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底物竞争性糖原合成酶激酶-3抑制剂——策略与影响

Substrate competitive GSK-3 inhibitors - strategy and implications.

作者信息

Eldar-Finkelman Hagit, Licht-Murava Avital, Pietrokovski Shmuel, Eisenstein Miriam

机构信息

Department of Human Molecular Genetics and Biochemistry, Sackler School of Medicine, Tel Aviv University, Tel Aviv 69978, Israel.

出版信息

Biochim Biophys Acta. 2010 Mar;1804(3):598-603. doi: 10.1016/j.bbapap.2009.09.010. Epub 2009 Sep 18.

Abstract

Glycogen synthase kinase-3 (GSK-3) is a highly conserved protein serine/threonine kinase ubiquitously distributed in eukaryotes as a constitutively active enzyme. Abnormally high GSK-3 activity has been implicated in several pathological disorders, including diabetes and neuron degenerative and affective disorders. This led to the hypothesis that inhibition of GSK-3 may have therapeutic benefit. Most GSK-3 inhibitors developed so far compete with ATP and often show limited specificity. Our goal is to develop inhibitors that compete with GSK-3 substrates, as this type of inhibitor is more specific and may be useful for clinical applications. We have employed computational, biochemical, and molecular analyses to gain in-depth understanding of GSK-3's substrate recognition. Here we argue that GSK-3 is a promising drug discovery target and describe the strategy and practice for developing specific substrate-competitive inhibitors of GSK-3.

摘要

糖原合酶激酶-3(GSK-3)是一种高度保守的蛋白丝氨酸/苏氨酸激酶,作为一种组成型活性酶广泛分布于真核生物中。GSK-3活性异常升高与多种病理疾病有关,包括糖尿病、神经退行性疾病和情感障碍。这引发了一种假设,即抑制GSK-3可能具有治疗益处。迄今为止开发的大多数GSK-3抑制剂与ATP竞争,且往往表现出有限的特异性。我们的目标是开发与GSK-3底物竞争的抑制剂,因为这类抑制剂更具特异性,可能对临床应用有用。我们采用了计算、生化和分子分析方法,以深入了解GSK-3的底物识别。在此,我们认为GSK-3是一个有前景的药物发现靶点,并描述了开发GSK-3特异性底物竞争性抑制剂的策略和实践。

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