Phycobiliprotein-linker peptide complex fluorescent tracer and methods of using the same

• US 6,020,212 A
• Filed: 02/23/1998
• Issued: 02/01/2000
• Est. Priority Date: 06/09/1995
• Status: Expired due to Fees

• Current Assignee: CIS Bio International (Institut National Radio-Elements et D'Util Pub)
• Original Assignee: CIS Bio International (Institut National Radio-Elements et D'Util Pub)
• Inventors: Mathis, Gerard
• Primary Examiner(s): CEPERLEY, MARY
• Application Number:
  US08/973,364
• Time in Patent Office: 708 Days
• Field of Search: 436/546, 436/519, 436/800, 436/813, 436/531, 530/391.3
• US Class Current: 436/546
• CPC Class Codes: C07K 14/195 from bacteria
• CPC Class Codes: G01N 33/533 with fluorescent label
• CPC Class Codes: Y10S 436/80 Fluorescent dyes, e.g. rhodamine
• CPC Class Codes: Y10S 436/813 Cancer

Abstract

The use of a phycobiliprotein-linker peptide complex as a fluorescent tracer in a fluorescent method of detecting and/or determining an analyte in a medium in which it may be present, is disclosed. Fluorescent conjugates consisting of said complex covalently bonded to one of the elements of a ligand/receptor specific binding pair, are also disclosed.

Claims

1. A fluorescent method of detecting and/or determining an analyte in a medium in which it may be present, characterised in that a phycobiliprotcin-linker peptide complex is used as a fluorescent tracer.

2. The method according to claim 1, characterised in that the phycobiliprotein of said phycobiliprotein-linker peptide complex is selected from phycocrythrin, phycoerythrocyanine, phycocyanine, allophycocyanine and allophycccyanine B.

3. The method according to claim 1 characterised in that the phycobiliprotein-linker peptide complex is extracted from a cyanobacterium selected from Mastigoclodus Laminosus, Synechocystis 6701, Synechococcus, 6301, Anabaena variabilis and Nostoc spec.

4. The method according to claim 1, characterised in that the linker peptide of said phycobiliprotein-linker peptide complex is selected from the peptides L_R, L_C, L_RC and L_CM.

5. The method according to claim 1, characterised in that the phycobiliprotein-linker peptide complex is selected from the complexes

(α

^PEC, β

^PEC)₆ L_R, (α

^PEC, β

^PEC)₃ L_R,

(α

^PC, β

^PC)₆ L_R, (α

^PC, β

^PC)₆ L_RC, (α

^PC, β

^PC)₃ L_R,

(α

^AP, β

^AP)₃ L_C, (α

^APB, [α

2]α

₂^AP, [B3]β

₃^AP)L_C and (α

^AP, β

^AP)₂ L_CM.

14. A method of amplification of the emission signal of a rare earth cryptate or chelate used as fluorescent donor compound in a fluorescent assay according to claim 1, in which a fluorescent acceptor compound is also used, characterised in that the rare earth clyptate or chelate possesses a low overall quantum yield, and in that the quantum yield of radiative deactivation from the emission level of the rare earth is lower than the quantum yield of the acceptor being constituted by a phycobiliprotein-linker peptide complex.

15. The method according to claim 1, characterised in that the phycobiliprotein-linker peptide complex is used in combination with one or more different fluorescent tracers.

6. A homogenous fluorescent method of detecting and/or determining an analyte in a medium in which it may be present, by displaying the product of the reaction between the analyte and at least one corresponding receptor, consisting of:

1) adding to said medium a first reagent constituted of at least one receptor of said analyte,

2) adding a second reagent selected from the analyte or at least one of its receptors, one of said first reagent or said second reagent coupled with a flourescent donor compound constituted by a rare earth cryptate, chelate or macrocyclic complex and other reagent being coupled with a fluorescent acceptor compound, it being possible for the order of addition of the reagents to be the reverse order and, after excitation of the mixture by a source of light at the excitation wavelength of the fluorescent donor compound,

3) measuring the emission signal of the fluorescent acceptor compould, and

4) correlating the measured emission signal of the fluorescent acceptor compound to the presence and/or amount of analyte, characterised in that a phycobiliprotein-linker peptide complex is used as a fluorescent acceptor compound.

7. The method according to claim 6 which consists of an excess method, characterised in that it consists of:

1) adding to said medium containing the analyte sought after a first reagent constituted by at least one receptor of said analyte coupled with a fluorescent donor compound constituted by a rare earth cryptate, chelate or macrocyclic complex,

2) adding a second reagerit constituted by one or more other receptors of said analyte, said second reagent being coupled with a fluorescent acceptor compound constituted by a phycobiliprotein-linker peptide complex,

3) incubating said medium after each addition of reagents or after the addition of the second reagent,

4) exciting the resulting medium at the excitation wavelength of the fluorescent donor compound,

5) measuring the signal emitted by the fluorescent acceptor compound.

8. The method according to claim 6 consisting of a competitive method, characterised in that it consists of:

1) adding to said medium containing the analyte sought after a first reagent constituted by a receptor of said analyte, coupled with a fluorescent donor compound constituted by a rare earth cryptate, chelate or macrocyclic complex,

2) adding a second reagent constituted of the analyte coupled with a fluorescent acceptor compound constituted by a phycobiliprotein-linker peptide complex,

3) incubating said medium after each addition of reagents or after the addition of the second reagent,

4) exciting the resulting medium at the excitation wavelength of the fluorescent donor compound,

5) measuring the signal emitted by the fluorescent acceptor compound.

9. The method according to claim 6 consisting of a competitive method, characterised in that it consists of:

1) adding to said medium containing the analyte sought after a first reagent constituted by a receptor of said analyte, said receptor being coupled with a fluorescent acceptor compound constituted by a phycobiliprotein-linker peptide complex,

2) adding a second reagent constituted of the analyte coupled with a fluorescent donor compound constituted by a rare earth cryptate or chelate,

3) incubating said medium either after the addition of each reagent, or after the addition of the second reagent,

4) exciting the resulting medium at the excitation wavelength of he fluorescent donor compound,

5) measuring the signal emitted by the fluorescent acceptor compound.

10. The method according to any one of claims 6 to 9, characterised in that the first reagent and the second reagent are added simultaneously to the medium containing the analyte sought after.

11. The method according to any one of claims 6 or 7, characterised in that one sole receptor of the analyte is used which is coupled either with the fluorescent donor compound, or with the fluorescent acceptor compound.

12. The method according to any one of claims 6 to 9, characterised in that the fluorescent donor compound is a terbium or europium chelate, cryptate or macrocyclic complex.

13. The method according to any one of claims 6 to 9 characterised in that the fluorescent donor compound is an Eu³⁺ chelate, cryptate or macrocyclic complex and the fluorescent acceptor compound is the (α

^AP, β

^AP)₃ L_C complex.

24. The method of claim 6 wherein phycobiliprotein of said phycobiliprotein-linker peptide complex is selected from phycoerythrin, phycoerythrocyanine, phycocyanine, allophycocyanine and allophycocyanine B.

25. The method of claim 6 wherein said phycobiliprotein-linker peptide complex is extracted from a cyanobacterium selected from Mastigoclodus Laminosus, Synechocystis 6701, Synechococcus, 6301, Anabaena variabilis and Nostoc spec.

26. The method of claim 6 wherein the linker peptide of said phycobiliprotein-linker peptide complex is selected from the peptides L_R, L_C, L_RC and L_CM.

27. The method of claim 6 wherein said phycobiliprotein-linker peptide complex is selected from the complexes

(α

^PEC, β

^PEC)₆ L_R, (α

^PEC, β

^PEC)₃ L_R,

(α

^PC, β

^PC)₆ L_R, (α

^PC, β

^PC)₆ L_RC, (α

^PC, β

^PC)₃ L_R,

(α

^AP, β

^AP)₃ L_C, (α

^APB, α

2^AP, B3^AP)L_C and (α

^AP, β

^AP)₂ L_CM.

16. A fluorescent conjugate constituted of a phycobiliprotein-linker peptide complex covalently bound to one of the elements of a ligand/receptor specific binding pair.

17. The conjugate according to claim 16, characterized in that the phycobiliprotein of said phycobiliprotein-linker peptide complex is selected from phycoerythrin, phycoerythrocyanine, phycocyanine, allophycocyanine and allophycocyanine B.

18. The conjugate according to claim 16 or 17, characterized in that the linker peptide of said phycobiliprotcin-linkcr peptide complex is selected from the peptides L_R, L_C, L_RC and L_CM.

19. The conjugate according to one of claims 16 or 17, characterised in that the phycobiliprotein-linker peptide complex is selected from the complexes

(α

^PEC, β

^PEC)₆ L_R, (α

^PEC, β

^PEC)₃ L_R,

(α

^PC, β

^Pc)₆ L_R, (α

^PC, β

^PC)₆ L_RC, (α

^PC, β

^PC)₃ L_R,

(α

^AP, β

^AP)₃ L_C, (α

^APB, [α

2]α

₂^AP ;

[B3]β

₃^AP)L_C and (α

^AP, β

^AP)₂ L_CM.

20. The conjugate according to one of claims 16 or 17, characterised in that the phycobiliprotein-linker peptide complex is extracted from a c),anobacterium selectcd from Mastigoclodus Laminosus, Synechocystis 6701, Synechococcis 6301, Anabaena variabilis and Nostoc spec.

21. The conjugate according to claim 16, characterised in that the element of the ligand/receptor specific binding pair is a receptor.

22. The conjugate according to claim 16, characterised in that the element of the ligand/receptor specific binding pair is a ligand.

23. A flow cytometry method characterized by the use of the conjugate of claim 16 or 17.

28. The conjugate of claim 21 wherein said receptor is a cell receptor or an antibody.

29. The conjugate of claim 22 wherein said ligand is an analyte.