Methods of using inductively coupled plasma mass spectroscopy systems for analyzing a cellular sample
The invention relates to the use of inductively coupled plasma mass spectroscopy for cellular sample analysis. In some embodiments a method of performing mass spectroscopy analysis using an inductively coupled plasma mass spectroscopy system is provided. The method may include introducing a cellular sample comprising one or more cells or cellular particles into an inductively coupled plasma of the inductively coupled plasma mass spectroscopy system. The method may further include using the inductively coupled plasma mass spectroscopy system to assess the cellular sample by detecting and measuring one or more element tags in the cellular sample based on the element or isotopic compositions of the one or more element tags.
1. A kit comprising:
an element tag comprising a plurality of atoms of a single isotope of an element selected from the group consisting of a rare earth element, and a lanthanide, and further comprising a molecular structure supporting the plurality of atoms, wherein the element tag is distinguishable based on its isotopic composition; and
a nucleic acid probe labeled with the element tag; and
wherein the nucleic acid probe specifically hybridizes to a target nucleic acid.
2. The kit of claim 1 , further comprising the target nucleic acid.
3. The kit of claim 2 , wherein the target nucleic acid or the nucleic acid probe is bound to a support.
4. The kit of claim 1 , wherein the target nucleic acid is endogenous to a cell.
5. The kit of claim 1 , further comprising a target nucleic acid that is chemically synthesized.
6. The kit of claim 1 , wherein the target nucleic acid is amplified.
7. The kit of claim 1 , further comprising an affinity reagent.
8. The kit of claim 7 , wherein the affinity reagent is element tagged.
9. The kit of claim 1 , further comprising a plurality of distinguishable element tags.
10. A biological sample comprising:
a target nucleic acid;
an element tag comprising a plurality of atoms of a single isotope of an element selected from the group consisting of a rare earth element, and a lanthanide, and further comprising a molecular structure supporting the plurality of atoms, wherein the element tag is distinguishable based on its isotopic composition; and
a nucleic acid probe labeled with the element tag; and
wherein the nucleic acid probe is specifically hybridized to the to the target nucleic acid.
11. The sample of claim 10 , wherein the target nucleic acid is endogenous to a cell.
12. The sample of claim 10 , wherein the target nucleic acid is chemically synthesized.
13. The sample of claim 10 , further comprising an affinity reagent.
14. The sample of claim 13 , wherein the affinity reagent is element tagged.
15. The sample of claim 10 , further comprising a solid support bound to the nucleic acid probe or the target nucleic acid.
16. The sample of claim 10 , further comprising a tissue.
17. The sample of claim 10 , further comprising a suspension of cells.
18. A method comprising:
analyzing an isotopic composition of a biological sample by mass spectrometric atomic spectroscopy;
wherein the biological sample comprises:
a target nucleic acid;
an element tag comprising a plurality of atoms of a single isotope of an element selected from the group consisting of a rare earth element, and a lanthanide, and further comprising a molecular structure supporting the plurality of atoms, wherein the element tag is distinguishable based on its isotopic composition; and
a nucleic acid probe labeled with the element tag; and
wherein the nucleic acid probe is specifically hybridized to the to the target nucleic acid.
19. The method of claim 18 , further comprising hybridizing the nucleic acid probe to the target nucleic acid.
20. The method of claim 18 , further comprising analyzing the isotopic composition of the sample by inductively coupled plasma mass spectroscopy.