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首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Interaction of the red pigment-concentrating hormone of the crustacean Daphnia pulex, with its cognate receptor, Dappu-RPCHR: A nuclear magnetic resonance and modeling study
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Interaction of the red pigment-concentrating hormone of the crustacean Daphnia pulex, with its cognate receptor, Dappu-RPCHR: A nuclear magnetic resonance and modeling study

机译:甲壳动物的红色颜料浓缩激素的相互作用 Daphnia pulex ,具有其同源受体,Dappu-RPCHR:核磁共振和建模研究

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AbstractThe primary sequence of the red pigment-concentrating hormone (RPCH) receptor of the water flea,Daphnia pulex,was used in homology modeling to construct the first 3D model of a crustacean G-protein coupled receptor, Dappu-RPCHR. This receptor was found to belong to the class A subfamily of GPCRs with a disulfide bridge between Cys72and Cys150and an ionic lock between Arg97and Thr224and Thr220. NMR restrained molecular dynamics was used to determine the structure of an agonist, Dappu-RPCH, in a membrane-mimicking environment. The agonist was found to be flexible but has two main conformations in solution, both having β-turns. Docking of the predominant structure was used to find a binding pocket on the receptor. The pocket’s spatial location was similar to that of the AKH receptor ofAnopheles gambiae. The binding affinity was ?69kcalmol?1with the N-terminus of Dappu-RPCH inserted between helices 4 and 6, and the C-terminus interacting with extra-cellular loop, ECL2. Upon binding, H-bonding to the peptide may activate the receptor. This development of the first Dappu-RPCH/Dappu-RPCHR model could be useful for understanding ligand-receptor interactions in crustaceans.]]>
机译:<![cdata [ 抽象 水跳蚤的红色颜料浓缩激素(RpCh)受体的主要序列, daphnia pulex,用于同源模型,构建甲壳类族酰蛋白偶联受体,Dappu-RPCHR的第一3D模型。发现该受体属于Cys 72之间的二硫化物桥(Cys 和cys 150 < / ce:sup>和arg 97 和thr 224 和thr < CE:sup =“post”> 220 。 NMR限制分子动力学用于确定膜模拟环境中的激动剂Dappu-RPCH的结构。发现激动剂是灵活的,但在溶液中具有两个主要构象,两者都具有β-转。使用主要结构的对接用于在受体上找到粘合口袋。口袋的空间位置类似于 anopheles gambiae 的Akh受体。结合亲和力是α69kcalmol 1 ce> sup>,用拔螺旋4和6之间插入的dappu-rpch的n-末端,以及与细胞间相互作用的c-末端循环,ECL2。结合后,对肽的H键可活化受体。该第一个Dappu-RPCH / Dappu-RPCHR模型的发展可用于理解甲壳类动物中的配体受体相互作用。 ]]>

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