ARHGAP10 inhibitors are a class of chemical compounds that specifically target and modulate the activity of ARHGAP10, a Rho GTPase-activating protein (GAP). ARHGAP10 is involved in the regulation of small GTPase proteins, particularly those in the Rho family, which play critical roles in controlling the dynamics of the cytoskeleton. These small GTPases act as molecular switches, cycling between active GTP-bound and inactive GDP-bound states, with ARHGAP10 accelerating the transition to the inactive state. By inhibiting ARHGAP10, these compounds prevent the protein from promoting the inactivation of Rho GTPases, leading to prolonged signaling and extended activity of GTPases like RhoA, Rac1, and Cdc42. This extended activity can have significant effects on cellular functions such as actin cytoskeleton remodeling, cell shape, and motility.
Researchers often utilize ARHGAP10 inhibitors to explore the molecular mechanisms underlying cytoskeletal organization, as Rho GTPases play a crucial role in the formation of stress fibers, lamellipodia, and filopodia, which are important for cellular movement and morphological changes. The inhibition of ARHGAP10 can also alter processes such as cell division, adhesion, and migration, as the modulation of Rho GTPase activity directly influences how cells interact with their surrounding environment. Additionally, ARHGAP10 inhibitors can be valuable in studies of intracellular signaling pathways, particularly those related to cell polarity and vesicle trafficking, where Rho GTPases have essential roles. By blocking ARHGAP10 activity, scientists can dissect the functional contributions of these pathways in various cellular contexts, providing insights into the regulation of complex protein networks.
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