Biopolymer sequences by MALDI granddaughter ion spectra
View Patent ↗The invention relates to the acquisition of spectra of biopolymers, especially of proteins, in tandem mass spectrometers with ionization using matrix-assisted laser desorption (MALDI) for the examination or determination of sequence patterns. The invention consists of a method of measuring granddaughter spectra of terminal fragment ions of the bipolymers in tandem mass spectrometers, wherein a so-called in-source fragmentation to generate a first generation of fragment or daughter ions of a biopolymer is coupled with a subsequent measurement of granddaughter ions, which have been obtained by a further fragmentation of a selected type of daughter ions. The method according to the invention enables the determination of the terminal sequences which are otherwise very difficult to measure.
1. Method for the acquisition of a mass spectrum containing information about sequences of a biopolymer, in a tandem mass spectrometer with an ion source for the ionization of the biopolymer by means of matrix-assisted laser desorption, the method comprising:
(a) preparing the biopolymer together with a matrix substance as a sample on a sample support;
(b) placing the sample support in the ion source;
(c) bombarding the sample on the sample support with light pulses from a pulsed laser with such a high energy density that it causes spontaneous fragmentations of a part of the biopolymer molecules whereby different species of in-source decay ISD fragment ions are formed;
(d) accelerating the ions and injecting them into a first mass spectrometer of the tandem mass spectrometer;
(e) selecting one species of the ISD fragment ions in the first mass spectrometer of the tandem mass spectrometer;
(f) fragmenting the selected ISD fragment ions at least partially to granddaughter ions by means of gas collisions (CID), surface collisions (SID) photon collisions (PID) or metastable decay (LID); and
(g) measuring the granddaughter ions in a second mass spectrometer of the tandem mass spectrometer to form a granddaughter mass spectrum.
2. Method according to claim 1 wherein the tandem mass spectrometer is a tandem in time mass spectrometer.
3. Method according to claim 1 wherein the tandem mass spectrometer is a tandem in space mass spectrometer.
4. Method according to claim 3 , wherein the tandem in space mass spectrometer comprises one of the grourp consisting of magnetic sector mass spectrometers, quadrupole filter mass spectrometers, ion trap mass spectrometers and time-of-flight mass spectrometers.
5. Method according to claim 1 , wherein the tandem mass spectrometer comprises a quadrupole filter as the first mass spectrometer and a time-of-flight mass spectrometer with orthogonal ion injection as the second mass spectrometer.
6. Method according to claim 1 , wherein the tandem mass spectrometer comprises two coaxially aligned time-of-flight mass spectrometers (TOF/TOF).
7. Method according to claim 1 , wherein the formation of the granddaughter mass spectrum is preceded by an acquisition of a mass spectrum of ISD fragment ions generated in the ion source by the laser bombardment and wherein the mass spectrum of the ISD fragment ions serves as a base for the selection of the one species of ISD fragment ions for the formation of the granddaughter mass spectrum.
8. Method according to claim 7 , wherein the biopolymers are proteins and wherein more than one mass spectrum of the ISD fragment ions is acquired prior to the formation of the granddaughter mass spectrum, and for each one of the mass spectra of the ISD fragment ions, a different matrix substance is used to form ISD fragment ions.
9. Method according to claim 7 , wherein the biopolymers are proteins and prior to the formation of the granddaughter mass spectrum, cross links of the proteins are dissolved.
10. Method according to claim 9 , wherein disulfide bridges between cysteines are dissolved by reduction and alkylation, or by oxidation.
11. Method according to claim 1 , wherein the tandem mass spectrometer is an ion trap mass spectrometer and wherein the selection, fragmentation and measuring of the granddaughter ions are carried out in the ion trap mass spectrometer consecutively.
12. Method for the determination of terminal sequences of a protein using a tandem mass spectrometer, the method comprising:
(a) acquiring granddaughter mass spectra of different species of in-source decay ISD fragment ion of the same fragmentation series, each granddaughter mass spectrum being acquired by
(i) preparing the protein together with a matrix substance as a sample on a sample support;
(ii) placing the sample support in the ion source;
(iii) bombarding the sample on the sample support with light pulses from a pulsed laser with such a high energy density that it causes spontaneous fragmentations of a part of the protein whereby different species of ISD fragment ions are formed;
(iv) accelerating the ions and injecting them into a first mass spectrometer of the tandem mass spectrometer;
(v) selecting one species of the ISD fragment ions in the first mass spectrometer of the tandem mass spectrometer;
(vi) fragmenting the selected ISD fragment ions at least partially to granddaughter ions by means of gas collisions (CID), surface collisions (SID) photon collisions (PID) or metastable decay (LID); and
(vii) measuring the granddaughter ions in a second mass spectrometer of the tandem mass spectrometer to form a granddaughter mass spectrum;
(b) comparing the granddaughter mass spectra to determine one fixed ion fragmentation series that is not shifted on all of the granddaughter mass spectra; and
(c) using the mass differences of the fixed ion fragmentation series to read out the terminal sequence of the protein.
13. Method according to claim 12 , wherein a computer program is used to identify the fixed ion fragmentation series in the granddaughter mass spectra.
14. Method according to claim 13 , wherein the determination read out of the terminal sequence is also performed by means of a computer program.