Antipenko Alexander, Himanen Juha-Pekka, van Leyen Klaus, Nardi-Dei Vincenzo, Lesniak Jacob, Barton William A, Rajashankar Kanagalaghatta R, Lu Min, Hoemme Claudia, Püschel Andreas W, Nikolov Dimitar B
Cellular Biochemistry and Biophysics Program, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021, USA.
Neuron. 2003 Aug 14;39(4):589-98. doi: 10.1016/s0896-6273(03)00502-6.
The semaphorins are a large group of extracellular proteins involved in a variety of processes during development, including neuronal migration and axon guidance. Their distinctive feature is a conserved 500 amino acid semaphorin domain, a ligand-receptor interaction module also present in plexins and scatter-factor receptors. We report the crystal structure of a secreted 65 kDa form of Semaphorin-3A (Sema3A), containing the full semaphorin domain. Unexpectedly, the semaphorin fold is a variation of the beta propeller topology. Analysis of the Sema3A structure and structure-based mutagenesis data identify the neuropilin binding site and suggest a potential plexin interaction site. Based on the structure, we present a model for the initiation of semaphorin signaling and discuss potential similarities with the signaling mechanisms of other beta propeller cell surface receptors, such as integrins and the LDL receptor.
信号素是一大类细胞外蛋白,参与发育过程中的多种进程,包括神经元迁移和轴突导向。它们的独特特征是一个保守的由500个氨基酸组成的信号素结构域,这是一种配体-受体相互作用模块,也存在于丛状蛋白和分散因子受体中。我们报道了一种分泌型65 kDa的信号素-3A(Sema3A)的晶体结构,其包含完整的信号素结构域。出乎意料的是,信号素折叠是β-螺旋桨拓扑结构的一种变体。对Sema3A结构及基于结构的诱变数据的分析确定了神经纤毛蛋白结合位点,并提示了一个潜在的丛状蛋白相互作用位点。基于该结构,我们提出了一个信号素信号传导起始的模型,并讨论了与其他β-螺旋桨细胞表面受体(如整合素和低密度脂蛋白受体)信号传导机制的潜在相似性。