Epitope mapping method

Patent metadata

Field	Value
Publication number	US-11217328-B2
Application number	US-201916388681-A
Country	US
Kind code	B2
Filing date	Apr 18, 2019
Priority date	Apr 19, 2018
Publication date	Jan 4, 2022
Grant date	Jan 4, 2022

Abstract

Provided herein are methods for mapping antibody binding to an immunogen, comprising: immunizing a subject with an immunogen and obtaining sera from the immunized subject at multiple time intervals following immunization, wherein the sera comprises antibodies that are used to form one or more immune complexes with the immunogen; isolating the one or more immune complexes formed by the serum derived antibodies bound to the immunogen; imaging, by electron microscopy, the one or more immune complexes in each of the time intervals, to obtain structural images formed between the immunogen and serum antibodies; determining, from the plurality of structural images, immunogen-antibody binding site for each of the immune complexes obtained at the plurality of time intervals; mapping immunogen-antibody binding by measuring differences in structural images obtained at different time intervals to determine immunogen-antibody binding over multiple time intervals.

First claim

What is claimed is:

1. A method of mapping antibody binding to an immunogen, the method comprising:
immunizing a subject with an immunogen;
obtaining sera from the immunized subject at multiple time intervals following immunization, wherein the sera comprises antibodies that bind to the immunogen;
isolating one or more antibodies from the sera;
contacting the one or more antibodies with the immunogen to form one or more immune complexes;
imaging, by electron microscopy, the one or more immune complexes from each of the multiple time intervals to obtain structural images;
determining, from a plurality of structural images, immunogen-antibody binding sites for each of the immune complexes obtained at the multiple time intervals;
mapping immunogen-antibody binding by comparing structural images obtained at the multiple time intervals to determine changes in immunogen-antibody binding over the multiple time intervals.

2. The method of claim 1 , wherein the serum antibodies comprise IgA (immunoglobin A), IgD (immunoglobin D), IgE (immunoglobin E), IgG (immunoglobin G), IgM (immunoglobin M), or combinations thereof.

3. The method of claim 1 , wherein the immune complex is purified by a chromatographic method prior to imaging.

4. The method of claim 3 , wherein the chromatographic method comprises size exclusion chromatography (SEC).

5. The method of claim 1 , wherein the electron microscopy comprises cyro electron microscopy or negative stain electron microscopy.

6. The method of claim 1 , wherein the immune complex is further analyzed by Mass Spectrometry, next generation sequencing (NGS), MS/MS and/or NGS-assisted MS/MS.

7. The method of claim 1 , wherein the subject is a human, mouse, humanized mouse, rat, or humanized rat.

8. The method of claim 1 , further comprising characterizing the antibody type and quantifying the antibody response to the immunogen.

9. The method of claim 1 , wherein the subject is a mammal.

10. The method of claim 1 , wherein the immunogen is a recombinant immunogen.

11. The method of claim 1 , wherein the immunogen is an epitope and/or an antigen.

12. The method of claim 1 , wherein the method maps the epitope binding sites on the antibody.

Assignees

• Scripps Research Inst

Inventors

• Hangartner Lars
• Ward Andrew
• Bianchi Matteo
• Turner Hannah

Classifications

• G01N33/6878 Primary

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• H01J37/26

  Electron or ion microscopes; Electron or ion diffraction tubes · CPC title

• H01J49/00

  Particle spectrometers or separator tubes · CPC title

• G16B25/20

  Polymerase chain reaction [PCR]; Primer or probe design; Probe optimisation · CPC title

• H01J49/0027

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