The invention generally relates to quadrupole ion traps and more particularly to two dimensional (2-D) quadrupole ion traps.
Tandem mass spectrometry methods (MS/MS) are very useful for characterizing and/or quantifying a component of interest in a complex mixture and/or for deriving enhanced structural information from an analyte that yields limited fragmentation and/or has a feature that complicates quantification. Linear ion traps are one type of instrumentation commonly used for MS/MS. The term “linear ion trap” may include three dimensional ion traps (e.g. 3-D ion traps) made up of ring and end-cap electrodes forming a near ideal quadrupole field or ion traps comprising four pole rods (e.g., 2-D ion traps). In an ideal 3-D ion trap quadrupole field, a radio frequency (RF) field strength increases linearly both radially and axially and the repulsing pseudo-forces also increase linearly. The 2-D ion traps are made up of four rod electrodes in which the quadrupole field only changes along two coordinates (x, y) and remains constant along the third coordinate (z).
Typically, 3-D ion traps have a small octopole field in addition to the quadrupole field. The octopole component makes the 3-D ion trap a substantially non-linear resonating system (A. A. Makarov, Anal. Chem. 1996, 68, p. 4257-4263, Franzen, et al., Practical aspects of Ion Trap Mass Spectrometry, volume 1 p. 69 edited by R. E. March and J.F.J. Todd). This means that isolation is asymmetrical both below the m/z of interest and above it. With a positive sign of the octopole field the isolation window can be very sharp for m/z below the nominal m/z value and quite diffused above the nominal m/z value.
Isolation techniques such as those described in U.S. Pat. No. 5,324,939 do not recognize the non-linearity of the ion trap and focus on the construction of the ejection waveforms based on the assumption of a linear resonance system. As a result the isolation procedure requires a substantial amount of time (i.e., on the order of 20 to 60 ms) and the width of the isolation window is typically greater than 1 Da.
Franzen in U.S. Pat. No. 5,331,157 (the '157 Patent) recognized the non-linear behavior and non-symmetrical ion behavior around the m/z of interest and disclosed the use of a non-linear resonance to facilitate the ejection of M+1 species from an ion trap. However when using the technique of the '157 Patent, it is typically difficult to obtain an isolation window width better then 1Da. Further the ejection of ions with masses higher than the m/z of interest typically requires repeating the procedure. When using the technique of the '157 Patent, it is desirable to have a lower number of ions stored in the ion trap. Thus, typically the total number of ions that can be stored in the ion trap prior to isolation (e.g., the “isolation storage capacity”) is limited.
U.S. Pat. No. 6,649,911 discloses a complex specially designed wave function used, with phase inversion at around the frequency that corresponds to the mass to be isolated, for trapping ions. Repeating application of the scan function is typically necessary to provide isolation of a well resolved ion species.
Superimposing a substantial contribution of an octopole field onto the pure quadrupole field of a 2-D ion trap has been suggested recently. (See Linear Quadrupoles with Added Octopole Fields, Sudakov at the Proceedings of the 51 ASMS, Canada, Jun. 8-12, 1993; and Franzen, U.S. Patent Publication U.S. 2004/0051036 A1). However, adding an octopole component in a 2-D ion trap utilizing prior art isolation methods typically results in a diffused isolation edge on the one side of the isolation window.
Accordingly, there is a need for isolation apparatus and methods for a 2-D ion trap with a superimposed octopole field.
The present invention includes a 2-D ion trap comprising, a trapping chamber. The ion trap includes a plurality of electrodes defining the trapping volume, a circuit for providing a substantially quadrupole radio frequency field (RF field) having a planar x-y geometry in the trapping volume and a circuit for providing an octopole field for distorting the planar x-y geometry of the quadrupole RF field. The ion trap may further include a means for introducing or forming ions in the trapping volume, and a means for forcing ion motion in a first direction and a second direction independently and sequentially.
The means for forcing ion motion in a first direction and a second direction independently may include a first means for generating an excitation wave frequency that provides an excitation wave frequency wherein the excitation wave frequency changes from a high frequency to a low frequency over time and a second means for generating an excitation wave frequency that provides an excitation wave frequency wherein the excitation wave frequency changes from a low frequency to a high frequency over time.
The means for distorting the planar quadrupole x-y geometry may be an octopole field. The ratio of the octapole field contribution to the quadrupole field contribution may be about 0.2% to about 5%.
The invention further comprises a method for trapping ions using the apparatus of the invention.
The present invention provides an apparatus and method for isolation of selected ions of interest in a 2-D ion trap. The apparatus and method provide for isolation resolution characterized by symmetrical sharp edges for the isolation window and, typically, a decrease in the time needed for isolation of ions. The apparatus comprises a trapping chamber including a plurality of electrodes defining a trapping volume, a circuit for providing an RF field in the trapping volume, a circuit for providing an octopole field in the trapping volume, and first and second supplemental wave form generators. Further, the present invention provides a method for improved ion isolation that is substantially insensitive to the presence of large number of ions within the 2-D trap (e.g., the method has high ion capacitance with respect to the isolation procedure).
An exemplary prior art 2-D ion trap comprising a quadrupole filter with input and exit plates and rod electrodes is shown in
where U and V are the DC and RF voltages applied to the opposite electrodes of the electrode pairs, and v is the frequency of the RF voltage. For the example shown in
In practice the actual electric field is slightly different from theoretical quadropole field described by the equation (1) due to the truncation of the hyperbolic surfaces of the electrodes. It is convenient to represent the actual electric field by the following expansion series:
Where A0, A2, A4 and A6 are expansion coefficients, P6 (x,y) is a polynomial function of the sixth degree and o(x,y) represents the sum of higher than sixth degree terms in the expansion series, U is the DC voltage applied the opposite pair of electrodes and V is the amplitude of the main RF voltage applied to the electrodes. The coefficients A2 and A4 are called quadrupole and octopole weighting coefficients, respectively. The percentage ratio A4/A2 defines the weighted contribution of the octopole field with respect to the contribution of the quadrupole field and can be used as a quantitative measure for the field distortion from the pure quadrupole field (referred to herein as the ratio of octopole field to the quadrupole field). Typically, for commercially available 2-D ion traps the quadrupole RF field is between approximately 0.5 Mhz and 2 Mhz. For such ion traps it is desirable to modify ion trap geometry from the ideal by adding an octopole field contribution to give an octopole field to quadrupole field ratio of about 0.2% to about 5% while minimizing higher order components of the expansion series. In some embodiments an octopole field to quadrupole field ratio of about 0.5% to about 2% is desirable. Typically, the optimum ratio is determined experimentally by identifying the ratio which yields the best resolution. Sufficient octopole contribution must be present to impact ion motion. Too much octopole contribution creates additional motion components that degrade resolution. The octopole contribution in combination with the method of applying supplemental resonance fields described herein allows one to achieve an improved isolation for the selected ions when eliminating unwanted ions from the ion trap.
More particularly, the ion trap geometry shown in
X′=k1X
Y′=k2Y (3)
where X′ and Y′ are the x and y axis dimensions of the modified electrode, X and Y are the ideal electrode dimensions along the z and y axis and k1, and k2 are scaling coefficients. The hyperbolic electrodes thus modified in shape and dimension such that the asymptotes no longer form a 90 degree angle are referred to hereinafter as stretched electrodes 31, 32, 33, 34.
In an exemplary embodiment k2=1/k1 and the value of k1 is typically in the range of 1.01 to 1.2 to provide a suitable octopole field contribution. For the example shown in
Stretched electrodes or round rod electrodes may be used as electrodes in the 2-D ion trap of the invention. In general, the round rod electrodes are somewhat less expensive as compared to hyperbolic or stretched electrodes. Thus, round rod electrodes may offer an economic advantage.
Referring to
In one exemplary embodiment of a modified geometry 2-D ion trap 120 with round rod electrodes, an octopole field contribution is introduced without introducing any substantial higher order components to the quadropole field by scaling the radii of the two opposite pairs of electrodes in inverse proportion while keeping the same Ro. This transformation can be described mathematically by the set of equations:
Rxn=Rd/J1
Ryn=Rd J1
Ron=Ro, (4)
where Rxn is the radius of the pair of rods aligned with the x axis, Ryn is the radius of the pair of rods aligned with the y axis, Ron is the inscribed radius for the final geometry, Ro is the inscribed radius for the undistorted geometry and J1 is the scaling coefficient. In an exemplary embodiment, J1 is selected to be about 1.0 to about 1.2.
In another embodiment as shown in
Alternatively, the electrode geometry modification may be accomplished by placing one or more slits in at least one of the electrodes of the electrode pairs and/or etching or engraving an indentation in the inner surface of one or more electrodes and/or adding a bulge to an inner surface of one or more electrodes.
The methods of modifying the physical geometry of electrodes that form the quadrupole field of a 2-D ion trap to provide an octopole contribution discussed herein are exemplary. Any other method that provides a suitable octapole field contribution to the quadropole field may be used.
Terminology used herein for the sign of the octopole field contribution as related to the main quadrupole field along a certain axis is as follows: The octopole contribution is positive along a certain coordinate axis if the sign of the coefficients of the expansion series as presented by equation 2 for the second power and the fourth power of that axis coordinate are the same. Accordingly, as equation 2 reveals, if the octopole field contribution is positive around one axis then it is negative around the orthogonal axis. For example, for the embodiments illustrated in
Generally, trapping ions in an ion trap comprises either forming ions in the ion trap or admitting them to the ion trap from an ion source external to the quadrupole trapping volume. Typically, the ions have a range of m/z (e.g. mass to charge) values and include some ions of interest and other ions which may have m/z values larger or smaller than the ions of interest. To perform an MS/MS experiment or an ion/molecule reaction or the like, for example, it is best to remove the ions with m/z values larger or smaller than the ions of interest from the ion trap. This is generally done in a systematic manner by manipulating the motion of the ions. The systematic application of changing conditions to eject unwanted ions from the ion trap may be referred to as scanning. Once the ions of the m/z of interest are isolated, the MS/MS analyses or ion/molecule investigation or the like may be performed.
Typically, MS/MS experiments are performed in a 2-D ion trap by applying one or several supplemental wave-forms to one pair of opposite electrodes to isolate the ions of interest. The applied wave-forms are selected to resonate with unwanted ions and eject the unwanted ions out of the ion trap, while attempting to preserve the ions of interest within the trapping volume. The wave forms may be quite complex and the process can be repeated several times to achieve the desired degree of isolation.
Ideally, the selection for the ions of interest in an MS/MS analyses should be as narrow as possible with respect to the nominal mass-to-charge (e.g. m/z) ratio of the ions of interest. This provides good discrimination and specificity. However if the isolation step is too narrow, then it may decrease the abundance of ions of interest and lower sensitivity. The desirable mass resolution for the isolation of the ions of interest is determined by the ratio of the m/z of the ions of interest to the width of the smallest window that does not discriminate against the intensity of the ions of interest to more than a 90% level. Another important parameter for ion isolation is total time that is required to complete the isolation. In general, the shortest possible isolation time is the most preferable, since it allows one to do a fast analysis with high duty cycle and also improves overall sensitivity of the apparatus.
Ion motion in a linear ion trap can be described as follows: When the DC voltage is zero (U=0), ion motion within the x-y plane of a linear ion trap in the presence of a supplemental sine wave, can be described using a pseudo-potential well approximation with assumption of decoupled x and y coordinates by the following equations:
where μ is the coefficient representing molecular drag or ion collisions with neutral molecules, due to the presence of the collisional gas in the ion trap, A4′ is the octopole normalized term, and Ex and Ey are the coefficients representing the amplitude of the supplemental excitation field along the x and y axis (e.g. coordinates), respectively.
If Ex or Ey are non-zero at the same time, Equations (5a) and (5b) can be treated independently. The resonance curves for these equations are presented in
For the modified ion traps 120 of the invention the resonance curves are non-linear resonance curves as shown in
In one embodiment, forcing ion motion in the x and the y directions independently is accomplished by using two supplemental wave form generators. A supplemental wave-form generator is attached to each pair of rod electrodes. In this embodiment as shown in
Optionally, an arbitrary wave form generator may be used as the supplemental wave form generator. An arbitrary wave form generator is a device that is capable of generating a computer generated pre-calculated signal.
For the embodiment shown in
More specifically, in the exemplary time sequence presented in
An exemplary chirp wave form that can be used in the practice of the invention may be described by the equation sin (ν(t)t), where ν=νi+αt. Alternatively, a chirp-like wave form such as the wave form that can be obtained using the SWIFT technique may be used. In SWIFT the wave form is obtained by addition of a plurality of sine waves with quadratic modulation for the phases with an increase of the average spectral frequencies in time during the wave-form duration. When the chirp or chirp-like wave form is applied, ions with an m/z larger than the m/z of the ions of interest will fall into resonance by intercepting the sharp edge of the reversed y-resonance curve (see
In practice, a complex arbitrary wave is designated as having a wave form with a frequency change from a low frequency to high frequency if the original frequency wave form can be segmented mathematically into a finite number of time segments and after taking Fourier transformation for each of the segments the resulting frequencies of the wave form components substantially increase from one segment to another, respectively. Similarly, a complex arbitrary wave is designated as having a wave form with a frequency change from a high frequency to low frequency if the original frequency wave form can be segmented mathematically into a finite number of time segments and after taking Fourier transformation for each of the segments the resulting frequencies of the wave form components substantially decrease from one segment to another, respectively. For this designation, only major frequency components that are presented with substantial intensities that can effect ion motion are considered.
For both ions with m/z smaller than the m/z of the ions of interest and for ions with m/z larger than the m/z of the ions of interest, it is possible to achieve non-linear resonance ejection though the sharp (near vertical) edge of a resonance curve. This yields the end result of an isolation window with a symmetrical shape. Typically, it also provides faster rates of ramping resonance parameters than with a conventional 2-D ion trap and typically overall shorter isolation times. The procedure, as described herein, can be repeated in sequence to eliminate nearly all ions that may result due to ion molecule reactions, ions/ion reactions or dissociation reactions within the trap.
For many applications, a single isolation sequence may be sufficient. However, after the initial isolation of the ion of interest, sequential repetition of this isolation procedure can be beneficial in some applications, for example, to address large space charge conditions. Optionally, in applications where space charge conditions are an issue, a first round initial isolation including only a T1 step executed at relatively high ramp rates (such as 50-100 Kda/s) using a wide isolation window (e.g., the order of 20 Da) can be used. In an exemplary embodiment, the time for this initial isolation procedure may be about 10 to 20 ms. A second isolation round can then be performed as shown in
where wx and wy, are ion oscillation fundamental frequencies along the x and the y axis respectively and the other terms are as defined for equations (5a) and (5b). Equations 5a and 5b assume an approximation of small coupling between x and y motions. To satisfy this condition, the initial ion position has to be close to (0,0). The x-y coupling makes the resonance curves somewhat time dependent and somewhat diffused. In some applications x-y coupling can compromise the resolution of the isolation. Coupling between x and y oscillations is inversely proportional to the difference (Δ) in frequencies for the x and y fundamental oscillations. Accordingly, providing an additional DC voltage can provide decoupling between x and y motions and yield higher isolation resolution. Additionally, the DC voltage provides a parameter that facilitates fine adjustments of the contribution of the octopole terms (A′4DCx and A′4DCx) without changing the trap electrodes' physical geometry.
In some applications, it is desirable to detect ions ejected from the ion trap. As
In one exemplary embodiment of the 2-D ion trap, it is possible to use a fast ejection of all the ions below the m/z of the ion of interest by utilizing the border of the main stability region without using the supplemental generator 64. An exemplary time diagram for this embodiment is shown in
The foregoing discussion discloses and describes many exemplary methods and embodiments of the present invention. As will be understood by those familiar with the art, the invention may be embodied in other specific forms without departing from the spirit or essential characteristics thereof. Accordingly, the disclosure of the present invention is intended to be illustrative, but not limiting, of the scope of the invention, which is set forth in the following claims.
Number | Name | Date | Kind |
---|---|---|---|
4761545 | Marshall et al. | Aug 1988 | A |
5324939 | Louris et al. | Jun 1994 | A |
5331157 | Franzen | Jul 1994 | A |
5420425 | Bier et al. | May 1995 | A |
5679951 | Kelley et al. | Oct 1997 | A |
5696376 | Doroshenko et al. | Dec 1997 | A |
6649911 | Kawato | Nov 2003 | B2 |
6897438 | Soudakov et al. | May 2005 | B2 |
20040051036 | Franzen et al. | Mar 2004 | A1 |
20060038123 | Quarmby et al. | Feb 2006 | A1 |
Number | Date | Country | |
---|---|---|---|
20070057175 A1 | Mar 2007 | US |