Time-of-flight mass spectrometry analysis of biomolecules

• US 5,627,369 A
• Filed: 06/07/1995
• Issued: 05/06/1997
• Est. Priority Date: 05/19/1995
• Status: Expired due to Term

• Current Assignee: Applied Biosystems LLC (Thermo Fisher Scientific Incorporated)
• Original Assignee: Perseptive Biosystems Incorporated (Ecovyst, Inc.)
• Inventors: Vestal, Marvin L., Juhasz, Peter
• Primary Examiner(s): ANDERSON, BRUCE C
• Application Number:
  US08/488,127
• Time in Patent Office: 699 Days
• Field of Search: 250/281, 250/282, 250/287, 250/286, 250/423 P
• US Class Current: 250/287
• CPC Class Codes: H01J 49/164 Laser desorption/ionisation, e.g. matrix-assisted laser desorption/ionisation [MALDI] sample holders H01J49/0418
• CPC Class Codes: H01J 49/403 characterised by the acceleration optics and/or the extraction fields

Abstract

A time-of-flight mass spectrometer for measuring the mass-to-charge ratio of a sample molecule is described. The spectrometer provides independent control of the electric field experienced by the sample before and during ion extraction. Methods of mass spectrometry utilizing the principles of this invention reduce matrix background, induce fast fragmentation, and control the transfer of energy prior to ion extraction.

Claims

1. A time-of-flight mass spectrometer for measuring the mass-to-charge ratio of ions generated from a sample comprising:

a) a sample holder;

b) a sample ionizer for generating a pulse of sample ions from a sample disposed on the holder;

c) a first element spaced apart from the sample holder;

d) a power source electrically coupled to the first element and the holder for

i) applying a variable potential to each of the first element and the holder to establish a first electric field wherein the first element and holder potentials are variable independently before ion extraction, and

ii) applying a second variable potential to each of the first element and the holder to establish a second electric field for ion extraction, wherein the second variable potential is applied at a predetermined time subsequent to establishing the first electric field and the first element and holder potentials are variable independently; and

e) an ion reflector spaced apart from the first element,

wherein a flight time of extracted ions of like mass-to-charge ratio from the reflector to a detector will be independent to second order of the initial velocity.

2. The mass spectrometer of claim 1 further comprising means for controlling the power source to set the potential of the first element with respect to the potential of the holder more positive when measuring positive ions and more negative for measuring negative ions prior to ion extraction.

3. The mass spectrometer of claim 1 further comprising a second element, spaced apart from the first element, for producing an electric field for accelerating sample ions.

4. The mass spectrometer of claim 1 wherein the ionizer is a pulsed light source.

5. The mass spectrometer of claim 1 wherein the ionizer is a laser which generates a pulse of energy.

6. The mass spectrometer of claim 1 further comprising a sample electrically coupled to the holder, the sample comprising one or more molecules to be analyzed and a matrix substance which absorbs radiation at a wavelength substantially corresponding to the pulse of energy, the matrix facilitating desorption and ionization of molecules.

7. The mass spectrometer of claim 6 wherein the sample comprises at least one compound of biological interest selected from the group consisting of DNA, RNA, polynucleotides and synthetic variants thereof.

8. The mass spectrometer of claim 6 wherein the sample comprises at least one biomolecule selected from the group consisting of peptides, proteins, PNA, carbohydrates, glycoconjugates and glycoproteins.

9. The mass spectrometer of claim 1 wherein the first element comprises a grid.

10. The mass spectrometer of claim 1 wherein the first element comprises an electrostatic lens.