Katanin p80 BL1 inhibitors represent a class of chemical compounds specifically designed to target and hinder the activity of the Katanin p80 subunit BL1, a regulatory protein involved in microtubule severing and regulation. This protein plays a crucial role in cellular processes such as mitosis, meiosis, and neuronal function by modulating the dynamics of microtubules, the structural elements essential for cell shape, intracellular transport, and cell division. Inhibition of Katanin p80 BL1 disrupts the usual microtubule severing activity, thereby affecting the cell's cytoskeleton organization and stability. The compounds in this class bind to the Katanin p80 BL1 subunit with high specificity, altering its interaction with the catalytic p60 subunit and other microtubule-associated proteins, which can lead to the stabilization of microtubules against severing. This specific inhibition is believed to result from changes in the conformation of the p80 BL1 subunit, which affects its ability to regulate the activity of the p60 subunit, the ATP-dependent protease responsible for the severing action.
The action of Katanin p80 BL1 inhibitors is not limited to a single domain or interaction but encompasses a range of effects on the microtubule network within the cell. By preventing proper regulation of microtubule severing, these inhibitors can cause alterations in the normal cellular architecture and the timing of mitotic events. The resulting cellular phenotype may include abnormal spindle formation, defective chromosome segregation, and a potential block in the progression of the cell cycle. These changes are brought about by the direct inhibition of Katanin p80 BL1 function, which, in turn, directly impacts the microtubule severing process. As a result, the cytoskeletal organization is compromised, leading to broader implications for cellular function and integrity. The specificity of these inhibitors for Katanin p80 BL1 ensures that the effects are targeted, providing a clear delineation of the role of Katanin p80 BL1 in microtubule dynamics and cell cycle progression.
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