Methods and compositions in particle-based detection of target molecules using linking molecules
Methods and compositions which can be used to increase the strength and/or probability of forming a binding complex comprising a target molecule and a substrate are disclosed. In one aspect, linking molecules are disclosed which can be used to increase the number of intra-complex binding interactions. Covalent bonds can be introduced to further increase the strength of these binding interactions. Inter-complex cross-linking can be utilized in connection with these methods to further strengthen and stabilize the disclosed binding complexes.
1. A method of generating a complex comprising a nucleic acid target molecule, said method comprising:
combining in a reaction mixture
a substrate surface, wherein said substrate surface comprises at least one target-immobilization probe bound thereto;
a detectable particle having a diameter of from 0.2 μm to 5 μm, wherein said detectable particle comprises a plurality of capture probes bound thereto;
a sample suspected of containing a nucleic acid target molecule; and
a linking molecule, wherein said linking molecule comprises
a plurality of non-continuous target-specific binding sequences which specifically bind to said nucleic acid target molecule, when present, wherein each of said non-continuous target-specific binding sequences specifically binds to a different region of said nucleic acid target molecule when present, and
a plurality of non-continuous capture probe-specific binding sequences, wherein each of said non-continuous capture probe-specific binding sequences specifically binds to one of said plurality of capture probes,
wherein said combining is under reaction conditions sufficient to provide for specific binding of said nucleic acid target molecule, if present, to said target-immobilization probe, and
wherein said combining is under reaction conditions sufficient to provide for specific binding of said linking molecule to said nucleic acid target molecule, if present, and to a plurality of said capture probes,
wherein, when said nucleic acid target molecule is present in said sample, said target-immobilization probe specifically binds to said nucleic acid target molecule, said nucleic acid target molecule specifically binds to said linking molecule, and said linking molecule specifically binds to a plurality of the capture probes bound to the detectable particle, thereby forming a complex comprising said substrate surface, said target immobilization probe, said nucleic acid target molecule, said linking molecule and said detectable particle, and
wherein said complex does not comprise more than one of said detectable particle.
2. The method of claim 1 , further comprising adding to the reaction mixture a cross-linking agent to form covalent bonds between specifically bound nucleic acid molecules, if present.
3. The method of claim 1 , wherein the linking molecule has a branched structure.
4. The method of claim 1 , wherein the linking molecule has a linear structure.
5. The method of claim 1 , wherein the plurality of non-contiguous target-specific binding sequences are covalently linked to the plurality of non-contiguous capture probe-specific binding sequences in the linking molecule.
6. A reaction mixture comprising:
a substrate surface, wherein said substrate surface comprises at least one target-immobilization probe bound thereto;
a detectable particle having a diameter of from 0.2 μm to 5 μm, wherein said detectable particle comprises a plurality of capture probes bound thereto;
a sample suspected of containing a nucleic acid target molecule; and
a linking molecule, wherein said linking molecule comprises
a plurality of non-contiguous target-specific binding sequences which specifically bind to said nucleic acid target molecule, when present, wherein each of said non-contiguous target-specific binding sequences specifically binds to a different region of said nucleic acid target molecule when present, and
a plurality of non-contiguous capture probe-specific binding sequences, wherein each of said non-contiguous capture probe-specific binding sequences specifically binds to one of said plurality of capture probes,
wherein, when said nucleic acid target molecule is present in said sample, said target-immobilization probe specifically binds to said nucleic acid target molecule, said nucleic acid target molecule specifically binds to said linking molecule, and said linking molecule specifically binds to a plurality of the capture probes bound to the detectable particle, thereby forming a complex comprising said substrate surface, said target immobilization probe, said nucleic acid target molecule, said linking molecule and said detectable particle, and
wherein said complex does not comprise more than one of said detectable particle.
7. The reaction mixture of claim 6 , wherein said detectable particle is a magnetic particle.
8. The reaction mixture of claim 6 , wherein the linking molecule has a branched structure.
9. The reaction mixture of claim 6 , wherein the linking molecule has a linear structure.
10. The reaction mixture of claim 6 , wherein the plurality of non-contiguous target-specific binding sequences are covalently linked to the plurality of non-contiguous capture probe-specific binding sequences in the linking molecule.
11. A method of generating a complex comprising a nucleic acid target molecule, said method comprising:
combining in a reaction mixture
a substrate surface, wherein said substrate surface comprises at least one target-immobilization probe bound thereto;
a detectable particle having a diameter of from 0.2 μm to 5 μm, wherein said detectable particle comprises a plurality of capture probes bound thereto;
a sample suspected of containing a nucleic acid target molecule; and
a plurality of linking molecules, wherein each member of said plurality of linking molecules is independently present in one or more copies, and wherein each member comprises
a target-specific binding sequence which specifically binds to a different region of said nucleic acid target molecule, when present, and
a capture probe-specific binding sequence which specifically binds to a capture probe of said plurality of capture probes,
wherein said combining is under reaction conditions sufficient to provide for specific binding of said nucleic acid target molecule, if present, to said target-immobilization probe, and
wherein said combining is under reaction conditions sufficient to provide for specific binding of said plurality of linking molecules to said nucleic acid target molecule, if present, and to a plurality of the capture probes bound to the detectable particle,
wherein, when said nucleic acid target molecule is present in said sample, said target-immobilization probe specifically binds to said nucleic acid target molecule, and said plurality of linking molecules specifically binds to a plurality of different regions of said nucleic acid target molecule and a plurality of the capture probes bound to the detectable particle, thereby forming a complex comprising said substrate surface, said target immobilization probe, said nucleic acid target molecule, said plurality of linking molecules, and said detectable particle, and
wherein said complex does not comprise more than one of said detectable particle.
12. The method of claim 11 , further comprising adding to the reaction mixture a cross-linking agent to form covalent bonds between specifically bound nucleic acid molecules, if present.
13. The method of claim 11 , wherein the target-specific binding sequence and the capture probe-specific binding sequence are covalently linked in each member of the plurality of linking molecules.
14. A reaction mixture comprising:
a substrate surface, wherein said substrate surface comprises at least one target-immobilization probe bound thereto;
a detectable particle having a diameter of from 0.2 μm to 5 μm, wherein said detectable particle comprises a plurality of capture probes bound thereto;
a sample suspected of containing a nucleic acid target molecule; and
a plurality of linking molecules, wherein each member of said plurality of linking molecules is independently present in one or more copies, and wherein each member comprises
a target-specific binding sequence which specifically binds to a different region of said nucleic acid target molecule, when present; and
a capture probe-specific binding sequence which specifically binds to a capture probe of said plurality of capture probes,
wherein when said nucleic acid target molecule is present in said sample, said target-immobilization probe specifically binds to said nucleic acid target molecule, and said plurality of linking molecules specifically binds to a plurality of different regions of said nucleic acid target molecule and a plurality of the capture probes bound to the detectable particle, thereby forming a complex comprising said substrate surface, said target immobilization probe, said nucleic acid target molecule, said plurality of linking molecules, and said detectable particle, and
wherein said complex does not comprise more than one of said detectable particle.
15. The reaction mixture of claim 14 , wherein said detectable particle is a magnetic particle.
16. The reaction mixture of claim 14 , wherein the target-specific binding sequence and the capture probe-specific binding sequence are covalently linked in each member of the plurality of linking molecules.
17. A method of generating a complex comprising a nucleic acid target molecule, said method comprising:
combining in a reaction mixture
a substrate surface, wherein said substrate surface comprises a plurality of capture probes bound thereto;
a detectable particle having a diameter of from 0.2 μm to 5 μm, wherein said detectable particle comprises a plurality of capture probes bound thereto;
a sample suspected of containing a nucleic acid target molecule;
a first linking molecule, wherein said first linking molecule comprises
a plurality of non-continuous target-specific binding sequences which specifically bind to said nucleic acid target molecule, when present, wherein each of said non-continuous target-specific binding sequences specifically binds to a different region of said nucleic acid target molecule when present, and
a plurality of non-continuous capture probe-specific binding sequences, wherein each of said non-continuous capture probe-specific binding sequences specifically binds to one of the plurality of capture probes bound to the detectable particle;
and
a second linking molecule, wherein said second linking molecule comprises
a plurality of non-continuous target-specific binding sequences which specifically bind to said nucleic acid target molecule, when present, wherein each of said non-continuous target-specific binding sequences specifically binds to a different region of said nucleic acid target molecule when present, and
a plurality of non-continuous capture probe-specific binding sequences, wherein each of said non-continuous capture probe-specific binding sequences specifically binds to one of the plurality of capture probes bound to the substrate surface,
wherein said combining is under reaction conditions sufficient to provide for specific binding of said first linking molecule to said nucleic acid target molecule, if present, and to a plurality of said capture probes bound to the detectable particle, and
wherein said combining is under reaction conditions sufficient to provide for specific binding of said second linking molecule to said nucleic acid target molecule, if present, and to a plurality of said capture probes bound to the substrate surface, and
wherein, when said nucleic acid target molecule is present in said sample, said first linking molecule specifically binds to said nucleic acid target molecule and a plurality the capture probes bound to the detectable particle, and said second linking molecule specifically binds to said nucleic acid target molecule and a plurality of the capture probes bound to the substrate surface, thereby forming a complex comprising said detectable particle, said first linking molecule, said nucleic acid target molecule, said second linking molecule and said substrate surface, and
wherein said complex does not comprise more than one of said detectable particle.
18. The method of claim 17 , further comprising adding to the reaction mixture a cross-linking agent to form covalent bonds between specifically bound nucleic acid molecules, if present.
19. The method of claim 17 , wherein the first linking molecule and/or the second linking molecule has a branched structure.
20. The method of claim 17 , wherein the first linking molecule and/or the second linking molecule has a linear structure.
21. The method of claim 17 , wherein the plurality of non-contiguous target-specific binding sequences of the first linking molecule are covalently linked to the plurality of non-contiguous capture probe-specific binding sequences of the first linking molecule, and wherein the plurality of non-contiguous target-specific binding sequences of the second linking molecule are covalently linked to the plurality of non-contiguous capture probe-specific binding sequences of the second linking molecule.
22. A reaction mixture comprising:
a substrate surface, wherein said substrate surface comprises a plurality of capture probes bound thereto;
a detectable particle having a diameter of from 0.2 μm to 5 μm, wherein said detectable particle comprises a plurality of capture probes bound thereto;
a sample suspected of containing a nucleic acid target molecule;
a first linking molecule, wherein said first linking molecule comprises
a plurality of non-continuous target-specific binding sequences which specifically bind to said nucleic acid target molecule, when present, wherein each of said non-contiguous target-specific binding sequences specifically binds to a different region of said nucleic acid target molecule when present, and
a plurality of non-contiguous capture probe-specific binding sequences, wherein each of said non-contiguous capture probe-specific binding sequences specifically binds to one of the plurality of capture probes bound to the detectable particle;
and
a second linking molecule, wherein said second linking molecule comprises
a plurality of non-contiguous target-specific binding sequences which specifically bind to said nucleic acid target molecule, when present, wherein each of said non-contiguous target-specific binding sequences specifically binds to a different region of said nucleic acid target molecule when present, and
a plurality of non-contiguous capture probe-specific binding sequences wherein each of said non-contiguous capture probe-specific binding sequences specifically binds to one of the plurality of capture probes bound to the substrate surface,
wherein, when said nucleic acid target molecule is present in said sample, said first linking molecule specifically binds to said nucleic acid target molecule and a plurality of the capture probes bound to the detectable particle, and said second linking molecule specifically binds to said nucleic acid target molecule and a plurality of the capture probes bound to the substrate surface, thereby forming a complex comprising said detectable particle, said first linking molecule, said nucleic acid target molecule, said second linking molecule and said substrate surface, and
wherein said complex does not comprise more than one of said detectable particle.
23. The reaction mixture of claim 22 , wherein said detectable particle is a magnetic particle.
24. The reaction mixture of claim 22 , wherein the first linking molecule and/or the second linking molecule has a branched structure.
25. The reaction mixture of claim 22 , wherein the first linking molecule and/or the second linking molecule has a linear structure.
26. The reaction mixture of claim 22 , wherein the plurality of non-contiguous target-specific binding sequences of the first linking molecule are covalently linked to the plurality of non-contiguous capture probe-specific binding sequences of the first linking molecule, and wherein the plurality of non-contiguous target-specific binding sequences of the second linking molecule are covalently linked to the plurality of non-contiguous capture probe-specific binding sequences of the second linking molecule.
27. A method of generating a complex comprising a nucleic acid target molecule, said method comprising:
combining in a reaction mixture
a substrate surface, wherein said substrate surface comprises a plurality of capture probes bound thereto;
a detectable particle having a diameter of from 0.2 μm to 5 μm, wherein said detectable particle comprises a plurality of capture probe bound thereto;
a sample suspected of containing a nucleic acid target molecule;
a first plurality of linking molecules, wherein each member of said first plurality of linking molecules is independently present in one or more copies, and wherein each member comprises
a target-specific binding sequence which specifically binds to a different region of said nucleic acid target molecule, when present, and
a capture probe-specific binding sequence which specifically binds to a capture probe of said plurality of capture probes bound to the detectable particle; and
a second plurality of linking molecules, wherein each member of said second plurality of linking molecules is independently present in one or more copies, and wherein each member comprises
a target-specific binding sequence which specifically binds to a different region of said nucleic acid target molecule, when present, and
a capture probe-specific binding sequence which specifically binds to a capture probe of said plurality of capture probes bound to the substrate surface,
wherein said combining is under reaction conditions sufficient to provide for specific binding of said first plurality of linking molecules to said nucleic acid target molecule, if present, and to a plurality of the capture probes bound to the detectable particle, and
wherein said combining is under reaction conditions sufficient to provide for specific binding of said second plurality of linking molecules to said nucleic acid target molecule, if present, and to a plurality of the capture probes bound to the substrate surface, and
wherein, when said nucleic acid target molecule is present in said sample, said first plurality of linking molecules specifically binds to a plurality of different regions of said nucleic acid target molecule and a plurality of the capture probes bound to the detectable particle, and said second plurality of linking molecules specifically binds to a plurality of different regions of said nucleic acid target molecule and a plurality of the capture probes bound to the substrate surface, thereby forming a complex comprising said detectable particle, said first plurality of linking molecules, said nucleic acid target molecule, said second plurality of linking molecules and said substrate surface, and
wherein said complex does not comprise more than one of said detectable particle.
28. The method of claim 27 , further comprising adding to the reaction mixture a cross-linking agent to form covalent bonds between specifically bound nucleic acid molecules, if present.
29. The method of claim 27 , wherein the target-specific binding sequence and the capture probe-specific binding sequence for each member of the first plurality of linking molecules are covalently linked in each member of the first plurality of linking molecules, and wherein the target-specific binding sequence and the capture probe-specific binding sequence for each member of the second plurality of linking molecules are covalently linked in each member of the second plurality of linking molecules.
30. A reaction mixture comprising:
a substrate surface, wherein said substrate surface comprises a plurality of capture probes bound thereto;
a detectable particle having a diameter of from 0.2 μm to 5 μm, wherein said detectable particle comprises a plurality of capture probes bound thereto;
a sample suspected of containing a nucleic acid target molecule;
a first plurality of linking molecules, wherein each member of said first plurality of linking molecules is independently present in one or more copies, and wherein each member comprises
a target-specific binding sequence which specifically binds to a different region of said nucleic acid target molecule, when present, and
a capture probe-specific binding sequence which specifically binds to a capture probe of said plurality of capture probes bound to the detectable particle; and
a second plurality of linking molecules, wherein each member of said second plurality of linking molecules is independently present in one or more copies, and wherein each member comprises
a target-specific binding sequence which specifically binds to a different region of said nucleic acid target molecule, when present, and
a capture probe-specific binding sequence which specifically binds to a capture probe of said plurality of capture probes bound to the substrate surface,
wherein, when said nucleic acid target molecule is present in said sample, said first plurality of linking molecules specifically binds to a plurality of different regions of said nucleic acid target molecule and a plurality of the capture probes bound to the detectable particle, and said second plurality of linking molecules specifically binds to a plurality of different regions of said nucleic acid target molecule and a plurality of the capture probes bound to the substrate surface, thereby forming a complex comprising said detectable particle, said first plurality of linking molecules, said nucleic acid target molecule, said second plurality of linking molecules and said substrate surface, and
wherein said complex does not comprise more than one of said detectable particle.
31. The reaction mixture of claim 30 , wherein said detectable particle is a magnetic particle.
32. The reaction mixture of claim 30 , wherein the target-specific binding sequence and the capture probe-specific binding sequence for each member of the first plurality of linking molecules are covalently linked in each member of the first plurality of linking molecules, and wherein the target-specific binding sequence and the capture probe-specific binding sequence for each member of the second plurality of linking molecules are covalently linked in each member of the second plurality of linking molecules.