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Substrate Competitive GSK-3 Inhibitors - strategy and Implications
被引:47
|作者:
Eldar-Finkelman, Hagit
[1
]
Licht-Murava, Avital
[1
]
Pietrokovski, Shmuel
[2
]
Eisenstein, Miriam
[3
]
机构:
[1] Tel Aviv Univ, Sackler Sch Med, Dept Human Mol Genet & Biochem, IL-69978 Tel Aviv, Israel
[2] Weizmann Inst Sci, Dept Mol Genet, IL-76100 Rehovot, Israel
[3] Weizmann Inst Sci, Dept Chem Res Support, IL-76100 Rehovot, Israel
来源:
关键词:
Protein kinase;
Phosphorylation;
GSK-3;
Inhibitors;
Substrate recognition;
GLYCOGEN-SYNTHASE KINASE-3;
NF-KAPPA-B;
BETA-CATENIN;
PROTEIN-KINASE;
SEQUENTIAL PHOSPHORYLATION;
MOLECULAR-MECHANISM;
INSULIN-RESISTANCE;
POTENT INHIBITORS;
WNT;
SPECIFICITY;
D O I:
10.1016/j.bbapap.2009.09.010
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
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. (C) 2009 Elsevier B.V. All rights reserved.
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页码:598 / 603
页数:6
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