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Inhibition of Fungal β-1,3-Glucan Synthase and Cell Growth by HM-1 Killer Toxin Single-Chain Anti-Idiotypic Antibodies

机译:HM-1杀伤毒素单链抗独特型抗体对真菌β-1,3-葡聚糖合酶的抑制和细胞生长

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摘要

Single-chain variable-fragment (scFv) anti-idiotypic antibodies of an HM-1 killer toxin (HM-1) from the yeast Williopsis saturnus var. mrakii IFO 0895 have been produced by recombinant DNA technology from the splenic lymphocytes of mice immunized by idiotypic vaccination with a neutralizing monoclonal antibody (nMAb-KT). The fungicidal activity of scFv anti-idiotypic antibodies against the isolates of four Candida species was assessed by MIC analysis. scFv antibodies were fungicidal at concentrations of 1.56 to 12.5 μg/ml in vitro against four Candida species. The scFv antibodies exerted a strong candidacidal activity in vitro, with 50% inhibitory concentration (IC50) values ranging from 7.3 × 10−8 to 16.0 × 10−8 M, and were neutralized by adsorption with nMAb-KT. Furthermore, all scFv antibodies effectively inhibited fungal β-1,3-glucan synthase activity in vitro, with IC50 values ranging from 2.0 × 10−8 to 22.7 × 10−8 M, values which almost coincide with the values that are inhibitory to the growth of fungal cells. Binding assays showed that the scFv antibodies specifically bind to nMAb-KT, and this binding pattern was confirmed by surface plasmon resonance analysis. The binding ability was further demonstrated by the competition observed between scFv antibodies and HM-1 to bind nMAb-KT. To the best of our knowledge, this is the first study to show that an antifungal anti-idiotypic antibody, in the form of recombinant scFv, potentially inhibits β-1,3-glucan synthase activity.
机译:酵母Williopsis saturnus var的HM-1杀手毒素(HM-1)的单链可变片段(scFv)抗独特型抗体。 mrakii IFO 0895已通过重组DNA技术从通过用中和性单克隆抗体(nMAb-KT)进行的独特型疫苗接种而免疫的小鼠的脾淋巴细胞中产生。通过MIC分析评估了scFv抗独特型抗体对四种念珠菌的分离物的杀真菌活性。 scFv抗体在体外对四种念珠菌具有杀菌作用,浓度为1.56至12.5μg/ ml。 scFv抗体在体外具有很强的候选酸活性,其50%抑制浓度(IC50)值范围为7.3×10-8至16.0×10-8 M,并通过nMAb-KT吸附进行中和。此外,所有scFv抗体在体外均能有效抑制真菌β-1,3-葡聚糖合酶活性,IC50值范围为2.0×10-8至22.7×10-8 M,该值几乎与抑制该酶的值相符。真菌细胞的生长。结合试验表明,scFv抗体与nMAb-KT特异性结合,这种结合方式通过表面等离振子共振分析得到证实。通过scFv抗体和HM-1之间竞争结合nMAb-KT的竞争进一步证明了结合能力。据我们所知,这是第一个显示重组scFv形式的抗真菌抗独特型抗体潜在抑制β-1,3-葡聚糖合酶活性的研究。

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