Apparatus and methods for determining biomolecular interactions

• US 6,710,877 B2
• Filed: 07/23/2001
• Issued: 03/23/2004
• Est. Priority Date: 07/23/2001
• Status: Expired due to Fees

• Current Assignee: Corning Incorporated
• Original Assignee: Corning Incorporated
• Inventors: Shi, Youchun, Quesada, Mark A., Chase, Christopher J., Kalal, Peter J.
• Primary Examiner(s): Lee, Diane I.
• Assistant Examiner(s): Kim, Ahshik
• Application Number:
  US09/911,119
• Publication Number:
  US 20030016360A1
• Time in Patent Office: 974 Days
• Field of Search: 356/432, 356/335, 356/336, 256/445
• US Class Current: 356/432
• CPC Class Codes: G01N 21/4788 Diffraction for sizing particles G01N15/0205

Abstract

Methods, apparatus and substrates for the detection of reactions between biomolecules or cells and a second compound are disclosed. The invention detects interactions between ligands and receptors by utilizing detecting the diffusion of a species proximate a sensing area. Absorbance detection and diffraction sensors are utilized to monitor the rate of diffusion from the sensing area.

Claims

1. A molecular detection apparatus comprising:

a first compartment containing at least a ligand or a receptor;

a second compartment adjacent said first compartment;

a boundary area disposed between said first and second compartments;

a sensing area; and

means for detecting the diffusion of a molecule proximate the sensing area;

wherein said ligand is smaller than said receptor and wherein the boundary area includes a membrane operative to allow said ligands to pass therethrough and to prevent passage of said receptors.

2. The molecular detection apparatus of claim 1, further comprising a means for detecting a rate of diffusion of said molecule proximate the sensing area.

3. The molecular detection apparatus of claim 1, wherein said means for detecting the diffusion of the molecule proximate the sensing area further includes a means for detecting variation of molecular concentration as a result of diffusion and interaction proximate the sensing area.

4. The molecular detection apparatus of claim 1, wherein the first compartment contains a matrix material.

5. The molecular detection apparatus of claim 1, wherein said ligand is a drug molecule having a molecular weight less than 1000 Daltons.

6. The molecular detection apparatus of claim 5, wherein the receptor molecule has a molecular weight greater than 5 kiloDaltons.

7. The molecular detection apparatus of claim 6, wherein the receptor molecule includes a protein molecule.

8. The molecular detection apparatus of claim 7, wherein the second compartment contains a buffer solution.

9. The molecular detection apparatus of claim 8, wherein the means for measuring molecular concentration of the molecule further comprises an optical detector.

10. The molecular detection apparatus of claim 9, wherein the optical detector includes a light source and a light detector.

11. The molecular detection apparatus of claim 10, wherein the light source includes a UV light source, the light detector includes a charge-coupled device detector, and the optical detector is operative to measure the light absorbed by the second compartment.

12. The molecular detection apparatus of claim 2, wherein the means for measuring the variation of molecular concentration comprises a refractive index detector and a diffraction device including three laterally spaced openings in a substrate.

13. The molecular detection apparatus of claim 12, wherein the means for measuring the molecular concentration further comprises detecting the change in the far field diffraction pattern generated by the three laterally spaced openings.

14. The molecular detection apparatus of claim 13, wherein the three laterally spaced openings includes a central opening containing a ligand and a receptor in solution.

15. The molecular detection apparatus of claim 14, further including means for detecting the change in the concentration of the ligand or the receptor contained in the central opening.

16. The molecular detection apparatus of claim 15, wherein the means for detecting the change in concentration of ligand and the receptor comprises a charge-coupled device camera.

17. An apparatus for detecting interaction between a ligand and a receptor comprising:

a first compartment containing a matrix, a ligand and a receptor; and

a second compartment adjacent the first compartment, the second compartment containing a buffer solution; and

a light source and a detector arranged to measure the diffusion of the ligand into the second compartment;

wherein the ligand is a drug molecule having a molecular weight less than 1000 Daltons and the receptor has a molecular weight greater than 5 kiloDaltons.

18. The apparatus of claim 17, wherein the matrix includes a polymer.

19. The apparatus of claim 17, wherein the light source and the detector determines the amount of light absorbed in the second compartment.

20. An apparatus for measuring the interaction between a ligand and a receptor comprising:

a light source;

a detector; and

a substrate including at least three laterally spaced optical openings adapted to generate a diffraction pattern;

wherein the three-laterally spaced openings are positioned on the opposite surface of a substrate containing a Y-shaped element including a sensing area.

21. The apparatus of claim 20, wherein the three laterally spaced openings includes a central opening.

22. The apparatus of claim 20, wherein the sensing area of the Y-shaped element is optically aligned with the central opening.

23. A substrate for use in a biological sensing system comprising three laterally spaced openings adapted to generate a diffraction pattern;

wherein a first surface contains the laterally spaced openings and a surface opposite the first surface includes a Y-shaped element including a sensing area optically aligned with the central opening.

24. The substrate of claim 23, wherein the three laterally spaced openings are adapted to generate a Fraunhofer diffraction pattern.

25. A method for analyzing biomolecular interactions comprising:

providing a ligand and a receptor either within or proximate to a slotted diffraction surface;

placing the ligand and the receptor in a Y-shaped element having a sensing area;

detecting the diffusion of biomolecules.

26. The method of claim 25, wherein the diffraction surface comprises three laterally spaced slots.

27. The method of claim 25, further comprising monitoring the diffraction pattern generated by the diffraction surface.

28. The method of claim 25, further comprising providing a ligand and a receptor within or proximate a central slot.

29. The method of claim 25, further comprising filling the Y-shaped element with a solution.

30. The method of claim 29, further comprising electrokinetically pumping the ligand and the receptor across the sensing area.

31. A method of analyzing biomolecular interactions comprising:

providing a ligand and a receptor either within or proximate to a slotted diffraction surface;

placing the ligand and the receptor in a Y-shaped element having a sensing area; and

monitoring the rate of diffusion of biomolecules from an upstream area towards a downstream area.

32. The method of claim 31, wherein the upstream area includes and upstream compartment containing a mixture of a ligand and a receptor separated from the downstream compartment by a membrane.

33. The method of claim 31, wherein the biomolecules are contained in a porous matrix.

34. The method of claim 31, wherein the downstream area includes means for measuring the absorbance of light in the downstream compartment.