Selective capture and release of analytes
The described subject matter includes techniques and components for minimally invasive, selective capture and release of analytes. An aptamer is selected for its binding affinity with a particular analyte(s). The aptamer is functionalized on a solid phase, for example, microbeads, polymer monolith, microfabricated solid phase, etc. The analyte is allowed to bind to the aptamer, for example, in a microchamber. Once the analyte has been bound, a temperature control sets the temperature to an appropriate temperature at which the captured analyte is released.
1. A method for selectively increasing the concentration of an analyte, comprising:
(a) functionalizing a solid phase with an aptamer;
(h) introducing the analyte to the aptamer in an impure form;
(c) binding the analyte to the aptamer;
(d) washing the bound aptamer analyte complex to remove impurities;
(e) repeating (a)-(d) until a desired analyte concentration is reached;
(f) decreasing the temperature of the aptamer such that the analyte is released from the aptamer; and
(g) re-using the aptamer for capture and release of analytes.
2. The method of claim 1 , wherein analyte capture and release occurs in an aqueous medium without altering solvent composition.
3. A method for using aptamers for the capture and selective release of an analyte, comprising:
(a) binding an analyte to an aptamer, the aptamer functionalized on a solid phase;
(b) adjusting a temperature to release the analyte from the aptamer; and
(c) re-using the aptamer for capture and release of analytes,
wherein the binding the analyte to the aptamer comprises binding the analyte to the aptamer at a first temperature, and wherein adjusting the temperature comprises reducing the temperature of the aptamer to a second temperature which is lower than the first temperature.
4. The method of claim 3 , further comprising introducing the analyte to the aptamer in impure form and washing the bound analyte to remove impurities.
5. The method of claim 3 , further comprising collecting and detecting the analyte.
6. The method of claim 5 , wherein the detecting comprises performing mass spectrometry on the released analyte.
7. The method of claim 5 , wherein detecting comprises detecting fluorescence intensity.
8. The method of claim 3 , wherein the analyte comprises an oligonucleotide.
9. The method of claim 3 , wherein the analyte comprises a cell.
10. The method of claim 3 , wherein the second temperature is between 15° C. and 30° C.
11. The method of claim 3 , wherein the second temperature is between 50° C. and 65° C.
12. The method of claim 3 , wherein analyte capture and release occurs in an aqueous medium without altering solvent composition.
13. A method for using aptamers for the capture and selective release of an analyte, comprising:
(a) binding an analyte to the aptamer, the aptamer being functionalized on a solid phase; and
(b) adjusting a temperature to release the analyte from the aptamer,
wherein binding the analyte to the aptamer comprises binding the analyte to the aptamer at a first temperature, and wherein adjusting the temperature comprises reducing the temperature of the aptamer to a second temperature which is lower than the first temperature.
14. The method of claim 13 , further comprising:
(c) introducing the analyte to the aptamer in an impure form;
(d) washing the bound analyte to remove impurities; and
(e) repeating (c), (a), and (d) such that the amount of bound analyte is increased.
15. The method of claim 13 , further comprising collecting and detecting the analyte.
16. The method of claim 15 , wherein the detecting comprises performing mass spectrometry on the released analyte.
17. The method of claim 15 , wherein the detecting comprises detecting fluorescence intensity.
18. The method of claim 13 , wherein the solid phase comprises a microbead.
19. The method of claim 13 , wherein the analyte includes an oligonucleotide.
20. The method of claim 13 , wherein the analyte comprises a cell.
21. The method of claim 13 , wherein analyte capture and release occurs in an aqueous medium without altering solvent composition.