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A Pan-GTPase Inhibitor as a Molecular Probe
Author(s) -
Hong Lin,
Yuna Guo,
Soumik BasuRay,
Jacob O. Agola,
Elsa Romero,
Denise S. Simpson,
Chad E. Schroeder,
Peter C. Simons,
Anna Waller,
Matthew Garcia,
Mark Carter,
Oleg Ursu,
Kristine Gouveia,
Jennifer E. Golden,
Jeffrey Aubé,
Angela WandingerNess,
Larry A. Sklar
Publication year - 2015
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0134317
Subject(s) - gtpase , rab , biology , microbiology and biotechnology , chemical biology , biochemistry , chemistry , computational biology
Overactive GTPases have often been linked to human diseases. The available inhibitors are limited and have not progressed far in clinical trials. We report here a first-in-class small molecule pan-GTPase inhibitor discovered from a high throughput screening campaign. The compound CID1067700 inhibits multiple GTPases in biochemical, cellular protein and protein interaction, as well as cellular functional assays. In the biochemical and protein interaction assays, representative GTPases from Rho, Ras, and Rab, the three most generic subfamilies of the GTPases, were probed, while in the functional assays, physiological processes regulated by each of the three subfamilies of the GTPases were examined. The chemical functionalities essential for the activity of the compound were identified through structural derivatization. The compound is validated as a useful molecular probe upon which GTPase-targeting inhibitors with drug potentials might be developed.

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