Multiplex immuno screening assay

Patent metadata

Field	Value
Publication number	US-9638692-B2
Application number	US-201213883339-A
Country	US
Kind code	B2
Filing date	Dec 10, 2012
Priority date	Dec 9, 2011
Publication date	May 2, 2017
Grant date	May 2, 2017

Abstract

The present invention provides kits and assay methods for the early detection of pathogens, precise identification of the etiologic agent, and improved disease surveillance. More specifically, the present invention discloses an immunoassay leading to the rapid and simultaneous detection of antibodies to a wide range of infectious pathogens in biological fluids of infected patients. This immunoassay involves the covalent and oriented coupling of fusion proteins comprising an AGT enzyme and a viral antigen on an identifiable solid support (e.g. fluorescent microspheres), said support being previously coated with an AGT substrate. This coupling is mediated by the irreversible reaction of the AGT enzyme on its substrate. The thus obtained antigen-coupled microspheres show enhanced capture of specific antibodies as compared to antigen-coupled microspheres produced by standard amine coupling procedures. The methods of the invention possess the ability to multiplex, minimize the amount of biological sample, and have enhanced sensitivity and specificity toward target antibodies as compared with classical ELISA or Radio-Immunoprecipitation assays.

First claim

The invention claimed is:

1. A method for detecting at least two target antibodies in a biological sample comprising:
(a) contacting said biological sample with at least one first solid support bound to a 6-alkylguanine-DNA-alkyltransferase (AGT) substrate covalently coupled to a first fusion protein comprising a 6-alkylguanine-DNA-alkyltransferase (AGT) polypeptide comprising SEQ ID NO:2 having a O6-alkylguanine-DNA alkyltransferase activity and a first epitope that is recognized by a first target antibody;
(b) contacting said biological sample with at least one second solid support bound to a 6-alkylguanine-DNA-alkyltransferase (AGT) substrate covalently coupled to a second fusion protein comprising a 6-alkylguanine-DNA-alkyltransferase (AGT) polypeptide having a O6-alkylguanine-DNA alkyltransferase activity and a second epitope that is recognized by a second target antibody, but not by said first target antibody; and
(c) detecting the presence or absence of the two target antibodies by detecting the binding or lack of binding of the two target antibodies to the two fusion proteins.

2. The method of claim 1 , wherein each of said solid supports is covalently coupled to said substrate of 6-alkylguanine-DNA-alkyltransferase (AGT) polypeptide.

3. The method of claim 2 , wherein each of the said solid supports is a magnetic microparticle internally labeled with a fluorescent dye.

4. The method of claim 3 , wherein said biological sample is selected from the group consisting of whole blood, serum, plasma, urine, seminal fluid, cerebrospinal fluid and saliva.

5. The method of claim 1 , wherein each of said solid supports is selected from the group consisting of test tubes, microtiter wells, sheets, beads, chips, and microparticles.

6. The method of claim 1 , wherein each of the said solid supports is magnetic.

7. The method of claim 1 , wherein each of the said solid supports is a microparticle.

8. The method of claim 1 , wherein each of said solid supports is labeled with a label selected from the group consisting of a fluorochrome, a chromophore, a radioisotope, and a mass tag.

9. The method of claim 1 , wherein each of the said solid supports is a microparticle internally labeled with a fluorescent dye with magnetite encapsulated in a functional polymer outer coat containing surface carboxyl groups for covalent coupling of ligands.

10. The method of claim 1 , comprising contacting said biological sample with at least 10 differently coupled-solid supports.

11. The method of claim 1 , further comprising detecting the presence or absence of the two target antibodies with secondary antibodies recognizing the constant part of the target antibodies.

12. The method of claim 1 , wherein said first or second epitope is selected from the group consisting of the amino acid sequences encoded by: SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:6, SEQ ID NO:7, SEQ ID NO:8, SEQ ID NO:9, SEQ ID NO:10, SEQ ID NO:11, SEQ ID NO:12, SEQ ID NO:13, SEQ ID NO:14, SEQ ID NO:54, SEQ ID NO:55, SEQ ID NO:56, SEQ ID NO:57, and SEQ ID NO:58.

13. The method of claim 1 , wherein said first and second fusion proteins that are coupled with said first and second solid supports are selected from the group consisting of: SEQ ID NO:21, SEQ ID NO:42, SEQ ID NO:49, SEQ ID NO:51, SEQ ID NO:53, SEQ ID NO:60, SEQ ID NO:62, SEQ ID NO:64, SEQ ID NO:66, SEQ ID NO:68, SEQ ID NO:70, SEQ ID NO:72, SEQ ID NO:74, SEQ ID NO:76, SEQ ID NO:78, SEQ ID NO:80, SEQ ID NO:82, SEQ ID NO:84, SEQ ID NO:86, SEQ ID NO:88, SEQ ID NO:90, SEQ ID NO:92, SEQ ID NO:94, SEQ ID NO:96, SEQ ID NO:98, SEQ ID NO:100, SEQ ID NO:102, SEQ ID NO:104, SEQ ID NO:109, SEQ ID NO:111, SEQ ID NO:113, SEQ ID NO:115, SEQ ID NO:117, SEQ ID NO:119, SEQ ID NO:121, SEQ ID NO:123, SEQ ID NO:125, SEQ ID NO:127, SEQ ID NO:129, SEQ ID NO:131, SEQ ID NO:133, SEQ ID NO:135, SEQ ID NO:137, SEQ ID NO:139, SEQ ID NO:141, SEQ ID NO:143, SEQ ID NO:145, SEQ ID NO:147, SEQ ID NO:149 and SEQ ID NO:151.

Assignees

• Pasteur Institut

Inventors

• Manuguerra Jean-Claude
• Vanhomwegen Jessica
• Despres Philippe
• Paulous Sylvie

Classifications

• G01N33/56983

  Viruses · CPC title

• G01N2333/185

  Flaviviruses or Group B arboviruses, e.g. yellow fever virus, japanese encephalitis, tick-borne encephalitis, dengue · CPC title

• G01N33/54353

  with ligand attached to the carrier via a chemical coupling agent (coatings G01N33/54393) · CPC title

• G01N33/6845

  Methods of identifying protein-protein interactions in protein mixtures · CPC title

• G01N33/564 Primary

  for pre-existing immune complex or autoimmune disease {, i.e. systemic lupus erythematosus, rheumatoid arthritis, multiple sclerosis, rheumatoid factors or complement components C1-C9} · CPC title