Fab segment of human-source human immunodeficiency virus (HIV) antibody and coded gene and application thereof
A technology that encodes genes and antibodies, used in applications, antibodies, gene therapy, etc.
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Embodiment 1
[0043] Example 1 is the screening and preparation method of HY498; Example 2 is the neutralizing activity of HY498 against HIV; Examples 3-5 are the reactivity of HY498; Example 6 is the screening and epitope analysis of HY498 epitope mimetic peptides.
[0044] Example 1, Preparation of Fab Fragment of Human Anti-HIV Antibody
[0045] 1. Obtaining the gene sequence and amino acid sequence of the Fab fragment of the human anti-HIV antibody
[0046] 1. Construction of phage antibody library
[0047]The database construction technology mainly refers to the method introduced by Barbas et al. (Carbos F.Barbas III, Dennis R.Burton, Jamie K.Scott, Gregg J.Siverman.Phage Display-A Laboratory Manual.Cold Spring Harbor Laboratory Press.New York), Such as primer design and PCR amplification of antibody gene, preparation of phage expression vector, etc. Firstly, the PCR amplification of the human IgG Fab segment gene was carried out. The steps are: use lymphocyte separation fluid to is...
Embodiment 2
[0055] Example 2, Expression and Purification of Fab Fragment of Human Anti-HIV Antibody
[0056] Transform the recombinant vector pComb3XSS-Fab containing the coding gene of the Fd fragment of HY498 shown in Sequence 2 and the light chain coding gene of HY498 shown in Sequence 1 obtained from the above screening into Escherichia coli TOP10F' competent cells, and pick a single colony Add to 500ml containing 20mM MgCl 2 and 50 μg / ml ampicillin in SB medium at 37°C at 250rpm for 5-8 hours (OD 600 =1), add 1ml 0.5M IPTG, shake at 37°C 250rpm for 16 hours, freeze-thaw bacteria at -80°C, add 25μl polymyxin B solution, shake well on ice with 0.5μl nuclease for 1 hour, centrifuge at 10000 rpm for 30 Minutes, the supernatant was purified with Ni-NTA Superflow N column or protein G column (according to the method provided in the manual). The Fab fragment (HY498) of the purified human anti-HIV antibody was obtained.
Embodiment 3
[0057] Example 3, HY498 neutralizing activity detection of HIV
[0058] The antiviral activity of Fab fragments of human anti-HIV antibodies was evaluated by HIV pseudovirus infection system. The specific steps are, the plasmid pcDNA3.1-ENV expressing the ENV protein of HIV strain SF162 or HXB2 and the backbone plasmid pSG3 ΔENV (Express all proteins in the HIV genome except ENV), transfect 293T cells at a mass ratio of 1:2, and set pSG3ΔENV control at the same time, that is, only transfect the same amount of pSG3 ΔENV . At 37°C, 5% CO 2After incubating in the cell incubator for 6 hrs, the plasmid entered the cells, then changed the medium, continued to incubate in the cell incubator for 48 hr, and the pseudovirus was secreted into the supernatant. Use a pipette to suck out the supernatant in the cell culture flask or plate as much as possible, filter through a 0.45 μm filter or centrifuge at 1000g for 10 minutes to get the supernatant, add FBS to it to make the final conce...
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