Method and reagent for identifying antibody combined with mutant antigen

A mutation and antigen technology, applied in the field of immune detection, can solve the problems of high incidence

Pending Publication Date: 2022-08-05
GUANGDONG FAPON BIOTECH CO LTD
View PDF18 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although preliminary assessments show that the new coronavirus B.1.1.7 mutant strain does not increase disease severity, it can lead to higher morbidity, resulting in more hospitalizations and deaths

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Method and reagent for identifying antibody combined with mutant antigen
  • Method and reagent for identifying antibody combined with mutant antigen
  • Method and reagent for identifying antibody combined with mutant antigen

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0047] Example 1 Identification of mutants by colloidal gold platform

[0048] The amino acid sequence of H83 antigen is shown in SEQ ID NO: 1, the amino acid sequence of H84 antigen is shown in SEQ ID NO: 2, Ab13 antibody is an antibody that binds to a reference antigen (such as H83 antigen); Ab13 antibody, human ACE2 can be purchased from Feipeng Biological; other reagents and materials are commercially available.

[0049] 1. Mark

[0050] (1) Preparation of colloidal gold: adopt the traditional sodium citrate reduction method, first heat the chloroauric acid solution to boiling, quickly add a certain proportion of trisodium citrate solution, stir evenly, and wait until the color of the solution becomes wine red and no longer changes Stop heating, cool to room temperature to obtain a colloidal gold solution with a concentration of 4 / 10,000;

[0051] (2) Labeling: Add 0.2M K to the colloidal gold solution 2 CO 3 The solution is adjusted to pH 6.0-7.5;

[0052] (3) Centri...

Embodiment 2

[0069] Example 2 Identification of mutants by colored microspheres

[0070] 1. Mark

[0071] Take colored microspheres, after 300W ultrasound, add 0.1ml of latex particles to 0.9ml of 100mM MES, vortex and mix; centrifuge at 15000rmp for 15min, then remove the supernatant; add 1.0ml of 100mM MES for ultrasound, add appropriate amount of MES and NHS to activate the microspheres 10min; centrifuge at 15000rmp for 15min, then remove the supernatant; add 1.0ml of 100mM MES for ultrasound, add an appropriate amount of ACE2, vortex overnight at 37°C; centrifuge at 15,000rmp for 15min, remove the supernatant, add BSA to block, sonicate, and react at 37°C for 4h; 15000rmp for 15min Centrifuge, remove the supernatant, wash, and sonicate; centrifuge at 15,000 rmp for 15 min, remove the supernatant and resuspend; dilute the resuspended concentrate, spread it on glass cellulose membrane, and then put it in a freeze dryer for lyophilization (1-2h) Or put it in a drying room at 37°C to dry ...

Embodiment 3

[0091] Example 3 Identification of mutants by colored microspheres

[0092] The H85 antigen amino acid sequence is shown in SEQ ID NO:3. The H85 antigen was coated on the T1 detection line, the H83 antigen was coated on the T2 detection line, and other labeling, coating, and detection processes were the same as those in Example 2. When the test sample is negative serum, the color development of the T1 and T2 detection lines is equivalent; when the detection sample contains an antibody that binds to the non-mutated antigen including the 456-position phenylalanine of the spike protein, the color development of the T2 detection line is weakened. The color of the T1 detection line is stronger than that of the T2 by at least 2 color cards; when the test sample contains an antibody that binds to the 456-position alanine of the spike protein, the color development of the T1 detection line is weakened and almost disappears, and the color of the T2 detection line is developed Stronger...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention provides a method and a reagent for identifying an antibody combined with a mutant antigen. According to the method, the antibody combined with the mutant antigen can be rapidly and accurately identified, the detection timeliness is ensured, the detection efficiency is high, the cost is low, and the method has important significance for guiding prevention and control of the current-stage new crown epidemic situation with epidemic situation outbreak and rapid antigen variation.

Description

technical field [0001] The invention belongs to the field of immunodetection. More specifically, it relates to a method and reagent for identifying antibodies that bind to mutant antigens. Background technique [0002] Since the outbreak of the new coronavirus (SARS-CoV-2) in 2019, various types of mutant strains have been discovered one after another. On December 14, 2020, the United Kingdom first notified the WHO of the new coronavirus mutant strain and named it the new coronavirus B.1.1.7 mutant strain. Although preliminary assessments suggest that the 2019-nCoV B.1.1.7 mutant does not increase disease severity, it does lead to higher morbidity, hospitalizations and deaths. The new coronavirus B1.351 mutant strain was first discovered in South Africa in mid-October 2020. In addition to the same N501Y mutation on the S antigen as the new coronavirus B.1.1.7 mutant strain, this mutant strain also contains the same N501Y mutation. Mutations at two key sites in the S prote...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
IPC IPC(8): G01N33/569G01N33/558
CPCG01N33/56983G01N33/558G01N2333/165
Inventor 何志强李瑞净潘少丽袁水林覃丽芳
Owner GUANGDONG FAPON BIOTECH CO LTD
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap