Activation of bioluminescene by structural complementation
Provided herein are compositions and methods for the assembly of a bioluminescent complex from two or more non-luminescent (e.g., substantially non-luminescent) peptide and/or polypeptide units. In particular, bioluminescent activity is conferred upon a non-luminescent polypeptide via structural complementation with another, complementary non-luminescent peptide.
1. A method comprising, combining:
(a) a first fusion of:
(i) a first binding moiety capable of binding to a target analyte, and
(ii) a complementary polypeptide comprising an amino acid sequence having less than 100% and greater than 40% sequence identity with SEQ ID NO: 440;
(b) a second fusion of:
(i) a second binding moiety capable of binding to a target analyte, and
(ii) a complementary peptide comprising an amino acid sequence having less than 100% and greater than 40% sequence identity with SEQ ID NO: 2;
(c) the target analyte; and
(d) a substrate for a bioluminescent complex formed between the peptide and polypeptide;
wherein a bioluminescent signal produced by the bioluminescent complex in the presence of the substrate is substantially increased when the first and second binding moieties are bound to the target analyte than in the absence of the target analyte.
2. The method of claim 1 , wherein the substrate is coelenterazine, or a coelenterazine derivative.
3. The method of claim 2 , wherein the substrate is furimazine.
4. The method of claim 1 , wherein the complementary peptide comprises an amino acid sequence having greater than 70% sequence identity with SEQ ID NO: 2271.
5. The method of claim 4 , wherein the complementary peptide comprises an amino acid sequence having 90% or greater sequence identity with SEQ ID NO: 2271.
6. The method of claim 5 , wherein the complementary peptide comprises an amino acid sequence of SEQ ID NO: 2271.
7. The method of claim 1 , wherein the complementary polypeptide comprises an amino acid sequence having greater than 70% sequence identity with SEQ ID NO: 2150.
8. The method of claim 7 , wherein the complementary polypeptide comprises an amino acid sequence having 90% or greater sequence identity with SEQ ID NO: 2150.
9. The method of claim 8 , wherein the complementary polypeptide comprises an amino acid sequence of SEQ ID NO: 2150.
10. The method of claim 1 , wherein the target analyte is a protein, small molecule, peptide, carbohydrate, nucleic acid, lipid, cell, or protein complex.
11. The method of claim 1 , wherein the first and second binding moieties are independently selected from the group consisting of: an antibody, a receptor domain that binds a target ligand, a domain of protein A, protein A, protein G, a domain of protein G, a polyclonal antibody, a monoclonal antibody, a single chain variable fragment, an antibody variable heavy chain, and an antibody variable light chain.
12. The method of claim 1 , wherein the first binding moiety and the second binding moiety are configured to bind to different epitopes on the target analyte.
13. The method of claim 1 , wherein the first binding moiety and the second binding moiety are brought into close proximity in the presence of the target analyte, thereby bringing the complementary peptide and complementary polypeptide into contact with each other.