Date published: 2025-9-7

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Alix Inhibitors

Alix, also known as ALG-2-interacting protein X, is a multifunctional protein involved in various cellular processes, including endosomal sorting, membrane trafficking, and cell signaling. As a component of the endosomal sorting complex required for transport (ESCRT) machinery, Alix plays a crucial role in the formation of multivesicular bodies (MVBs) and the sorting of ubiquitinated cargo proteins for degradation in lysosomes. Additionally, Alix interacts with numerous cellular proteins and regulates diverse signaling pathways implicated in cell proliferation, apoptosis, and cytoskeletal dynamics. Through its interactions with ESCRT proteins, Alix participates in the abscission phase of cytokinesis, facilitating the final separation of daughter cells during cell division. Moreover, Alix is involved in the repair of damaged DNA, contributing to genome stability and cellular integrity.

Inhibition of Alix function can occur through various mechanisms that disrupt its interactions with binding partners or interfere with its cellular localization and activity. One approach to inhibiting Alix involves the disruption of its interaction with ESCRT proteins, thereby impairing its function in endosomal sorting and membrane trafficking. This can be achieved through the use of small molecule inhibitors or peptides that target the Alix binding interface or disrupt protein-protein interactions critical for ESCRT assembly and function. Additionally, inhibition of Alix activity can be achieved through modulation of its post-translational modifications, such as phosphorylation or ubiquitination, which regulate its stability and subcellular localization. Furthermore, targeting upstream regulators or downstream effectors of Alix-mediated signaling pathways may also represent strategies for inhibiting Alix function and modulating cellular processes in which it is involved. Overall, understanding the mechanisms of Alix inhibition offers insights into strategies for targeting cellular processes dysregulated in various diseases.

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