Enhanced detection of biological and bioactive components by resonance Raman spectroscopy
A method for the detection of compounds, including biological macromolecules and cells, using changes in Raman spectroscopic properties upon binding of at least one analyte binding partner. The method comprises contacting at least one analyte with at least one analyte binding partner, binding at least one analyte to at least one analyte binding partner to form a complex, and detecting the complex using the change in Raman light scattering.
1 . A method for the detection of at least one analyte comprising
a. contacting at least one analyte with at least one analyte binding partner,
b. binding at least one analyte to at least one analyte binding partner to form a complex, wherein at least one unbound binding partner is not separated from at least one binding partner bound in a complex,
c. detecting the complex using the change in Raman light scattering wherein the detection does not rely upon surface enhanced Raman light scattering.
2 . The method of claim 1 wherein the complex is detected using resonant Raman light scattering.
3 . The method of claim 1 wherein a Raman signal at a single wavenumber is used to detect the presence of the complex.
4 . The method of claim 1 wherein a Raman signal at 250 cm −1 is used to detect the presence of the complex.
5 . The method of claim 1 wherein a Raman signal at 860 cm −1 is used to detect the presence of the complex.
6 . The method of claim 1 wherein Raman signals at more than one wavenumber are used to detect the presence of the complex.
7 . The method of claim 1 wherein Raman signals at 250 cm −1 and 860 cm −1 are used to detect the presence of the complex.
8 . The method of claim 1 wherein the at least one binding partner is chosen from proteins, peptides, naturally occurring antibodies, bioengineered antibodies, artificially produced antibodies, binding proteins, transport proteins, and enzymes.
9 . The method of claim 1 wherein the at least one binding partner is chosen from DNA primers, RNA primers, cDNA sequences, DNA sequences, and RNA sequences.
10 . The method of claim 1 wherein the at least one binding partner is chosen from feature selective dyes and feature selective molecules.
11 . The method of claim 1 wherein the at least one binding partner is chosen from nanoparticles with or without chemical modifications to render or increase their structural detectability upon adduct formation.
12 . The method of claim 1 wherein the at least one analyte is a molecule
13 . The method of claim 1 wherein the at least one analyte is a biological macromolecule.
14 . The method of claim 1 wherein the at least one analyte is a cell.
15 . The method of claim 1 wherein the at least one analyte is a bacteria.
16 . The method of claim 1 wherein the at least one analyte is a pathological bacteria.
17 . A method for the detection of at least one analyte comprising
a. contacting at least one analyte with at least one analyte binding partner,
b. binding at least one analyte to at least one analyte binding partner to form a complex,
c. detecting the complex using the change in Raman light scattering wherein the detection does not rely upon surface enhanced Raman light scattering.
18 . A method for the detection of at least one analyte comprising
a. contacting at least one analyte with at least one analyte binding partner,
b. binding at least one analyte to at least one analyte binding partner to form a complex, wherein at least one unbound binding partner is not separated from at least one binding partner bound in a complex,
c. detecting the complex using the change in Raman light scattering.