Suppr超能文献

生产和使用A组Paks的细胞渗透性抑制剂(TAT-PID)来分析信号转导。

Production and use of a cell permeable inhibitor of group A Paks (TAT-PID) to analyze signal transduction.

作者信息

Beeser Alexander, Chernoff Jonathan

机构信息

Tumor Cell Biology Program, Fox Chase Cancer Center, 333 Cottman Ave., Philadelphia, PA 19111, USA.

出版信息

Methods. 2005 Oct;37(2):203-7. doi: 10.1016/j.ymeth.2005.05.017.

Abstract

The Rho-family GTPases Cdc42 and Rac regulate a large number of important cellular processes, including motility, adhesion, proliferation, and survival. Among the key effectors for these GTPases are the p21-activated kinases. Although no specific chemical inhibitor has been developed against these enzymes, an inhibitory peptide derived from the N-terminus of these kinases is able to act in trans to suppress the activity of the full-length kinase. Here, we describe a method to deliver the inhibitory fragment into cells, using the recently described TAT system for protein transduction. This method is easy to use and is effective for transducing many different cell types, including those refractory to standard plasmid transfection. Use of the TAT-based inhibitor provides a specific means to suppress a single group of Cdc42 and Rac effectors, which is useful in analyzing their function.

摘要

Rho家族GTP酶Cdc42和Rac调节大量重要的细胞过程,包括运动性、黏附、增殖和存活。这些GTP酶的关键效应器之一是p21激活激酶。尽管尚未开发出针对这些酶的特异性化学抑制剂,但源自这些激酶N端的抑制性肽能够反式作用以抑制全长激酶的活性。在此,我们描述了一种使用最近描述的用于蛋白质转导的TAT系统将抑制性片段递送至细胞的方法。该方法易于使用,对转导许多不同类型的细胞有效,包括那些对标准质粒转染有抗性的细胞。使用基于TAT的抑制剂提供了一种特异性手段来抑制Cdc42和Rac效应器的单个组,这在分析它们的功能时很有用。

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