首页> 外文期刊>Hybridoma and hybridomics >Production of functional ScFv inhibiting Streptococcus mutans glucosyltransferase activity from a hybridoma P126.
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Production of functional ScFv inhibiting Streptococcus mutans glucosyltransferase activity from a hybridoma P126.

机译:从杂交瘤P126产生功能性ScFv抑制变形链球菌葡糖基转移酶活性。

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摘要

Streptococcus mutans has been considered the principal etiologic agent of dental caries in humans. The glucosyltransferase-I (GTF-I), which synthesized adhesive water-insoluble glucans from sucrose, has been demonstrated to be an important cariogenic property. Water-insoluble glucans (WIG) synthesized by S. mutans GTF-I can mediate sucrose-enhanced colonization on tooth surfaces and form dental plaque. It has been suggested that inhibition of WIG synthesis decreases bacterial colonization and cariogenicity. Indeed, the use of GTF enzymes as a vaccine antigen resulted in protection from experimental dental caries in rodents. However, it is preferable to eliminate unwanted immune response during active immunization of humans. To prevent this incidence, we attempted to produce the single-chain variable fragment (ScFv) antibody against GTF-I to develop passive immunization for dental caries. Hybridomas producing monoclonal antibody (MAb) that inhibited WIG synthesis by GTF-I have been constructed. Using mRNA from an IgG1 hybridoma P126, cDNAs encoding the variable fragments of the L and H chains of IgG1 from the hybridoma P126 were cloned by RT-PCR-based techniques and then transformed into an Escherichia coli expression system. The purified ScFv antibody recognized the recombinant (r) GTF-I proteins and was capable of inhibiting the WIG synthesis of rGTF-I.
机译:变形链球菌被认为是人类龋齿的主要病原体。由蔗糖合成粘性的水不溶性葡聚糖的葡糖基转移酶-I(GTF-1)已被证明是重要的致龋性。由变形链球菌GTF-1合成的水不溶性葡聚糖(WIG)可介导蔗糖增强的在牙齿表面上的定植并形成牙菌斑。已经提出,抑制WIG合成会降低细菌定植和致龋性。确实,使用GTF酶作为疫苗抗原可以保护啮齿动物免受实验性龋齿的侵害。但是,优选在人的主动免疫期间消除不需要的免疫应答。为了防止这种情况的发生,我们尝试生产抗GTF-1的单链可变片段(ScFv)抗体,以开发龋齿的被动免疫。已经构建了产生单克隆抗体(MAb)的杂交瘤,该单克隆抗体抑制了GTF-1的WIG合成。使用来自IgG1杂交瘤P126的mRNA,通过基于RT-PCR的技术克隆编码来自杂交瘤P126的IgG1的L和H链的可变片段的cDNA,然后将其转化到大肠杆菌表达系统中。纯化的ScFv抗体识别重组(r)GTF-1蛋白,并能够抑制rGTF-1的WIG合成。

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