Small molecule biosensors
Biosensors for small molecules can be used in applications that range from metabolic engineering to orthogonal control of transcription. Biosensors are produced based on a ligand-binding domain (LBD) using a method that, in principle, can be applied for any target molecule. The LBD is fused to either a fluorescent protein or a transcriptional activator and is destabilized by mutation such that the fusion accumulates only in cells containing the target ligand. The power of this method is illustrated by developing biosensors for digoxin and progesterone. Addition of ligand to cells expressing a biosensor activates transcription in yeast, mammalian cells and plants, with a dynamic range of up to about 100-fold or more. The biosensors are used to improve the biotransformation of pregnenolone to progesterone in yeast and to regulate CRISPR activity in mammalian cells. This work provides a general methodology to develop biosensors for a broad range of molecules.
1. A conditionally stable biosensor comprising a homodimeric ligand binding domain (LBD) having conditionally-destabilizing mutations that is fused to a trans-activation domain (TAD) and a DNA binding domain (DBD), wherein the conditionally stable biosensor is stabilized when the ligand binding domain is bound to a cognate steroid, and wherein the DNA binding domain (DBD) binds to DNA and the trans-activation domain (TAD) activates transcription of a target gene.
2. The conditionally stable biosensor of claim 1 , wherein the conditionally stable biosensor retains function when ported directly between yeast and mammalian cells.
3. The conditionally stable biosensor of claim 1 , wherein the ligand binding domain is between an N-terminal DNA binding domain and a C-terminal transcriptional activation domain.
4. The conditionally stable biosensor of claim 1 , wherein the ligand binding domain binds to digoxigenin.
5. The conditionally stable biosensor of claim 1 , wherein the ligand binding domain binds to progesterone.
6. The conditionally stable biosensor of claim 1 , wherein the trans-activation domain (TAD) is VP16.
7. The conditionally stable biosensor of claim 1 , wherein the trans-activation domain (TAD) is VP64.
8. A cell line comprising the conditionally stable biosensor of claim 1 .
9. The conditionally stable biosensor of claim 1 wherein the DNA binding domain (DBD) is a homodimeric DNA binding domain (DBD).