Capture ligand controls, blocking probes, masking probes and methods of using the same
The invention, depending on aspect and embodiment, relates to capture probe controls, and capture and signal probe configurations and combinations of configurations that can facilitate accurate and efficient multiplex analyte detection, especially in electrochemical detection schemes.
1. A composition comprising:
a. a capture binding ligand bound to a solid support, the capture binding ligand comprising a first detectable label emitting a first signal; and
b. an analyte bound to a signal binding ligand and the capture binding ligand, the signal binding ligand comprising a second detectable label emitting a second signal wherein the first detectable label has a first potential, wherein the second detectable label has a second potential, and wherein the first potential and the second potential are different..
2. The composition of claim 1 , wherein the capture binding ligand is covalently bound to the first detectable label.
3. The composition of claim 1 , wherein the first detectable label comprises a redox active label.
4. The composition of claim 3 , wherein the redox active label comprises a ferrocene or a ferrocene derivative.
5. The composition of claim 1 , wherein the solid support comprises a plurality of detection electrodes.
6. The composition of claim 5 , wherein the capture binding ligand is specific for a different analyte as between different detection electrodes.
7. The composition of claim 1 , wherein the solid support comprises an electrode, and wherein the first signal is detected when the electrode is functional.
8. The composition of claim 1 , wherein the capture binding ligand has a nucleic acid sequence and the signal binding ligand has a nucleic acid sequence, and wherein the nucleic acid sequence of the capture binding ligand does not cross-hybridize with the nucleic acid sequence of the signal binding ligand.
9. The composition of claim 1 , wherein the analyte has a first nucleic acid sequence and a second nucleic acid sequence, wherein the first nucleic acid sequence binds to the capture binding ligand, and wherein the second nucleic acid sequence binds to the signal binding ligand.
10. The composition of claim 1 , wherein the first detectable label is emitting a signal in the presence and absence of an analyte and wherein the second detectable label is emitting a signal only when bound to the analyte.
11. A composition comprising:
a solid support affixed to a first capture binding ligand bound to a first analyte, the first capture binding ligand comprising a first detectable label emitting a first signal at a first potential, wherein the first analyte is bound to a first signal binding ligand, and wherein the first signal binding ligand comprises a second detectable label emitting a second signal at a second potential, wherein the first and second potentials are different.
12. The composition of claim 11 the composition further comprising a detector for the first and second signal.
13. The composition of claim 11 , further comprising a second capture binding ligand bound to the first analyte, wherein the second capture binding ligand is not bound to a detectable label.
14. The composition of claim 11 , further comprising a second capture binding ligand, wherein the first capture binding ligand is specific for a first nucleic acid sequence of the first analyte, and wherein the second capture binding ligand is specific for a second nucleic acid sequence of the first analyte.
15. The composition of claim 11 , further comprising a second capture binding ligand, wherein the first capture binding ligand is specific for a first nucleic acid sequence of the first analyte, and the second capture binding ligand is specific for a first nucleic acid sequence of a second analyte.
16. The composition of claim 11 , wherein the first analyte is an amplicon from a Bacillus, Vibrio, Escherichia, Shigella, Salmonella, Mycobacterium, M. leprae, Clostridium, C. tetani, C. difficile, C. perfringens, Cornyebacterium, Streptococcus, S. pyogenes, S. pneumoniae, Staphylococcus, Haemophilus, Neisseria, N. gonorrhoeae, Yersinia, Pseudomonas, P. putida, Chlamydia, Bordetella , or Treponema microorganism.
17. The composition of claim 11 , further comprising a second signal binding ligand, wherein the first signal binding ligand is specific for a first nucleic acid sequence of the first analyte, and the second signal binding ligand is specific for a second nucleic acid sequence of the first analyte.
18. The composition of claim 11 , further comprising a second signal binding ligand, wherein the first signal binding ligand is specific for a first nucleic acid sequence of the first analyte and the second signal binding ligand is specific for a first nucleic acid sequence of a second analyte.
19. A method for detecting a target nucleic acid molecule comprising:
a. providing a solid support comprising a plurality of electrodes bound to a first capture binding ligand, the first capture binding ligand comprising a first detectable label;
b. contacting the solid support with a sample comprising the target nucleic acid molecule bound to a signal binding ligand, the signal binding ligand comprising a second detectable label
c. generating a first and second signal from the first and second detectable labels;
d. detecting the presence of the first signal to confirm the electrode is functional; and
e. detecting the presence of the second signal to confirm the presence of the target nucleic acid molecule wherein the first detectable label has a first potential, wherein the second detectable label has a second potential, and wherein the first potential and the second potential are different.
20. A composition comprising:
a. a capture binding ligand on a solid support, the capture binding ligand comprising a first detectable label and a linker connecting the capture binding ligand to the solid support wherein the linker is covalently attached to the solid support; and
b. an analyte bound to a signal binding ligand and the capture binding ligand, the signal binding ligand comprising a second detectable label wherein the first detectable label has a first potential, wherein the second detectable label has a second potential, and wherein the first potential and the second potential are different.