Multi-wavelength analyses of sol-particle specific binding assays
The present invention discloses methods for detecting the presence of a complex between a first reagent and a second reagent in solution. In particular, the invention provides methods for qualitative or quantitative detection of an analyte or its specific binding partner in complex biological samples. The invention further discloses algorithms using summary rate changes at selected wavelengths in the absorbance spectra of colloidal metal-labeled analytes or specific binding partners to identify intermolecular interactions between the analyte and its binding partner.
1. A method for determining the presence or absence of a complex of a first reagent and a second reagent in a mixture comprising
determining a first absorbance value at a first wavelength and a second absorbance value at a second wavelength upon mixing the first reagent with the second reagent, wherein the first reagent or the second reagent is conjugated to a metal nanoparticle or nanoshell, and wherein the first wavelength is within the absorbance wavelength region of the absorption spectrum for the metal nanoparticle or nanoshell and the second wavelength is within a scattering wavelength region of the absorption spectrum for the metal nanoparticle or nanoshell;
determining the ratio of the first absorbance value to the second absorbance value; and
comparing the ratio of the absorbance values to a pre-determined value, wherein the comparison is indicative of the presence of the complex of the first reagent and the second reagent.
2. The method of claim 1 , wherein the first and second absorbance values are determined relative to a reference absorbance value at a reference wavelength.
3. The method of claim 1 , wherein the first and second absorbance values are normalized to the maximum absorbance value at a wavelength corresponding to λ max .
4. The method of claim 1 further comprising obtaining at least one measurement of reagent integrity, wherein the at least one measurement is indicative of non-specific signals.
5. The method of claim 4 , wherein the at least one measurement comprises determining a transmittance value at a reference wavelength at an initial time point of mixing the first reagent with the second reagent; and comparing the transmittance value to a pre-determined limit value.
6. The method of claim 4 , wherein the at least one measurement comprises determining a maximum absorbance value at a wavelength corresponding to λ max at an initial time point of mixing the first reagent with the second reagent; and comparing the maximum absorbance to a pre-determined high absorbance limit value or a pre-determined low absorbance limit value.
7. The method of claim 1 , comprising
determining a first group of absorbance values at a first wavelength for a plurality of time points in an initial reaction period for mixing the first reagent with the second reagent,
determining a second group of absorbance values at a second wavelength for said plurality of time points, wherein the first wavelength is within the absorbance wavelength region of the absorption spectrum for the metal nanoparticle or nanoshell and the second wavelength is within a scattering wavelength region of the absorption spectrum for the metal nanoparticle or nanoshell;
determining the average ratio of the first group of absorbance values to the second group of absorbance values; and
comparing the average ratio to a pre-determined value, wherein the comparison is indicative of the presence of the complex of the first reagent and the second reagent.
8. The method of claim 7 , wherein the pre-determined value is a pre-determined threshold value.
9. The method of claim 7 , further comprising comparing the average ratio to a pre-determined high ratio limit value or a pre-determined low ratio limit value.
10. The method of claim 7 , wherein the first group of absorbance values are adjusted based on a first group of control absorbance values at the first wavelength for each of said plurality of time points and the second group of absorbance values are adjusted based on a second group of control absorbance values at the second wavelength for each of said plurality of time points.
11. The method of claim 1 , wherein the first reagent is an analyte in a biological sample.
12. The method of claim 1 , wherein the first reagent is an analyte in a biological sample and the second reagent is an entity that specifically binds to the first reagent.
13. The method of claim 1 , wherein the first reagent is an analyte in a biological sample and the second reagent is an antibody that specifically binds to the first reagent.
14. The method of claim 1 , wherein the first reagent is an analyte in a biological sample selected from the group consisting of epitopes of heartworm, Ehrlichia canis, Borrelia burgdorferi, Borrelia afzelii, Borrelia garinii, Anaplasma phagocytophilum , feline leukemia virus, parvovirus, influenza A strain, influenza B strain, avian influenza virus, respiratory syncytial virus, Legionella , adenovirus, and Group A Streptococcus.
15. The method of claim 1 , wherein the second reagent is an antibody that specifically binds to an epitope of heartworm, Ehrlichia canis, Borrelia burgdorferi, Borrelia afzelii, Borrelia garinii, Anaplasma phagocytophilum , feline leukemia virus, parvovirus, influenza A strain, influenza B strain, avian influenza virus, respiratory syncytial virus, Legionella , adenovirus, or Group A Streptococcus.
16. The method of claim 1 , wherein the metal nanoparticle or nanoshell is selected from the group consisting of gold particles, silver particles, copper particles, platinum particles, composite particles, gold hollow spheres, gold-coated silica nanoshells, and silica-coated gold shells.
17. The method of claim 1 , wherein the pre-determined value is a standard curve and the quantity of the complex of the first reagent and the second reagent is determined based on the comparison of the ratio to the standard curve.
18. The method of claim 7 , wherein the pre-determined value is a standard curve and the quantity of the complex of the first reagent and the second reagent is determined based on the comparison of the average ratio to the standard curve.
19. The method of claim 1 , wherein the pre-determined value is a pre-determined threshold value.
20. The method of claim 1 , wherein the pre-determined value is a standard curve.
21. The method of claim 7 , wherein the pre-determined value is a standard curve.