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 antibodie
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.
대표청구항▼
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-alkylguan
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.
연구과제 타임라인
LOADING...
LOADING...
LOADING...
LOADING...
LOADING...
이 특허에 인용된 특허 (17)
Felgner Philip L. (Rancho Santa Fe CA) Kumar Raj (San Diego CA) Basava Channa (San Diego CA) Border Richard C. (Poway CA) Hwang-Felgner Jiin-Yu (Rancho Santa Fe CA), Cationic lipids for intracellular delivery of biologically active molecules.
Daniel Jean-Claude (Fontenay/Sous/Bois FRX) Schuppiser Jean-Luc (Claye-Souilly FRX) Tricot ; deceased Marc (late of Andilly FRX by Nicole Tricot ; heir), Magnetic polymer latex and preparation process.
Ugelstad John (Trondheim NOX) Ellingsen Turid (Trondheim NOX) Berge Arvid (Trondheim NOX) Helgee Oskar B. (Mlnlycke SEX), Magnetic polymer particles and process for the preparation thereof.
Charmot Dominique (Paris FRX) Vidil Christine (Paris FRX), Magnetizable composite microspheres of hydrophobic crosslinked polymer, process for preparing them and their application.
Ugelstad John (Trondheim NOX) Ellingsen Turid (Trondheim NOX) Berge Arvid (Trondheim NOX) Helgee Oskar B. (Mnlycke SEX), Process for preparing magnetic polymer particles.
※ AI-Helper는 부적절한 답변을 할 수 있습니다.