Date published: 2025-11-6

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eIF3ε Activators

eIF3ε, a subunit of the eukaryotic initiation factor 3 (eIF3) complex, plays a crucial role in the initiation phase of protein synthesis. As a part of this multiprotein complex, eIF3ε contributes to the binding of the 40S ribosomal subunit to mRNA, thereby facilitating the assembly of the active 80S ribosome that is essential for the translation process. The regulation of eIF3ε is integral to the control of protein synthesis, which is a fundamental cellular process affecting growth, proliferation, and the maintenance of cellular functions. Understanding the expression patterns of eIF3ε and identifying compounds that can increase its expression is of significant interest in the context of cellular biology and gene expression regulation.

Several chemical compounds have been identified to potentially induce the expression of eIF3ε. These activators could operate through diverse mechanisms, each intersecting with intricate cellular pathways. Compounds like Epigallocatechin gallate (EGCG) and Resveratrol, for example, are known for their antioxidant properties and could upregulate eIF3ε by engaging cellular defense mechanisms against oxidative stress. This upregulation forms part of a broader cellular strategy to maintain protein homeostasis under adverse conditions. Similarly, Metformin, commonly recognized for its role in metabolic processes, might prompt the expression of eIF3ε by activating AMP-activated protein kinase (AMPK), an enzyme that plays a key role in cellular energy homeostasis. On another front, chemicals like lithium, which is known to alter intracellular signaling, could lead to the enhancement of eIF3ε expression by modulating gene expression profiles that are associated with cellular resilience and neuroprotection. These activators, while diverse in their primary functions, share the common potential to upregulate eIF3ε, highlighting the multifaceted nature of cellular regulation and the broad scope of interactions that can influence protein synthesis at the translational initiation level.

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