ion detector 5. The ion detector 5 includes a conversion dynode and a secondary electron multiplier, for example, and outputs the electric charges corresponding to the amount of detected ions as a detection signal. The detection signal that is output from the ion detector 5 is supplied to the output unit 6. The output unit 6 produces a mass spectrum (hereinafter abbreviated as a spectrum) by converting the detection signal into digital data. The display 9 displays the spectrum supplied by the output unit 6 through the controller 7 and various data. A user uses the operation unit 8 to give various instructions to the controller 7.
The spectrum calculation processing device 30 is constituted by an input output I/F (interface) 31, a CPU (Central Processing Unit) 32, a RAM (Random Access Memory) 33, a ROM (Read Only Memory) 34 and a storage device 35, and is a personal computer or a server, for example. The input output I/F 31, the CPU 32, the RAM 33, the ROM 34 and the storage device 35 are connected to a bus 38. The input output I/F 31 is connected to the output unit 6 and the controller 7 of the ion trap mass spectrometer 10.
The operation unit 36 includes a keyboard, a pointing device and so on, and is used for inputting various data, etc., and various types of operations. The display 37 includes a liquid crystal display, an organic electroluminance display or the like, and displays spectrums and various information and images. The operation unit 36 and the display 37 may be constituted by a touch panel display.
The storage device 35 includes a storage medium such as a hard disc, an optical disc, a magnetic disc, a semiconductor memory or a memory card, and stores the spectrum calculation processing program, which is a computer program. The RAM 33 is used as a work area for the CPU 32. A system program is stored in the ROM 34. The CPU 32 executes the spectrum calculation processing program stored in the storage device 35 on the RAM 33, whereby the spectrum calculation processing, described below, is performed.
As shown in
The user designates the specific m/z range (hereinafter abbreviated as an m/z range) using the operation unit 36. The m/z range setter 307 sets the m/z range designated using the operation unit 36. Further, the user designates a selection range of the specific physical quantity using the operation unit 36. In the present embodiment, the selection range of the integral charge quantity is set.
The spectrum acquirer 301 acquires a plurality of spectrums that are obtained by analysis that is carried out a plurality of times with respect to the same sample from the output unit 6 of the ion trap mass spectrometer 10 of
The specific physical quantity calculator 302 calculates the physical quantity of peaks in the set m/z range in each spectrum acquired by the spectrum acquirer 301 as the specific physical quantity. In the present embodiment, the specific physical quantity calculator 302 calculates an integral charge quantity with respect to each spectrum by calculating the area of peaks in the set m/z range in each spectrum acquired by the spectrum acquirer 301.
The spectrum sorter 303 sorts a plurality of spectrums based on the integral charge quantity calculated by the specific physical quantity calculator 302 with respect to each spectrum. Specifically, the spectrum sorter 303 sorts (rearranges) the plurality of spectrums in descending or ascending order of the integral charge quantity. The spectrum selector 304 selects a plurality of spectrums having specific physical quantities in the selection range set by the selection range setter 308. The post-selection spectrum integrator 305 integrates the data of the plurality of spectrums selected by the spectrum selector 304. The spectrum obtained by integration by the post-selection spectrum integrator 305 is referred to as a post-selection integrated spectrum. In the present embodiment, the post-selection spectrum integrator 305 is an example of a spectrum integrator.
The storage 309 stores the post-selection integrated spectrum, the type of specific physical quantity (the integral charge quantity in the present embodiment) and the selection range (the designated range of the integral charge quantity in the present embodiment). The display controller 310 allows the display 37 to display the plurality of spectrums acquired by the spectrum acquirer 301, the pre-selection integrated spectrum obtained by the pre-selection spectrum integrator 306, the plurality of spectrums sorted by the sorter 303, the plurality of spectrums selected by the spectrum selector 304, and the post-selection integrated spectrum obtained by the post-selection spectrum integrator 305. In the present embodiment, the display controller 310 constitutes a first display controller and a second display controller.
The spectrum calculation processing method is performed by execution of the spectrum calculation processing program.
The ion trap mass spectrometer 10 of
First, the spectrum acquirer 301 of
In the display screen of
The user designates the m/z range using the operation unit 36. Thus, the m/z range setter 307 sets the designated m/z range (step S4). In the example of
Next, the specific physical quantity calculator 302 calculates the specific physical quantity in the m/z range with respect to each spectrum (step S5). In the present embodiment, the specific physical quantity is an integral charge quantity, so that the specific physical quantity calculator 302 calculates the integral charge quantity in the m/z range MR with respect to each spectrum.
In the display screen of
In the example of
In the display screen of
The selection range setter 308 sets the designated selection range of the specific physical quantity (step S8). The spectrum selector 304 selects spectrums having specific physical quantities in the set selection range (step S9). In the example of
The display controller 310 allows the display 37 to display the plurality of spectrums selected by the spectrum selector 304 (step S10). When the user operates the integration instruction button 503 in the display screen of
Further, the post-selection spectrum integrator 305 integrates the data of the plurality of selected spectrums (step S11). Thus, the post-selection integrated spectrum is calculated. The display controller 310 allows the display 37 to display the post-selection integrated spectrum (step S12). In the example of
The spectrum calculation processing device 30 according to the present embodiment sorts the plurality of spectrums in the order of the specific physical quantity reflecting the amount of ions, and displays the plurality of spectrums in the sorted order. Thus, the user can identify the specific physical quantity range in which a good spectrum can be obtained by viewing the plurality of spectrums displayed in the order of the specific physical quantity. The plurality of spectrums having the specific physical quantities in the selection range designated by the user are selected, and the plurality of selected spectrums are integrated. Thus, a good post-selection integrated spectrum is obtained.
Generally, when the MALDI ion source is used, variations in amount of ions that are produced each time a sample is irradiated with laser light and production of ions in a wide range make influence by the space charges in the ion trap 2 be unstable. As a result, the value of the mass-to-charge ratio of each peak in a spectrum is unstable, or a plurality of peaks in the integrated spectrum are not sufficiently separated. Here, although such a spectrum is considered to be corrected, it is difficult to correct the spectrum due to the following reasons. First, because ion detection efficiency has mass dependency, it is difficult to calculate a correct amount of ions from a spectrum. Further, in the case where resonance excitation is used for discharge of ions from the ion trap 2, when the influence by space charges in the ion trap 2 becomes too large, the discharge of ions from the ion trap 2 changes from the resonance excitation discharge to the LMCO (Low Mass Cut off) discharge. In this case, the spectrum changes largely. Therefore, it is difficult to correct the spectrum accurately. As such, it is considered that the irradiated position with laser light and the power of laser light are adjusted such that influence by the space charges in the ion trap 2 is reduced. However, adjustment of the irradiated position with laser light and the power of laser light requires much labor or time. In particular, in consideration of consumption of the sample 12 due to continuous irradiation of the same position with laser light, the above-mentioned adjustment work requires even more labor or time.
In contrast, the spectrum calculation processing device 30 according to the present embodiment does not require the correction of a spectrum or the adjustment work of an irradiated position with laser light or the like. Therefore, a good post-selection integrated spectrum can be obtained easily based on the plurality of spectrums obtained by the ion trap mass spectrometry.
Further, because the post-selection integrated spectrum and the selection range of the specific physical quantity for obtaining the post-selection integrated spectrum are stored, a plurality of mass spectrums to be used for integration can be selected based on the stored selection range of the specific physical quantity at the time of analysis of another sample of the same type. Therefore, in the analysis that is carried out a plurality of times, the reference for selection of the plurality of spectrums to be used for integration is constant. Further, an analysis method including the selection range of the specific physical quantity as one of the analysis conditions can be created easily.
Further, the integral charge quantity used as the specific physical quantity sufficiently reflects the amount of ions in the ion trap 2, so that it is possible to obtain a good post-selection integrated spectrum by selecting a plurality of spectrums having integral charge quantities in an appropriate range.
While the integral charge quantity is used as the specific physical quantity in the above-mentioned embodiment, another physical quantity reflecting the amount of ions may be used as the specific physical quantity. For example, the total height of one or a plurality of peaks in the specific m/z range of the spectrum may be used as the specific physical quantity. When the space charges quantity in the ion trap 2 is large, the height and width of a peak in a spectrum tend to be large. Thus, the height of the peak reflects the amount of ions. Therefore, even when the total height of the one or plurality of peaks in the specific m/z range is used as the specific physical quantity, a good post-selection integrated spectrum can be obtained.
While the ion source 1 is the MALDI ion source in the above-mentioned embodiment, the present invention is not limited to this. For example, the ion source 1 may be an ion source using Electrospray Ionization (ESI) or an ion source using Atmospheric Pressure Chemical Ionization (APCI).
While the ion trap mass spectrometer 10 according to the above-mentioned embodiment is a MALDI-DIT-MS, the present invention is not limited to this. For example, the present invention is applicable to another ion trap mass spectrometer such as an Ion Trap Time of Flight (IT-TOF: Time of Flight) mass spectrometer.
While the ion detector 5 using a secondary electron multiplier is used in the above-mentioned embodiment, the ion detector in the present invention is not limited to this. The ion detector in the present invention may be another ion detector such as an ion detector using a multi-channel plate.
In the above-mentioned embodiment, the spectrum acquirer 301 saves a plurality of spectrums that are obtained each time a sample is irradiated with laser light. However, when the amount of data to be saved is large, every certain number of spectrums out of a plurality of spectrums acquired by the spectrum acquirer 301 may be integrated, data processing such as moving average may be performed on each integrated spectrum, and each spectrum on which the data processing has been performed may be saved.
As each of various elements recited in the claims, various other elements having configurations or functions described in the claims can be also used.
While preferred embodiments of the present invention have been described above, it is to be understood that variations and modifications will be apparent to those skilled in the art without departing the scope and spirit of the present invention. The scope of the present invention, therefore, is to be determined solely by the following claims.
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