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双阿片肽:双价配体的基础。

Biphalin: The Foundation of Bivalent Ligands.

作者信息

Cowell Scott M, Lee Yeon Sun

机构信息

1306 E. University Blvd, Tucson, AZ 85721.

出版信息

Curr Med Chem. 2016;23(29):3267-3284. doi: 10.2174/0929867323666160510122731.

Abstract

Seldom in medicinal chemistry does one ligand present the ability to study two separate phenomena in a pharmacological process. The discovery of biphalin with other homodimeric ligands has given scientists a tool that not only explores how to increase the efficacy of the ligand, but also explore the possible interactions of hetero and homo dimerization of the receptors themselves. As a straight ligand, biphalin has allowed scientists to increase efficacy by direct modification of the residues to affect the message-address interactions with receptors. This led to the exploration of ligand linkers to increase efficacy and it was this modification of the linkers led to discoveries that suggested dimerization of receptor system occurs as a secondary modulation of signal transduction. Even more recently, exploration of the advances in linkers through the discovery of bitopicity seems to modulate the actual receptors to increase the binding and signal transdcution of the ligand. This is accomplished by possible slight conformational changes in the receptors before binding of the ligand located at the end of the linker. These advances were made by the work of the late Prof. Andrzej W. Lipkowski. This review gives the foundation of biphalin and in turn celebrates the contributions of Prof. Lipkowski made in this area.

摘要

在药物化学中,一种配体很少能在药理过程中展现出研究两种不同现象的能力。双啡肽与其他同二聚体配体的发现为科学家提供了一种工具,它不仅能探索如何提高配体的功效,还能探究受体自身异源和同源二聚化的可能相互作用。作为一种直接配体,双啡肽使科学家能够通过直接修饰残基来影响与受体的信息 - 靶点相互作用,从而提高功效。这引发了对配体连接子的探索以提高功效,正是这种连接子的修饰带来了一些发现,表明受体系统的二聚化是信号转导的一种二级调节。就在最近,通过双位性的发现对连接子进展的探索似乎能调节实际的受体,以增加配体的结合和信号转导。这是通过在连接子末端的配体结合之前受体可能发生的轻微构象变化来实现的。这些进展是由已故的安杰伊·W·利普科夫斯基教授的工作取得的。本综述奠定了双啡肽的基础,进而颂扬了利普科夫斯基教授在这一领域所做的贡献。

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