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蛋白激酶的小分子底物磷酸化位点抑制剂:方法与挑战

Small molecule substrate phosphorylation site inhibitors of protein kinases: approaches and challenges.

作者信息

Breen Meghan E, Soellner Matthew B

机构信息

Department of Medicinal Chemistry and ‡Department of Chemistry, University of Michigan , 930 N. University Avenue, Ann Arbor, Michigan 48109, United States.

出版信息

ACS Chem Biol. 2015 Jan 16;10(1):175-89. doi: 10.1021/cb5008376. Epub 2014 Dec 23.

Abstract

Protein kinases are important mediators of cellular communication and attractive drug targets for many diseases. Although success has been achieved with developing ATP-competitive kinase inhibitors, the disadvantages of ATP-competitive inhibitors have led to increased interest in targeting sites outside of the ATP binding pocket. Kinase inhibitors with substrate-competitive, ATP-noncompetitive binding modes are promising due to the possibility of increased selectivity and better agreement between biochemical and in vitro potency. However, the difficulty of identifying these types of inhibitors has resulted in significantly fewer small molecule substrate phosphorylation site inhibitors being reported compared to ATP-competitive inhibitors. This review surveys reported substrate phosphorylation site inhibitors and methods that can be applied to the discovery of such inhibitors, including a discussion of the challenges inherent to these screening methods.

摘要

蛋白激酶是细胞通讯的重要介质,也是许多疾病颇具吸引力的药物靶点。尽管在开发ATP竞争性激酶抑制剂方面已取得成功,但ATP竞争性抑制剂的缺点促使人们对靶向ATP结合口袋以外的位点越来越感兴趣。具有底物竞争性、ATP非竞争性结合模式的激酶抑制剂很有前景,因为它们有可能提高选择性,并使生化活性与体外效力之间的一致性更好。然而,识别这类抑制剂的难度导致与ATP竞争性抑制剂相比,报道的小分子底物磷酸化位点抑制剂要少得多。本文综述了已报道的底物磷酸化位点抑制剂以及可用于发现此类抑制剂的方法,包括对这些筛选方法所固有的挑战的讨论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d19c/4301090/f04fee1e99af/cb-2014-008376_0008.jpg

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