Graduate School of Science and Engineering, Saitama University, 255 Shimo-Okubo, Sakura-ku, Saitama 338-8570, Japan.
School of Environmental and Chemical Engineering, Shanghai University, 99 Shangdalu, Baoshan District, Shanghai 200444, China.
Int J Environ Res Public Health. 2022 Aug 31;19(17):10881. doi: 10.3390/ijerph191710881.
House dust mite (HDM) is a globally ubiquitous domestic cause of allergic diseases. There is a pressing demand to discover efficient, harmless, and eco-friendly natural extracts to inhibit HDM allergens that are more likely to trigger allergies and challenging to be prevented entirely. This study, therefore, is aimed at assessing the inhibition of the allergenicity of major HDM allergen Der f 2 by todomatsu oil extracted from residues of . The inhibition was investigated experimentally (using enzyme-linked immunosorbent assay (ELISA), surface plasmon resonance (SPR), and sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE)) and in silico using molecular docking. The results showed that todomatsu oil inhibits the allergenicity of Der f 2 by reducing its amount instead of the IgG binding capacity of a single protein. Moreover, the compounds in todomatsu oil bind to Der f 2 via alkyl hydrophobic interactions. Notably, most compounds interact with the hydrophobic amino acids of Der f 2, and seven substances interact with CYS27. Contrarily, the principal compounds fail to attach to the amino acids forming the IgG epitope in Der f 2. Interestingly, chemical components with the lowest relative percentages in todomatsu oil show high-affinity values on Der f 2, especially β-maaliene (-8.0 kcal/mol). In conclusion, todomatsu oil has been proven in vitro as a potential effective public health strategy to inhibit the allergenicity of Der f 2.
屋尘螨(HDM)是一种在全球范围内普遍存在的引起过敏疾病的室内过敏原。因此,迫切需要发现高效、无害且环保的天然提取物来抑制 HDM 过敏原,这些过敏原更有可能引发过敏,而且很难完全预防。本研究旨在评估从 残留物中提取的柏木油对主要 HDM 过敏原 Der f 2 的变应原性抑制作用。通过实验(酶联免疫吸附测定(ELISA)、表面等离子体共振(SPR)和十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE))和计算分子对接来研究抑制作用。结果表明,柏木油通过减少 Der f 2 的含量而不是单个蛋白质的 IgG 结合能力来抑制其变应原性。此外,柏木油中的化合物通过烷基疏水相互作用与 Der f 2 结合。值得注意的是,大多数化合物与 Der f 2 的疏水性氨基酸相互作用,有七种物质与 CYS27 相互作用。相反,主要化合物不能与 Der f 2 中形成 IgG 表位的氨基酸结合。有趣的是,柏木油中相对百分比最低的化学物质在 Der f 2 上表现出高亲和力值,特别是 β-maaliene(-8.0 kcal/mol)。总之,柏木油已在体外被证明是一种潜在有效的公共卫生策略,可以抑制 Der f 2 的变应原性。