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基于活性分析的核转运蛋白α/β核输入途径肽抑制剂的设计

Design of peptide inhibitors for the importin alpha/beta nuclear import pathway by activity-based profiling.

作者信息

Kosugi Shunichi, Hasebe Masako, Entani Tetsuyuki, Takayama Seiji, Tomita Masaru, Yanagawa Hiroshi

机构信息

Institute for Advanced Biosciences, Keio University, Tsuruoka, Japan.

出版信息

Chem Biol. 2008 Sep 22;15(9):940-9. doi: 10.1016/j.chembiol.2008.07.019.

Abstract

Despite the current availability of selective inhibitors for the classical nuclear export pathway, no inhibitor for the classical nuclear import pathway has been developed. Here we describe the development of specific inhibitors for the importin alpha/beta pathway using a novel method of peptide inhibitor design. An activity-based profile was created via systematic mutational analysis of a peptide template of a nuclear localization signal. An additivity-based design using the activity-based profile generated two peptides with affinities for importin alpha that were approximately 5 million times higher than that of the starting template sequence. The high affinity of these peptides resulted in specific inhibition of the importin alpha/beta pathway. These peptide inhibitors provide a useful tool for studying nuclear import events. Moreover, our inhibitor design method should enable the development of potent inhibitors from a peptide seed.

摘要

尽管目前已有针对经典核输出途径的选择性抑制剂,但尚未开发出针对经典核输入途径的抑制剂。在此,我们描述了一种使用新型肽抑制剂设计方法开发针对输入蛋白α/β途径的特异性抑制剂的过程。通过对核定位信号肽模板进行系统的突变分析,创建了基于活性的图谱。利用基于活性的图谱进行基于加和性的设计,产生了两种对输入蛋白α具有亲和力的肽,其亲和力比起始模板序列高约500万倍。这些肽的高亲和力导致了对输入蛋白α/β途径的特异性抑制。这些肽抑制剂为研究核输入事件提供了一个有用的工具。此外,我们的抑制剂设计方法应该能够从一个肽种子开发出强效抑制剂。

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