Mass spectrometer system
View Patent ↗During the structural analysis of a protein or peptide by tandem mass spectroscopy, a peptide ion derived from a protein that has already been measured and that is expressed in great quantities is avoided as a tandem mass spectroscopy target. A peptide derived from a minute amount of protein, which has heretofore been difficult to analyze, can be automatically determined as a tandem mass spectroscopy target within the real time of measurement. Data concerning a protein that has already been measured and a peptide derived from the protein is automatically stored in an internal database. The stored data is collated with measured data with high accuracy to determine an isotope peak. In this way, the process of selecting a peptide peak that has not been measured as the target for the next tandem analysis can be performed within the real time of measurement and a redundant measurement of peptides derived from the same protein can be avoided. The information contained in the MS n spectrum is effectively utilized in each step of the MS n involving a multi-stage dissociation and mass spectroscopy (MS n ), so that the flows for the determination of the next analysis content and the selection of the parent ion for the MS n+1 analysis, for example, can be optimized within the real time of measurement and with high efficiency and accuracy. Thus, a target of concern to the user can be subjected to tandem mass spectroscopy without wasteful measurement.
1. A mass spectroscopy system comprising:
ionization means for ionizing a substance as an object of measurement for a mass spectrometer; and
means for selecting an ion species with a specific mass-to-charge ratio m/z from ions produced by said ionization means and dissociating the same, wherein the selection, dissociation and measurement of the ion species as the measurement object are repeated in a plurality of stages, said mass spectroscopy system further comprising:
mass spectroscopy data acquisition means for performing the selection and dissociation of an ion species n−1 times (n≧1, where n is an integer) and acquiring a peak of measurement intensity against the mass-to-charge ratio of the ion that has been selected and dissociated;
correspondence determination means for comparing the peak of measurement intensity against the mass-to-charge ratio of the ion that is obtained by the mass spectroscopy data acquisition means with the characteristics data of a certain ion species in order to determine the possibility of correspondence of the ion that has been selected and dissociated to the certain ion species;
next-analysis content determination means for determining the analysis content in an n-th stage mass spectroscopy based on the result of determination by said correspondence determination means; and
a data processing unit configured such that the combined time required by the correspondence determination means and the next-analysis content determination means is 10 milliseconds or less.
2. The mass spectroscopy system according to claim 1 , wherein the next-analysis content determination means determines the implementation of an MS 3 analysis based on the number of contiguous amino acid residues that can be decoded from an acquired MS 2 spectrum.
3. The mass spectroscopy system according to claim 1 , wherein the substance as the object of measurement is a protein, a peptide, a sugar chain, a polymer, a metabolite, or a lipid.
4. The mass spectroscopy system according to claim 1 , wherein the next-analysis content determination means performs an MS 2 analysis when the amount of the ion that has been determined to be in correspondence by the correspondence determination means fluctuates by more than a certain value.
5. The mass spectroscopy system according to claim 1 , wherein said data processing unit is one CPU.
6. The mass spectroscopy system according to claim 1 , wherein said data processing unit includes a parallel computer or a CPU cluster.