首页    期刊浏览 2024年11月10日 星期日
登录注册

文章基本信息

  • 标题:Structural insights into the aPKC regulatory switch mechanism of the human cell polarity protein lethal giant larvae 2
  • 本地全文:下载
  • 作者:Lior Almagor ; Lior Almagor ; Ivan S. Ufimtsev
  • 期刊名称:Proceedings of the National Academy of Sciences
  • 印刷版ISSN:0027-8424
  • 电子版ISSN:1091-6490
  • 出版年度:2019
  • 卷号:116
  • 期号:22
  • 页码:10804-10812
  • DOI:10.1073/pnas.1821514116
  • 出版社:The National Academy of Sciences of the United States of America
  • 摘要:Metazoan cell polarity is controlled by a set of highly conserved proteins. Lethal giant larvae (Lgl) functions in apical-basal polarity through phosphorylation-dependent interactions with several other proteins as well as the plasma membrane. Phosphorylation of Lgl by atypical protein kinase C (aPKC), a component of the partitioning-defective (Par) complex in epithelial cells, excludes Lgl from the apical membrane, a crucial step in the establishment of epithelial cell polarity. We present the crystal structures of human Lgl2 in both its unphosphorylated and aPKC-phosphorylated states. Lgl2 adopts a double β-propeller structure that is unchanged by aPKC phosphorylation of an unstructured loop in its second β-propeller, ruling out models of phosphorylation-dependent conformational change. We demonstrate that phosphorylation controls the direct binding of purified Lgl2 to negative phospholipids in vitro. We also show that a coil–helix transition of this region that is promoted by phosphatidylinositol 4,5-bisphosphate (PIP2) is also phosphorylation-dependent, implying a highly effective phosphorylative switch for membrane association.
  • 关键词:Lgl ; cell polarity ; aPKC
国家哲学社会科学文献中心版权所有