Fusion protein having luminescence activity
The fusion protein comprising (1) a first region comprising the amino acid sequence of SEQ ID NO: 18 and (2) a second region comprising an amino acid sequence for a polypeptide containing at least one cysteine residue for binding to other useful compound via the thiol group can be modified by chemical modification, and thus has a high catalytic ability for a luminescence activity and is highly available for general purposes.
1. A fusion protein comprising:
(1) a first region selected from the group consisting of (a) to (d) below:
(a) a region consisting of the amino acid sequence of SEQ ID NO: 18;
(b) a region consisting of the amino acid sequence of SEQ ID NO: 18 wherein 1 to 10 amino acids are deleted, substituted, inserted and/or added and having a catalytic ability for a luminescence activity with a luciferin which is a substrate;
(c) a region consisting of an amino acid sequence having at least 90% homology to the amino acid sequence of SEQ ID NO: 18 and having a catalytic ability for a luminescence activity with a luciferin which is a substrate; and,
(d) a region consisting of an amino acid sequence encoded by a polynucleotide which hybridizes under high stringent conditions to a polynucleotide consisting of a nucleotide sequence complementary to the nucleotide sequence of SEQ ID NO: 17 and having a catalytic ability for a luminescence activity with a luciferin which is a substrate,
wherein the high stringent conditions are 5×SSC, 5× Denhardt's solution, 0.5% (w/v) SDS, 50% (v/v) formamide and 50° C.; and,
(2) a second region consisting of an amino acid sequence for a polypeptide having at least one cysteine residue for binding to other useful compound via its thiol group, wherein the second region is selected from the group consisting of (e) to (h) below:
(e) a region consisting of the amino acid sequence of SEQ ID NO: 20;
(f) a region comprising the amino acid sequence of SEQ ID NO: 20 wherein 1 to 3 amino acids are deleted, substituted, inserted and/or added and having at least one cysteine residue for binding to other useful compound via the thiol group;
(g) a region comprising an amino acid sequence having at least 90% homology to the amino acid sequence of SEQ ID NO: 20 and having at least one cysteine residue for binding to other useful compound via the thiol group; and,
(h) a region comprising an amino acid sequence encoded by a polynucleotide which hybridizes under high stringent conditions to a polynucleotide consisting of a nucleotide sequence complementary to the nucleotide sequence of SEQ ID NO: 19 and having at least one cysteine residue for binding to other useful compound via the thiol group, wherein the high stringent conditions are 5×SSC, 5× Denhardt's solution, 0.5% (w/v) SDS, 50% (v/v) formamide and 50° C.
2. The fusion protein according to claim 1 , wherein:
(1) the first region is a region consisting of the amino acid sequence of SEQ ID NO: 18, and,
(2) the second region is a region consisting of the amino acid sequence of SEQ ID NO: 20.
3. The fusion protein according to claim 1 , further comprising an amino acid sequence for promoting translation and/or an amino acid sequence for purification.
4. A fusion protein consisting of an amino acid sequence of SEQ ID NO: 4, 6 or 8.
5. A complex comprising the fusion protein according to claim 1 and other useful compound bound to the fusion protein via the thiol group of the cysteine residue in the second region.
6. The complex according to claim 5 , wherein other useful compound is a ligand specific to a fluorescent substance and/or an analyte.
7. A kit comprising the fusion protein according to claim 1 .
8. A kit comprising the complex of claim 5 .
9. The kit according to claim 7 , further comprising a luciferin.
10. The kit according to claim 9 , wherein the luciferin is a coelenterazine analogue.
11. The kit according to claim 10 , wherein the coelenterazine analogue is coelenterazine.