Abstract
Formins are potent actin assembly factors. Diaphanous formins, including mDia1, mDia2, and mDia3 in mammals, are implicated in mitosis and cytokinesis, but no chemical interactors have been reported. We developed an in vitro screen for inhibitors of actin assembly by mDia1 and identified an inhibitor of mDia1 and mDia2 that does not inhibit mDia3 at the concentrations tested. These results establish the druggability of mDia formins and introduce a first-generation inhibitor.
Publication types
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Research Support, N.I.H., Extramural
MeSH terms
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Actins / antagonists & inhibitors*
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Actins / metabolism
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Adaptor Proteins, Signal Transducing / antagonists & inhibitors*
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Adaptor Proteins, Signal Transducing / chemistry
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Adaptor Proteins, Signal Transducing / physiology
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Animals
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Carrier Proteins / antagonists & inhibitors*
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Carrier Proteins / chemistry
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Carrier Proteins / physiology
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Fetal Proteins / antagonists & inhibitors
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Formins
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Humans
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Mice
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Microfilament Proteins / antagonists & inhibitors
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Microtubule-Associated Proteins / antagonists & inhibitors*
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Microtubule-Associated Proteins / chemistry
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Microtubule-Associated Proteins / physiology
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NADPH Dehydrogenase / antagonists & inhibitors*
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NADPH Dehydrogenase / chemistry
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NADPH Dehydrogenase / physiology
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Nuclear Proteins / antagonists & inhibitors
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Protein Isoforms / antagonists & inhibitors
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Protein Isoforms / chemistry
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Protein Isoforms / physiology
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Protein Structure, Tertiary / physiology
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Pyrenes / chemistry
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Sequence Homology, Amino Acid
Substances
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Actins
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Adaptor Proteins, Signal Transducing
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Carrier Proteins
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DIAPH1 protein, human
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DIAPH2 protein, human
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Diap2 protein, mouse
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Fetal Proteins
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Formins
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Microfilament Proteins
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Microtubule-Associated Proteins
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Nuclear Proteins
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Protein Isoforms
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Pyrenes
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Dia2 protein, mouse
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NADPH Dehydrogenase