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双特异性 DNA 适体非遗传重编程生长因子受体的配体特异性。

Nongenetic Reprogramming of the Ligand Specificity of Growth Factor Receptors by Bispecific DNA Aptamers.

机构信息

Department of Chemistry and Biotechnology, Graduate School of Engineering, The University of Tokyo , 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656, Japan.

出版信息

J Am Chem Soc. 2017 May 17;139(19):6554-6557. doi: 10.1021/jacs.7b02411. Epub 2017 May 8.

Abstract

The reprogramming of receptor-ligand interactions affords an opportunity to direct cells to respond to user-defined external cues. Although this has often been achieved via the genetic engineering of receptors, an alternative, nongenetic approach is highly demanded. In this article, we propose the design of oligonucleotide-based synthetic switches that feature the ability to reprogram the ligand specificity of the growth factor receptor. We demonstrated that our synthetic switches induced growth factor signaling via the formation of the dynamic complex with specific external cues that would otherwise not induce the signaling. This chemical approach may be applied to designing a new class of chemical tools that can control the activities of native cells and represent smart and safer regenerative drugs.

摘要

受体-配体相互作用的重编程提供了一个机会,可以指导细胞对用户定义的外部信号做出反应。虽然这通常是通过受体的基因工程来实现的,但人们非常需要一种替代的非遗传方法。在本文中,我们提出了基于寡核苷酸的合成开关的设计,其具有重新编程生长因子受体配体特异性的能力。我们证明,我们的合成开关通过与特定外部信号形成动态复合物来诱导生长因子信号,而这些外部信号否则不会诱导信号。这种化学方法可用于设计一类新的化学工具,可以控制天然细胞的活性,代表智能和更安全的再生药物。

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