Cox4i1: A Novel Target for Diabetes Treatment
Researchers at the University of Pittsburgh have identified Cytochrome c oxidase subunit 4 isoform 1 (Cox4i1) as a novel molecular target of metformin, a widely used antihyperglycemic agent. This discovery opens new avenues for the development of first-in-class small molecules for the treatment of diabetes, potentially revolutionizing diabetes therapy. The identification of Cox4i1 as a target could lead to more specific and efficacious treatments for both Type 1 and Type 2 diabetes.
Description
The technology is based on proteomic analysis of mouse liver protein isolates treated with metformin, revealing that Cox4i1 is stabilized via direct binding of the ligand. This binding limits the activity of Complex IV, leading to an increase in the AMP to ATP ratio and triggering AMP-Activated Protein Kinase (AMPK) activity. This dual mechanism is believed to contribute to the beneficial diabetes-related effects of metformin. The technology includes methods for drug screening against Cox4i1 to identify potential therapeutic compounds.Applications
• Development of new antidiabetic drugs targeting Cox4i1• Therapeutic intervention for Type 1 and Type 2 diabetes
• Drug screening for compounds that modulate Cox4i1 activity
