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Molecular dynamics simulation studies and in vitro site directed mutagenesis of avian beta-defensin Apl_AvBD2

机译:分子动力学仿真研究和体外型观点定向诱变禽β - 防御素APL_AVBD2

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Background: Defensins comprise a group of antimicrobial peptides, widely recognized as important elements of the innate immune system in both animals and plants. Cationicity, rather than the secondary structure, is believed to be the major factor defining the antimicrobial activity of defensins. To test this hypothesis and to improve the activity of the newly identified avian (3-defensin Apl_AvBD2 by enhancing the cationicity, we performed in silico site directed mutagenesis, keeping the predicted secondary structure intact. Molecular dynamics (MD) simulation studies were done to predict the activity. Mutant proteins were made by in vitro site directed mutagenesis and recombinant protein expression, and tested for antimicrobial activity to confirm the results obtained in MD simulation analysis. Results: MD simulation revealed subtle, but critical, structural variations between the wild type Apl_AvBD2 and the more cationic in silico mutants, which were not detected in the initial structural prediction by homology modelling. The C-terminal cationic 'claw' region, important in antimicrobial activity, which was intact in the wild type, showed changes in shape and orientation in all the mutant peptides. Mutant peptides also showed increased solvent accessible surface area and more number of hydrogen bonds with the surrounding water molecules. In functional studies, the Escherichia coli expressed, purified recombinant mutant proteins showed total loss of antimicrobial activity compared to the wild typeprotein. Conclusion: The study revealed that cationicity alone is not the determining factor in the microbicidal activity of antimicrobial peptides. Factors affecting the molecular dynamics such as hydrophobicity, electrostatic interactions and the potential for oligomerization may also play fundamental roles. It points to the usefulness of MD simulation studies in successful engineering of antimicrobial peptides for improved activity and other desirable functions.
机译:背景:防御素包括一组抗微生物肽,广泛认识为动物和植物中的先天免疫系统的重要元素。据信,阳离子,而不是二级结构,是定义防御素的抗微生物活性的主要因素。为了测试这一假设并通过增强阳离子的新鉴定的禽(3-Defensin APL_AVBD2的活动,我们在硅网站定向诱变中进行,保持预测的二级结构完整。分子动力学(MD)模拟研究进行了预测该活性。通过体外位点定向诱变和重组蛋白表达制备突变蛋白,并测试抗微生物活性以确认在MD模拟分析中获得的结果。结果:MD仿真揭示了野生型APL_AVBD2之间的微妙,但批判性的结构变化并且在硅突变体中更阳离子,这些突变体在同源造型的初始结构预测中未检测到。C末端阳离子'爪区域,在野生类型中完整的抗微生物活性重要性,表现出形状和方向的变化在所有突变肽中。突变肽还显示出增加的溶剂可接近的表面积和更多与周围水分子的氢键数。在功能性研究中,纯化的重组突变体蛋白表达了大肠杆菌,与野生蛋白相比,纯化的重组突变体蛋白显示出抗微生物活性的总丧失。结论:该研究表明,单独的阳离子不是抗微生物肽的微生物活性的决定因素。影响疏水性,静电相互作用等分子动力学的因素也可能起到基本作用。它指出了MD模拟研究在成功工程中的抗微生物肽的工程,以改善活性和其他理想的功能。

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