Biosensors including lipid bilayer doped with ion channels anchored to a recording electrode by bridging molecules

• US 5,204,239 A
• Filed: 01/09/1991
• Issued: 04/20/1993
• Est. Priority Date: 01/09/1990
• Status: Expired due to Term

• Current Assignee: Yeda Research and Development Co. Ltd. (Weizmann Institute of Science)
• Original Assignee: Yeda Research and Development Co. Ltd. (Weizmann Institute of Science)
• Inventors: Yuli, Itzhak, Gitler, Carlos
• Primary Examiner(s): Nucker, Christine
• Assistant Examiner(s): PRESTON, DAVID
• Application Number:
  US07/638,488
• Time in Patent Office: 832 Days
• Field of Search: 435/877, 435/7.1, 435/817, 435/288, 435/291, 436/525, 436/527, 436/526, 436/501
• US Class Current: 435/7.1
• CPC Class Codes: B01J 2219/00734 Lipids
• CPC Class Codes: G01N 33/5438 Electrodes
• CPC Class Codes: Y10S 435/817 Enzyme or microbe electrode

Abstract

Biosensors for qualitative and quantitative analysis comprise an amphipathic liquid crystalline membrane composed of a lipid bilayer attached to a recording electrode via bridging anchoring molecules. The lipid bilayer is doped with biologic or synthetic ion channels and is in continuous contact with a bulk aqueous medium on both its surfaces. The bridging anchoring molecules may contain a phospholipid moiety linked to a polyoxylakylene chain terminated with a thiol or thioether residue.

Claims

1. A biosensor for qualitative and quantitative analysis of an anylate comprising a container defining a containment chamber having at least one wall comprised of apolar material exposed to the containment chamber;

bulk aqueous electrolyte medium contained in said containment chamber;

a reference electrode located in an upper part of the containment chamber immersed in said electrolyte medium;

a recording electrode located at the bottom of said containment chamber;

a liquid crystalline membrane comprised of a lipid bilayer doped with ion channels wherein said liquid crystalline membrane is immersed in the electrolyte medium between the reference electrode and the recording electrode; and

bridging anchoring molecules attached to the recording electrode on one side and to the lipid bilayer on the other side to anchor the lipid bilayer to the recording electrode in a spaced relationship so that the lipid bilayer is in continuous contact with the bulk aqueous electrolyte medium on both the upper and lower surfaces of the lipid bilayer with the boundaries of the lipid bilayer being sealed by apolar contact with the apolar material of the at least one wall.

2. A biosensor according to claim 1 wherein the lipid bilayer is comprised of a solvated phospholipid bilayer and the bridging anchoring molecules are comprised of a hydrophilic spacer arm joined to a phospholipid moiety.

3. A biosensor according to claim 2 wherein the bridging anchoring molecules comprise a phosphatidylethanolamine residue linked to a polyoxyalkylene chain terminated by a thiol or thioether residue for attachment to the recording electrode.

4. A biosensor according to claim 3 wherein the bridging anchoring molecule has the formula

5. A biosensor according to claim 1 wherein the ion channels are proteins selected from a group consisting of natural receptors and hybrid receptors having a receptive part which interacts with a ligand and a channel-forming part of a second protein.

6. A biosensor according to claim 1 wherein the ion channels are synthetic mellitin-like peptides having a hapten as the receptive part and an antibody directed against a hapten as an inhibitory ligand component, the hapten being an analyte or analyte-like moiety.

7. A biosensor according to claim 6 wherein the ion channel is the peptide CH-1 of the formula

8. A method for the analysis of a ligand comprising contacting a sample containing the ligand with a biosensor according to claim 5 wherein the ion channels comprise the receptor to said ligand or comprise at least its receptive part attached to a channel-forming part of a hybrid protein, and the binding of the ligand triggers the opening of the ion channel in the lipid bilayer leading to a change in electric conductivity, and measuring the change in electric conductivity by the recording electrode.

9. A method for the analysis of an analyte comprising contacting a sample containing said analyte with a biosensor according to claim 6 wherein the ion channels are mellitin-like peptides, containing said analyte or analyte-like moiety as the hapten, and which are bound to an antibody directed against the hapten, whereby the antibody molecules are released thus triggering the opening of the ion channels in the lipid bilayer leading to a change in electric conductivity, and measuring the change in electric conductivity by the recording electrode.

10. A method for the analysis of an analyte comprising contacting a sample containing said analyte with a biosensor according to claim 7 wherein the ion channels are mellitin-like peptides, containing said analyte or analyte-like moiety as the hapten, and which are bound to an antibody directed against it the hapten, whereby the antibody molecules are released thus triggering the opening of the ion channels in the lipid bilayer leading to a change in electric conductivity, and measuring the change in electric conductivity by the recording electrode.