Conjugates of sulforhodamine fluorophores with enhanced fluorescence

• US 5,846,737 A
• Filed: 07/26/1996
• Issued: 12/08/1998
• Est. Priority Date: 07/26/1996
• Status: Expired due to Term

• Current Assignee: Molecular Probes Incorporated (Thermo Fisher Scientific Incorporated)
• Original Assignee: Molecular Probes Incorporated (Thermo Fisher Scientific Incorporated)
• Inventors: Kang, Hee Chol
• Primary Examiner(s): Wilson, James O.
• Application Number:
  US08/686,858
• Time in Patent Office: 865 Days
• Field of Search: 549/224, 549/227, 549/394, 435/7.1, 435/7.5, 435/7.72, 435/7.8, 530/300, 530/387.1, 530/388.9, 530/391.3, 530/391.5, 530/391.9, 536/23.1, 536/25.1, 536/25.2, 536/25.32, 536/26.26, 536/26.6, 536/26.7, 536/26.8, 436/501, 436/544, 436/546, 436/800
• US Class Current: 435/7.1
• CPC Class Codes: G01N 33/533 with fluorescent label
• CPC Class Codes: Y10S 436/80 Fluorescent dyes, e.g. rhodamine

Abstract

The invention describes useful conjugates of sulforhodamine, wherein the conjugated substance and the fluorophore are separated by an alkanoic acid spacer that is attached to the fluorophore via a sulfonamide bond. The increased length of the covalent linkage due to the spacer results in dye-conjugates having a number of surprisingly advantageous properties relative to previous sulforhodamine-labeled conjugates, including increased fluorescence.

Claims

1. A dye-conjugate comprising a conjugated substance that is a peptide, protein, polysaccharide, nucleotide, oligonucleotide or nucleic acid polymer to which is attached one or more dye molecules, which may be the same or different, having the formula ##STR6## or the formula ##STR7## wherein n=1-10;

R¹ is CH₃ or CH₂ CH₃ ; and

R² is the conjugated substance.

2. A dye-conjugate, as claimed in claim 1, wherein the conjugated substance is a peptide or a protein.

3. A dye-conjugate, as claimed in claim 2, wherein the conjugated substance is a peptide having 5-36 amino acids.

4. A dye-conjugate, as claimed in claim 2, wherein the conjugated substance is an antibody, a fragment of an antibody, an avidin or a streptavidin.

5. A dye-conjugate, as claimed in claim 2, wherein the conjugated substance is a lipoprotein or a glycoprotein.

6. A dye-conjugate, as claimed in claim 1, wherein the conjugated substance is a polysaccharide, a glycoprotein, the carbohydrate portion of a nucleotide, the carbohydrate portion of a nucleic acid polymer, or a periodate-oxidized ribonucleic acid.

7. A dye-conjugate, as claimed in claim 1, wherein the conjugated substance is a ribonucleotide, a deoxyribonucleotide, a dideoxyribonucleotide, an oligonucleotide or a nucleic acid polymer.

8. A dye-conjugate, as claimed in claim 7, wherein the conjugated substance is a uridine triphosphate or a deoxyuridine triphosphate.

9. A dye-conjugate, as claimed in claim 7, wherein said dye is bound to the conjugated substance at a purine or pyrimidine base through an amide, ester, ether or thioether bond.

10. A dye-conjugate, as claimed in claim 7, wherein said dye is bound to the conjugated substance via a phosphate, thiophosphate, phosphite, or phosphonate group through an ester or amide bond.

11. A dye-conjugate, as claimed in claim 1, where the conjugated substance is attached via an amide, ester or thioester linkage.

12. A dye-conjugate, as claimed in claim 1, wherein n=3-5.

13. A method of detecting a complementary member of a specific binding pair in a sample, comprising:

a) adding to said sample a dye-conjugate of a first member of a specific binding pair for which there is a complementary member, to which is attached one or more dye molecules, which may be the same or different, having the formula ##STR8## or the formula ##STR9## wherein n=1-10;

R¹ is CH₃ or CH₂ CH₃ ; and

R² is the first member of the specific binding pair;

b) allowing sufficient time for the dye-conjugate to form a complex with the complementary member; and

c) detecting the complex to locate the complementary member.

14. A method, as claimed in claim 13, wherein the first member of the specific binding pair is a peptide, a protein, a nucleotide, an oligonucleotide or a polysaccharide.

15. A method, as claimed in claim 13, wherein the complex is detected by its fluorescence response.

16. A method, as claimed in claim 13, wherein the first member of the specific binding pair is an antibody, an antibody fragment, avidin, streptavidin, or a conjugate of an antibody, an antibody fragment, avidin, or streptavidin and the complementary member is a hapten, an antigen or a biotin.

17. A method, as claimed in claim 16, wherein the first member of the specific binding pair is avidin or streptavidin or a conjugate of avidin or streptavidin.

18. A method, as claimed in claim 16, wherein the first member of the specific binding pair is an antibody or antibody fragment or a conjugate of an antibody or an antibody fragment.

19. A method, as claimed in claim 16, wherein the complementary member is a hapten having a molecular weight less than 1,000.

20. A method, as claimed in claim 19, wherein the complementary member is present in a cell, bacteria, virus or yeast cell.

21. A method, as claimed in claim 13, wherein the first member of the specific binding pair is an oligonucleotide or nucleic acid polymer.

22. A method, as claimed in claim 21, wherein the complementary member is present in a cell, bacteria, virus or yeast cell.

23. A method, as claimed in claim 21, wherein the complementary member is immobilized on a polymer, polymeric membrane or polymeric particle.

24. A method, as claimed in claim 21, wherein the complementary member is present in an electrophoretic gel.

25. A method, as claimed in claim 15, wherein the fluorescence response is detected using a flow cytometer, a fluorescence microscope, a fluorometer or a fluorescence plat reader.

26. A method, as claimed in claim 25, further comprising distinguishing the fluorescence response from that of a second fluorophore having detectably different optical properties.

27. A method, as claimed in claim 25, wherein the fluorescence response is detected using a flow cytometer, further comprising sorting said complex based on the fluorescence response.

28. A complex of a dye-conjugate of a first member of a specific binding pair and a complementary member of said complementary member, where the first member of the specific binding pair is attached to one or more dyes, which may be the same or different, having the formula ##STR10## or the formula ##STR11## wherein n=1-10;

R¹ is CH₃ or CH₂ CH₃ ; and

R² is the first member of the specific binding pair.

29. A complex, as claimed in claim 28, wherein the first member of the specific binding pair is a peptide or a protein.

30. A complex, as claimed in claim 29, wherein the first member of the specific binding pair is an antibody, toxin, lipoprotein, lectin, avidin, streptavidin, protein A or protein G.

31. A complex, as claimed in claim 28, wherein the first member of the specific binding pair is a polysaccharide.

32. A complex, as claimed in claim 28, wherein the first member of the specific binding pair is a drug or toxin.

33. A complex, as claimed in claim 28, wherein the first member of the specific binding pair is a nucleotide, oligonucleotide or a nucleic acid polymer.

34. A dye-conjugate, prepared by the reaction of a substance that is a peptide, protein, polysaccharide, nucleotide, oligonucleotide or nucleic acid polymer with a reactive dye having the formula ##STR12## or the formula ##STR13## or a mixture thereof, wherein n=1-10;

and

R¹ is CH₃ or CH₂ CH₃.