Ni Tao, Harlos Karl, Gilbert Robert
Division of Structural Biology, Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford OX3 7BN, UK.
Division of Structural Biology, Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford OX3 7BN, UK
Open Biol. 2016 May;6(5). doi: 10.1098/rsob.160053. Epub 2016 May 4.
The vertebrate-specific proteins astrotactin-1 and 2 (ASTN-1 and ASTN-2) are integral membrane perforin-like proteins known to play critical roles in neurodevelopment, while ASTN-2 has been linked to the planar cell polarity pathway in hair cells. Genetic variations associated with them are linked to a variety of neurodevelopmental disorders and other neurological pathologies, including an advanced onset of Alzheimer's disease. Here we present the structure of the majority endosomal region of ASTN-2, showing it to consist of a unique combination of polypeptide folds: a perforin-like domain, a minimal epidermal growth factor-like module, a unique form of fibronectin type III domain and an annexin-like domain. The perforin-like domain differs from that of other members of the membrane attack complex-perforin (MACPF) protein family in ways that suggest ASTN-2 does not form pores. Structural and biophysical data show that ASTN-2 (but not ASTN-1) binds inositol triphosphates, suggesting a mechanism for membrane recognition or secondary messenger regulation of its activity. The annexin-like domain is closest in fold to repeat three of human annexin V and similarly binds calcium, and yet shares no sequence homology with it. Overall, our structure provides the first atomic-resolution description of a MACPF protein involved in development, while highlighting distinctive features of ASTN-2 responsible for its activity.
脊椎动物特有的astrotactin-1和2蛋白(ASTN-1和ASTN-2)是整合膜穿孔素样蛋白,已知在神经发育中起关键作用,而ASTN-2与毛细胞中的平面细胞极性通路有关。与它们相关的基因变异与多种神经发育障碍和其他神经病理学有关,包括阿尔茨海默病的早发。在这里,我们展示了ASTN-2大部分内体区域的结构,表明它由多种多肽折叠的独特组合构成:一个穿孔素样结构域、一个最小的表皮生长因子样模块、一种独特形式的纤连蛋白III型结构域和一个膜联蛋白样结构域。穿孔素样结构域与膜攻击复合物-穿孔素(MACPF)蛋白家族其他成员的结构域不同,这表明ASTN-2不会形成孔。结构和生物物理数据表明,ASTN-2(而非ASTN-1)结合肌醇三磷酸,这提示了一种其活性的膜识别或第二信使调节机制。膜联蛋白样结构域在折叠上与人类膜联蛋白V的第三个重复序列最接近,同样能结合钙,但与它没有序列同源性。总体而言,我们的结构首次提供了对参与发育的MACPF蛋白的原子分辨率描述,同时突出了ASTN-2负责其活性的独特特征。