Fluorescent proteins

1. An isolated fluorescent protein having chemiluminescence activity, comprising in a complex an apoprotein that is a component of a calcium-binding photoprotein, a coelenteramide or an analog thereof, and a calcium ion or a divalent or trivalent ion that can be substituted for the calcium ion;

wherein the coelenteramide remains coordinated inside the apoprotein,

wherein the calcium ion or the divalent or trivalent ion that can be substituted for the calcium ion is bound to EF-hand of the apoprotein, and

wherein the sulfhydryl groups of the cysteine residues of the apoprotein exists without forming a disulfide bond such that the isolated fluorescent protein maintains chemiluminescence activity.

2. The fluorescent protein having chemiluminescence activity of claim 1 , wherein, in the complex of the apoprotein and the coelenteramid or the analog thereof, the ratio of the number of molecules of the apoprotein to the number of molecules of the coelenteramid or the analog thereof is 1:1; and wherein, in the complex of the apoprotein and the calcium ion or the divalent or trivalent ion that can be substituted for the calcium ion, the ratio of the number of molecules of the apoprotein to the number of molecules of the calcium ion or the divalent or trivalent ion is 1:1 to 1:4.

3. The fluorescent protein having chemiluminescence activity of claim 1 , wherein the apoprotein is an protein selected from the group consisting of apoaequorin, apoclytin, apoobelin, apomitrocomin, apomineopsin, and apobervoin.

4. The fluorescent protein having chemiluminescence activity of claim 1 , wherein the apoprotein is an apoaequorin having the amino acid sequence shown in SEQ ID NO: 1 or a mutant apoaequorin in which one or more amino acids are deleted, substituted, or added in the sequence shown in SEQ ID NO: 1.

5. The fluorescent protein having chemiluminescence activity of claim 1 , wherein the apoprotein is an apoobelin having the amino acid sequence shown in SEQ ID NO: 2 or a mutant apoobelin in which one or more amino acids are deleted, substituted, or added in the sequence shown in SEQ ID NO: 2.

6. The fluorescent protein having chemiluminescence activity of claim 1 , wherein the apoprotein is an apoclytin having the amino acid sequence shown in SEQ ID NO: 3 or a mutant apoclytin in which one or more amino acids are deleted, substituted, or added in the sequence shown in SEQ ID NO: 3.

7. The fluorescent protein having chemiluminescence activity of claim 1 , wherein the apoprotein is an apomitrocomin having the amino acid sequence shown in SEQ ID NO: 4 or a mutant apomitrocomin in which one or more amino acids are deleted, substituted, or added in, the sequence shown in SEQ ID NO: 4.

8. An isolated fluorescent protein having chemiluminescence activity, comprising in a complex an apoprotein that is a component of a calcium-binding photoprotein, a coelenteramid or an analog thereof, and a calcium ion or a divalent or trivalent ion that can be substituted for the calcium ion,

wherein the coelenteraminde or the analog thereof is represented by the following formula (1) or (2):

wherein

R 1 is a substituted or unsubstituted aryl group, a substituted or unsubstituted arylated alkyl group, or a straight or branched chain alkyl group that may be substituted by an aliphatic cyclic group;

R 2 is a substituted or unsubstituted aryl group, a substituted or unsubstituted arylated alkyl group, a substituted or unsubstituted aryl alkenyl group, a straight or branched chain alkyl group that may be substituted by an aliphatic cyclic group, a straight or branched chain alkenyl group that may be substituted by an aliphatic cyclic group, or a heterocyclic group;

R 3 is a hydrogen atom, a substituted or unsubstituted alkyl group;

X 1 is a hydrogen atom, a hydroxyl group, a halogen atom, an alkoxyl group, or an amino group;

X 2 is a hydrogen atom or a hydroxyl group; and

is a divalent hydrocarbon group having 1 to 4 carbon atoms;

wherein the coelenteraminde remains coordinated inside the apoprotein,

wherein the calcium ion or the divalent or trivalent ion that can be substituted for the calcium ion is bound to an EF-hand of the apoprotein, and

wherein the sulflydryl groups of the cysteine residues of the apoprotein exists without forming a disulfide bond such that the isolated fluorescent protein maintains chemiluminescence activity.

9. The fluorescent protein having chemiluminescence activity of claim 8 ,

wherein, in the formula (1) or (2),

R 1 is an unsubstituted aryl group, an unsubstituted arylated alkyl group, an arylated alkyl group substituted by a hydroxyl group or a halogen atom, or a straight or branched chain alkyl group that may be substituted by a cyclohexyl group;

R 2 is an unsubstituted aryl group, an aryl group substituted by a hydroxyl group, an unsubstituted arylated alkyl group, an arylated alkyl group substituted with a hydroxyl group, an unsubstituted aryl alkenyl group, an unsubstituted straight or branched chain alkyl group, a straight chain alkyl group that may be substituted by an aliphatic cyclic group, a branched chain alkenyl group, a heterocyclic group containing sulfur;

R 3 is a hydrogen atom, a methyl group, or 2-hydroxyethyl group;

X 1 is a hydrogen atom, a hydroxyl group, a fluorine atom, a methoxy group, or an amino group; and

Y is a methylene group, ethylene group, a propylene group, or a vinylene group.

10. The fluorescent protein (bFP) having

chemiluminescence activity of claim 8 ,

wherein, in the formula (1) or (2),

R 1 is a phenyl group, a benzyl group, a p-hydroxybenzyl group, a p-fluorobenzyl group, a p-chlorobenzyl group, a p-bromobenzyl group, a p-iodinebenzyl group, a 3,4-difluorobenzyl group, a pentafluorobenzyl group, a phenylethyl group, a phenylpropyl group, a naphthylmethyl group, a cyclohexylmethyl group, a methyl group, a 1-methylpropyl group, or a 2-methylpropyl group; and

R 2 is a phenyl group, a p-hydroxy phenyl group, a benzyl group, an <alpha>-hydroxybenzyl group, a phenylethyl group, a phenylvinyl group, a cyclohexyl group, a cyclohexylmethyl group, a cyclohexylethyl group, a methyl group, an ethyl group, a propyl group, a 2-methylpropyl group, a 2-methylpropenyl group, an adamantylmethyl group, a cyclopentyl ethyl group, or a thiophene-2-yl group.

11. The fluorescent protein having chemiluminescence activity of claim 1 , wherein the divalent or trivalent ion that can be substituted for the calcium ion is one selected from the group consisting of a strontium ion and a lead ion.

12. A method for detecting a target substance, comprising:

a step of binding a ligand for the target substance to a fluorescent protein having chemiluminescence activity to provide a ligand bound fluorescent protein having chemiluminescence activity, wherein the fluorescent protein comprises in a complex an apoprotein that is a component of a calcium-binding photoprotein, a coelenteramide or an analog thereof, and a calcium ion or a divalent or trivalent ion that can be substituted for the calcium ion,

a step of binding the ligand bound fluorescent protein having chemiluminescence activity to the target substance to be bound via the ligand,

a step of emitting light by adding a coelenterazine or an analog thereof, and

a step of detecting the emitted light;

wherein the coelenteramide remains coordinated inside the apoprotein,

wherein the calcium ion or the divalent or trivalent ion that can be substituted for the calcium ion is bound to an EF-hand of the apoprotein, and

wherein the sulfhydryl groups of the cysteine residues of the apoprotein exists without forming a disulfide bond such that the fluorescent protein maintains chemiluminescence activity.

13. A method for enhancing thermal stability of a fluorescent protein having chemiluminescence activity, wherein the fluorescent protein comprises in a complex an apoprotein that is a component of a calcium-binding photoprotein, a coelenteramide or an analog thereof, and a calcium ion or a divalent or trivalent ion that can be substituted for the calcium ion,

wherein a reducing agent is added to a solution in which the fluorescent protein is dissolved;

wherein the coelenteramide remains coordinated inside the apoprotein; wherein the calcium ion or the divalent or trivalent ion that can be substituted for the calcium ion is bound to an EF-hand of the apoprotein, and

wherein the sulflydryl group of the cysteine residues of the apoprotein exists without forming a disulfide bond such that the fluorescent protein maintains chemiluminescence activity.

14. The method for enhancing thermal stability of claim 13 , wherein the reducing agent is dithiothreitol or mercaptoethanol.

15. A chemiluminescence method, comprising a step of reacting a coelenterazine or an analog thereof with a fluorescent protein, wherein the fluorescent protein comprises in a complex an apoprotein that is a component of a calcium-binding photoprotein, a coelenteramide or an analog thereof, and a calcium ion or a divalent or trivalent ion that can be substituted for the calcium ion;

wherein the coelenteramide or the analog thereof remains coordinated inside the apoprotein;

wherein the calcium ion or the divalent or trivalent ion that can be substituted for the calcium ion is bound to an EF-hand of the apoprotein, and

wherein the sulflydryl group of the cysteine residues of the apoprotein exists without forming a disulfide bond such that the fluorescent protein maintains chemiluminescence activity.

16. The chemiluminescence method of claim 15 , wherein the coelenterazine or the analog thereof is made to react in the presence of a reducing agent.

17. The chemiluminescence method of claim 15 , wherein the coelenterazine or the analog thereof is represented in the following formula (3) or (4):

wherein

R 1 is a substituted or unsubstituted aryl group, a substituted or unsubstituted arylated alkyl group, or a straight or branched chain alkyl group that may be substituted by an aliphatic cyclic group;

R 2 is a substituted or unsubstituted aryl group, a substituted or unsubstituted arylated alkyl group, a substituted or unsubstituted aryl alkenyl group, a straight or branched chain alkyl group that may be substituted by an aliphatic cyclic group, a straight or branched chain alkenyl group that may be substituted by an aliphatic cyclic group, or a heterocyclic group;

R 3 is a hydrogen atom, a substituted or unsubstituted alkyl group;

X 1 is a hydrogen atom, a hydroxyl group, a halogen atom, an alkoxyl group, or an amino group;

X 2 is a hydrogen atom or a hydroxyl group; and

Y is a divalent hydrocarbon group having 1 to 4 carbon atoms.

18. The chemiluminescence method of claim 17 , wherein, in the formula (3) or formula (4),

R 1 is an unsubstituted aryl group, an unsubstituted arylated alkyl group, an arylated alkyl group substituted by a hydroxyl group or a halogen atom, or a straight or branched chain alkyl group that may be substituted by a cyclohexyl group;

R 2 is an unsubstituted aryl group, an aryl group substituted by a hydroxyl group, an unsubstituted arylated alkyl group, an arylated alkyl group substituted with a hydroxyl group, an unsubstituted aryl alkenyl group, an unsubstituted straight or branched chain alkyl group, a straight chain alkyl group that may be substituted by an aliphatic cyclic group, a branched chain alkenyl group, a heterocyclic group containing sulfur;

R 3 is a hydrogen atom, a methyl group, or 2-hydroxyethyl group;

X 1 is a hydrogen atom, a hydroxyl group, a fluorine atom, a methoxy group, or an amino group: and

Y is a methylene group, ethylene group, a propylene group, or a vinylene group.

19. The chemiluminescence method of claim 17 ,

wherein, in the formula (3) or (4),

R 1 is a phenyl group, a benzyl group, a p-hydroxybenzyl group, a p-fluorobenzyl group, a p-chlorobenzyl group, a p-bromobenzyl group, a p-iodinebenzyl group, a 3,4-difluorobenzyl group, a pentafluorobenzyl group, a phenylethyl group, a phenylpropyl group, a naphthylmethyl group, a cyclohexylmethyl group, a methyl group, a 1-methylpropyl group, or a 2-methylpropyl group; and

R 2 is a phenyl group, a p-hydroxy phenyl group, a benzyl group, an α-hydroxybenzyl group, a phenylethyl group, a phenylvinyl group, a cyclohexyl group, a cyclohexylmethyl group, a cyclohexylethyl group, a methyl group, an ethyl group, a propyl group, a 2-methylpropyl group, a 2-methylpropenyl group, an adamantylmethyl group, a cyclopentylmethyl group, or a thiophene-2-yl group.

20. A luminescence kit comprising the isolated fluorescent protein having chemiluminescence activity of claim 1 and a coelenterazine or an analog thereof.

21. The luminescence kit of claim 20 , further comprising a reducing agent.