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Anti-human β2 microglobulin single domain antibody and its preparation method and use

A β2 microglobulin and single-domain antibody technology, applied in the field of anti-β2 microglobulin antibodies, can solve problems such as increased sensitivity, high production costs, and impact on test results, so as to improve diagnosis and treatment, promote diagnosis and treatment, The effect of high specific binding capacity

Active Publication Date: 2016-08-31
CROWN MEDICAL TECH DALIAN CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The use of IgG in the field of β2 microglobulin detection has the following defects: (1) the larger molecular weight limits the immobilization density of antibodies on the surface of the matrix, and also increases the difficulty of directional immobilization of antibodies, which limits the improvement of the sensitivity of the above detection methods
(2) Monoclonal IgG is difficult to prepare in large quantities, and the production cost is high, while the binding ability of polyclonal IgG is unstable
(3) The Fc segment of IgG is easy to bind to the Fc receptor of non-target cells, which affects the detection results
Although the existing antibody ligand adsorbents are still in the research stage and there are no commercial products yet, this kind of adsorbents have shown good application prospects in the field of hemoperfusion

Method used

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  • Anti-human β2 microglobulin single domain antibody and its preparation method and use
  • Anti-human β2 microglobulin single domain antibody and its preparation method and use
  • Anti-human β2 microglobulin single domain antibody and its preparation method and use

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0037] Example 1 Screening of monoclonal phage antibodies

[0038] Using phage display technology to carry out multiple rounds of enrichment and screening of the alpaca phage antibody library, the purified β 2 Microglobulin has undergone four rounds of "adsorption-elution-amplification" enrichment screening for antigens, and the recovery rate of each round of screening shows an increasing trend, indicating that after screening, there is β 2 Microglobulin-specific phages were highly enriched.

[0039] The specific method is as follows:

[0040] 1. Establishment of alpaca phage antibody library

[0041] The names and sequences of the primers used are shown in Table 1, and the underlined part is the enzyme cutting site.

[0042] Table 1. Primer names and their sequences

[0043]

[0044]

[0045] (1) Separation of lymphocytes and isolation of total RNA

[0046] Take 100ml of peripheral blood from a 3-year-old female alpaca, put it into an anticoagulant tube, add an equ...

Embodiment 2

[0084] Example 2 Detection of monoclonal phage antibodies:

[0085] (1) Randomly pick 80 single bacterial clones from the TY-AG plate cultured overnight after the fourth round of screening, mix BLT5615 with phage preservation solution / lysate (1‰ to 0.1‰), and culture on a shaker at 37°C until After lysing and lysing the bacteria, immediately add NaCl to a concentration of 0.5M in the solution, centrifuge at 10000rpm for 10min, take the supernatant, and recover the phage liquid. ELISA method for detection: Antigen β 2 Microglobulin was coated on the microtiter plate (0.4 μg / well), and after blocking, 100 μl of monoclonal phage solution was added to each well, and incubated at 37° C. for 2 hours. After washing, 1:5000 HRP-labeled mouse anti-M13 antibody was added and incubated at 37°C for 1h. The positive control was the primary antibody (mouse anti-human β 2 Microglobulin), secondary antibody (goat anti-mouse IgG); negative control only added 2% MPBS. O-phenylenediamine was...

Embodiment 3

[0087] Example 3 DNA sequence determination of positive clones:

[0088] The phagemids of A and B positive clones were extracted respectively, and the sdAb DNA was sequenced by the dideoxy terminal termination method using sdAb DNA sequencing primers (upstream primers and downstream primers were from T7select cloning kit).

[0089] The nucleotide sequences of clones A and B were obtained, and the obtained sequences were compared with the single domain antibody variable region genes in Gene Bank using Blast software. The analysis results showed that the variable region genes of the obtained A and B clones were consistent with the SdAb antibody gene, the deduced amino acid sequence had a typical antibody variable region structure, and the protein sequence determined the start and end of the CDR according to the blast and Kabat codes parts. The amino acid composition and sequence of the complementarity determining regions (CDRs) are highly variable. The three CDRs together form...

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Abstract

The invention discloses a novel anti-human β2 microglobulin single-domain antibody and its preparation method and application. The present invention utilizes phage display technology to perform multiple rounds of screening on the alpaca phage antibody library to enrich phages with β2 microglobulin specificity, prepare antibodies by culturing the phages, identify positive clones, and obtain their corresponding coding sequences by sequencing. Then expressed in E. coli to obtain soluble antibody fragments. The antibody of the present invention has the amino acid sequence shown in SEQ ID NO.1 or SEQ ID NO.10. The antibody provided by the invention has high binding ability to β2 microglobulin, can be used in the fields of blood purification and β2 microglobulin detection, and helps to promote and improve the diagnosis and treatment of diseases such as dialysis-related amyloidosis.

Description

technical field [0001] The present invention relates to an anti-β2 microglobulin antibody, in particular to a novel anti-β2 microglobulin specific single-domain antibody, the amino acid sequence and DNA coding sequence of its variable region, and a method for preparing the single-domain antibody and uses. Background technique [0002] β2 microglobulin is a small molecular globulin produced by lymphocytes, platelets, and polymorphonuclear leukocytes, with a molecular mass of 11.8 kDa. It is a single-chain polypeptide), and widely exists in plasma, urine, cerebrospinal fluid, saliva and colostrum, and the content is very low. In healthy people, β2 microglobulin is synthesized at a relatively stable rate, and the serum concentration of healthy people is relatively stable, generally 1.5-3mg / l (Tilman B, et.al, Massy beta2-microglobulin progress in uremic toxin research, Seminars indialysis200922 , 4, 378–380). The synthesis rate of β2 microglobulin in healthy people is about ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C07K16/18C12N15/13C12N15/70C12N1/21G01N33/68
Inventor 贾凌云暴晓博徐丽任军
Owner CROWN MEDICAL TECH DALIAN CO LTD
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