Recognition of cellular target binding by a bioactive agent using intracellular bioluminescence resonance energy transfer
View Patent ↗The present invention provides compositions and methods for detection and analysis of intracellular binding of a bioactive agent to a cellular target. In particular, provided herein are bioactive agents tethered to fluorophores, cellular targets fused to bioluminescent reporters, and methods of detecting and analyzing the interaction of bioactive agents with cellular targets therewith.
1. A system comprising:
(a) a bioactive small molecule conjugated to a small molecule fluorophore;
(b) a cell that expresses a protein fusion of: (i) a protein of interest and (ii) a luciferase, wherein the bioactive small molecule is capable of binding non-covalently to the protein of interest upon interaction therewith, wherein the emission spectrum of the luciferase overlaps with the excitation spectrum of the small molecule fluorophore; and
(c) a substrate for the luciferase.
2. The system of claim 1 , wherein the small molecule fluorophore is a carboxy rhodamine analog.
3. The system of claim 1 , wherein the luciferase comprises a polypeptide with at least 70% sequence identity with SEQ ID NO.: 1.
4. The system of claim 1 , wherein the substrate for the luciferase is coelenterazine or a coelenterazine derivative.
5. The system of claim 4 , wherein the substrate is 2-furanylmethyl-deoxy-coelenterazine.
6. The system of claim 1 , wherein the bioactive small molecule conjugated to the small molecule fluorophore is within a cell.
7. The system of claim 1 , wherein the bioactive small molecule conjugated to the small molecule fluorophore is cell permeable.
8. The system of claim 1 , further comprising a permeabilization agent to potentiate entry of the bioactive small molecule conjugated to the small molecule fluorophore into the cell.
9. The system of claim 1 , wherein the bioactive small molecule conjugated to the small molecule fluorophore is part of a library of different bioactive small molecules tethered to fluorophores.
10. The system of claim 1 , wherein the protein fusion is one of a plurality of different proteins of interest fused to luciferase.
11. The system of claim 1 , wherein the bioactive small molecule is produced by non-natural chemical synthesis.
12. The system of claim 1 , wherein:
(i) said luciferase has a first emission spectrum with a first peak emission;
(ii) said small molecule fluorophore has an excitation spectrum that overlaps said first emission spectrum; and
(iii) said small molecule fluorophore has a second emission spectrum with a second peak emission, said second peak emission being substantially separated from said first peak emission.
13. The system of claim 12 , wherein substantially separated is at least 80 nm.
14. The system of claim 12 , wherein the Forster distance of the small molecule fluorophore and luciferase pair is less than 20 nm.
15. The system of claim 14 , wherein the Forster distance of the small molecule fluorophore and luciferase pair is less than 5 nm.
16. The system of claim 12 , wherein upon binding of the bioactive small molecule to the protein of interest, conversion of the substrate to a reaction product by the luciferase results in excitation of the small molecule fluorophore by BRET and fluorescence emission from the small molecule fluorophore.
17. The system of claim 1 , wherein upon binding of the bioactive small molecule to the protein of interest, conversion of the substrate to a reaction product by the luciferase results in excitation of the small molecule fluorophore by BRET and fluorescence emission from the small molecule fluorophore.
18. The system of claim 1 , wherein the protein of interest of the fusion protein is displayed on the cell surface or the protein of interest of the fusion protein is intracellular and the bioactive small molecule conjugated to a small molecule fluorophore is cell permeable.