Sensitive intracavity biosensing platform and methods for detection therewith
View Patent ↗The present disclosure provides a method of detecting a target analyte, by binding the target analyte and a probe with at least one fluorophore to form a fluid composition. The fluid composition is excited within a laser cavity. The method comprises measuring a laser emission from the fluid composition based on an interaction between the target analyte and the probe. In certain aspects, the method provides hybridizing the target analyte and the probe, prior to the exciting. In certain variations, the methods comprise detecting a target analyte by measuring a laser emission from the fluid composition based on an interaction between the target analyte, where the interaction is probe energy transfer, intercalation, hybridization of the target analyte and the probe, or combinations thereof. The energy transfer can include fluorescence resonance energy transfer (FRET), FRET with a molecular-beacon, or cavity-assisted radiative energy transfer, by way of non-limiting example.
1. A method of detecting a target analyte, the method comprising:
binding the target analyte and a probe comprising at least one fluorophore to form a fluid composition;
exciting the fluid composition within a laser cavity; and
measuring a laser emission from the fluid composition based on an interaction between the target analyte and the probe.
2. The method of claim 1 , further comprising hybridizing the target analyte and the probe, prior to the exciting.
3. The method of claim 2 , wherein the fluorophore is a saturation dye, an acceptor fluorophore, a donor fluorophore or a fluorescent protein.
4. The method of claim 1 , wherein the laser cavity is an optofluidic ring resonator (OFRR) microlaser with an intracavity biosensing platform.
5. The method of claim 1 , wherein the interaction is selected from the group consisting of an energy transfer, intercalation, hybridization of the target analyte and the probe, and combinations thereof.
6. The method of claim 5 , wherein the energy transfer occurs when an acceptor fluorophore and a donor fluorophore are separated by a distance of greater than or equal to about 1 nm to less than or equal to about 20 nm when the target analyte hybridizes with the probe.
7. The method of claim 5 , wherein the energy transfer comprises one of fluorescence resonance energy transfer (FRET), or fluorescence resonance energy transfer (FRET) with a molecular-beacon.
8. The method of claim 1 , wherein the target analyte is selected from the group consisting of a protein, an enzyme, a receptor, an antibody fragment, a peptide, a carbohydrate, nucleic acids, single-stranded DNA, double-stranded DNA, RNA, an oligonucleotide, a single-nucleotide polymorphism (SNP) sequence, and any combination thereof.
9. The method of claim 1 , further comprising exposing the target analyte to an activity, wherein the activity causes a detectable change in the target analyte.
10. The method of claim 9 , wherein the detectable change is one of binding, dissociation, enzymatic cleavage, or a conformational change.
11. A method of detecting a DNA molecule, the method comprising:
labeling the DNA molecule with an acceptor fluorophore;
labeling at least one probe with a donor fluorophore;
hybridizing the DNA molecule and the probe to create a fluid composition, wherein upon hybridization the acceptor fluorophore and the donor fluorophore are separated by greater than or equal to about 1 nm to less than or equal to about 20 nm;
exciting the fluid composition within a laser cavity;
transferring energy between the donor fluorophore and the acceptor fluorophore by fluorescence resonance energy transfer (FRET) to generate a laser emission from the fluid composition and the laser cavity; and
measuring the laser emission to thereby detect the DNA molecule.
12. A method of detecting a DNA molecule, the method comprising:
combining a single-stranded DNA molecule and a single-stranded probe with a saturation dye to form a fluid composition;
exciting the fluid composition within a laser cavity; and
measuring a laser emission from the fluid composition based on an interaction between the single-stranded DNA molecule and the single-stranded probe.
13. A method of detecting a target analyte, the method comprising:
binding the target analyte and a probe comprising a gain medium to form a fluid composition;
exciting the fluid composition within a laser cavity; and
measuring a laser emission from the fluid composition based on an interaction between the target analyte and the probe.
14. The method of claim 13 , wherein the gain medium comprises a fluorophore or a dye.
15. The method of claim 13 , wherein exciting the fluid composition within a laser cavity comprises exciting the fluid composition within a laser cavity that is a cross-section of a capillary that forms a ring resonator that supports a whispering gallery mode (WGM).
16. The method of claim 15 , wherein the WGM has a Q-factor great than 10 7 .
17. The method of claim 15 , wherein the capillary comprises capillary walls with a thickness of less than or equal to about 10 μm.
18. The method of claim 15 , wherein exciting the fluid composition further comprises interacting the WGM with the gain medium to generate the laser emission.
19. The method of claim 13 , wherein measuring a laser emission from the fluid composition comprises measuring a laser emission from the fluid composition through free space with a detector.
20. The method of claim 13 , wherein measuring a laser emission from the fluid composition comprises contacting an optical fiber, a fiber prism or a waveguide to the laser cavity and measuring the laser emission through the optical fiber, fiber prism or waveguide with a detector.