Suppr超能文献

核蛋白转运途径。

Nuclear protein transport pathways.

作者信息

Köhler M, Haller H, Hartmann E

机构信息

Charité, Franz Volhard Clinic, Humboldt University, Berlin, Germany.

出版信息

Exp Nephrol. 1999 Jul-Aug;7(4):290-4. doi: 10.1159/000020616.

Abstract

Nuclear proteins like transcription factors and ribosomal proteins are synthesized in the cytoplasm and have to be transported into the nucleus to fulfill their functions. The transport of proteins >20-60 kD through the nuclear pore complex (NPC) into the nucleus is an active, energy-requiring process. Transport substrates are recognized by their transport proteins via certain signals. The best-characterized protein import pathway is the 'classical' nuclear localization signal-dependent pathway with importin alpha and beta carrying the substrate to the NPC. The transport of the importin-substrate complex into the nucleus is regulated by the small GTPase Ran/TC4. During the last years more than ten proteins have been discovered which have already been proven or are very likely to be nuclear transport factors of distinct import pathways: members of the importin alpha protein family are very similar and transport in complex with importin beta nuclear localization signal-bearing proteins into the nucleus. Members of the Ran-binding protein family show some weak similarity to importin beta. Sharing a common domain at the amino terminus, they are able to bind RanGTP, a prerequisite for their function as nuclear import or export factors for distinct proteins or RNAs. However, Ran/TC4 seems to play a key regulatory role in all nuclear transport pathways described so far, although the molecular mechanism of the translocation step through the NPC is still unclear.

摘要

像转录因子和核糖体蛋白这样的核蛋白在细胞质中合成,必须转运到细胞核中才能发挥其功能。分子量大于20 - 60 kDa的蛋白质通过核孔复合体(NPC)进入细胞核是一个需要能量的主动过程。转运底物通过特定信号被其转运蛋白识别。最具特征的蛋白质导入途径是“经典的”依赖核定位信号的途径,其中输入蛋白α和β将底物携带到NPC。输入蛋白 - 底物复合物进入细胞核的转运受小GTP酶Ran/TC4调节。在过去几年中,已经发现了十多种蛋白质,它们已被证明或极有可能是不同导入途径的核转运因子:输入蛋白α蛋白家族的成员非常相似,并与携带核定位信号的输入蛋白β一起将蛋白质转运到细胞核中。Ran结合蛋白家族的成员与输入蛋白β有一些微弱的相似性。它们在氨基末端共享一个共同结构域,能够结合RanGTP,这是它们作为不同蛋白质或RNA的核输入或输出因子发挥功能的前提条件。然而,Ran/TC4似乎在迄今为止描述的所有核转运途径中都起着关键的调节作用,尽管通过NPC的转运步骤的分子机制仍不清楚。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验