Enzyme-based fluorescence biosensor for chemical analysis

• US 5,952,236 A
• Filed: 10/25/1996
• Issued: 09/14/1999
• Est. Priority Date: 10/26/1995
• Status: Expired due to Fees

• Current Assignee: Marcia W. Patchan, Richard B. Thompson, Zhengfang Ge
• Original Assignee: University of Maryland
• Inventors: Thompson, Richard B., Patchan, Marcia W., Ge, Zhengfang
• Primary Examiner(s): Achutamurthy, Ponnathapura
• Assistant Examiner(s): WESSENDORF, TERESA D
• Application Number:
  US08/736,904
• Time in Patent Office: 1,054 Days
• Field of Search: 436/74, 436/501, 436/73, 436/76, 436/77, 530/413, 530/412, 530/350
• US Class Current: 436/77
• 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 for testing an aqueous sample for the presence of a metal ion comprising the steps of:

reacting a macromolecule with said sample, said macromolecule having a binding site for binding a metal ion, being able to reversibly bind said metal ion, and further having a suitable photoluminescent donor label bound thereto, said label being optimally and accessibly positioned with respect to the metal ion binding site the distance between said photoluminescent donor label and said metal ion is <

R₀, wherein R₀ is the Forster distance where energy transfer is fifty percent efficient, resulting in a macromolecule-metal ion complex, wherein said metal ion is capable of reacting with said donor label to quench the photoluminescence,

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

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

relating the degree of quenching to the fraction of macromolecules with bound metal ion, and to the binding affinity of said macromolecule, thereby determining the presence of said metal ion.

2. The method of claim 1, wherein said metal ion is selected from the group consisting of Zn(II), Co(II), Ni(II), Hg(II), Fe(II), Mn(II), Pb(II), Cd(II), and Cu(II).

3. The method of claim 1, wherein the macromolecule is a protein.

4. The method of claim 3, wherein said protein is selected from the group consisting carbonic anhydrase, alkaline phosphatase, leucine aminopeptidase, carboxypeptidase, laccase, azurin, and urease.

5. The method of claim 1, wherein the distance between said photoluminescent donor label and said metal ion is r≦

0.75 R₀.

6. The method of claim 1, wherein said metal ion is selected from the group consisting of Zn(II), Co(II), Ni(II), Cd(II), and Cu(II).

7. The method of claim 1, wherein the photoluminescent label is selected from the group consisting of fluorescein, isothiocyanate, rhodamine iodoacetamide, CY3 iodoacetamide, and Green Fluorescent Protein.