首页> 美国卫生研究院文献>PLoS Computational Biology >Relationships between Th1 or Th2 iNKT Cell Activity and Structures of CD1d-Antigen Complexes: Meta-analysis of CD1d-Glycolipids Dynamics Simulations
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Relationships between Th1 or Th2 iNKT Cell Activity and Structures of CD1d-Antigen Complexes: Meta-analysis of CD1d-Glycolipids Dynamics Simulations

机译:Th1或Th2 iNKT细胞活性与CD1d-抗原复合物结构之间的关系:CD1d-糖脂动力学模拟的荟萃分析

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摘要

A number of potentially bioactive molecules can be found in nature. In particular, marine organisms are a valuable source of bioactive compounds. The activity of an α-galactosylceramide was first discovered in 1993 via screening of a Japanese marine sponge (Agelas mauritanius). Very rapidly, a synthetic glycololipid analogue of this natural molecule was discovered, called KRN7000. Associated with the CD1d protein, this α-galactosylceramide >1 (KRN7000) interacts with the T-cell antigen receptor to form a ternary complex that yields T helper (Th) 1 and Th2 responses with opposing effects. In our work, we carried out molecular dynamics simulations (11.5 µs in total) involving eight different ligands (conducted in triplicate) in an effort to find out correlation at the molecular level, if any, between chemical modulation of >1 and the orientation of the known biological response, Th1 or Th2. Comparative investigations of human versus mouse and Th1 versus Th2 data have been carried out. A large set of analysis tools was employed including free energy landscapes. One major result is the identification of a specific conformational state of the sugar polar head, which could be correlated, in the present study, to the biological Th2 biased response. These theoretical tools provide a structural basis for predicting the very different dynamical behaviors of α-glycosphingolipids in CD1d and might aid in the future design of new analogues of >1.
机译:在自然界中可以发现许多潜在的生物活性分子。特别地,海洋生物是生物活性化合物的宝贵来源。 α-半乳糖苷神经酰胺的活性于1993年通过筛选日本海洋海绵(Agelas mauritanius)首次发现。很快,就发现了这种天然分子的合成糖脂类似物,称为KRN7000。该α-半乳糖基神经酰胺> 1 (KRN7000)与CD1d蛋白相关,与T细胞抗原受体相互作用,形成三元复合物,产生具有相反作用的T辅助(Th)1和Th2反应。在我们的工作中,我们进行了分子动力学模拟(总共11.5 µs),涉及八个不同的配体(一式三份进行),以发现> 1 的化学调制之间在分子水平上的相关性。以及已知的生物学反应Th1或Th2的方向。已对人与小鼠以及Th1与Th2数据进行了比较研究。使用了大量的分析工具,包括自由能景观。一个主要结果是鉴定了糖极头的特定构象状态,在本研究中,这可能与生物学的Th2偏倚反应有关。这些理论工具为预测CD1d中α-糖鞘脂的非常不同的动力学行为提供了结构基础,并可能有助于将来> 1 的新类似物的设计。

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