The first group of chemicals, which includes Taxol and Epothilone B, enhances KIF4's activity by stabilizing microtubules. KIF4 is a kinesin protein that relies on microtubules to transport cellular cargo. By stabilizing the microtubules, these compounds increase the efficiency of KIF4's transport activity, thereby enhancing its function.
A second group of compounds, including Nocodazole, Vinblastine, Colchicine, Combretastatin A4, Podophyllotoxin, Estramustine, 2-methoxyestradiol, Maytansine, Noscapine, and Albendazole, works differently. These compounds disrupt microtubule dynamics, either by destabilizing microtubules or by inhibiting their assembly. While this may seem counterintuitive, it is important to note that in cellular systems, destabilization of microtubules can paradoxically enhance the activity of kinesin proteins like KIF4. This is because the disruption of microtubules increases the demand for KIF4's cargo transport activity to maintain cellular homeostasis. As a result, these compounds indirectly enhance the activity of KIF4 by increasing its functional demand within the cell.
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