Eldar-Finkelman Hagit, Licht-Murava Avital, Pietrokovski Shmuel, Eisenstein Miriam
Department of Human Molecular Genetics and Biochemistry, Sackler School of Medicine, Tel Aviv University, Tel Aviv 69978, Israel.
Biochim Biophys Acta. 2010 Mar;1804(3):598-603. doi: 10.1016/j.bbapap.2009.09.010. Epub 2009 Sep 18.
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.
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。