Force-controlled nanoswitch assays for single-molecule detection in complex biological fluids
Provided herein are methods and products for detecting analytes in a sample. The analytes may be rare analytes such as biomarkers in a biological sample. These methods make use of nucleic acid nanoswitches that adopt a particular conformation and have a particular length in the presence of an analyte.
1. A method for detecting an analyte in a sample comprising
(a) contacting a sample with a plurality of nanoswitches for a time and under conditions sufficient for binding of an analyte to the nanoswitch,
(b) enriching and isolating closed nanoswitches bound to the analyte,
(c) tethering the closed nanoswitches to a surface, and
(d) measuring length of a single surface-tethered closed nanoswitch and/or detecting a rupture event in a single surface-tethered closed nanoswitch, under force,
wherein the nanoswitch is a nucleic acid conjugated to a first and a second analyte-binding agent which when bound to the analyte adopts a looped conformation and a shorter length as compared to the length of the nanoswitch when it is not bound to the analyte, and
wherein the closed nanoswitches are enriched and isolated by
(i) cleaving open and closed nanoswitches present after (a) with one or more endonucleases between the first and second analyte-binding agents,
(ii) end-conjugating the cleaved nanoswitches with a particle,
(iii) isolating the particle-conjugated nanoswitches, and
(iv) binding the particle-conjugated nanoswitches to a surface.
2. The method of claim 1 , wherein the method measures length of the surface-tethered closed nanoswitch.
3. The method of claim 2 , wherein the length of the surface-tethered closed nanoswitch is measured under constant force.
4. The method of claim 1 , wherein the method detects a rupture event in the surface-tethered closed nanoswitch.
5. The method of claim 4 , wherein the rupture event is detected under dynamic force.
6. The method of claim 1 , wherein the method detects a plurality of rupture events in the same surface tethered closed nanoswitch under dynamic force, and the method then identifies the force at which the maximum number of rupture events occur.
7. The method of claim 1 , wherein the one or more endonucleases is two endonucleases.
8. The method of claim 1 , wherein the particle is a magnetic particle.
9. The method of claim 1 , wherein the particle is a fluorescent particle.
10. The method of claim 1 , wherein the particle is a quantum dot.
11. The method of claim 1 , wherein the nanoswitch is labeled with detectable stain or dye.
12. The method of claim 1 , wherein the analyte-binding agents are antibodies or antigen-binding antibody fragments.
13. A method for detecting an analyte in a sample comprising
(a) contacting a sample with a plurality of nanoswitches each end-conjugated to a bead for a time and under conditions sufficient for binding of an analyte to a nanoswitch thereby forming a mixture of closed and open nanoswitches,
(b) tethering closed and open nanoswitches to a surface,
(c) identifying surface-tethered closed nanoswitches having symmetrical trajectories under forward and reverse forces, and
(d) measuring length of single surface-tethered closed nanoswitches and/or detecting rupture event of single surface-tethered closed nanoswitch, under force,
wherein the nanoswitch is a nucleic acid conjugated to a first and a second analyte-binding agent which when bound to the analyte adopts a looped conformation and a shorter length as compared to the length of the nanoswitch when it is not bound to the analyte.
14. The method of claim 13 , further comprising, between steps (a) and (b), enriching and isolating closed nanoswitches bound to the analyte.
15. A method for detecting an analyte in a sample comprising
(a) contacting a sample with a plurality of nanoswitches, each nanoswitch conjugated at a first end to a lipid and at a second end to a particle, for a time and under conditions sufficient for binding of an analyte to a nanoswitch, thereby forming a mixture of closed and open nanoswitches,
(b) aligning and extending the closed and open nanoswitches in a fluid lipid bilayer using force, and
(c) identifying, and optionally measuring, closed nanoswitches based on length,
wherein the nanoswitch is a nucleic acid conjugated to a first and a second analyte-binding agent which when bound to the analyte adopts a looped conformation and has a shorter length as compared to the length of the nanoswitch when it is not bound to the analyte.
16. The method of claim 15 , wherein the nanoswitches of (a) are in solution, and after the time sufficient for binding to an analyte are inserted into the lipid bilayer.
17. The method of claim 15 , wherein the nanoswitches are labeled with a detectable stain or dye.
18. A method for detecting an analyte in a sample comprising
(a) providing a surface-tethered complex, wherein the complex comprises an analyte bound to a first and a second analyte binding agent, wherein the first analyte-binding agent is coupled to a bead and the second analyte-binding agent is coupled to a surface,
(b) applying a force to the complex, and optionally identifying surface-tethered complexes having symmetrical trajectories under forward and reverse forces,
(c) measuring, for individual surface-tethered complexes, length of the complex under force, and/or the force required to rupture the bead from the second analyte-binding agent under dynamic force, and/or lifetime of the complex under constant force.
19. The method of claim 18 , wherein the first analyte-binding agent is coupled to the bead with a nucleic acid.
20. The method of claim 18 , wherein the second analyte-binding agent is coupled to the surface with a nucleic acid.