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葫芦[8]脲诱导的超分子 4,4'-联吡啶-肽二聚体可逆控制 DNA 结合。

Reversible Control of DNA Binding with Cucurbit[8]uril-Induced Supramolecular 4,4'-Bipyridinium-Peptide Dimers.

机构信息

Departamento de Química, Facultade de Ciencias and Centro de Investigacións Científicas Avanzadas (CICA), Universidade da Coruña, 15071 A Coruña, Spain.

出版信息

Bioconjug Chem. 2021 Mar 17;32(3):507-511. doi: 10.1021/acs.bioconjchem.1c00063. Epub 2021 Mar 8.

Abstract

Many cellular processes in living organisms are regulated by complex regulatory networks, built from noncovalent interactions between relatively few proteins that perform their functions by switching between homo- and heterooligomeric assemblies or mono- and bivalent states. Herein, we demonstrate that the conjugation of a 4,4'-bipyridinium scaffold to the basic region of the GCN4 bZip transcription factor can be exploited to control the dimerization of the conjugate by formation of a supramolecular complex with cucurbit[8]uril. Importantly, this supramolecular complex is able to specifically recognize its target dsDNA, and this binding can be reversibly switched by the application of external stimuli.

摘要

许多生物体中的细胞过程受到复杂的调控网络的调节,这些网络是由相对较少的蛋白质通过同聚和异聚组装或单和二价状态之间的转换来发挥功能的非共价相互作用构建而成。在这里,我们证明了将 4,4'-联吡啶支架连接到 GCN4 bZip 转录因子的碱性区域,可以通过与瓜环[8]脲形成超分子复合物来控制共轭物的二聚化。重要的是,这种超分子复合物能够特异性地识别其靶双链 DNA,并且这种结合可以通过施加外部刺激来可逆地切换。

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