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Alpaca-derived nano antibody combined with SARS-CoV-2 RBD

A sars-cov-2rbd, antibody technology, applied in the direction of antibodies, antiviral agents, hybrid immunoglobulins, etc., to achieve the effect of high expression, high stability, and high affinity

Active Publication Date: 2022-03-29
UNIV OF SCI & TECH OF CHINA
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

We isolated and obtained 7 nanobody strains

Method used

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  • Alpaca-derived nano antibody combined with SARS-CoV-2 RBD
  • Alpaca-derived nano antibody combined with SARS-CoV-2 RBD
  • Alpaca-derived nano antibody combined with SARS-CoV-2 RBD

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0108] Example 1 Using SARS-CoV-2 RBD to Immunize Alpacas and Screen Nanobodies

[0109] 1) The purified SARS-CoV-2 RBD (QKV42562.1, aa 321-591) expressed in HEK293F cells (ATCC, CBP60437) was mixed with Freund's adjuvant, and the alpaca was subcutaneously injected with 500 μg / time for three times, Two 6-month-old female alpacas were vaccinated at intervals of 2 weeks.

[0110] 2) Two weeks after the third immunization, blood was collected from a vein and white blood cells in the blood were separated. Total RNA was extracted using the RNA extraction kit from Omegabiotek, and genomic DNA was removed using DNase. Using TAKARA's PrimeScript TM II 1st Strand cDNA Synthesis Kit performs reverse transcription on RNA and reverse transcribes RNA into cDNA.

[0111] 3) Preparation of nanobody phagemid library: use the alpaca VHH-specific primers we designed to amplify the coding gene fragment of VHH using the above cDNA as a template, and clone the amplified VHH sequence into a pha...

Embodiment 2

[0122] Example 2 Expression and purification of nanobodies and their Fc fusion proteins

[0123] 1) Design primers, fuse the N-terminus of the gene sequence of the Nanobody to IFNα protein signal peptide to guide secreted expression, fuse the C-terminus of the gene sequence of the Nanobody to human IgG1 Fc, and introduce a TEV restriction enzyme between them site, and then cloned into the mammalian expression vector pTT5. The constructed vector was transiently transfected into mammalian HEK293F cells with PEI, and the supernatant was collected after 3 days of culture. The fusion protein in the supernatant was purified by Protein A column, and SDS-PAGE electrophoresis was performed. The results are as follows: figure 2 As shown in A, from the supernatant, we obtained highly pure Nanobody Fc fusion protein.

[0124] 2) Digest the fusion protein with TEV, then flow the digested products through Protein G column and nickel column respectively, so as to remove the undigested prot...

Embodiment 3

[0125] Example 3 Characterization of the Nanobodies

[0126] 1) Use circular dichroism (CD) to characterize the stability of nanobodies: replace the nanobody solutions of the examples with PBS and dilute to QD 280nm It is about 0.6, and then detected by a circular dichroism spectrometer, the detection wavelength range is 280nm-180nm, and the temperature is from 20-95°C. Each assay was repeated twice. Prism software was used to process the data, and the variation of the spectral value at 205 nm with temperature was selected, and the Tm value was further fitted. The result is as image 3 As shown, the Tm values ​​of aRBD-2-Fc, aRBD-3-Fc, aRBD-5-Fc, aRBD-7-Fc, aRBD-41-Fc, aRBD-42-Fc and aRBD-54-Fc were 72.33 , 75.44, 73.37, 78.98, 71.26, 98.23 and 71.07°C.

[0127] 2) Preliminary characterization of the binding of the Nanobody Fc fusion protein to the extracellular segment of the SARS-CoV-2 spike protein (S1+S2) by non-competitive ELISA: the SARS-CoV-2 SARS-CoV-2 spike protei...

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Abstract

The present disclosure relates to an alpaca-derived antibody or an antigen-binding fragment thereof that binds to SARS-CoV-2 RBD, and in particular, to an alpaca-derived nanoantibody or an antigen-binding fragment thereof that can bind to a new coronavirus (SARS-CoV-2) receptor binding region (RBD) with high affinity, which can be used for the prevention, treatment and / or diagnosis of SARS-CoV-2 infection.

Description

technical field [0001] The invention belongs to the field of biotechnology, and in particular relates to an anti-SARS-CoV-2 RBD nanobody sequence for treatment and diagnosis. Background technique [0002] SARS-CoV-2 is a coronavirus, and the pneumonia it causes is called COVID-19. SARS-CoV-2 enters cells through the receptor binding domain (RBD) of its surface spike protein (spike) and angiotensin-converting enzyme 2 (ACE2) on the surface of epithelial cells, and completes the infection. [0003] Fully human antibodies isolated from recovered patients have been proven to have good antiviral effects, but these are traditional monoclonal antibodies consisting of 2 heavy chains and 2 light chains. It has the limitations of large molecular weight, complex production process, and difficult processing and transformation. [0004] In camelids, there is an antibody that naturally lacks light chains, that is, heavy chain antibodies. Its variable region is only composed of heavy cha...

Claims

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Application Information

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IPC IPC(8): C07K16/10C07K16/46C12N15/13G01N33/569G01N33/577A61K39/42A61P31/14
CPCC07K16/10G01N33/56983G01N33/577A61P31/14C07K2317/569C07K2317/565C07K2317/31C07K2317/92C07K2317/94C07K2317/76C07K2317/71C07K2317/52G01N2333/165A61K2039/505
Inventor 金腾川马欢曾威红
Owner UNIV OF SCI & TECH OF CHINA
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