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人血小板生成素受体复合物的结构模型。

A structural model of the human thrombopoietin receptor complex.

作者信息

Deane C M, Kroemer R T, Richards W G

机构信息

Physical and Theoretical Chemistry Laboratory, University of Oxford, United Kingdom.

出版信息

J Mol Graph Model. 1997 Jun;15(3):170-8, 185-8. doi: 10.1016/s1093-3263(97)00102-2.

Abstract

Thrombopoietin (TPO) is a glycoprotein hormone that regulates red blood cell production. Presented here is a modeling study of the extracellular region of the human thrombopoietin receptor complex, in particular the TPO-receptor interface. The models were developed from structural homology to other cytokines and their receptors. Experimental evidence suggests that the receptor is homodimeric and it was modeled accordingly. Key interactions are shown that correlate with previous cytokine receptor complexes, and the pattern of cysteine bonding (Cys7-Cys151 and Cys29-Cys85) agrees with that experimentally determined for thrombopoietin. These models pave the way for possible mutagenesis experimentation and the design of (ant)agonists.

摘要

血小板生成素(TPO)是一种调节红细胞生成的糖蛋白激素。本文展示了一项关于人血小板生成素受体复合物细胞外区域,特别是TPO-受体界面的建模研究。这些模型是基于与其他细胞因子及其受体的结构同源性构建的。实验证据表明该受体是同二聚体,并据此进行了建模。文中展示了与先前细胞因子受体复合物相关的关键相互作用,并且半胱氨酸键合模式(Cys7-Cys151和Cys29-Cys85)与血小板生成素实验测定的结果一致。这些模型为可能的诱变实验以及(抗)拮抗剂的设计铺平了道路。

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