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解码 WW 结构域串联介导的组织生长和细胞极性中的靶标识别。

Decoding WW domain tandem-mediated target recognitions in tissue growth and cell polarity.

机构信息

Division of Life Science, State Key Laboratory of Molecular Neuroscience, Hong Kong University of Science and Technology, Hong Kong, China.

Department of Pharmacology and Moores Cancer Center, University of California, San Diego, La Jolla, United States.

出版信息

Elife. 2019 Sep 5;8:e49439. doi: 10.7554/eLife.49439.

Abstract

WW domain tandem-containing proteins such as KIBRA, YAP, and MAGI play critical roles in cell growth and polarity via binding to and positioning target proteins in specific subcellular regions. An immense disparity exists between promiscuity of WW domain-mediated target bindings and specific roles of WW domain proteins in cell growth regulation. Here, we discovered that WW domain tandems of KIBRA and MAGI, but not YAP, bind to specific target proteins with extremely high affinity and exquisite sequence specificity. Via systematic structural biology and biochemistry approaches, we decoded the target binding rules of WW domain tandems from cell growth regulatory proteins and uncovered a list of previously unknown WW tandem binding proteins including β-Dystroglycan, JCAD, and PTPN21. The WW tandem-mediated target recognition mechanisms elucidated here can guide functional studies of WW domain proteins in cell growth and polarity as well as in other cellular processes including neuronal synaptic signaling.

摘要

WW 结构域串联蛋白,如 KIBRA、YAP 和 MAGI,通过与特定亚细胞区域的靶蛋白结合并定位靶蛋白,在细胞生长和极性中发挥关键作用。WW 结构域介导的靶蛋白结合的随意性与 WW 结构域蛋白在细胞生长调节中的特定作用之间存在巨大差异。在这里,我们发现 KIBRA 和 MAGI 的 WW 结构域串联,而不是 YAP,与特定的靶蛋白具有极高的亲和力和极其精确的序列特异性结合。通过系统的结构生物学和生物化学方法,我们从细胞生长调节蛋白中解码了 WW 结构域串联的靶蛋白结合规则,并发现了一系列以前未知的 WW 串联结合蛋白,包括β-Dystroglycan、JCAD 和 PTPN21。这里阐明的 WW 串联介导的靶识别机制可以指导 WW 结构域蛋白在细胞生长和极性以及神经元突触信号等其他细胞过程中的功能研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37df/6744271/518a95e42114/elife-49439-fig1.jpg

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