Chemical structure-guided design of dynapyrazoles, cell-permeable dynein inhibitors with a unique mode of action

Author:

Steinman Jonathan B1ORCID,Santarossa Cristina C1,Miller Rand M1,Yu Lola S1,Serpinskaya Anna S2,Furukawa Hideki3,Morimoto Sachie3,Tanaka Yuta3,Nishitani Mitsuyoshi4,Asano Moriteru3,Zalyte Ruta5,Ondrus Alison E6,Johnson Alex G7,Ye Fan8,Nachury Maxence V8,Fukase Yoshiyuki3,Aso Kazuyoshi3,Foley Michael A3,Gelfand Vladimir I2,Chen James K7,Carter Andrew P5,Kapoor Tarun M1ORCID

Affiliation:

1. Laboratory of Chemistry and Cell Biology, Rockefeller University, New York, United States

2. Department of Cell and Molecular Biology, Feinberg School of Medicine, Northwestern University, Chicago, United States

3. Tri-Institutitional Therapeutics Discovery Institute, New York, United States

4. Pharmaceutical Research Division, Takeda Pharmaceuticals Ltd, Kanagawa, Japan

5. Medical Research Council Laboratory of Molecular Biology, Cambridge, United Kingdom

6. Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, United States

7. Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, United States

8. Department of Molecular and Cellular Physiology, Stanford University, Stanford, United States

Abstract

Cytoplasmic dyneins are motor proteins in the AAA+ superfamily that transport cellular cargos toward microtubule minus-ends. Recently, ciliobrevins were reported as selective cell-permeable inhibitors of cytoplasmic dyneins. As is often true for first-in-class inhibitors, the use of ciliobrevins has in part been limited by low potency. Moreover, suboptimal chemical properties, such as the potential to isomerize, have hindered efforts to improve ciliobrevins. Here, we characterized the structure of ciliobrevins and designed conformationally constrained isosteres. These studies identified dynapyrazoles, inhibitors more potent than ciliobrevins. At single-digit micromolar concentrations dynapyrazoles block intraflagellar transport in the cilium and lysosome motility in the cytoplasm, processes that depend on cytoplasmic dyneins. Further, we find that while ciliobrevins inhibit both dynein's microtubule-stimulated and basal ATPase activity, dynapyrazoles strongly block only microtubule-stimulated activity. Together, our studies suggest that chemical-structure-based analyses can lead to inhibitors with improved properties and distinct modes of inhibition.

Funder

National Institutes of Health

Robertson Therapeutic Development Fund

Damon Runyon Cancer Research Foundation

Medical Research Council

Wellcome

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

Reference68 articles.

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