Characterizing macromolecules interacting with at least three ligands on a sensor

• US 5,554,541 A
• Filed: 12/30/1994
• Issued: 09/10/1996
• Est. Priority Date: 11/10/1988
• Status: Expired due to Term

• Current Assignee: GE Healthcare Bio-Sciences AB (GE Healthcare Technologies, Inc.)
• Original Assignee: Pharmacia Biosensor AB (General Electric Company)
• Inventors: Larsson, Anita, Sjodal, Jorgen, Karlsson, Robert, Malmqvist, Magnus
• Primary Examiner(s): Housel, James C.
• Assistant Examiner(s): Chin, Christopher L.
• Application Number:
  US08/366,443
• Time in Patent Office: 620 Days
• Field of Search: 422/82.05, 422/82.08, 422/82.11, 436/165, 436/518, 436/527, 436/536, 436/805
• US Class Current: 436/518
• CPC Class Codes: G01N 21/211 Ellipsometry optical thickness measurement G01B11/06
• CPC Class Codes: G01N 21/553 and using surface plasmons fluorescence excitation G01N21/648; enhanced Raman G01N21/658
• CPC Class Codes: G01N 33/54373 involving physiochemical end-point determination, e.g. wave-guides, FETS, gratings
• CPC Class Codes: G01N 33/6878 in eptitope analysis
• CPC Class Codes: Y10S 436/805 Optical property

Abstract

A method of characterizing a macromolecule by studying its interactions with ligands comprises the determination of the mutual influence of ligand interactions by, after the macromolecule has interacted with at least one ligand, contacting the macromolecule with at least one additional ligand, either the macromolecule or the additional ligand or ligands having been bound to a sensor surface, determining interaction by detecting a consequential change in the physico-chemical properties of the sensor surface, and on the basis of the determined mutual dependence between the ligand interactions discriminating between epitopes of the macromolecule and mapping their relative positions.

Claims

1. A method of discriminating between and mapping epitopes of a macromolecule by studying its interactions with ligands, comprising the steps of:

determining blocking or non-blocking of the epitopes by the ligands by, after the macromolecule has interacted with at least one ligand, sequentially contacting the macromolecule with at least two additional ligands, either the macromolecule or one of the at least two additional ligands having been bound to a sensor surface;

determining ligand binding interaction by detecting a change in the physico-chemical properties of the sensor surface; and

discriminating between epitopes of the macromolecule and mapping their relative positions on the basis of the determined blocking or non-blocking of the epitopes by the ligands.

2. The method according to claim 1, further comprising the steps of:

a) binding the macromolecule to a sensor surface;

b) sequentially contacting at least three ligands with the macromolecule bound to the sensor surface; and

c) determining the ligand binding interaction after each one of the at least three ligands is contacted with the macromolecule by detecting the change in the physico-chemical properties of the sensor surface after each one of the at least three ligands is contacted with the macromolecule bound to the sensor surface.

3. The method according to claim 2, wherein steps b) and c) are repeated one or more times with the ligands in an altered sequence.

4. The method according to claim 1, further comprising the steps of:

a) binding the at least one ligand, specific to the macromolecule to the sensor surface;

b) permitting the macromolecule to interact with the at least one ligand bound to the sensor surface for binding the macromolecule to the sensor surface;

c) sequentially contacting the at least two additional ligands with the macromolecule bound to the sensor surface; and

d) determining the ligand binding interaction after each one of the at least two additional ligands is contacted with the macromolecule by detecting the change in the physico-chemical properties of the sensor surface after each one of the at least two ligands is contacted with the macromolecule bound to the sensor surface.

5. The method according to claim 4, wherein steps c) and d), and optionally also a), are repeated one or more times with the ligands in an altered sequence.

6. The method according to claim 1, further comprising contacting the macromolecule with the at least one ligand and the at least two additional ligands at least one more time in an altered sequence.

7. The method according to claim 1, wherein a plurality of ligands is used, and the method is performed repeatedly with a subset of the ligands.

8. The method according to claim 1, wherein said change in the physico-chemical properties of the sensor surface is a change in the refractive index of the sensor surface.

9. The method according to claim 1, wherein the macromolecule is a protein.

10. The method according to claim 1, wherein the ligands comprise antibodies.

11. The method of claim 1, further comprising structurally modifying the macromolecule and studying influences of the structural modification on ligand binding properties of the macromolecule.

12. The method of claim 1, wherein the macromolecule is from a patient and said discriminating between and mapping epitopes of the macromolecule is used for diagnostic or prognostic clinical purposes.

13. The method of claim 12, which comprises characterizing the macromolecule with a subset of ligands defining different possible epitopes on the macromolecule, the presence or absence, respectively, of one or more of said epitopes on the macromolecule being indicative of a pathological condition.

14. The method according to claim 12, which comprises analyzing immune response by first contacting a macromolecule having defined epitopes with a patient sample, and then determining the possible blocking of one or more of the epitopes by macromolecules present in the sample by contacting the macromolecule having defined epitopes with a subset of ligands binding to said epitopes.