Methods and composition for measuring the amount of Vitamin D derivatives
Methods and compositions for measuring the amount of vitamin D derivatives are disclosed. Fluorescence Resonance Energy Transfer (FRET) in combination with a modified ligand-binding domain of the vitamin D receptor (LBD-VDR) to measure vitamin D derivatives are also disclosed.
1. A method for measuring the amount or concentration of a vitamin D derivative in a sample comprising:
a) contacting a sample with a polypeptide comprising a modified VDR ligand-binding domain (VDR-LBD) and a donor-acceptor pair of fluorophores; and
b) measuring the amount of fluorescence, wherein said amount of fluorescence is detectably higher or lower in the presence of the vitamin D derivative relative to the amount of fluorescence in the absence of the vitamin D derivative;
wherein the modified VDR comprises at least one mutation causing said modified VDR to have a higher binding affinity to 25-hydroxyvitamin D relative to calcitriol, and wherein said at least one mutation comprises a substitution at one or more amino acid positions selected from the group consisting of 274, 147, 150, 227, 230, 233, 234, 271, 275, 286, 288, 300, 309, 313, 418, 237, 143, 278, 305 and 397 of SEQ ID NO: 1.
2. The method according to claim 1 wherein the vitamin D derivative is 25-hydroxyvitamin D.
3. The method according to claim 2 wherein the modified VDR has at least a 10-fold higher affinity for 25-hydroxyvitamin D than to other vitamin D derivatives.
4. The method according to claim 1 wherein the sample is from a mammalian subject.
5. The method according to claim 4 wherein the mammalian subject is a human.
6. The method according to claim 5 wherein the human is suffering from chronic kidney disease (CKD).
7. The method according to claim 1 wherein said mutation at position 274 comprises a substitution of a basic amino acid residue for an aliphatic amino acid residue.
8. The method according to claim 1 wherein said at least one mutation comprises Arg274Leu.
9. The method according to claim 1 wherein the fluorescence is measured using Fluorescence Resonance Energy Transfer (FRET).
10. The method according to claim 9 wherein the donor-acceptor pair of fluorophores is selected from the group consisting of green fluorescent protein (GFP), red fluorescent protein (RFP), cyan-fluorescent protein (CFP), yellow-fluorescent protein (YFP), and active fragments thereof.