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信号转导抑制剂研发中的磷酸酪氨酸模拟物

Phosphotyrosyl mimetics in the development of signal transduction inhibitors.

作者信息

Burke Terrence R, Lee Kyeong

机构信息

Laboratory of Medicinal Chemistry, Center for Cancer Research, National Cancer Institute, National Institutes of Health, NCI-Frederick, Frederick, Maryland, USA.

出版信息

Acc Chem Res. 2003 Jun;36(6):426-33. doi: 10.1021/ar020127o.

Abstract

Phosphotyrosyl (pTyr) residues play important roles in cellular signal transduction by facilitating recognition and binding necessary for critical protein-protein interactions, and for this reason pTyr motifs represent attractive starting points in the development of signaling antagonists. Although the pTyr phosphoryl moiety is central in these phenomena, its incorporation into signaling inhibitors is contraindicated due to enzymatic lability and limited bioavailability associated with phosphate esters. To address these limitations, an entire field of study has arisen devoted to the design and utilization of pTyr mimetics. This Account provides a perspective on the roles of pTyr residues in signal transduction and approaches to pTyr mimetic development.

摘要

磷酸酪氨酸(pTyr)残基通过促进关键蛋白质-蛋白质相互作用所需的识别和结合,在细胞信号转导中发挥重要作用。因此,pTyr基序是信号拮抗剂开发中有吸引力的起始点。尽管pTyr磷酸基团在这些现象中起核心作用,但由于磷酸酯相关的酶不稳定性和有限的生物利用度,其不能用于信号抑制剂。为了解决这些限制,一个致力于pTyr模拟物设计和应用的研究领域应运而生。本综述阐述了pTyr残基在信号转导中的作用以及pTyr模拟物的开发方法。

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