Process and device for assaying a hapten

• US 5,849,480 A
• Filed: 03/16/1995
• Issued: 12/15/1998
• Est. Priority Date: 06/11/1993
• Status: Expired due to Term

• Current Assignee: Bio Merieux
• Original Assignee: Bio Merieux
• Inventors: Kurfurst, Robin, Cros, Philippe, Battail, Nicole, Piga, Nadia
• Primary Examiner(s): Housel, James C.
• Assistant Examiner(s): ASHTON, ROSEMARY E
• Application Number:
  US08/379,593
• Time in Patent Office: 1,370 Days
• Field of Search: 422/57, 422/60, 435/7.1, 435/7.9, 435/7.92-7.95, 435/961, 435/6, 435/969, 436/527, 436/531, 436/532, 436/810, 427/2.11, 427/2.13
• US Class Current: 435/6.14
• CPC Class Codes: C12Q 1/6804 Nucleic acid analysis using immunogens immunoassay G01N33/53
• CPC Class Codes: G01N 33/54306 Solid-phase reaction mechanisms
• CPC Class Codes: Y10S 435/961 including a step of forming, releasing, or exposing the antigen or forming the hapten-immunogenic carrier complex or the antigen per se
• CPC Class Codes: Y10S 435/969 Multiple layering of reactants

Abstract

A device for assaying haptens includes a solid support linked through a nucleic acid fragment to a reagent that can compete with the hapten for binding to antibodies that bind to the hapten. A process for assaying a hapten uses this device.

Claims

1. Hapten assay device for assaying a first hapten comprising a solid support and a reagent covalently linked to a nucleic acid fragment to form a conjugate immobilized or immobilizable on said solid support by means of said fragment, wherein said reagent is a second hapten that competes with said first hapten for specific binding to antibodies that bind to said first hapten.

2. Device according to claim 1, wherein said conjugate is immobilized by passive adsorption of said fragment onto the solid support.

3. Device according to claim 1, wherein said conjugate is immobilized by covalent coupling of said fragment onto the solid support.

4. Device according to claim 1, wherein said conjugate is immobilized onto the solid support by hybridization with a second nucleic acid fragment hybridizable with said nucleic acid fragment of said conjugate, said second nucleic acid fragment being immobilized on the support.

5. Device according to claim 1, wherein said conjugate is immobilized on the support by an antibody or an antibody fragment directed against said nucleic acid fragment of said conjugate, said antibody or antibody fragment being immobilized on said solid support.

6. Device according to claim 1, wherein said device comprises a protein immobilized on the support said protein having an affinity for binding with said fragment.

7. Device according to claim 1, wherein the nucleic acid fragment is selected from the group consisting of a DNA fragment and an RNA fragment.

8. Device according to claim 7, wherein said nucleic acid fragment is a deoxyribonucleotide, a ribonucleotide, a deoxyribonucleoside or a ribonucleoside.

9. Device according to claim 7, wherein the nucleic acid fragment is an oligodeoxyribonucleotide or an oligoribonucleotide with a length of between 2 and 100 nucleotides.

10. Device according to claim 9, wherein the length is between 10 and 50 nucleotides.

11. Device according to claim 7, wherein the nucleic acid fragment comprises a naturally modified base.

12. Device according to claim 11, wherein the naturally modified base is selected from the group consisting of 6-ketopurine, xanthine, 5-methyl-cytosine and 2-aminopurine.

13. Device according to claim 7, wherein the nucleic acid fragment comprises an unnatural modified base.

14. Device according to claim 7, wherein the unnatural modified base is selected from the group consisting of thioguanine and 8-oxoguanine.

15. Device according to claim 13, wherein the nucleic acid fragment is modified on a glycosidic portion.

16. Device according to claim 7, wherein the nucleic acid fragment is modified in a phosphodiester skeleton.

17. Device according to claim 7, wherein the nucleic acid fragment comprises nucleosides that are each alpha or each beta anomers.

18. Device according to claim 7, wherein nucleosides of the nucleic acid fragment are selected from the group consisting of D-nucleosides and L-nucleosides.

19. Device according to claim 11, wherein said second hapten is identical to said first hapten.

20. Process for assaying a first hapten in a liquid sample comprising:

adding to said sample a predetermined quantity of antibodies to which said first hapten specifically binds;

contacting the sample with the device as defined in claim 1;

evaluating the quantity of antibody attached to the solid support of the device; and

deducing the quantity of first hapten present in the sample.

21. Process according to claim 20, wherein said conjugate is immobilized by passive adsorption of said fragment onto the solid support.

22. Process according to claim 20, wherein said conjugate is immobilized by covalent coupling of said fragment onto the solid support.

23. Process according to claim 20, wherein said conjugate is immobilized onto the solid support by hybridization with a second nucleic acid fragment hybridizable with said nucleic acid fragment of the said conjugate, said second nucleic acid fragment being immobilized on the support.

24. Process according to claim 20, wherein said conjugate is immobilized on the support by an antibody or an antibody fragment directed against said nucleic acid fragment of said conjugate, said antibody or antibody fragment being immobilized on said solid support.

25. Process according to claim 20, wherein said device comprises a protein immobilized on the support by said fragment, said protein having an affinity for binding with said fragment.

26. Process according to claim 20, wherein the nucleic acid fragment is selected from the group consisting of a DNA fragment and an RNA fragment.

27. Process according to claim 20, wherein said nucleic acid fragment is a deoxyribonucleotide, a ribonucleotide, a deoxyribonucleoside or a ribonucleoside.

28. Process according to claim 20, wherein the nucleic acid fragment is an oligodeoxyribonucleotide or an oligoribonucleoside with a length of between 2 and 100 nucleotides.

29. Process according to claim 28, wherein the length is between 10 and 50 nucleotides.

30. Process according to claim 20, wherein the nucleic acid fragment comprises a naturally modified base.

31. Process according to claim 30, wherein the naturally modified base is selected from the group consisting of 6-ketopurine, xanthine, 5-methyl-cytosine and 2-aminopurine.

32. Process according to claim 20, wherein the nucleic acid fragment comprises an unnatural modified base.

33. Process according to claim 32, wherein the unnatural modified base is selected from the group consisting of thioguanine and 8-oxoguanine.

34. Process according to claim 20, wherein the nucleic acid fragment is modified on a glycosidic portion.

35. Process according to claim 20, wherein the nucleic acid fragment is modified in a phosphodiester skeleton.

36. Process according to claim 20, wherein the nucleic acid fragment comprises nucleosides that are each alpha or each beta anomers.

37. Process according to claim 20, wherein nucleosides of the nucleic acid fragment are selected from the group consisting of D-nucleosides and L-nucleosides.

38. Hapten assay device for assaying a first hapten consisting essentially of a solid support and a reagent covalently linked to a nucleic acid fragment to form a conjugate immobilized or immobilizable on said solid support by means of said fragment, wherein said reagent is a second hapten that competes with said first hapten for specific binding to antibodies that bind to said first hapten.