Split pleckstrin homology domain-mediated cytoplasmic-nuclear localization of PI3-kinase enhancer GTPase |
| |
Authors: | Yan Jing Wen Wenyu Chan Ling-Nga Zhang Mingjie |
| |
Institution: | Department of Biochemistry, Molecular Neuroscience Center, Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong, P.R. China |
| |
Abstract: | Cytoplasm-nucleus shuttling of phosphoinositol 3-kinase enhancer (PIKE) is known to correlate directly with its cellular functions. However, the molecular mechanism governing this shuttling is not known. In this work, we demonstrate that PIKE is a new member of split pleckstrin homology (PH) domain-containing proteins. The structure solved in this work reveals that the PIKE PH domain is split into halves by a positively charged nuclear localization sequence. The PIKE PH domain binds to the head groups of di- and triphosphoinositides with similar affinities. Lipid membrane binding of the PIKE PH domain is further enhanced by the positively charged nuclear localization sequence, which is juxtaposed to the phosphoinositide head group-binding pocket of the domain. We demonstrate that the cytoplasmic-nuclear shuttling of PIKE is dynamically regulated by the balancing actions of the lipid-binding property of both the split PH domain and the nuclear targeting function of its nuclear localization sequence. |
| |
Keywords: | PI3 phosphoinositol 3 PIKE PI3-kinase enhancer PH pleckstrin homology PIP phosphoinositide PLC phospholipase C NLS nuclear localization signal HSQC heteronuclear single quantum coherence NOE nuclear Overhauser enhancement PC phosphatidylcholine PS phosphatidylserine NOESY NOE spectroscopy |
本文献已被 ScienceDirect PubMed 等数据库收录! |