Labeling dye for detecting biomolecule, labeling kit, and method for detecting biomolecule

1. A labeling dye used for detecting a biomolecule by measurement of fluorescence, wherein the dye comprises a coloring portion comprising an organic EL-dye, a bonding portion to be bonded with the biomolecule and a spacer portion for linking the coloring portion and the bonding portion,

wherein said spacer portion is represented by the following general formula (I)

—(CHR′) p —X—(CHR″) q —  (I)

wherein X represents a direct bond, or at least one functional group selected from the group consisting of —NHCOO—, —CONH—, —COO—, —SO 2 NH—, —HN—C(═NH)—NH—, —O—, —S—, —NR—, —CH═CH—, —C≡C—, —AR— and —CO—Ar—NR—; R′ and R″ each independently represent a hydrogen atom, an aliphatic hydrocarbon group, or an aromatic hydrocarbon group, and wherein the aliphatic hydrocarbon group or the aromatic hydrocarbon group is optionally substituted with any one charge group selected from the group consisting of a sulfonyl group, hydroxyl group, quaternary ammonium group and carboxyl group; Ar represents an aryl group; and p and q each independently represent an integer of 0 to 20, wherein the value of “p+q” is greater than or equal to 1.

2. A labeling dye used for detecting a biomolecule by measurement of fluorescence, wherein the dye comprises a coloring portion comprising an organic EL-dye, a bonding portion to be bonded with the biomolecule and a spacer portion for linking the coloring portion and the bonding portion,

wherein said spacer portion is an amino acid or a peptide linker comprising 2 to 20 amino acids.

3. The labeling dye according to claim 1 , wherein said organic EL-dye comprises a condensed poly-ring compound consisting of a 5-membered ring compound containing one or more hetero atom(s), selenium atom(s) or boron atom(s) and a 6-membered ring compound having a conjugate system.

4. The labeling dye according to claim 2 , wherein said organic EL-dye comprises a condensed poly-ring compound consisting of a 5-membered ring compound containing one or more hetero atom(s), selenium atom(s) or boron atom(s) and a 6-membered ring compound having a conjugate system.

5. The labeling dye according to claim 2 , wherein said condensed poly-ring compound is an azole derivative of the following general formula (1), (2) or (3):

wherein, R 1 , R 2 , R 3 and R 4 each independently represent a hydrogen atom, an aromatic hydrocarbon group, hydrocarbon group, heterocyclic group or aromatic group containing a hetero atom in the ring, optionally having a substituent; X represents a nitrogen atom, sulfur atom, oxygen atom, selenium atom or boron atom; R′ represents an aliphatic hydrocarbon group, optionally having a substituent, or an aromatic hydrocarbon group; and An − represents a halide ion.

6. The labeling dye according to claim 5 , wherein R 2 and R 3 each independently represent any one compound selected from the group consisting of a thiophene derivative, furan derivative, pyrole derivative, imidazole derivative, oxazole derivative, thiazole derivative and pyridine derivative.

7. The labeling dye according to claim 5 , wherein R 2 and R 3 represent an aryl group having a sulfonyl group.

8. The labeling dye according to claim 2 , wherein said condensed poly-ring compound is an imidazole derivative of the following general formula (4), (5), (6), (7) or (8):

wherein, R 1 , R 2 , R 3 , R 4 and R 5 each independently represent a hydrogen atom, an aromatic hydrocarbon group, hydrocarbon group, heterocyclic group or aromatic group containing a hetero atom in the ring, optionally having a substituent; R 1 , R 2 , R 3 , R 4 and R 5 may be the same or different; R′ and R″ represent an aliphatic hydrocarbon group, optionally having a substituent, or an aromatic hydrocarbon group; and An represents a halide ion.

9. The labeling dye according to claim 8 , wherein R 2 and R 3 each independently represent any one compound selected from the group consisting of a thiophene derivative, furan derivative, pyrole derivative, imidazole derivative, oxazole derivative, thiazole derivative and pyridine derivative.

10. The labeling dye according to claim 8 , wherein R 2 and R 3 represent an aryl group having a sulfonyl group.

11. The labeling dye according to claim 1 , wherein said bonding portion is any one reactive group selected from the group consisting of a carboxyl group, isocyanate group, isothiocyanate group, epoxy group, halogenated alkyl group, triazine group, carbodiimide group and active ester carbonyl group.

12. The labeling dye according to claim 2 , wherein said bonding portion is any one reactive group selected from the group consisting of a carboxyl group, isocyanate group, isothiocyanate group, epoxy group, halogenated alkyl group, triazine group, carbodiimide group and active ester carbonyl group.

13. The labeling dye according to claim 2 , wherein said spacer is a natural amino acid or synthetic amino acid.

14. The labeling dye according to claim 13 , wherein said amino acid is any one selected from the group consisting of cysteine acid, 2-amino-sulfosulfanylpropanic acid, 2-amino-amino-3-sulfoxypropanic acid, tyrosine, threonine, 4-amino-2-hydroxybutanic acid, homo-serine and serine.

15. The labeling dye according to claim 2 , wherein said spacer is a peptide linker comprising at least one charge group selected from the group consisting of a sulfonyl group, hydroxyl group, quaternary ammonium group and carboxyl group.

16. The labeling dye according to claim 15 , wherein said peptide linker comprises at least one amino acid selected from the group consisting of cysteine acid, 2-amino-sulfosulfanylpropanic acid, 2-amino-amino-3-sulfoxypropanic acid, tyrosine, threonine, 4-amino-2-hydroxybutanic acid, homo-serine and serine.

17. A labeling kit used to detect a biomolecule by fluorescence measurement, wherein said labeling kit includes a labeling dye comprising a coloring portion comprising an organic EL-dye, a bonding portion to be bonded with a biomolecule and a spacer portion for linking the coloring portion and the bonding portion,

wherein said spacer portion is represented by the following general formula (I)

—(CHR) p —X—(CHR″) q —  (I)

wherein X represents a direct bond, or at least one functional group selected from the group consisting of —NHCOO—, —CONH—, —COO—, —SO 2 NH—, —HN—C(═NH)—NH—, —O—, —S—, —NR—, —CH═CH—, —C≡—, —Ar— and —CO—Ar—NR—; R′ and R″ each independently represent a hydrogen atom, an aliphatic hydrocarbon group, or an aromatic hydrocarbon group, and wherein the aliphatic hydrocarbon group or the aromatic hydrocarbon group is optionally substituted with any one charge group selected from the group consisting of a sulfonyl group, hydroxyl group, quaternary ammonium group and carboxyl group; Ar represents an aryl group; and p and q each independently represent an integer of 0 to 20, wherein the value of “p+q” is greater than or equal to 1.

18. A labeling kit used to detect a biomolecule by fluorescence measurement, wherein said labeling kit includes a labeling dye comprising a coloring portion comprising an organic EL-dye, a bonding portion to be bonded with a biomolecule and a spacer portion for linking the coloring portion and the bonding portion,

wherein said spacer portion is an amino acid or a peptide linker comprising 2 to 20 amino acids.

19. The labeling kit according to claim 17 , said labeling kit comprising a reactive group introducing reagent to introduce a reactive group into the labeling dye selected from the group consisting of a carboxyl group, isocyanate group, isothiocyanate group, epoxy group, halogenated alkyl group, triazine group, carbodiimide group and active ester carbonyl group.

20. The labeling kit according to claim 18 , said labeling kit comprising a reactive group introducing reagent to introduce a reactive group into the labeling dye selected from the group consisting of a carboxyl group, isocyanate group, isothiocyanate group, epoxy group, halogenated alkyl group, triazine group, carbodiimide group and active ester carbonyl group.

21. A method of detecting a biomolecule, comprising reacting the biomolecule with a labeling dye comprising a coloring portion including an organic EL-dye, a bonding portion to be bonded with a biomolecule and a spacer portion for linking the coloring portion and the bonding portion, and measuring the fluorescence of the labeled biomolecule,

wherein said spacer portion is represented by the following general formula (I)

—(CHR) p —X—(CHR″) q —  (I)

wherein X represents a direct bond, or at least one functional group selected from the group consisting of —NHCOO—, —CONH—, —COO—, —SO 2 NH—, —HN—C(═NH)—NH—, —O—, —S—, —NR—, —CH═CH—, —C≡—, —Ar— and —CO—Ar—NR—; R′ and R″ represent each independently a hydrogen atom, an aliphatic hydrocarbon group, or an aromatic hydrocarbon group, and wherein the aliphatic hydrocarbon group or the aromatic hydrocarbon group is optionally substituted with any one charge group selected from the group consisting of a sulfonyl group, hydroxyl group, quaternary ammonium group and carboxyl group; Ar represents an aryl group; and p and q each independently represent an integer of 0 to 20, wherein the value of “p+q” is greater than or equal to 1.

22. A method of detecting a biomolecule, comprising reacting the biomolecule with a labeling dye comprising a coloring portion including an organic EL-dye, a bonding portion to be bonded with a biomolecule and a spacer portion for linking the coloring portion and the bonding portion, and measuring the fluorescence of the labeled biomolecule,

wherein said spacer portion is an amino acid or a peptide linker comprising 2 to 20 amino acids.

23. The method according to claim 21 , wherein said biomolecule is any one selected from the group consisting of nucleic acids, proteins, peptides and saccharides.

24. The method according to claim 22 , wherein said biomolecule is any one selected from the group consisting of nucleic acids, proteins, peptides and saccharides.