Free solution measurement of molecular interactions by backscattering interferometry
Disclosed are methods, systems, and apparatuses for the free solution measurement of molecular interactions by backscattering interferometry. In one aspect, the invention relates to method and systems for detecting molecular interaction between analytes in free-solution wherein the analytes are label-free and detection is performed by back-scattering interferometry. Also disclosed are label-free, free-solution, and/or real-time measurements of characteristic properties and/or chemical events using the disclosed techniques. The disclosed methods can have very low detection limits and/or very low sample volume requirements. Also disclosed are various biosensor applications of the disclosed techniques. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
1. A method for real-time, free-solution determination of molecular interactions, the method comprising detecting one or more interaction products of two unlabeled, non-immobilized analytes via refractive index changes, wherein at least one of the interaction products is present during the determination at a concentration of less than about 5.0×10 −5 M and/or wherein at least one of the interaction products is present during the determination in a solution with a volume in a detection zone of less than about 500 nL.
2. The method of claim 1 , wherein further comprising introducing one of the analytes at a concentration of less than about 5.0×10 −7 M.
3. The method of claim 1 , wherein further comprising introducing one of the analytes at a concentration of less than about 5.0×10 −9 M.
4. The method of claim 1 , wherein the interaction is a biomolecular interaction.
5. The method of claim 1 , wherein the volume in the detection zone is less than about 300 nL.
6. The method of claim 1 , wherein the volume in the detection zone is less than about 100 nL.
7. The method of claim 1 , further comprising introducing both of the analytes at a concentration of less than about 5.0×10 −5 M.
8. The method of claim 1 , further comprising introducing both of the analytes at a concentration of less than about 5.0×10 −7 M.
9. The method of claim 1 , further comprising introducing both of the analytes at a concentration of less than about 5.0×10 −9 M.
10. The method of claim 1 , further comprising introducing both of the analytes in a solution with a volume in the detection zone of less than about 300 nL.
11. The method of claim 1 , wherein the interaction is a binding event between one or more of antibody-antigen, protein-protein, small molecule-small molecule; small molecule-protein, drug-receptor; antibody-cell; protein-cell; oligonucleotide-cell; carbohydrate-cell; cell-cell; enzyme-substrate; protein-DNA; protein-aptamer; DNA-DNA; RNA-RNA; DNA-RNA; protein-RNA; small molecule-nucleic acid; biomolecule-molecular imprint; biomolecule-protein mimetic; biomolecule-antibody derivatives; lectin-carbohydrate; biomolecule-carbohydrate; small molecule-micelle; small molecule-cell membrane; and enzyme-substrate.
12. The method of claim 1 , wherein the interaction is a binding event involving a protein associated with plasma or organelle membranes.
13. The method of claim 1 , wherein the interaction is a binding event involving calmodulin.
14. The method of claim 1 , wherein the interaction creates a conformational change in at least one of the analytes.
15. The method of claim 1 , wherein the interaction is the formation of one or more covalent bonds, electrostatic bonds, hydrogen bonds, or hydrophobic interactions.
16. The method of claim 1 , wherein the method further comprises introducing each analyte to a channel, and wherein each analyte is introduced simultaneously.
17. The method of claim 1 , wherein the method further comprises introducing each analyte to a channel, and wherein each analyte is introduced sequentially.
18. The method of claim 1 , wherein each analyte is present in the same sample.
19. The method of claim 1 , wherein each analyte is present in a different sample.
20. The method of claim 1 , wherein the analytes form interaction products prior to introduction to a channel.