Enzyme-based fluorescence biosensor for chemical analysis

• US 6,225,127 B1
• Filed: 03/15/1999
• Issued: 05/01/2001
• Est. Priority Date: 10/26/1995
• Status: Expired due to Fees

• Current Assignee: Richard B. Thompson
• Original Assignee: University of Maryland Baltimore County (University of Maryland)
• Inventors: Patchan, Marcia W., Ge, Zhenfang, Thompson, Richard B.
• Primary Examiner(s): WESSENDORF, TERESA D
• Application Number:
  US09/270,308
• Time in Patent Office: 778 Days
• Field of Search: 436/77, 436/76, 436/74, 436/73, 436/501, 530/413, 530/412, 530/350
• US Class Current: 436/76
• CPC Class Codes: G01N 31/22 using chemical indicators G01N31/02 takes precedence
• CPC Class Codes: G01N 33/542 with steric inhibition or signal modification, e.g. fluorescent quenching
• CPC Class Codes: G01N 33/84 involving inorganic compounds or pH

Abstract

This invention generally relates to the detection, determination, and quantitation of certain ions and small molecules involving the quenching of a fluorescent label attached to a macromolecule, often due to fluorescence energy transfer to a colored inhibitor or certain metal ions bound to the macromolecule.

Claims

1. A method of testing a sample for the presence of an anion comprising the steps of:

reacting a metallo-enzyme attached to a photoluminescent donor label with said sample, said metallo-enzyme being able to reversibly bind said anion, resulting in a metallo-enzyme-anion complex, to quench the photoluminescence,

altering the degree of quenching of said photoluminescent donor label in a proximity-dependent quenching process by binding of said anion,

measuring the degree of said quenching by determining the change in intensity or lifetime of photoluminescent emission,

relating the degree of quenching to the fraction of said metallo-enzyme with bound anion, and to the binding affinity of said metallo-enzyme, thereby determining the presence of said anion wherein the proximity between said donor label and said anion is r≦

0.75R₀, wherein R₀is the Fö

rster distance where energy transfer is fifty percent efficient.

2. The method of claim 1, wherein the presence of said anion is determined by measuring the concentration of the anion.

3. The method of claim 1, wherein said anion is selected from the group consisting of OH⁻

, CN⁻

, CNO⁻

, NO₃⁻

, CH₃COO⁻

, HCOO⁻

, HCO₃⁻

, C₆H₅O⁻

, N₃⁻

, C₆H₃O₅N₂⁻

, SCN⁻

, HS⁻

.

4. A method of testing a sample for the presence of a metal ion comprising the steps of:

reacting an enzyme attached to a photoluminescent donor label with said sample in the presence of a colored ligand wherein said colored ligand is selected from the group consisting of azosulfamide, 4-(4, dimethylaminophenyl) azophenyl sulfonamide and salicylazobenzenesulfonamide, creating a metallo-enzyme,

wherein the presence of said metal ion in a binding site of the enzyme permits the colored ligand to bind, thereby bringing it into closer proximity to said photoluminescent donor label,

altering the degree of quenching of said photoluminescent donor label in a proximity-dependent quenching process by binding of said metal ion,

measuring the degree of said quenching by determining the change in intensity or lifetime of photoluminescent emission,

relating the degree of quenching to the fraction of said metallo-enzyme with bound metal ion, and to the binding affinity of said metallo-enzyme, thereby determining the presence of said metal ion wherein the proximity between said donor label and said metal ion is r≦

0.75R₀, wherein R₀ is the Fö

rster distance where energy transfer is fifty percent efficient.

5. The method of claim 4, wherein said colored ligand is azosulfamide.

6. The method of claim 4, wherein the presence of said metal ion in said sample is determined by measuring the concentration of said metal ion.

7. The method of claim 6, wherein said enzyme is selected from the group consisting of carbonic anhydrase, alkaline phosphatase, leucine aminopeptidase, carboxypeptidase, laccase, azurin and urease.

8. The method of claim 7 wherein said enzyme is a mutant enzyme.