Song Yanyi, Jian Shuyi, Teng Junlin, Zheng Pengli, Zhang Zhe
State Key Laboratory of Membrane Biology, Peking University-Tsinghua University-National Institute of Biological Sciences Joint Graduate Program, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, China.
MOE Key Laboratory of Cell Proliferation and Differentiation, School of Life Sciences, Peking University, Beijing, China.
Nat Commun. 2025 Jan 3;16(1):132. doi: 10.1038/s41467-024-55396-3.
Planar cell polarity (PCP) is an evolutionarily conserved process for development and morphogenesis in metazoans. The well-organized polarity pattern in cells is established by the asymmetric distribution of two core protein complexes on opposite sides of the cell membrane. The Van Gogh-like (VANGL)-PRICKLE (PK) pair is one of these two key regulators; however, their structural information and detailed functions have been unclear. Here, we present five cryo-electron microscopy structures of human VANGL1, VANGL2, and their complexes with PK1 at resolutions of 2.2-3.0 Å. Through biochemical and cell imaging experiments, we decipher the molecular details of the VANGL-PK interaction. Furthermore, we reveal that PK1 can target VANGL-containing intracellular vesicles to the peripheral cell membrane. These findings provide a solid foundation to understand the explicit interaction between VANGL and PK while opening new avenues for subsequent studies of the PCP pathway.
平面细胞极性(PCP)是后生动物发育和形态发生过程中一个进化上保守的过程。细胞中组织良好的极性模式是由两种核心蛋白复合物在细胞膜两侧的不对称分布所建立的。类梵高(VANGL)-刺(PK)对是这两个关键调节因子之一;然而,它们的结构信息和详细功能尚不清楚。在这里,我们展示了人类VANGL1、VANGL2及其与PK1复合物的五个冷冻电子显微镜结构,分辨率为2.2-3.0埃。通过生化和细胞成像实验,我们破译了VANGL-PK相互作用的分子细节。此外,我们发现PK1可以将含有VANGL的细胞内囊泡靶向到外周细胞膜。这些发现为理解VANGL和PK之间的明确相互作用提供了坚实的基础,同时为随后对PCP途径的研究开辟了新的途径。