Constructing and expressing a recombinant protective antigen (PA) involves gene cloning protective antigen PA63 structural in DNA plasmid, and using DNA chimeras bearing a set of signal sequences targets protective antigen PA63 to subcellular locations
2024-03-30
专利权人SUKINDER P S (SUKI-Individual) ; HARSHIL K (HARS-Individual) ; KHANSAHAB H M S (KHAN-Individual) ; NILESHBHAI N (NILE-Individual) ; CHODAVADIYA C (CHOD-Individual) ; CHAUHAN D (CHAU-Individual) ; PAREKH V (PARE-Individual) ; SINGH C (SING-Individual)
申请日期2024-03-30
专利号IN202421026424-A
成果简介NOVELTY - Constructing and expressing a recombinant protective antigen (PA) involves: (a) gene cloning a protective antigen PA63 structural in a DNA plasmid; (b) using DNA chimeras bearing a set of signal sequences targets protective antigen PA63 to multiple subcellular locations, and expressing multiple forms of protease-cleaved PA63 fragment; (c) using an expressed recombinant protective antigen rPA63 protein to mediate and function as the receptor binding moiety of anthrax toxin complex for producing higher anti-protective antigen (PA) immunoglibulin (Ig)G1 antibody in a individual; (d) inducing a cellular and humoral immune response by expressed recombinant protective antigen rPA63 protein, where the DNA chimeras bearing a set of signal sequences includes lysosome-associated membrane protein 1 (LAMP1), tissue plasminogen activator (TPA) and ubiquitin. USE - Method for constructing and expressing a recombinant protective antigen (PA). ADVANTAGE - The recombinant protective antigen (PA) when administered produces multiple immune responses, where immune response include B and T-cell responses, Th-cell response, Cytotoxic T lymphocyte (CTL) response and α-(L)-threofuranosyl nucleic acid (TNA) response. The TNA titers to predict any correlation between the presence of TNA in the serum and protection against lethal challenge. The high end-point titers of IgG antibodies are maintained until 24 week by high avidity toxin neutralizing antibodies (TNA) and effective cellular adaptive immunity in the systemic compartment. DETAILED DESCRIPTION - Constructing and expressing a recombinant protective antigen (PA) involves: (a) gene cloning a protective antigen PA63 structural in a DNA plasmid; (b) using DNA chimeras bearing a set of signal sequences targets protective antigen PA63 to multiple subcellular locations, and expressing multiple forms of protease-cleaved PA63 fragment; (c) using an expressed recombinant protective antigen rPA63 protein to mediate and function as the receptor binding moiety of anthrax toxin complex for producing higher anti-protective antigen (PA) immunoglibulin (Ig)G1 antibody in a individual; (d) inducing a cellular and humoral immune response by expressed recombinant protective antigen rPA63 protein, where the DNA chimeras bearing a set of signal sequences includes lysosome-associated membrane protein 1 (LAMP1), tissue plasminogen activator (TPA) and ubiquitin, and the DNA plasmid include Protein Phosphatase 2 Phosphatase Activator-protective antigen-63 (pTPA-PA63), pPA63-Native, pLAMP1-PA63, pTPA-PA63-LAMP1, pUQ-PA63 and pTPA-P, and DNA plasmid encoding multiple forms of protease-cleaved PA63 fragment is expressed.
IPC 分类号C12N-001/21 ; C12N-015/70 ; C12N-015/80 ; C12P-021/02
国家印度
专业领域医药卫生
语种英语
成果类型专利
文献类型科技成果
条目标识符http://119.78.100.226:8889/handle/3KE4DYBR/17444
专题中国科学院新疆生态与地理研究所
作者单位
1.SUKINDER P S (SUKI-Individual)
2.HARSHIL K (HARS-Individual)
3.KHANSAHAB H M S (KHAN-Individual)
4.NILESHBHAI N (NILE-Individual)
5.CHODAVADIYA C (CHOD-Individual)
6.CHAUHAN D (CHAU-Individual)
7.PAREKH V (PARE-Individual)
8.SINGH C (SING-Individual)
推荐引用方式
GB/T 7714
SUKINDER P S,HARSHIL K,KHANSAHAB H M S,et al. Constructing and expressing a recombinant protective antigen (PA) involves gene cloning protective antigen PA63 structural in DNA plasmid, and using DNA chimeras bearing a set of signal sequences targets protective antigen PA63 to subcellular locations. IN202421026424-A[P]. 2024.
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