Methods for target molecule detection using siderophores and related compositions
View Patent ↗The invention provides methods for isolating a target molecule from a sample. In an embodiment, the method involves contacting a sample with a capture agent, the agent comprising a siderophore and a transition metal cation, under conditions wherein the agent is capable of binding a target molecule to form a target molecule-capture agent complex, wherein the target molecule is selected from the group consisting of a phosphorylated molecule, a nitrotyrosine-containing molecule and a sulfated molecule, and separating the target molecule-capture agent complex from the sample, thereby isolating the target molecule from the sample. Also provided are methods for determining the presence of a target molecule in a sample, that involve contacting a sample with a capture agent, the agent comprising a siderophore and a transition metal cation.
1. A method for determining the presence of a target molecule in a biological sample at physiological pH, comprising:
(a) contacting a biological sample with a capture agent at physiological pH, the capture agent comprising a hydroxamate siderophore complexed with a transition metal cation as a binding moiety, under conditions wherein the binding moiety of the capture agent is capable of selectively binding a target molecule to form a target molecule-capture agent complex, wherein the target molecule is selected from the group consisting of a phosphorylated molecule, a nitrotyrosine-containing molecule and a sulfated molecule, and
(b) detecting formation of the target molecule-capture agent complex in the biological sample at physiological pH, thereby determining the presence of the target molecule in the biological sample;
wherein the biological sample is not washed or purified prior to detecting formation of the target molecule-capture agent complex in the biological sample.
2. The method of claim 1 , wherein the detecting is performed by measuring binding between the capture agent and the target molecule.
3. The method of claim 2 , wherein the measuring comprises a mode selected from the group of absorbance, transmission, mass measurement, fluorescence intensity, fluorescence polarization, time-resolved fluorescence, resonance light scattering, surface-enhanced Raman scattering, inductively-coupled plasma mass spectrometry, electron paramagnetic resonance, refractive index absorbance, nuclear magnetic resonance, microcalorimetry, Fourier transform infrared spectrometry, atomic spectrometry, surface plasmon resonance, refractive index changes, spectropolarimetry and ellipsometry.
4. The method of claim 1 , wherein the hydroxamate siderophore portion of the target molecule-capture agent complex is detected.
5. The method of claim 1 , wherein the transition metal portion of the target molecule-capture agent complex is detected.
6. The method of claim 1 , wherein the phosphorylated molecule portion of the target molecule-capture agent complex is detected.
7. The method of claim 1 , wherein the target molecule is a phosphorylated molecule.
8. The method of claim 1 , wherein the hydroxamate siderophore is desferrioxamine.
9. The method of claim 1 , wherein the transition metal cation is iron (III).
10. The method of claim 1 , wherein the hydroxamate siderophore is desferrioxamine, the transition metal cation is iron (III), and the target molecule is a phosphorylated molecule.
11. The method of claim 1 , wherein the phosphorylated molecule comprises a polypeptide.
12. The method of claim 1 , wherein the phosphorylated molecule comprises a peptide.
13. The method of claim 10 , wherein the phosphorylated molecule comprises a polypeptide.
14. The method of claim 10 , wherein the phosphorylated molecule comprises a peptide.
15. The method of claim 1 , wherein the physiological pH is about 7.4.
16. The method of claim 1 , wherein the biological sample is selected from the group consisting of biological fluids, whole organisms, organs, tissues, cells, culture medium, subcellular organelles, protein complexes, individual proteins, recombinant proteins, fusion proteins, viruses, viral particles, biopsy samples, peptides and amino acids.