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Immunoaffinity material specifically adsorbing c-Myc label single domain heavy chain antibody

A single-domain heavy chain antibody and adsorption material technology, applied in the field of immunoaffinity adsorption materials, can solve the problems of reduced antibody activity and non-reusable use, and achieve the effects of easy acquisition, avoiding production methods, and reducing production costs

Inactive Publication Date: 2017-08-15
NANCHANG UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Since the monoclonal antibody or polyclonal antibody is composed of heavy chain and light chain, acid-base elution will inevitably lead to a decrease in antibody activity, so it cannot be reused

Method used

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  • Immunoaffinity material specifically adsorbing c-Myc label single domain heavy chain antibody
  • Immunoaffinity material specifically adsorbing c-Myc label single domain heavy chain antibody

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0022] Construction of an immune library of anti-c-Myc tag single domain heavy chain antibody (ie single domain heavy chain antibody against c-Myc tag)

[0023] The c-Myc tag was covalently coupled to bovine serum albumin (BSA) to obtain the c-Myc artificial antigen c-Myc-BSA. After emulsifying 300 μg of c-Myc-BSA with Freund's complete adjuvant, Alpacas (Lama pacos) were immunized by subcutaneous multipoint injection. For booster immunization, 150 μg c-Myc-BSA was emulsified with Freund's incomplete adjuvant at intervals of 2 weeks. Blood was collected from the 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 accor...

Embodiment 2

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

[0034] The single domain heavy chain antibody against c-Myc tag was panned from the anti-c-Myc tag single domain heavy chain antibody immune library obtained in Example 1 by solid phase affinity panning. Add 120 μL of Myc-GST fusion protein (the fusion protein of Myc tag and glutathione) diluted with PBS to each enzyme-labeled well, coat at 4°C overnight, and the coating concentration of each round of panning is 100 , 75, 50 μg / mL; aspirate the coating solution, wash the plate 5 times with PBS, add 300 μL 3% BSA-PBS to each well, block for 2 hours at 37°C; wash the plate 5 times with PBS, add 100 μL phage antibody library (containing about 1× 10 11 CFU), 37°C, incubate for 2.0 h; aspirate unbound phage, wash the plate with PBST (containing 0.5% Tween-20) for 3-5 times (increase 5 times for each round), and then wash the plate with PBS for 15-25 times; Use 100 μL eluent (glycine-hydrochlor...

Embodiment 3

[0044] Scale Production of Anti-c-Myc Tag Single Domain Heavy Chain Antibody

[0045] Obtaining the DNA fragment encoding the anti-c-Myc tag single-domain heavy-chain antibody: 1. Using restriction endonuclease SfiI / NotI, double-digest the phagemid pHEN-anti-c-Myc single-domain heavy-chain antibody gene, and agar Glycogel electrophoresis to recover the anti-c-Myc tag single domain heavy chain antibody gene; 2. Directly send the anti-c-Myc tag single domain heavy chain antibody coding sequence to a biotechnology service company for chemical synthesis; 3. Design specific primers, through PCR technology amplifies from a cDNA library derived from alpaca (Lama pacos).

[0046] The obtained anti-c-Myc tag single domain heavy chain antibody gene fragment was cloned into the expression vector pET25-flag (the c-Myc tag carried by the vector itself was replaced with the Flag tag: DYKDDDDK), identified by PCR and enzyme digestion, and constructed Complete the E. coli expression plasmid ...

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Abstract

The invention belongs to the field of genetic engineering and in particular relates to a single domain heavy chain antibody (also known as a nano antibody) specific to a c-Myc label, and the single domain heavy chain antibody has an amino acid sequence shown in SEQ ID NO.1. The amino acid sequence provided by the invention can be taken as a precursor, modification is carried out by virtue of a random or site-directed mutagenesis technology, a mutant with better properties (affinity, specificity, stability and the like) can be obtained, and the high-specificity nano antibody can serve as an immunoaffinity adsorption material specific to c-Myc and purify recombinant proteins containing the c-Myc label.

Description

technical field [0001] The invention relates to an immunoaffinity adsorption material based on a single-domain heavy chain antibody (also known as nanobody technology), especially an immunoaffinity adsorption material for c-Myc label. [0002] technical background [0003] The discovery of the c-Myc tagged protein originated in 1985 when Evan prepared a monoclonal antibody 9E10 against the human proto-oncogene product Myc protein. Later studies found that the epitope recognized by the antibody consists of 10 amino acid residues, and its sequence It is Glu-Gln-Lys-Leu-Ile-Ser-Glu-Glu-Asp-Leu, and these 10 amino acids can still maintain strong antigenic activity after fusion expression with other proteins, and can be recognized by corresponding antibodies without being affected by The effect of the protein framework. Therefore, the c-Myc tag system is widely used in the fields of immunological detection, cell imaging, affinity purification, and protein engineering. [0004] T...

Claims

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Application Information

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IPC IPC(8): B01J20/281B01J20/28B01J20/30C07K1/22
CPCB01J20/281B01J20/28009B01J20/28021B01J20/28054B01J2220/52B01J2220/58C07K1/22
Inventor 付金衡吴青松涂追许杨
Owner NANCHANG UNIV
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