Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Nano antibody for specifically identifying histidine label

A histidine tag, nanobody technology, applied in nanotechnology, nanotechnology, nanotechnology for materials and surface science, etc., can solve the complex, cumbersome development and production process of monoclonal antibody, and limited sources of polyclonal antibody And other issues

Inactive Publication Date: 2016-10-26
NANCHANG UNIV
View PDF2 Cites 10 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] At present, there are monoclonal or polyclonal antibodies against the His tag on the market for detection, but the development and production process of monoclonal antibodies is extremely cumbersome and complicated, and the sources of polyclonal antibodies are limited

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
  • Nano antibody for specifically identifying histidine label
  • Nano antibody for specifically identifying histidine label
  • Nano antibody for specifically identifying histidine label

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0022] Construction of an immune library of anti-His tag single domain heavy chain antibody (that is, single domain heavy chain antibody against His tag)

[0023] The 6×His tag was covalently coupled to bovine serum albumin (BSA) to obtain 6×His artificial antigen 6×His-BSA. After emulsifying 300 μg of 6×His-BSA with Freund’s complete adjuvant, Alpacas (Lamapacos) were immunized by subcutaneous multipoint injection. For booster immunization, 150 μg of 6×His-BSA was emulsified with Freund’s incomplete adjuvant at intervals of 2 weeks. Blood was collected from vein 7 days after each immunization, and the serum titer was determined by indirect ELISA method. The sample with the highest serum titer was selected to separate lymphocytes. cells, RNA was extracted.

[0024] The extraction of RNA was carried out according to the instruction manual of RNAiso reagent from TAKARA company. Using RNA as a template and oligo dT as a primer, the first strand of cDNA was synthesized according...

Embodiment 2

[0033] Panning and Identification of Anti-His Tag Single Domain Heavy Chain Antibody

[0034]The single domain heavy chain antibody against His tag was panned from the anti-His tag single domain heavy chain antibody immune library obtained in Example 1 by solid-phase affinity panning. 6×His was covalently coupled to ovalbumin (OVA) to obtain artificial antigen 6×His-OVA. Add 100 μL of artificial antigen 6×His-OVA diluted with PBS to each well, and coat overnight at 4°C. The coating concentration of each round of panning is 100, 75, and 50 μg / mL; suck out the coating solution, and wash the plate with PBS for 3 Add 300 μL 3% skim milk (in PBS) to each well, block for 2 hours at 37°C; wash the plate 6 times with PBS, add 100 μL phage antibody library (containing about 2×10 11 CFU), 37°C, incubate for 1.5 h; aspirate unbound phage, wash the plate with PBST (containing 0.5% Tween-20) 5 times (increase 5 times for each round), and then wash the plate with PBS for 10 times (the numb...

Embodiment 3

[0043] Scale production of anti-His tag single domain heavy chain antibody

[0044] Acquisition of the DNA fragment encoding the anti-His tag single domain heavy chain antibody: 1. Using restriction endonuclease SfiI / NotI, double digestion of phagemid pHEN-anti-His tag single domain heavy chain antibody gene, agarose gel electrophoresis Recover the anti-His tag single domain heavy chain antibody gene; 2. Directly send the anti-His tag single domain heavy chain antibody coding sequence to a biotechnology service company for chemical synthesis; 3. Design specific primers and use PCR technology from alpaca (Lama pacos ) was amplified from a cDNA library from the source.

[0045] The obtained anti-His tag single domain heavy chain antibody gene fragment was cloned into the expression vector pET25-flag (the His tag carried by the vector itself has been replaced with the Flag tag: DYKDDDDK), identified by PCR and enzyme digestion, and the anti-His tag single E. coli expression plas...

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 belongs to the field of genetic engineering and particularly relates to a single-domain heavy chain antibody specific to a histidine label, having an amino acid sequence shown as in SEQ ID NO: 1 and applicable to the fields such as immunodetection and antigen enrichment and purification. The amino acid sequence provided herein may function as a precursor, and by modifying through random or fixed-point mutation technology, it is possible to obtain a mutant with better properties (affinity, specificity, stability and the like), and the mutant is useful to develop proteins or polypeptides applied to medicine, industry and agriculture.

Description

technical field [0001] The present invention relates to single domain heavy chain antibody technology (also known as nanobody technology), and genetic engineering antibody technology, especially single domain heavy chain antibody or polypeptide for histidine tag. technical background [0002] Histidine (His) tag, usually composed of 6 and histidine, is also called polyhistidine tag, 6×His tag or hexa histidine tag. Histidine tags are often fused to the C-terminal or N-terminal of the target protein to facilitate the purification and detection of the target protein. Histidine residues can specifically bind to several types of immobilized ions (such as nickel, cobalt, and copper) under certain buffer conditions, and then elute from the stationary phase by changing the buffer conditions, thereby achieving purification containing His-tagged target protein. [0003] His tag is one of the most commonly used protein tags. By detecting the His tag, the status of the target protein...

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
Patent Type & Authority Applications(China)
IPC IPC(8): C07K16/00C07K1/22C12N15/13G01N33/53B01J20/24B01J20/281B01J20/30B01D15/38B82Y30/00
CPCC07K16/005B01D15/3804B01J20/24B01J20/281B82Y30/00C07K2317/565C07K2317/567C07K2317/569G01N33/53
Inventor 吴红静涂追付金衡许杨
Owner NANCHANG UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

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

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com