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首页> 外文期刊>Angewandte Chemie >Potent Th2 Cytokine Bias of Natural Killer T Cell by CD1d Glycolipid Ligands: Anchoring Effect of Polar Groups in the Lipid Component
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Potent Th2 Cytokine Bias of Natural Killer T Cell by CD1d Glycolipid Ligands: Anchoring Effect of Polar Groups in the Lipid Component

机译:CD1D糖脂配体的天然杀伤T细胞有效的TH2细胞因子偏差:极性基团在脂质组分中的锚定效应

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摘要

Th2-biasing CD1d ligands are attractive potential candidates for adjuvants and therapeutic drugs. However, the number of potent ligands is limited, and their biasing mechanism remain unclear. Herein, a series of novel Th2-biasing CD1d glycolipid ligands, based on modification of their lipid part, have been identified. These have shown high binding affinities and efficient Th2 cytokine production. Importantly, the truncated acyl chain containing variants still retain their binding affinities and agonistic activities, which can be associated with an anchoring effect, that is, formation of a buried hydrogen bond between a polar group on the acyl chain and the CD1d lipid-binding pocket. The analysis indicated that the appearance rates of ligand-CD1d complexes on the cell surface were involved in Th2-biasing responses. The designed ligands, having the anchor in the shorter lipid part, are one of the most potent Th2-biasing ligands among the known ligands.
机译:Th2-偏置CD1D配体是辅助和治疗药物的有吸引力的潜在候选者。 然而,有效配体的数量是有限的,并且它们的偏置机制仍然不清楚。 这里,已经鉴定了一系列基于其脂质部分的改性的新型Th2-偏置CD1D糖脂配体。 这些已经显示出高结合亲和力和有效的Th2细胞因子产生。 重要的是,截断的酰基链含有变体仍然保持其结合亲和力和激动活性,其可以与锚定效果相关,即,在酰基链和CD1D脂质结合口袋之间的极性基团之间形成掩埋氢键 。 该分析表明,C细胞表面上的配体-CD1D复合物的外观率涉及Th2-偏置响应。 在较短的脂质部分中具有锚的设计配体是已知配体中最有效的Th2偏置配体之一。

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